Introduction
Eosinophilic gastrointestinal disorders (EGIDs) are chronic allergic diseases of the
gastrointestinal (gastrointestinal) tract and are classified into eosinophilic esophagitis
(EoE), eosinophilic gastritis (EG), eosinophilic gastroenteritis (EGE), and eosinophilic
colitis (EC) according to the site of eosinophilic infiltration [1]
[2]. In the first Japanese study on EGIDs, 26 patients with EoE and 144 with EGE between
2004 and 2009 were included; it suggested that EoE is less prevalent than non-EoE
EGIDs, such as EG, EGE, and EC [3]. However, since then, the prevalence of EoE has been increasing [4]
[5], and the prevalence of non-EoE EGIDs is currently considered to be low in Japan.
Although the epidemiology of non-EoE EGIDs is unclear, a recent US study that used
the insurance database reported that EG, EGE, and EC are rare and have standardized
prevalence of 6.3/100,000, 8.4/100,000, and 3.3/100,000, respectively [6].
Diagnosis of EGIDs is based on the presence of gastrointestinal symptoms and dense
eosinophilic infiltration in the gastrointestinal tract [1]
[2]
[7]
[8]
[9]
[10]. However, endoscopic findings play a key role in the initial diagnosis of patients
refractory to standard treatment or those suspected to have EGIDs. Although endoscopic
findings in EoE such as edema, rings, white exudates, furrows, and strictures are
well established [8] and a grade system [11] is widely used in research, endoscopic findings of gastric lesions in EGIDs have
not been clearly described due to the rarity of EG and EGE and due to the non-specificity
of the endoscopic findings presented in earlier reports. In this study, we assessed
patients with EGIDs in our department and collected images of gastric lesions in patients
with EG or EGE to identify the associated endoscopic findings.
Patients and methods
Study subjects
A total of 298 patients suspected to have EGIDs were referred to our department between
January 2009 and January 2020. We excluded eight patients without tissue eosinophilia
and 12 with disorders of other etiologies. We assessed 278 patients with EGIDs and
biopsy confirmed gastric eosinophilia in 19 patients. As detailed endoscopic images
for one patient were missing, we assessed 18 patients with gastric lesions. We collected
clinical data such as age, sex, height, body weight, smoking and alcohol drinking
status, presence of allergic diseases, symptoms, disease duration, and blood test
parameters including peripheral eosinophil count, hemoglobin level, and albumin level
from medical charts. This study was approved by the ethics committee of Osaka City
University (approval number: 4141) and conducted in accordance with the ethical principles
of the Declaration of Helsinki. Written informed consent was obtained from all participants
before endoscopic examination. All patients were provided the opportunity to opt out
from this study.
Diagnosis of non-EoE EGIDs (EG, EGE, and EC)
Diagnosis of non-EoE EGIDs was based on the following guidelines from the Japanese
Ministry of Health, Labor and Welfare [1]
[12]: 1. presence of symptoms such as abdominal pain, diarrhea, and vomiting; 2. mucosal
eosinophilic infiltration of ≥ 20 eosinophils per high-power field (eos/hpf) on biopsy
of the stomach, small intestine, or large intestine; 3. exclusion of other diseases
such as inflammatory bowel disease, parasitic infections, and systemic diseases; and
4. presence of ascites and high number of eosinophils in ascites. Patients with any
gastrointestinal symptom and ≥ 20 eos/hpf on gastric biopsy were diagnosed with EG
or EGE, regardless of the presence of esophageal eosinophilia.
Endoscopic examination and biopsy protocol
Upper gastrointestinal endoscopy was performed using EGL600-LR7 (Fujifilm, Tokyo,
Japan) or Q240, Q260, H260, H290, or H290-Z (Olympus, Tokyo, Japan) endoscopes. Midazolam
was used for sedation in some patients. After careful examination of the esophagus,
stomach, and duodenum, biopsies were performed using single-use Radial Jaw 4 (Boston,
Scientific Japan, Tokyo, Japan). Targeted biopsies were performed when there were
abnormal endoscopic findings, and random biopsies were performed at the discretion
of each endoscopist.
