CC BY-NC-ND 4.0 · J Neurol Surg Rep 2024; 85(02): e29-e38
DOI: 10.1055/a-2267-1810
Case Report

Acute Paraplegia Caused by Spinal Epidural Empyema Following Infectious Cellulitis of the Hand: Case Report and Literature Review

Breno Nery
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Cláudio Brandão Filho
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
2   Department of Neurosurgery, Universitary Center Unifacisa, Campina Grande, Paraíba, Brazil
,
Lucas Nunes
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Eduardo Quaggio
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Fred Bernardes Filho
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Joaquim Alencar Neto
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Layssa Rhossana Melo
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Anna Carolyne Oliveira
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Rafael Rabello
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Victoria Rodrigues Durand
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Rayssa Rocha Silva
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
Rafael Emmanuel Costa
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
,
José Alencar Segundo
1   Department of Neurosurgery, Hospital Beneficiência Portuguesa de Ribeirão Preto, Ribeirão Preto, SP, Brazil
› Author Affiliations
 

Abstract

Background Spinal epidural abscess is a rare but serious condition that can cause spinal cord compression and neurological deficits.

Case Description and Methods The article reports a case of a 31-year-old patient who presented with an infectious cellulitis in the left hand, which progressed to a spinal epidural abscess. The diagnosis was confirmed by clinical examination and magnetic resonance imaging. Treatment involved laminectomy, after which the patient had complete recovery of neurological deficits. This article is a case report with a literature review. Patient data and images were collected by the researchers who participated in the patient's care. The literature was reviewed by one of the researchers based on the search for articles in the PubMed database. For the research, the following keywords were inserted: “Spinal epidural empyema,” “Spinal epidural abscess.”

Conclusion Spinal epidural abscess is often underdiagnosed, which can lead to delays in treatment and serious complications. The relationship between cellulitis and spinal epidural abscess may be related to the spread of infection through the lymphatic or blood system.


#

Introduction

Spinal epidural abscess (SEA) was first described in the medical literature in 1761 and represents a severe, generally pyogenic infection of the epidural space requiring emergent neurosurgical intervention to avoid permanent neurologic deficits.[1] The incidence of SEA is around 0.2 to 1.2 cases per 10,000 people per year,[1] [2] [3] [4] with a mortality rate of around 1 and 16%.[1] In recent years, there has been a significant increase in the incidence of SEA worldwide,[5] [6] possibly due to the increasing incidence of diseases such as acquired immune deficiency syndrome and the increased use of invasive devices in medical practice.[1] [7]

Young adults and elderly are the most commonly affected populations by SEA, with risk factors including diabetes, intravenous drug use, use of invasive devices, autoimmune diseases, cancer, and other conditions that affect the immune system.[1] [7] [8] [9] Staphylococcus aureus is the most common germ found in patients with SEA with methicillin-sensitive S. aureus more often identified than methicillin-resistant strains.[10] [11]

Common symptoms of SEA include back pain, fever, muscle weakness, and numbness in the limbs.[7] [12] It is considered a neurological emergency, as compression of the spinal cord can lead to serious neurological complications, including paraplegia and loss of limb function.[7] [12] Early diagnosis and immediate treatment may include antibiotics, surgical drainage, and treatment of the underlying cause of the infection and are essential to prevent permanent damage.[1] [7]

We present a case report of a young adult patient who developed SEA after presenting with an infectious cellulitis in the left hand. The patient subsequently developed fever, back pain, muscle weakness, sensory dysfunction, urinary and bowel dysfunction, and was diagnosed with SEA. This case report can contribute to the medical literature by adding another example of how infectious cellulitis can lead to the development of SEA. This may help physicians to quickly identify this complication in patients with severe skin infections, enabling earlier diagnosis and treatment.


#

Methods

This article is a case report with a literature review. Patient data and images were collected by the researchers who participated in the patient's care. The literature was reviewed by one of the researchers based on the search for articles in the PubMed database. For the research, the following keywords were inserted: “Spinal epidural empyema,” “Spinal epidural abscess.” The “Boolean Operator” “OR” was used to maximize the number of articles published. Inclusion criteria reached articles published in the 2020 to 2023, case reports, English, and humans. Thus, 41 articles were found based on the ones, of which 33 met the defined analysis criteria.


#

Case Description

A 31-year-old previously healthy man presented on September 25, 2018 flu symptoms and sought emergency care for initial treatment. At that time the initiated treatment included intravenous dexamethasone, subsequently leading to the development of cardiac arrhythmia. Intravenous amiodarone was administered following dexamethasone, with both medications given in the hand, as depicted in a picture. After the resolution of arrhythmia, the patient was discharged with outpatient follow-up. Three days after, the patient underwent a cardiology evaluation, ruling out cardiac causes for the arrhythmia, attributing it to intravenous medication. On the same night, the patient developed erythema and inflammatory signs at the venipuncture site ([Fig. 1]). Due to erythema, the patient returned to the emergency room on the fifth day with high fever, worsening erythema on the hand and forearm, and the onset of back pain. Laboratory analysis on this day showed mild leukocytosis of 12,500 with neutrophilia of 87.9%. Oral ciprofloxacin 500 mg twice a day was initiated. At this point, a vascular doctor performed local drainage of the abscess in the hand, and the patient was referred for outpatient follow-up with oral antibiotics. On the eighth day, the patient sought an orthopaedic doctor due to the onset of acute back pain, and analgesia and physical therapy were indicated. No imaging tests were requested at this time. On the ninth day, it was reported that after a physical therapy session, paresthesia began in the lower limbs without a defined territory, and the low back pain worsened in the early hours of the morning. Urinary incontinence and crural paraparesis started, progressing to paraplegia over the next 12 hours. The patient was in a secondary hospital and was transferred to our hospital for evaluation by the Neurosurgery service. Upon admission, the patient presented with a fever of 40 degrees, crural paraplegia, anesthesia with a dermatomal territory at T7, erythrocyte sedimentation rate (ESR) of 55 mm in the first hour, and 116 mm in the second hour, C-reactive protein (CRP) of 172.35 mm, urea of 48, creatinine of 1.5, worsening of leukocytosis to 14,100 with neutrophilia, lymphopenia, and the presence of toxic granulations. Spinal magnetic resonance imaging (MRI) showed the presence of a posterior abscess extending from the level of T4 to T8, causing anterior displacement of the spinal cord ([Figs. 2] and [3]). Surgery was performed urgently after the results of the MRI. Previous doctors did not order cultures. In surgery performed urgently, blood culture and swabs were collected from the site of the surgical wound. The patient underwent emergent spinal decompression with laminectomies from T4 to T8, and frank purulent fluid was drained. He started treatment empirically with meropenem 1 g 8/8 h and vancomycin 15 mg/kg 8/8 h, that were exchanged for ampicillin 1 g 6/6 h because the culture revealed Streptococcus pyogenes strain sensitive to ampicillin in blood and on the empyema material. Hematogenous spread from hand infectious cellulitis probably causes the SEA ([Figs. 4] and [5]). At the first hospital, an emergency physician initially considered hypotheses of Guillain–Barré syndrome and transverse myelitis. However, after a more in-depth evaluation, these conditions were ruled out. The hypothesis of SEA was strengthened based on the clinical presentation and imaging results, emphasizing the importance of a comprehensive and careful approach in identifying and discarding differential diagnoses. At a 6-week follow-up, the patient underwent a new MRI which did not show evidence of SEA, indicating that the abscess was completely drained by the surgical procedure and the patient had responded well to the antibiotic treatment ([Fig. 6]). The patient had no signs of infection and had fully recovered from neurological deficits.

