Keywords
lipoma - neuropathy - ulnar nerve - soft-tissue tumor
Introduction
Lipomas usually present in adults as isolated tumors, with no presence of pain and
with slow growth, more frequently in the thorax and extremities.[1] Lipomas are typically lobular and well-circumscribed, consisting of adipose tissue
cells. They are separated from the surrounding adipose tissue by a thin fibered capsule.[1]
[2]
[3] Complementary exams are important because they assist in the determination of the
type and location of the lipoma.[4] Lipomas can be classified as intramuscular, more frequent, and intermuscular, less
frequent. In addition, intramuscular lipomas are divided into infiltrative and well-circumscribed.[2] Lipomas are commonly isolated and rarely multiple, presenting in varying shapes
and sizes, being considered giant when its diameter exceeds 5 cm.[2]
[3]
The present work aims to describe the rare case of intermuscular lipoma in the left
upper limb hypothenar region with ulnar nerve compression. We also provide a brief
bibliographic review on the subjects involved in the studied case. For this, we used
recent material available in virtual libraries, in addition to analyzing the medical
records of the patient with unusual case presentation.
First, a review of the medical records of the patient was carried out to elaborate
the case report. Then, a bibliographic research was conducted in the literature, seeking
papers published in the last 47 years, in Portuguese, English and Spanish. The inclusion
criteria of the researched studies were: the appropriate methodology applied, the
update, and the similarity in some aspect with the present case. Exclusion criteria
were: low relevance of some articles, nonapproach to the area of interest, and lack
of important information.
The following descriptors were used: lipoma, deepseated lipoma, lipomatous tumor, liposarcoma, lipoma of the extremities and intramuscular lipoma. The digital libraries and open access electronic data sources accessed were the
Scienific Electronic Library Online (SciELO) and the Virtual Health Library (VHL).
The portal minhaUFMG was also used to access paid articles and a theme pertinent to
this research.
Case Report
Patient M. A. O., 68 years old, female, housewife, sought outpatient medical care
due to persistent headache. In her physical examination, it was detected a bulging
area in the hypothenar region of the left upper limb extremity. No cyanosis or phlogistic
signs were observed in the bulging region. The patient reported moderate-intensity
pain in the left-hand thenar region, with irradiation to digits IV and V. No Tinel
sign was found on the tumor lesion, and there were no sensitivity or motricity deficits
identified.
A hand ultrasonography was requested, which evidenced an echogenic nodular well-defined
image, without flow to the Doppler, encapsulated, measuring 24 mm, in the hypothenar
region ([Fig. 1]).
Fig. 1 Left hand ultrasonography evidencing a well-defined echogenic nodular image, without
flow to the Doppler, encapsulated, measuring 2.39 mm, in the hypothenar region. Note
the dashed lines skirting the lipoma.
Upon presentation of the examination, we opted for hospitalization, which was preceded
by the request for surgical risk exams. Local anesthesia was used with lidocaine without
vasoconstrictor medication. As surgical access, we opted for linear incision in the
V-digit axis, in the hypothenar region. Neurostimulation was performed during the
procedure, in order to preserve the distal motor branches of the ulnar nerve. The
lesion had a relatively well-delimited capsular structure, with a slightly oval shape
and yellowish staining ([Figs. 2a] and [2b]). After complete removal of the lesion, the common palmar digital nerves of the
ulnar nerve and the abductor muscle of the V finger were identified. In the postoperative
care, the patient presented pain improvement in the hypothenar region, and preservation
of the motor function was confirmed.
Fig. 2 (a) Perioperative photo showing voluminous lesion with a relatively well-delimited
capsular structure, with slightly oval shape, and yellowish staining. (B) Photography
of the lesion after its resection, confirming its oval and capsulated form.
The evaluation of the histopathologic sections of the tissue showed a benign neoplasia
consisting of 12 g of unilocular mature adipose tissue ([Fig. 3a]), with the presence of some muscular tissue ([Fig. 3b]) and blood vessels ([Fig. 3c] ), interwoven by connective tissue with collagen fibers ([Fig. 3d]) and fibroblasts, sometimes constituting a myxoid aspect. In addition, the absence
of atypia and of signs of malignancy was observed.
Fig. 3 Pictures of histological sections used for pathological study (Hematoxylin-eosin,
enlargement x250). (A) Adipocytes with nuclear hyperchromatism (arrows) in medium
to mature lipomatous background. (B) presence of muscle tissue (arrow). (C) blood
vessels (arrows). (D) fibrated capsule (arrow).
Discussion
Lipoma is described as a benign adipose tumor, separated from the adjacent adipose
tissue by a thin, well-circumscribed, well-defined film, that can occur in any region
of the body. When poorly circumscribed and very infiltrated, it can be mistaken for
well-differentiated liposarcoma. Well-differentiated liposarcomas, in turn, do not
cause metastases, and they are considered of low degree of malignancy, but they present
high recurrence rates.[5]
[6]
Among the main symptoms and signs of lipomas located in the hand are: local pain,
paresis, hypoesthesia and local bulging by tumor growth in the underlying tissues
([Table 1]).[5]
[6]
Table 1
|
Authors
|
Year
|
n
|
Tumor localization
|
Symptoms
|
Result of Surgical care
|
|
Rodriguez et al[18]
|
1970
|
15
|
12 in the hand and 3 on the wrist.
|
14 Asymptomatic tumors; 1 with pain; Limitation of movement.
|
Absence of recurrences and complications.
|
|
Ceballos et al[19]
|
2005
|
4
|
2 in the hand (1 in the palmar space, 1 in the thenar eminence) and 2 in the fingers.
|
Swelling and aesthetic discomfort.