Histological assessment
The biopsy samples were fixed in formalin, embedded in paraffin, cut into 4 μm sections,
and stained with hematoxylin-eosin. Intraepithelial eosinophils were counted using × 40
and × 10 objective lenses (BX50 optical microscope, Olympus, Tokyo, Japan). For each
specimen, peak eosinophil counts of easily recognizable areas of eosinophilia were
evaluated in a low-power field and expressed as the maximum number in a high-power
field (0.24 mm2). Diagnosis was made by experienced pathologists.
Endoscopic assessment
All pre-treatment endoscopic images of the stomach were collected, assessed, and categorized
into ulcer, erosion, erythema, nodularity, discoloration, or others. Each endoscopic
finding was defined and described as follows:
Ulcers and erosions
The number, size, shape, depth, and location of ulcers and erosions were evaluated.
Ulcers were subdivided into large ulcers (≥ 2 cm in diameter; [Fig. 1a]) and small ulcers (< 2 cm in diameter; [Fig. 1c]). Typical gastric erosions are shown in [Fig. 1d].
Fig. 1 Several endoscopic findings of gastric lesions in patients with eosinophilic gastrointestinal
disorders. a Submucosal tumor-like deep large ulcer. b Ulcer size and marginal elevation are reduced, and reddish regenerative mucosa is
observed after food elimination therapy. c Multiple shallow small ulcers. d Multiple erosions. e Localized diffuse redness. f Multiple white granular elevations. g Patchy discoloration. h Marked white coats. i Antral rings.
Erythema
Erythema was categorized according to the 2013 Kyoto gastritis classification of the
Japanese Gastroenterological Endoscopy Society, which has listed 19 endoscopic findings
related to gastritis [13]
[14]
[15]. Among these findings, diffuse redness, map-like redness, red streaks, patchy redness,
and spotty redness were proposed as characteristic of erythema. In addition, localized
diffuse redness, defined as strong redness in a restricted area, has been added in
this study ([Fig. 1e]).
Nodularity
Nodularity was categorized into two types. Multiple white granular elevation includes
small whitish nodules with a granular pattern on the surface ([Fig. 1f]). Antral Penthorum-like appearance includes small nodules radially lined toward the pyloric ring on
the antrum ([Fig. 2]) and some nodules with erosion or redness on the top, similar to the raised erosion
described in the Kyoto classification ([Fig. 2a], [Fig. 2b], [Fig. 2c]) [13]
[14]
[15]. Penthorum chinense Pursh, a rooted vascular plant distributed in eastern Asia, is frequently found in
the muddy wetland, riparian food plains and fallow paddy fields in Japan and resembles
the feet of octopus.
Fig. 2 Antral Penthorum-like appearances. a Small nodules lined radially toward to pyloric ring, hence the name antral Penthorum-like appearance. b Indigocarmine contrast image. c, d Other cases of antral Penthorum-like appearance.
Discoloration
Discoloration was classified into two types: multiple patchy type and muskmelon-like
appearances. The multiple patchy type is defined as several small patchy discolorations
not connected to each other ([Fig. 1g]), whereas muskmelon-like appearance is defined as discolored mucosa-composed mesh
patterns ([Fig. 3]).
Fig. 3 Muskmelon-like appearances. a, b , c Three cases of discolored mucosa-composed mesh pattern referred to as muskmelon-like
appearances are shown.
Cracks
Cracks were defined as crackled-like appearance of the gastric mucosa that was endoscopically
detected using multiple depressed lines [16]. The location of cracks was evaluated, and the crack patterns were divided into
linear type ([Fig. 4b] and [Fig. 4 d]) and mesh-like type ([Fig. 4a], [Fig. 4c]).