Zoom Image
Fig. 1 Left dorsal hand is erythematous, swollen, and tender. Dorsal metacarpal vein (circle) was the local of vein puncture for administration of amiodarone.
Zoom Image
Fig. 2 A thoracic spine T2-weighted axial MRI showing a fluid collection with hypersignal in the epidural space (arrowhead), displacing the spinal cord anteriorly, and also other discrete fluid collections with hypersignal on the intrathoracic paravertebral (red arrow) and extra-thoracic paraspinal (yellow arrow) areas. MRI, magnetic resonance imaging.
Zoom Image
Fig. 3 A thoracic spine T1-weighted sagittal MRI with fat saturation, obtained after the intravenous application of a Gd-containing contrast agent, shows intense marginal contrast enhancement of the epidural fluid collection in the vertebral canal (arrowhead). MRI, magnetic resonance imaging.
Zoom Image
Fig. 4 Schematic representation of the posterior view of the spinal column, indicating a purulent collection in the epidural space between T4 and T8 vertebrae, which is characteristic of spinal epidural abscess in this location.
Zoom Image
Fig. 5 Schematic drawing showing the route taken by the infectious process.
Zoom Image
Fig. 6 Sagittal T2-weighted magnetic resonance image showing the patient's spinal column after laminectomy and antibiotic treatment. No further evidence of SEA is detected, indicating successful treatment. SEA, spinal epidural abscess.

#

Discussion

SEA is a rare, but extremely serious condition, due to the potential for lethality and functional disability. There is a correlation between incidence and an increase in risk factors, with emphasis on aging, immunosuppressive conditions, intravenous drugs, spinal procedures.[13] It is rarely observed in individuals under 20 years of age (0.3 per 100,000 people), with incidence levels 20 times higher in older patients (6.5 per 100,000 people over 70 years of age), with relevance in the fifth to seventh decades of life and male.[6]

The diagnosis of SEA, when there is a classic triad of symptoms, fever, low back pain, and neurological deficit, raises the suspicion of this condition, which requires surgical intervention and early antibiotic therapy.[14] [15] [16] [17] Many studies report the classic triad of symptoms in SEA, as described in [Table 1]. Of the reported cases, 38.88% had the triad of symptoms. However, it was observed that the main challenge is the diagnosis, since most do not present in the classic way.[18] Some symptoms vary according to the site affected by SAE (for example, cases with cervical involvement may have dysphagia, while cases with thoracic involvement may have sphincter dysregulation).[19]

Table 1

Review of case reports about Spinal Epidural Abscess in the year 2020–2023

Author, year

Age, sex

Infectious source, cause

Clinical

presentation

Laboratory

test

Image exam

Treatment

Culture,

ATB therapy empirical

Outcome

Agrawal et al, 2022[12]

Woman,70

DM2

Fever, altered sensorium, back pain and upper limbs; hypertonia, exaggerated deep tendon reflexes; paraparesis

Not specified

MRI T10–L1 epidural abscess

Laminectomy and drainage

Streptococcus gallolyticus; ceftriaxone, doxycycline, and ampicillin

Recovery sensorium, power lower limbs partially improved; progressively debilitating condition; died

Scalia et al, 2022[39]

Female,54

Acute pyelonephritis

Lumbar pain, paraparesis spastic

Not specified

MRI T2–L5 anterior epidural abscess

Laminectomy and drainage

No specified culture; after drainage, local vancomycin powder.

Improved; MRI postoperative documented adequate canal decompression.

Kharbat et al, 2022[44]

Male, 53

Cellulitis right hand; DM

Fever, back pain, urinary dysfunction

Elevated WBC

MRI T5–T9 epidural abscess

Laminectomy and drainage

Methicillin-resistant Staphylococcus aureus (MRSA); vancomycin powder

The patient was thereafter managed with daptomycin. Partially improved

Ammar et al, 2022[45]

11 month, boy

Upper lobe pneumonia

Fever

Not specified

MRI C7–L2 posterior abscess epidural

Percutaneous drainage

MRSA

MRI postoperative showed adequate canal decompression; antibiotic therapy 1 month

Cao et al, 2022[3]

Male, 58

Fistula between the cervical abscess and the epidural abscess of the spinal canal

Neck pain, upper limbs and shoulders; fever, decrease muscle strength of the limbs

Not specified

MRI C1–C7 epidural abscess

Cervical decompression and drainage

S. aureus; vancomycin

Ceftriaxone for 5 weeks. Improved muscle strength. MRI postoperative showed adequate canal decompression

Rashid et al, 2022[22]

Female, 58

Not specified

Intermittent low back pain, spastic paraparesis, fever, and weight loss

Negative for leukocytosis or anemia; ERS 75 mm/h

MRI T11–T12 epidural abscess, and vertebral osteomyelitis

T11–T12 laminectomy and tissue removal

Histopathology showed Aspergillus spp; antifungal

Patient progressed well

Papaetis et al, 2022[47]

Male, 63

Osteomyelitis

Fever, altered level of consciousness, pain mid-back

WBC 16. 170/mm3, ERS 95 mm/h, CRP 16.8 mg/dL

MRI septic spondylodiscitis T6–T7; osteomyelitis T6–T7; anterior epidural abscess T6–T7

Laminectomy and drainage; foraminotomy and facetectomy.

Bacteroides fragilis; meropenem and teicoplanin

Ertapenem and metronidazole for 12 weeks. The patient improved consciousness and mobility

Göre et al, 2022[30]

Male, 56

COVID-19 infection

Fever, back pain, lower extremity muscle weakness, IgA nephropathy

WBC 8,100–11,600/

mm3, CRP (0.01–0.177 g/L)

MRI epidural abscess C7–T1 and T10–T11

Teicoplanin and ciprofloxacin. Neurosurgery not considered.

Coagulase negative S. aureus.

Clinic and symptoms improved. Control MRI showed regression of the formation of abscess.

Fujita et al, 2022[48]

Male, 71

Thoracoplasty for tuberculosis

Fever, back pain, lower extremity muscle weakness, tendon reflexes, reduced bilateral, Guillain–Barré syndrome

WBC 13,600 cell/μL, CRP 14.24 mg/dL, anti-ganglioside antibodies

MRI epidural abscess L5–S1

Surgical decompression and drainage

Campylobacter coli; levofloxacin

Immunoglobulin therapy attenuated the progression of the paralysis.

Xu et al, 2022[27]

Male, 56

Not specified

Fever, lower back, and extremity pain

WBC 12,200 cell/μL, CRP 89.2 mg/dL, ERS 61 mm/h

MRI epidural abscess T1–T2 and L3–L4

Laminectomies T1–T2 and L2–L3; drainage

Methicillin-resistant S. aureus; vancomycin empirically

Vancomycin 6 weeks; lower limb weakness not significantly improved.

Shin et al, 2022[18]

Male, 85

Diabetes mellitus, chronic kidney disease;

infectious urinary tract;

fracture lumbar vertebra

Fever, lower back pain

WBC 14,100 cell/μL, CRP 24.4 mg/dL, ERS 61 mm/h

MRI epidural abscess anterior L3–S1.

Laminectomy L4–S1 and drainage

E. coli; cefotaxime

Continuation 6 months antimicrobial. Improved.