|
Postoperatory period without intercurrences. No complications.
|
|
Kamath et al[20]
|
2006
|
1
|
Palmar region.
|
Swelling and discomfort for movement.
|
Recovery of the function and without recurrences.
|
|
Mohan et al[21]
|
2008
|
1
|
Between the thenar muscles.
|
Some difficulty in the seizure of objects (by important bulging).
|
Recovery of hand function.
|
|
Nadar et al[22]
|
2010
|
13
|
13 in the hand (5 on the back, 6 palmar, 1 on the wrist) and 1 on the forearm.
|
Bulging, pain, paresis and pruritus.
|
Remission of the feel-but. No recurrences were found.
|
|
Pagonis et al[23]
|
2011
|
1
|
Palmar region.
|
Compression of the median and ulnar nerves characteristic symptoms; Reduction of pulse
movement amplitude; flexion limitation of the distal phalanx (I finger).
|
Remission of pain and recovery of motricity.
|
|
Chatterton et al[24]
|
2013
|
1
|
Thenar eminence.
|
Left thumb pain and swelling in the hand.
|
After excision of the lipoma, the patient went through a trapezectomy to treat arthritis
of the carpometacarpal joints.
|
|
Ramirez et al[25]
|
2013
|
1
|
Third finger of the left hand.
|
Limitation of interphalangeal movement and digital paresthesia.
|
Complete motricity recovery and disappearance of paresthesia.
|
|
Radivojcevic et al[26]
|
2016
|
1
|
Ulnar region of the palm of the hand.
|
Pain and tingling in the fingers (IV and V).
|
Pain control.
|
|
Schmidt[27]
|
2017
|
1
|
Thenar region with extension to fingers.
|
Limitation of finger extension (I-III), paresthesia and pain.
|
Six months after surgery, function and sensitivity of the affected fingers were restored.
|
|
Ribeiro et al[28]
|
2017
|
1
|
Palmar region.
|
Paresthesia and pain in the fingers (I-III).
|
Reversal of the complaints of paresthesia and pain.
|
The best form of treatment for lipomatous tumors is complete surgical resection. Surgery
should be performed after complementary exams that allow the surgeon to locate the
tumor and plan their approach, since precipitated measures may contribute to the recurrence
of the tumor if it is not properly removed during surgery.[5] Although surgery is commonly indicated, there is little consensus on which is the
best surgical treatment for deep lipomatous tumors.[5]
[7] In the literature, in the case of suspicion of malignancy, the wide resection, with
margins of ∼ 1 cm, associated with annual follow-up with complementary imaging examination,
is presented.[7]
Lipomas can be commonly visualized in ultrasound as distinct echogenic masses, having
a varied reading; they may be: hyperechoic (20–52%), isoechoic (28–60%) or hypoechoic
(20%).[8]
[9]
[10] When encapsulated, the capsule may be difficult to identify in this imaging examination
mode.[11] In computed tomography (TC), lipomas are hypodense (∼ 65,120 units Hounsfield).[10]
[11] Magnetic resonance imaging (MRI) is often the modality of choice in the case of
lipomas, not only to confirm diagnosis, which is usually suggested by ultrasound and
TC, as well as better evaluating the atypical features suggesting the diagnosis of
liposarcoma. In MRI, lipomas show hyperintense in sequences T1 and T2. Furthermore,
magnetic resonance imaging allows a better definition of the anatomy adjacent to the
tumor.[11]
The histological aspect of lipomas is characteristic, with predominant amount of adipose
tissue, with adipocytes and negative image of fat. There is also the frequent presence
of a fibered capsule involving the superficial region of the tumor.[1] Less often, blood vessels are observed, often more abundant in the surrounding muscle
tissue than in the tumor region, being muscular capillaries.[1]
[8] In addition, there is a beam of muscular fibers in the middle of the tumor tissue.[8]
Despite the range of possibilities for histological tissue types, which may vary from
benign lipomas to liposarcomas, it is estimated that lipomatous neoplasms comprise
half of all soft tissue tumors.[1]
[5] Due to eventual similarities between benign and malignant affections, histological
analyses have been conducted, and studies report some characteristics that allow the
physician to assist in the correct diagnosis and in the efficient referral to appropriate
treatment. Advanced age, tumor of high dimensions, and localization at the extremity
instead of the thorax, for example, are characteristics that suggest an atypical lipomatous
tumor, instead of a giant lipoma.[5]
There are other types of lesions of a benign character that can be considered as a
differential diagnosis in the present case. The importance of mentioning these tumors
found in the hand is due to the complexity of the affected structures and, consequently,
the implications, such as loss of sensitivity, pain or even motor impairment of the
limb.[12] In the group of lesions that could be differential diagnosis are: synovial cyst,
giant cell tumor of the tendon sheath, cysts of epidermal inclusion, fibromas, Schwannomas
and neurofibromas.[12]
[13]
[14]
[15]
[16]
[17]
A table was elaborated relating rare and representative lipoma cases ([Table 1]). Most of them present mild symptomatology and/or presence of local bulging without
symptoms. Rare cases developed with neurological manifestations, and all revealed
resolution of the pain and motor symptoms when present.[18]
[19]
[20]
[21]
[22]
[23]
[24]
[25]
[26]
[27]
[28]
Conclusion
The presence of lipoma in the hand, besides being uncommon, may not generate early
clinical manifestations until the tumor reaches a larger volume and compresses the
adjacent structures. The surgical procedure corroborates the effectiveness reported
in the literature, being the recommended conduct. Due to the existence of lesions
of different natures that may compromise the hand, surgery also allows obtaining material
for histopathological confirmation.