Fig. 4 Cracks of several patterns observed in different parts of the stomach. a Cracks on the upper gastric body. b Cracks on the lesser curvature of the gastric body showing the linear furrows of
eosinophilic esophagitis. c Cracks on the antrum near the pylorus. d, e, f Cracks on the greater curvature of the antrum. d White-light image. e Indigocarmine contrast image. f Magnifying narrow-band image.
Other findings
We assessed other findings such as polyps including hyperplastic polyps and fundic
gland-type polyps, white coat ([Fig. 1 h]), and antral rings, revealing ring-shaped lines around the pylorus ([Fig. 1i]).
Efficacy of treatment on endoscopic findings
Pretreatment and post-treatment endoscopic images were evaluated and compared. Efficacy
was categorized into complete remission (healed mucosa or disappearance), remission
(decreased size or shape of the lesions or relatively normalized color of the mucosa),
and no change/worsening.
Helicobacter pylori infection status
H. pylori-positive infection was defined as the presence of H. pylori histologically and/or positive results of other diagnostic modalities such as serum
antibody and rapid urease test. H. pylori-negative infection was defined as the absence of H. pylori histologically and absence of atrophic gastritis on endoscopy. H. pylori infection status was classified as positive, negative, or post-eradication.
Statistical analysis
Data were expressed as mean ± standard deviation, median and interquartile range (IQR),
or number (frequency). Data were analyzed using one-way analysis of variance, followed
by Dunnett’s test for statistical comparisons. The level of statistical significance
was P < 0.05. All analyses were performed with EZR (Saitama Medical Center, Jichi Medical
University, Saitama, Japan), which is a graphical user interface for R (The R Foundation
for Statistical Computing, Vienna, Austria). More precisely, it is a modified version
of R commander designed to add statistical function frequently used in biostatistics
[17].
Results
Study subjects
Clinical characteristics of the study participants are shown in [Table 1]. Of the 18 patients assessed, 16 were categorized as EGE and two as EG. Most patients
(89 %) had allergic diseases, including bronchial asthma in seven patients, food allergy
in five, allergic rhinitis in four, and drug allergy in three. The patients had varied
symptoms because 16 patients had eosinophilia in different parts of the gastrointestinal
tract: the esophagus (n = 10), small intestine (n = 10), and colon (n = 2). The range
of gastric eosinophil count was 20–280 eos/hpf, and the mean peak number was 81.9
eos/hpf.
Table 1
Clinical characteristics of the study subjects.
|
Characteristic
|
|
Age (years)
|
46.7 ± 18.9
|
|
Sex (male/female)
|
5/13
|
|
Body mass index (kg/m2)
|
21.7 ± 5.1
|
|
Smoking habits (%)
|
1 (1 %)
|
|
Drinking habits (%)
|
5 (28 %)
|
|
Allergic diseases (%)
|
16 (89 %)
|
|
Symptoms (%)
|
|
|
7 (39 %)
|
|
|
4 (22 %)
|
|
|
3 (17 %)
|
|
|
2 (11 %)
|
|
|
1 (6 %)
|
|
|
1 (6 %)
|
|
Disease duration
|
1 month–10 years
|
|
Blood examination
|
|
|
14 (78 %)
|
|
|
12.7 ± 1.7
|
|
|
3.6 ± 0.7
|
|
Eosinophils of the stomach (eos/hpf)
|
48 (27–110.5)
|
|
H. pylori infection
|
|
|
2 (11 %)
|
|
|
13 (72 %)
|
|
|
3 (17 %)
|
Data were mean ± SD, median (IQR), or number (frequency).
Hb, hemoglobin; Alb, albumin; SD, standard deviation; IQR, interquartile range.
Endoscopic findings
The gastric lesions are summarized in [Table 2]. Erythema was most frequently observed (72 %), followed by ulcers (39 %), discoloration
(33 %), erosions (28 %), nodularity (28 %), and polyps (28 %).