Mor et al, 2021[34]

Female, 56

Not specified

Fever, back pain, paraplegia, confusion, and urinary incontinence

Not specified

MRI epidural abscess between l2 and the distal-most thecal sac

L3–l5 laminectomy

Pasteurella multocida; vancomycin and cefepime.

Ampicillin-sulbactam; full recovery paraplegia.

Sati et al, 2021[17]

Male, 23

Not specified

Fever, back pain, weakness of the left upper limb, and spastic paraplegia

Not specified

MRI epidural abscess C5/C6–T2/T3

C7–T1 hemilaminectomy

S. aureus

Muscle tone and power of the upper limb were recovered

Kim et al, 2021[21]

Female, 75

Not specified

Back pain, pulmonary edema, dyspnea

WBC 6700 cell/μL, PCR 7.718 mg/dL, ERS 59 mm/h

MRI epidural abscess l5 seconds

Ll5–S1 laminectomy; second surgery: lumbar corpectomy

S. hominis (blood culture) and S. epidermis (abscess culture); vancomycin 9 weeks; second surgery plus M. tuberculosis in the abscess culture.

Recovered completely

Kim et al, 2021[21]

Female, 79

Rheumatoid arthritis and DM2

Back pain, fever, weak legs.

WBC 14.360 cell/μL, CRP 7.57 mg/dL, ERS 83 mm/h

MRI epidural abscess T3-L5

Laminotomy t8 and t12 levels; 5-Fr pediatric.

Methicillin-resistant S. aureus; vancomycin

Motor strength improved

Nitinai et al, 2021[50]

Male, 71

Chemoradiation therapy, DM2.

Fever, neck pain

WBC 21,000 cell/μL, CRP 7.57 mg/dL, ERS 83 mm/h

MRI anterior epidural abscess C2–C7

Conservative therapy

Klebsiella pneumoniae; ceftriaxone

Progressively debilitating condition; died

Horiya et al, 2021[51]

Female, 62

Type 2 diabetes mellitus

Coma

WBC 9,600/μL (neutrophil 94.0%), CRP 29.76 mg/dL, and procalcitonin 19.48 ng/mL

CT L4–L5 fat-saturated T2-weighted imaging MRI L4–L5 left pyogenic psoas abscess and spontaneous discitis

Percutaneous drainage

Methicillin-susceptible S. aureus broad-spectrum (meropenem and daptomycin) >> others antibiotics

Recovery, but with severe bone destruction

Munasinghe et al, 2021[36]

Female, 67

Subarachnoid block (anesthesia)

Back pain

Not specified

Urgent MRI SEA with cauda equina compression

Bilateral L4 laminectomy and drainage

Methicillin-resistant S. aureus >> meropenem

Complete recovery after 6 weeks

Vig et al, 2021[38]

Female, 22 month old

Presumptive diagnosis of nonspecific viral illness

Fever, dry cough, back pain, and recusal food

WBC 7,500 mm3 (68% neutrophils, 22% lymphocytes, 9% monocytes on differential); ESR 73 mm/h;

CRP 92.5 mg/L

T2 STIR and T1 fat-suppression MRI with gadolinium contrast SEA T5–T11

T10–11 decompressive laminotomy and evacuation of abscess

Group A Streptococcus (S. pyogenes

empiric antibiotic (Ceftriaxone)

Total recovery with no neurological symptoms discharged on oral clindamycin.

Spennato et al, 2020[20]

Female, 9

Glycogen storage disease type 3b

Axial dorsal pain, fever, paraplegia, urinary and fecal incontinence

Elevated ERS

MRI posterior epidural mass at levels D5– D11 with hypointense signal in T1 and T2

T5–T11 laminotomy

Staphylococcus aureus methicillin sensitive.

Broad-spectrum antibiotic (ceftazidime and vancomycin) >> ceftriaxone and vancomycin

Total recovery, but motor deficits did not recover.

Spennato et al, 2020[20]

Female, 14

Paronychia and skin abscess in the knee

Back pain

Pain at the

mobilization of the neck and torticollis

Elevated C-reactive protein

(357.7 mg/L), procalcitonin and WBC

normal

MRI hyperintense signal in T2-weighted C4 to L1

T1–T12 laminotomy

Staphylococcus aureus methicillin sensitive.

Broad-spectrum antibiotic

(clindamycin, rifampicin, gentamicin, and ciprofloxacin)

She fully recovered from her symptoms. Postoperative MRI at 3 months did not show recurrence

Lodhi et al, 2020[53]

Male, 66

Cat bit

Unrelenting back pain, fever, chills, and severe back spasms

WBC 19,600 cells/mL, elevated CRP 5.3 mg/L, and elevated procalcitonin (1.43 ng/mL)

MRI with and without contrast SEA L3–L4

Nonsurgical

P. multocida

broad-spectrum IV antimicrobials.

(ampicillin-sulbactam >> ceftriaxone)

Total recovery

Altdorfer et al, 2020[54]

Woman, 76

Not specified

Back pain, lower limb, and loss of

sphincter control

CRP 322mg/L; WBC 16,700/mL (neutrophilic)

MRI with contrast (full spine) SEA T4–T6

Laminectomy with surgical drainage

Aggregatibacter aphrophilus (HACEK group)

broad spectrum (ceftazidime and vancomycin) >> ceftriaxone (2 g twice daily)

Total recovery with no pain or sensorimotor deficits

Hirai et al, 2020[33]

Male, 52

Not specified

Acute back pain and fever,

WBC 5,800 cells/mL (band cells 27%, segmented cells 58%, lymphocytes 10%, monocytes 4.5%); CPR: 29.0 mg/dL;

MRI SEA L2–L4

Laminectomy drainage abscess and antibiotic

Salmonella altona;

broad-spectrum (meropenem 1 g 8/8 h) >> ceftriaxone 2 g 24/24 h >> ceftriaxone 2 g 12/12 h and ciprofloxacin 400 mg 8/8 h >> oral ciprofloxacin for another 2 weeks

Discharged without signs of neurological dysfunction (neurological status improved)

Mallik et al, 2020[52]

Female, 20

Spinal anesthesia [cesarean]

Lower limb weakness, urinary retention, lower back pain

WBC 27,000, (90% neutrophils), CRP 13

MRI with contrast SEA T2–S1

L3 laminectomy with drainage of pus

Staphylococcus aureus

Broad-spectrum antibiotics (ceftriaxone + amikacin) >> (meropenem + linezolid)

Recovery after 3 weeks

Brunasso et al, 2020[55]

Female, 45

Therapeutic epidural spinal injections (ESIs) of steroids.

Constipation, leg pain, inability to walk, acute urinary retention, perineal hypoesthesia

WBC 19,790/mL

Lumbar MRI without gadolinium SEA L4–L5–S1

Laminectomy for debridement/decompression

Methicillin-resistant Staphylococcus aureus and Streptococcus parasanguinis;

broad-spectrum (vancomycin and ceftazidime) >> clindamycin and gentamicin

.

Partial recovery with 4/5 motor function without any residual sphincter dysfunction

Van baarsel et al, 2020[43]

Female, 77

Not specified

Lumbar back pain, fever

CRP 3.25 mg/L

MRI SEA L2–L3 with osteomyelitis spanning L2–L4

Expectant

E. coli (ertapenem) >> oral ciprofloxacin

Complete recovery with no neurological deficits

Van baarsel et al, 2020[43]

Male, 51

Not specified

Neck pain and stiffness

WBC 10,900/mL, lactate 2.14 U/L

CT head without contrast, no acute abnormalities; MRI SEA C5–C7

Urgent laminectomy by orthopaedic surgery

E. cloacae (cefepime)

Permanent paraplegia and decreased hand strength bilaterally.

Van baarsel et al, 2020[43]

Female, 63

Not specified

Bilateral lower extremity weakness and tingling, urinary and fecal incontinence

ESR 101 mm/h and CRP 12 mg/L

Spinal epidural abscess spanning T6–T9

T6–T9 laminectomy and decompression

B. fragilis (ertapenem)

Permanent paraplegia

Plancha da silva et al, 2020[56]

Female, 53

Not specified

Dorsal persistent pain, fever, loss of bowel and bladder control, and progressive paraparesis

WBC with left deviation (11,820/mL with 85.3% neutrophils)

CT T4–T9;

MRI T2–T9, with greater thickness at levels T4–T6

Urgent laminectomy and drainage of the abscess

Methicillin-susceptible S. aureus;

empiric antibiotic therapy (ceftriaxone and metronidazole) >> >> flucloxacillin.

Improvements in some motor and sensory deficits after physical therapy

Sahu and Chastain, 2020[24]

Female, 80

Neurostimulator implant

Back pain with different characteristics

Not specified

MRI epidural abscess C2–T8

Urgent neurosurgical evacuation

Group B streptococcus

Not specified

Maiese et al, 2020[57]

Male, 44

Mesotherapeutic

Lumbar pain, fever, and vomiting >> paraplegia and urinary incontinence

WBC and elevated PCR

MRI intramedullary lesion extended between multiple cervical and dorsal metamers

Start a rehabilitation program

Methicillin-sensitive S. aureus >> vancomycin

and meropenem

Paraplegia with

walking allowed only in a wheelchair.

Polsky et al, 2020[37]

Male, 65

Not specified

Unable to ambulate, perineal anesthesia, and urinary retention.

No data

MRI thoracic spinal epidural abscess.

Surgical decompression for his spinal epidural abscess

Multi-week course of antibiotics

Continued to progress with physical therapy and was able to regain strength and ambulate independently

Usuda et al, 2020[13]

Woman, 33

Not specified

Fever, back pain, and numbness

WBC increases CRP and ESR

MRI spinal epidural fluid L5 to S2 vertebral body level region

CT-guided percutaneous needle aspiration of the abscess

Piperacillin-tazobactam >> oral levofloxacin

MRI scan > improvements > discharged

Shikano et al, 2020[28]

Male, 70

Airway stent

Lower limb muscle weakness

and numbness of the left hand

High levels of

inflammatory markers

MRI epidural abscess

Hemilaminectomy for C7 and laminectomy for T1–T4.

Antibiotic therapy was made, but not specified

Muscle

weakness gradually progressed.

Abbreviations: CRP, C-reactive protein; CT, computed tomography; DM2, Type 2 diabetes mellitus; ESR, erythrocyte sedimentation rate; IgA, immunoglobulin A; MRI, magnetic resonance imaging; SEA, spinal epidural abscess; WBC, white blood cell.


An increased level of spinal cord compression is strongly correlated with a higher likelihood of experiencing neurological symptoms, which can lead to poor outcomes for the affected individual.[20] Abdelhakim et al developed a classification system for spinal cord compression and its association with neurological deficit in SEA. Grade 4 and 5 abscesses characterized by overt spinal cord compression have a significant correlation with motor weakness during initial presentation. Abscesses classified as Grade 5, which exhibit severe cord compression without visible cerebrospinal fluid around the cord, are more prone to have concurrent sensory deficit or paresthesias and are significantly linked with bladder dysfunction.[1] However, in some cases, the occurrence of deficits disproportionate to the degree of compression observed on imaging suggests a role of vascular compromise of the cord secondary to vascular thrombosis or thrombophlebitis, which may be classified as grade 1, 2, or 3 depending on the deformation of the thecal sac.[21] In our article, the patient had a grade 5 compression, resulting in motor weakness, paresthesia, urinary and bowel dysfunction.

Prompt diagnosis and treatment of SEA is essential as delay can result in paralysis or death.[1] [6] [17] [22] [23] [24] Due to its low incidence and nonspecific presentation, accurately diagnosing SEA can be challenging with up to 75% of cases being misdiagnosed, misdiagnosis is alarmingly common.[1] [18] [23] [25] [26] There is a significant reduction in diagnostic delays by implementing a novel decision guideline using risk factor assessment followed by ESR and CRP testing before obtaining definitive imaging for suspected SEA.[27] In the analysis of [Table 1], despite the small amount of data collected, of the 24 (66,6%) articles that specified laboratory analysis of inflammatory markers, ESR was elevated in 13 cases (54.16%) and CRP in 20 (83.3%). The white cell count also showed leukocytosis in 17 (70.83) % of cases.

Considering that with the research of risk factors, which can be more sensitive than the classic triad, associated with markers of inflammatory activity and white cell count, an imaging exam can be used to confirm the diagnosis of SEA.[28] Definitive diagnosis of SEA is best achieved with gadolinium-enhanced MRI, with a sensitivity and specificity greater than 90%.[23] Enhanced MRI is still considered the preferred imaging study for confirming the diagnosis of SEA, which is most commonly found in the thoracic region (48%), followed by the lumbar region (31%) and the cervical region.[29] [30] [31] [32] [33] As evidenced in [Table 1], the SEA involved multiple vertebral levels; the region of the thoracic vertebrae was affected in 50%, the lumbar region in 50%, and the cervical region in 27.7%.

Empiric antibiotic treatment is started in nearly all patients and is narrowed if speciation is possible. The most common causative organism, S. aureus, is present in 50 to 70% of cases. This S. aureus is followed by aerobic and anaerobic streptococcus species in 7% of the cases.[22] Despite little data collected, [Table 1] reveals Staphylococcus and Streptococcus are the most recurrent, although other genres and even fungi can be found. In this article, it was found, when analyzing the studies found, that the most prevalent microorganisms in epidural abscesses were 11 (33.33%) cases of methicillin-sensitive S. aureus, 6 (18.18%) cases of methicillin-resistant S. aureus, 4 (12.12%) cases of Streptococcus. Bacteria of the gastrointestinal tract, for example, Escherichia coli, are also related to the formation of such abscesses, despite a lower prevalence when compared with Staphylococcus and Streptococcus.

When there is suspicion of SEA, prompt treatment is crucial. Empirical antibiotic therapy is typically initiated in almost all patients, and if the causative agent can be identified, the treatment is then narrowed down to a more specific spectrum.[34] Patients who present with a focal motor deficit are more likely to experience neurological improvement with surgical intervention.[28] Laminectomy alone has the benefit of being less expensive and having a relatively lower risk profile when compared with laminectomy combined with fusion.[1] However, nonoperative management may be appropriate in patients with intact neurologic status, multiple medical comorbidities that preclude safe surgery, pan spinal involvement, or paralysis for 0.48 hours.[23] In most of the reviewed case reports, shown in [Table 1], the treatment involved surgical intervention in 83.3%, with only 3 cases undergoing percutaneous drainage of the SEA. In addition, 16.6% were treated with antibiotics alone. Two cases resulted in death (5.5%), with one undergoing surgical intervention and the other managed with antibiotics.

The single most important predictor of residual neurologic outcome is the patient's neurologic status before intervention.[13] [35] [36] More severe preoperative neurologic deficits are associated with worse outcomes.[1] In our case, despite the severe neurological condition, there was complete recovery of the deficits presented. As shown in [Table 1], out of the six cases that had paraplegia, two had complete recovery.

Cellulitis is an inflammatory condition, sometimes of infectious origin, where various tissues are affected, which can lead to pain, swelling, and functional loss. Risk factors include diabetes mellitus, intravenous drug use, alcohol consumption, steroids, gout, rheumatoid arthritis, peripheral vascular disease, and renal failure.[37] [38] Streptococcus pyogenes, in its invasive form, can have several listed etiologies, notably for cellulitis (39%).[22] Linked to this condition, several microorganisms can be disseminated via hematogenous or lymphatic routes, perpetuating the proliferation of bacteria in unusual places. Possible manifestations are SEAs, which, despite having a rare epidemiology, is extremely serious.[39]

The etiology in this case remains unknown, although we suggest dissemination through the venous plexus. The spinal epidural space is a potential space located between the dura mater and vertebral bone that contains adipose tissue and a rich venous plexus. Venous drainage of the spinal column and epidural space communicates with the systemic circulation via the Batson plexus, a valveless venous network that allows bidirectional flow and potential spread of infection from local or distant sources.[1] [40] [41] [42] The most likely pathway would be through the veins of the left upper extremity, which join the thoracic veins and then the superior vena cava, which carries blood to the heart. From there, the infection can spread to the thoracic vertebral column via the ascending lumbar veins and the posterior intercostal veins.[39]

Another possibility would be lymphatic spread. The lymphatics on the medial side of the hand follow the basilic vein and drain into the supratrochlear lymph nodes. The supratrochlear lymph nodes are located above the medial epicondyle of the humerus. The supratrochlear lymph nodes will eventually drain into the axillary lymph nodes, which will then travel to the heart through the thoracic duct, and may subsequently access the Batson plexus.[43] [44] [45] [46] [47] [48] [49] [50] [51] [52] [53] [54] [55] [56] [57]


#

Conclusion

SEA is a rare condition, but extremely relevant due to morbidity and mortality sequelae. Early interpretation of the patient's signs and symptoms is a diagnostic challenge due to the absence of a suggestive clinical picture in most cases. That said, cellulitis has been shown to be one of the most relevant causes for the development of empyema.

The doctor's suspicion should take into account the risk factors and symptoms, whether nonspecific or specific, in addition to a targeted anamnesis, so that the correct conduct is directed.

It is also important to point out that even making the correct diagnosis, the doctor should not delay his conduct, under the risk of permanent damage or even an unfavorable outcome, death. Thus, the indication of surgical or conservative management, combined with antibiotic therapy, must be carefully analyzed so that there is a favorable result.


#
#

Conflict of Interest

None declared.

  • References

  • 1 Reihsaus E, Waldbaur H, Seeling W. Spinal epidural abscess: a meta-analysis of 915 patients. Neurosurg Rev 2000; 23 (04) 175-204 , discussion 205
  • 2 Aycan A, Aktas OY, Guzey FK. et al. Rapidly progressive spontaneous spinal epidural abscess. Case Rep Infect Dis 2016; 2016: 7958291
  • 3 Cao J, Fang J, Shao X, Shen J, Jiang X. Case Report: a case of cervical spinal epidural abscess combined with cervical paravertebral soft tissue abscess. Front Surg 2022; 9: 967806
  • 4 Houshian S, Seyedipour S, Wedderkopp N. Epidemiology of bacterial hand infections. Int J Infect Dis 2006; 10 (04) 315-319
  • 5 Abdelhakim K, Bakir MS, Fargen KM, Raper DM. A classification system for spinal cord compression and its association with neurological deficit in spinal epidural abscess. J Neurosurg Spine 2017; 26 (05) 573-578
  • 6 Rosc-Bereza K, Arkuszewski M, Ciach-Wysocka E, Boczarska-Jedynak M. Spinal epidural abscess: common symptoms of an emergency condition. A case report. Neuroradiol J 2013; 26 (04) 464-468
  • 7 Zhang JH, Wang ZL, Wan L. Cervical epidural analgesia complicated by epidural abscess: a case report and literature review. Medicine (Baltimore) 2017; 96 (40) e7789
  • 8 Darouiche RO. Spinal epidural abscess. N Engl J Med 2006; 355 (19) 2012-2020
  • 9 Khanna RK, Malik GM, Rock JP, Rosenblum ML. Spinal epidural abscess: evaluation of factors influencing outcome. Neurosurgery 1996; 39 (05) 958-964
  • 10 Centers for Disease Control Prevention. Active bacterial core surveillance (ABCs) report. Emerging infections program net- work. Group A Streptococcus—2015. Accessed October 1, 2017 at: https://www.cdc.gov/abcs/reports-findings/survreports/gas15.pdf.
  • 11 Shah AA, Ogink PT, Harris MB, Schwab JH. Development of predictive algorithms for pre-treatment motor deficit and 90- day mortality in spinal epidural abscess. J Bone Joint Surg Am 2018; 100 (12) 1030-1038
  • 12 Agrawal V, Viswanathan S, Selvaraj J, Pillai V. Streptococcus gallolyticus-related spinal epidural abscess. BMJ Case Rep 2022; 15 (08) e250733
  • 13 Usuda D, Taki Y, Izumida T. et al. Disseminated spinal epidural abscess in an immunocompetent individual: a case report and review of the literature. J Med Cases 2020; 11 (12) 417-425
  • 14 Chenoweth CE, Bassin BS, Mack MR. et al. Vertebral Osteomyelitis, Discitis, and Spinal Epidural Abscess in Adults. Ann Arbor, MI:: Michigan State University;; 2018
  • 15 Connor Jr DE, Chittiboina P, Caldito G, Nanda A. Comparison of operative and nonoperative management of spinal epidural abscess: a retrospective review of clinical and laboratory predictors of neurological outcome. J Neurosurg Spine 2013; 19 (01) 119-127
  • 16 Darouiche RO, Hamill RJ, Greenberg SB, Weathers SW, Musher DM. Bacterial spinal epidural abscess. Review of 43 cases and literature survey. Medicine (Baltimore) 1992; 71 (06) 369-385
  • 17 Sati WO, Haddad M, Anjum S. A case of spinal epidural abscess presenting with horner syndrome. Cureus 2021; 13 (04) e14541
  • 18 Shin W, Oh JH, Cho AY. et al. A rare case of spinal epidural abscess following urinary tract infection caused by escherichia coli in a patient with pre-existing stress fractures of the lumbar spine. Korean J Fam Med 2022; 43 (02) 147-149
  • 19 Ameer MA, Knorr TL, Mesfin FB. Spinal Epidural Abscess. Mar 31, 2020. In: StatPearls [Internet]. Treasure Island, FL:: StatPearls Publishing;; 2020
  • 20 Spennato P, Renedo D, Cascone D. et al. Spinal epidural abscess in children: a case-based review. Childs Nerv Syst 2020; 36 (07) 1385-1392
  • 21 Kim C, Lee S, Kim J. Spinal epidural abscess due to coinfection of bacteria and tuberculosis: a case report. World J Clin Cases 2021; 9 (16) 4072-4080
  • 22 Rashid MH, Hossain MN, Ahmed N. et al. Aspergillus spinal epidural abscess: a case report and review of the literature. J Craniovertebr Junction Spine 2022; 13 (02) 204-211
  • 23 Rigamonti D, Liem L, Sampath P. et al. Spinal epidural abscess: contemporary trends in etiology, evaluation, and management. Surg Neurol 1999; 52 (02) 189-196 , discussion 197
  • 24 Sahu KK, Chastain I. A rare case of holocord spinal epidural abscess. QJM 2020; 113 (04) 302-303
  • 25 Davis DP, Salazar A, Chan TC, Vilke GM. Prospective evaluation of a clinical decision guideline to diagnose spinal epidural abscess in patients who present to the emergency department with spine pain. J Neurosurg Spine 2011; 14 (06) 765-770
  • 26 Davis DP, Wold RM, Patel RJ. et al. The clinical presentation and impact of diagnostic delays on emergency department patients with spinal epidural abscess. J Emerg Med 2004; 26 (03) 285-291
  • 27 Xu T, Du Y, Guo J. et al. Extensive spinal epidural abscess resulting in complete paraplegia treated by selective laminectomies and irrigation. Orthop Surg 2022; 14 (09) 2380-2385
  • 28 Shikano K, Ishii D, Umimura T. et al. Spondylodiscitis and spinal epidural abscess related to long-term placement of an airway stent for malignant central airway obstruction. Thorac Cancer 2020; 11 (08) 2343-2346
  • 29 Arko IV L, Quach E, Nguyen V, Chang D, Sukul V, Kim BS. Medical and surgical management of spinal epidural abscess: a systematic review. Neurosurg Focus 2014; 37 (02) E4
  • 30 Göre B, Yenigün EC, Cevher ŞK, Çankaya E, Aydın N, Dede F. IGA nephropathy and spinal epidural abscess after COVID-19 infection: a case report. Future Virol 2022; 17 (09) 611-615
  • 31 Gupta KM, Tay KY. Spinal epidural abscess in an infant presenting as fever and respiratory distress. Pediatr Emerg Care 2020; 36 (11) e649-e650
  • 32 Heusner AP. Nontuberculous spinal epidural infections. N Engl J Med 1948; 239 (23) 845-854
  • 33 Hirai N, Kasahara K, Yoshihara S. et al. Spinal epidural abscess caused by non-typhoidal Salmonella: a case report and literature review. J Infect Chemother 2020; 26 (10) 1073-1077
  • 34 Mor YS, Rizwan A, Frank A. Paraplegia from a spinal epidural abscess caused by pasteurella multocida. Cureus 2021; 13 (06) e15477
  • 35 Baker AS, Ojemann RG, Swartz MN, Richardson Jr EP. Spinal epidural abscess. N Engl J Med 1975; 293 (10) 463-468
  • 36 Munasinghe BM, Pathirage N, Hameed MS, Hapuarachchi CT. Pus in spinal needle: diagnosis and management of a long-segment spinal epidural abscess. Case Rep Infect Dis 2021; 2021: 9989847 ( Erratum in: Case Rep Infect Dis. 2021 Aug 11;2021:9893619. PMID: 34007497; PMCID: PMC8100421)
  • 37 Polsky Z, Dowling SK, Jacobs WB. Just the facts: risk stratifying non-traumatic back pain for spinal epidural abscess in the emergency department. CJEM 2020; 22 (06) 753-755
  • 38 Vig KS, Amarante M, Hutchinson I, Lawrence JP. Pediatric Group A streptococcal spinal epidural abscess presenting with recurrent symptoms of viral illness: an operative case report. N Am Spine Soc J 2021; 6: 100067
  • 39 Scalia G, Marrone S, Paolini F. et al. Spinal epidural abscess due to acute pyelonephritis. Surg Neurol Int 2022; 13: 159
  • 40 Last's Anatomy. 12th edition. England: Churchill Livingstone. 2011. ISBN:0702033944
  • 41 Ma CX, Pan WR, Liu ZA, Zeng FQ, Qiu ZQ, Liu MY. Anatomia linfática profunda do membro superior: estudo anatômico e implicações clínicas. Ana Anat 2019; 223: 32-42
  • 42 Radkowski CA, Richards RS, Pietrobon R, Moorman CT. Estudo anatômico da veia cefálica na abordagem do ombro deltopeitoral. Clin Orthop Relat Res 2006; 442: 139-142
  • 43 Van Baarsel ED, Kesbeh Y, Kahf HA, Patel V, Weng B, Sutjita M. Spinal epidural abscess secondary to gram-negative bacteria: case report and literature review. J Community Hosp Intern Med Perspect 2020; 10 (01) 60-64
  • 44 Kharbat AF, Cox CT, Purcell A, MacKay BJ. Methicillin-resistant Staphylococcus aureus spinal epidural abscess: local and systemic case management. Cureus 2022; 14 (03) e22831
  • 45 Ammar AA, Hamad MK, Obeidallah MS, Kobets AJ, Lee SK, Abbott IR. Successful treatment of pediatric holo-spinal epidural abscess with percutaneous drainage. Cureus 2022; 14 (05) e24735
  • 46 Chaker AN, Bhimani AD, Esfahani DR. et al. Epidural abscess: a propensity analysis of surgical treatment strategies. Spine 2018; 43 (24) E1479-E1485
  • 47 Papaetis GS, Petridis TA, Karvounaris SA, Demetriou T, Lykoudis S. Bacteroides fragilis bacteremia complicated by spondylodiscitis, spinal epidural abscess, and sepsis: a case report. Am J Case Rep 2022; 23: e936179
  • 48 Fujita M, Ueno T, Horiuchi M. et al. Campylobacter coli infection causes spinal epidural abscess with Guillain-Barré syndrome: a case report. BMC Neurol 2022; 22 (01) 9
  • 49 Davis DP, Wold RM, Patel RJ. et al. Spinal epidural abscess: diagnosis, management, and outcomes. West J Emerg Med 2014; 15 (01) 1-8
  • 50 Nitinai N, Punpichet M, Nasomsong W. Fatal cervical spinal epidural abscess and spondylodiscitis complicated with rhombencephalitis caused by klebsiella pneumoniae: a case report and literature review. Cureus 2021; 13 (12) e20100
  • 51 Horiya M, Anno T, Kawada M. et al. Pyogenic psoas abscess on the dorsal side, and bacterial meningitis and spinal epidural abscess on the ventral side, both of which were induced by spontaneous discitis in a patient with diabetes mellitus: a case report. J Diabetes Investig 2021; 12 (07) 1301-1305
  • 52 Mallik J, Motiani V, Pai MG. Spinal epidural abscess post spinal anesthesia: an uncommon complication of a common procedure. Asian J Neurosurg 2020; 15 (03) 730-732
  • 53 Lodhi FAK, Shogren SL, Haque N, Ishaq M, Rehman A. Spinal epidural abscess due to Pasteurella multocida infection. IDCases 2020; 21: e00801
  • 54 Altdorfer A, Gavage P, Moerman F. Aggregatibacter aphrophilus spinal epidural abscess. BMJ Case Rep 2020; 13 (07) e235320
  • 55 Brunasso L, Basile L, Gerardo Iacopino D. et al. All that glitters is not gold: a spinal epidural empyema following epidural steroid injection. Surg Neurol Int 2020; 11: 240
  • 56 Plancha da Silva T, Amaral Silva M, Santos Boaventura S, Castro Martins M, Teixeira Duro S, Carvalho F. Spinal cord disorder due to spinal epidural abscess secondary to thoracic facet joint septic arthritis-a rare case with a surprising evolution. Spinal Cord Ser Cases 2020; 6 (01) 102
  • 57 Maiese A, Volonnino G, Viola RV. et al. A rare case of Spinal Epidural Abscess following mesotherapy: a challenging diagnosis and the importance of clinical risk management. Considerations concerning uncommon risk factor for development of Spinal Epidural Abscess and its prevention. Clin Ter 2020; 170 (01) e15-e18

Address for correspondence

Cláudio Brandão Filho
Rua Francisco Alves Ramalho 997
Campina Grande, Paraíba 58408-308
Brazil   

Publication History

Received: 04 July 2023

Accepted: 14 January 2024

Accepted Manuscript online:
13 February 2024

Article published online:
08 April 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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Rüdigerstraße 14, 70469 Stuttgart, Germany

  • References

  • 1 Reihsaus E, Waldbaur H, Seeling W. Spinal epidural abscess: a meta-analysis of 915 patients. Neurosurg Rev 2000; 23 (04) 175-204 , discussion 205
  • 2 Aycan A, Aktas OY, Guzey FK. et al. Rapidly progressive spontaneous spinal epidural abscess. Case Rep Infect Dis 2016; 2016: 7958291
  • 3 Cao J, Fang J, Shao X, Shen J, Jiang X. Case Report: a case of cervical spinal epidural abscess combined with cervical paravertebral soft tissue abscess. Front Surg 2022; 9: 967806
  • 4 Houshian S, Seyedipour S, Wedderkopp N. Epidemiology of bacterial hand infections. Int J Infect Dis 2006; 10 (04) 315-319
  • 5 Abdelhakim K, Bakir MS, Fargen KM, Raper DM. A classification system for spinal cord compression and its association with neurological deficit in spinal epidural abscess. J Neurosurg Spine 2017; 26 (05) 573-578
  • 6 Rosc-Bereza K, Arkuszewski M, Ciach-Wysocka E, Boczarska-Jedynak M. Spinal epidural abscess: common symptoms of an emergency condition. A case report. Neuroradiol J 2013; 26 (04) 464-468
  • 7 Zhang JH, Wang ZL, Wan L. Cervical epidural analgesia complicated by epidural abscess: a case report and literature review. Medicine (Baltimore) 2017; 96 (40) e7789
  • 8 Darouiche RO. Spinal epidural abscess. N Engl J Med 2006; 355 (19) 2012-2020
  • 9 Khanna RK, Malik GM, Rock JP, Rosenblum ML. Spinal epidural abscess: evaluation of factors influencing outcome. Neurosurgery 1996; 39 (05) 958-964
  • 10 Centers for Disease Control Prevention. Active bacterial core surveillance (ABCs) report. Emerging infections program net- work. Group A Streptococcus—2015. Accessed October 1, 2017 at: https://www.cdc.gov/abcs/reports-findings/survreports/gas15.pdf.
  • 11 Shah AA, Ogink PT, Harris MB, Schwab JH. Development of predictive algorithms for pre-treatment motor deficit and 90- day mortality in spinal epidural abscess. J Bone Joint Surg Am 2018; 100 (12) 1030-1038
  • 12 Agrawal V, Viswanathan S, Selvaraj J, Pillai V. Streptococcus gallolyticus-related spinal epidural abscess. BMJ Case Rep 2022; 15 (08) e250733
  • 13 Usuda D, Taki Y, Izumida T. et al. Disseminated spinal epidural abscess in an immunocompetent individual: a case report and review of the literature. J Med Cases 2020; 11 (12) 417-425
  • 14 Chenoweth CE, Bassin BS, Mack MR. et al. Vertebral Osteomyelitis, Discitis, and Spinal Epidural Abscess in Adults. Ann Arbor, MI:: Michigan State University;; 2018
  • 15 Connor Jr DE, Chittiboina P, Caldito G, Nanda A. Comparison of operative and nonoperative management of spinal epidural abscess: a retrospective review of clinical and laboratory predictors of neurological outcome. J Neurosurg Spine 2013; 19 (01) 119-127
  • 16 Darouiche RO, Hamill RJ, Greenberg SB, Weathers SW, Musher DM. Bacterial spinal epidural abscess. Review of 43 cases and literature survey. Medicine (Baltimore) 1992; 71 (06) 369-385
  • 17 Sati WO, Haddad M, Anjum S. A case of spinal epidural abscess presenting with horner syndrome. Cureus 2021; 13 (04) e14541
  • 18 Shin W, Oh JH, Cho AY. et al. A rare case of spinal epidural abscess following urinary tract infection caused by escherichia coli in a patient with pre-existing stress fractures of the lumbar spine. Korean J Fam Med 2022; 43 (02) 147-149
  • 19 Ameer MA, Knorr TL, Mesfin FB. Spinal Epidural Abscess. Mar 31, 2020. In: StatPearls [Internet]. Treasure Island, FL:: StatPearls Publishing;; 2020
  • 20 Spennato P, Renedo D, Cascone D. et al. Spinal epidural abscess in children: a case-based review. Childs Nerv Syst 2020; 36 (07) 1385-1392
  • 21 Kim C, Lee S, Kim J. Spinal epidural abscess due to coinfection of bacteria and tuberculosis: a case report. World J Clin Cases 2021; 9 (16) 4072-4080
  • 22 Rashid MH, Hossain MN, Ahmed N. et al. Aspergillus spinal epidural abscess: a case report and review of the literature. J Craniovertebr Junction Spine 2022; 13 (02) 204-211
  • 23 Rigamonti D, Liem L, Sampath P. et al. Spinal epidural abscess: contemporary trends in etiology, evaluation, and management. Surg Neurol 1999; 52 (02) 189-196 , discussion 197
  • 24 Sahu KK, Chastain I. A rare case of holocord spinal epidural abscess. QJM 2020; 113 (04) 302-303
  • 25 Davis DP, Salazar A, Chan TC, Vilke GM. Prospective evaluation of a clinical decision guideline to diagnose spinal epidural abscess in patients who present to the emergency department with spine pain. J Neurosurg Spine 2011; 14 (06) 765-770
  • 26 Davis DP, Wold RM, Patel RJ. et al. The clinical presentation and impact of diagnostic delays on emergency department patients with spinal epidural abscess. J Emerg Med 2004; 26 (03) 285-291
  • 27 Xu T, Du Y, Guo J. et al. Extensive spinal epidural abscess resulting in complete paraplegia treated by selective laminectomies and irrigation. Orthop Surg 2022; 14 (09) 2380-2385
  • 28 Shikano K, Ishii D, Umimura T. et al. Spondylodiscitis and spinal epidural abscess related to long-term placement of an airway stent for malignant central airway obstruction. Thorac Cancer 2020; 11 (08) 2343-2346
  • 29 Arko IV L, Quach E, Nguyen V, Chang D, Sukul V, Kim BS. Medical and surgical management of spinal epidural abscess: a systematic review. Neurosurg Focus 2014; 37 (02) E4
  • 30 Göre B, Yenigün EC, Cevher ŞK, Çankaya E, Aydın N, Dede F. IGA nephropathy and spinal epidural abscess after COVID-19 infection: a case report. Future Virol 2022; 17 (09) 611-615
  • 31 Gupta KM, Tay KY. Spinal epidural abscess in an infant presenting as fever and respiratory distress. Pediatr Emerg Care 2020; 36 (11) e649-e650
  • 32 Heusner AP. Nontuberculous spinal epidural infections. N Engl J Med 1948; 239 (23) 845-854
  • 33 Hirai N, Kasahara K, Yoshihara S. et al. Spinal epidural abscess caused by non-typhoidal Salmonella: a case report and literature review. J Infect Chemother 2020; 26 (10) 1073-1077
  • 34 Mor YS, Rizwan A, Frank A. Paraplegia from a spinal epidural abscess caused by pasteurella multocida. Cureus 2021; 13 (06) e15477
  • 35 Baker AS, Ojemann RG, Swartz MN, Richardson Jr EP. Spinal epidural abscess. N Engl J Med 1975; 293 (10) 463-468
  • 36 Munasinghe BM, Pathirage N, Hameed MS, Hapuarachchi CT. Pus in spinal needle: diagnosis and management of a long-segment spinal epidural abscess. Case Rep Infect Dis 2021; 2021: 9989847 ( Erratum in: Case Rep Infect Dis. 2021 Aug 11;2021:9893619. PMID: 34007497; PMCID: PMC8100421)
  • 37 Polsky Z, Dowling SK, Jacobs WB. Just the facts: risk stratifying non-traumatic back pain for spinal epidural abscess in the emergency department. CJEM 2020; 22 (06) 753-755
  • 38 Vig KS, Amarante M, Hutchinson I, Lawrence JP. Pediatric Group A streptococcal spinal epidural abscess presenting with recurrent symptoms of viral illness: an operative case report. N Am Spine Soc J 2021; 6: 100067
  • 39 Scalia G, Marrone S, Paolini F. et al. Spinal epidural abscess due to acute pyelonephritis. Surg Neurol Int 2022; 13: 159
  • 40 Last's Anatomy. 12th edition. England: Churchill Livingstone. 2011. ISBN:0702033944
  • 41 Ma CX, Pan WR, Liu ZA, Zeng FQ, Qiu ZQ, Liu MY. Anatomia linfática profunda do membro superior: estudo anatômico e implicações clínicas. Ana Anat 2019; 223: 32-42
  • 42 Radkowski CA, Richards RS, Pietrobon R, Moorman CT. Estudo anatômico da veia cefálica na abordagem do ombro deltopeitoral. Clin Orthop Relat Res 2006; 442: 139-142
  • 43 Van Baarsel ED, Kesbeh Y, Kahf HA, Patel V, Weng B, Sutjita M. Spinal epidural abscess secondary to gram-negative bacteria: case report and literature review. J Community Hosp Intern Med Perspect 2020; 10 (01) 60-64
  • 44 Kharbat AF, Cox CT, Purcell A, MacKay BJ. Methicillin-resistant Staphylococcus aureus spinal epidural abscess: local and systemic case management. Cureus 2022; 14 (03) e22831
  • 45 Ammar AA, Hamad MK, Obeidallah MS, Kobets AJ, Lee SK, Abbott IR. Successful treatment of pediatric holo-spinal epidural abscess with percutaneous drainage. Cureus 2022; 14 (05) e24735
  • 46 Chaker AN, Bhimani AD, Esfahani DR. et al. Epidural abscess: a propensity analysis of surgical treatment strategies. Spine 2018; 43 (24) E1479-E1485
  • 47 Papaetis GS, Petridis TA, Karvounaris SA, Demetriou T, Lykoudis S. Bacteroides fragilis bacteremia complicated by spondylodiscitis, spinal epidural abscess, and sepsis: a case report. Am J Case Rep 2022; 23: e936179
  • 48 Fujita M, Ueno T, Horiuchi M. et al. Campylobacter coli infection causes spinal epidural abscess with Guillain-Barré syndrome: a case report. BMC Neurol 2022; 22 (01) 9
  • 49 Davis DP, Wold RM, Patel RJ. et al. Spinal epidural abscess: diagnosis, management, and outcomes. West J Emerg Med 2014; 15 (01) 1-8
  • 50 Nitinai N, Punpichet M, Nasomsong W. Fatal cervical spinal epidural abscess and spondylodiscitis complicated with rhombencephalitis caused by klebsiella pneumoniae: a case report and literature review. Cureus 2021; 13 (12) e20100
  • 51 Horiya M, Anno T, Kawada M. et al. Pyogenic psoas abscess on the dorsal side, and bacterial meningitis and spinal epidural abscess on the ventral side, both of which were induced by spontaneous discitis in a patient with diabetes mellitus: a case report. J Diabetes Investig 2021; 12 (07) 1301-1305
  • 52 Mallik J, Motiani V, Pai MG. Spinal epidural abscess post spinal anesthesia: an uncommon complication of a common procedure. Asian J Neurosurg 2020; 15 (03) 730-732
  • 53 Lodhi FAK, Shogren SL, Haque N, Ishaq M, Rehman A. Spinal epidural abscess due to Pasteurella multocida infection. IDCases 2020; 21: e00801
  • 54 Altdorfer A, Gavage P, Moerman F. Aggregatibacter aphrophilus spinal epidural abscess. BMJ Case Rep 2020; 13 (07) e235320
  • 55 Brunasso L, Basile L, Gerardo Iacopino D. et al. All that glitters is not gold: a spinal epidural empyema following epidural steroid injection. Surg Neurol Int 2020; 11: 240
  • 56 Plancha da Silva T, Amaral Silva M, Santos Boaventura S, Castro Martins M, Teixeira Duro S, Carvalho F. Spinal cord disorder due to spinal epidural abscess secondary to thoracic facet joint septic arthritis-a rare case with a surprising evolution. Spinal Cord Ser Cases 2020; 6 (01) 102
  • 57 Maiese A, Volonnino G, Viola RV. et al. A rare case of Spinal Epidural Abscess following mesotherapy: a challenging diagnosis and the importance of clinical risk management. Considerations concerning uncommon risk factor for development of Spinal Epidural Abscess and its prevention. Clin Ter 2020; 170 (01) e15-e18

Zoom Image
Fig. 1 Left dorsal hand is erythematous, swollen, and tender. Dorsal metacarpal vein (circle) was the local of vein puncture for administration of amiodarone.
Zoom Image
Fig. 2 A thoracic spine T2-weighted axial MRI showing a fluid collection with hypersignal in the epidural space (arrowhead), displacing the spinal cord anteriorly, and also other discrete fluid collections with hypersignal on the intrathoracic paravertebral (red arrow) and extra-thoracic paraspinal (yellow arrow) areas. MRI, magnetic resonance imaging.
Zoom Image
Fig. 3 A thoracic spine T1-weighted sagittal MRI with fat saturation, obtained after the intravenous application of a Gd-containing contrast agent, shows intense marginal contrast enhancement of the epidural fluid collection in the vertebral canal (arrowhead). MRI, magnetic resonance imaging.
Zoom Image
Fig. 4 Schematic representation of the posterior view of the spinal column, indicating a purulent collection in the epidural space between T4 and T8 vertebrae, which is characteristic of spinal epidural abscess in this location.
Zoom Image
Fig. 5 Schematic drawing showing the route taken by the infectious process.
Zoom Image
Fig. 6 Sagittal T2-weighted magnetic resonance image showing the patient's spinal column after laminectomy and antibiotic treatment. No further evidence of SEA is detected, indicating successful treatment. SEA, spinal epidural abscess.