Table 2
Endoscopic findings of gastric lesions in patients with EGIDs.
|
Lesions
|
Types
|
Number (%)
|
|
Ulcers
|
|
7 (39 %)
|
|
Large ulcers
|
5 (28 %)
|
|
Small ulcers
|
2 (11 %)
|
|
Erosions
|
|
5 (28 %)
|
|
Erythema
|
|
13 (72 %)
|
|
Patchy redness
|
10 (56 %)
|
|
Red streak
|
3 (17 %)
|
|
Localized diffuse redness
|
2 (11 %)
|
|
Spotty redness
|
1 (6 %)
|
|
Nodularity
|
|
5 (28 %)
|
|
Multiple white granular elevation
|
2 (11 %)
|
|
Antral Penthorum-like appearance
|
3 (17 %)
|
|
Discoloration
|
|
6 (33 %)
|
|
Multiple patchy discoloration
|
3 (17 %)
|
|
Muskmelon-like appearance
|
3 (17 %)
|
|
Cracks
|
|
5 (28 %)
|
|
Others
|
|
5 (28 %)[1]
|
|
Polyps
|
5 (28 %)
|
|
White coat
|
1 (6 %)
|
|
Antral rings
|
1 (6 %)
|
EGID, eosinophilic gastrointestinal disorder.
1 There were two findings in two patients.
Of the seven ulcers observed, five were large ulcers (3 in the antrum and 2 in the
gastric body) and two were small ulcers. A typical large ulcer is shown in [Fig. 1a] and [Fig. 1b]. A submucosal tumor (SMT)-like deep large ulcer was observed on the greater curvature
of the antrum ([Fig. 1a]). After food elimination therapy, symptoms improved, ulcer size and marginal elevation
reduced, and reddish regenerative mucosa was observed ([Fig. 1b]). Three of the five large ulcers were SMT-like deep ulcers, and the other two large
ulcers had no marginal elevation and were located in the pre-pylorus. Two patients
had multiple shallow small ulcers in the antrum ([Fig. 1c]), and five had multiple erosions located in the antrum (1 patient) and the gastric
body (4 patients). Several types of erythema were observed such as patchy redness
in 10 patients, red streaks in three, localized diffuse redness in two, and spotty
redness in 13 (72 %). Two patients had multiple white granular elevations on the gastric
body and three had small nodules radially lined toward the pyloric ring on the antrum,
referred to as a antral Penthorum-like appearance (two had nodules with raised erosion ([Fig. 2a], [Fig. 2b], [Fig. 2c]) and one had a relatively flat elevation ([Fig. 2 d]). Discoloration was found in six patients (33 %): three with multiple patchy type
and three with muskmelon-like appearances ([Fig. 3a], [Fig. 3b], [Fig. 3c]). Five patients (28 %) had cracks, and no patients received proton pump inhibitors
(PPIs). Cracks were located in the antrum (two patients), the body (two patients),
and both the antrum and the body (one patients). Of the three patients with cracks
in the antrum, two had a mesh-like pattern ([Fig. 4c]) and one had a linear pattern ([Fig. 4d], [Fig. 4e], [Fig. 4f]). One patient had a mesh-like pattern in the body ([Fig. 4a]) and linear furrows, which were similar to endoscopic findings in EoE found on the
lesser curvature of the gastric body in three patients with cracks ([Fig. 4b]). Five polyps consisting of two hyperplastic polyps and three fundic gland-type
polyps were observed, and one patient had multiple hyperplastic polyps. Other findings
included a marked white coat in one patient and antrum rings in one patient. Of the
two patients with H. pylori-positive infection, one had small ulcers with red streak and the other had antrum
rings with patchy redness. Of the three patients with post-eradication, one had erosion
and fundic gland-type polyps; one had muskmelon-like appearance, hyperplastic polyp,
and cracks; and one had multiple hyperplastic polyps with white coat and patchy redness.
Of these endoscopic findings of gastric lesions in patients with EG or EGE, SMT-like
deep ulcers, antral Penthorum-like appearance, muskmelon-like appearance, multiple white granular elevations, cracks,
and antral rings were considered relatively unique endoscopic findings.
Association between endoscopic findings and gastric eosinophilia
In this study, 73 biopsies were performed and the mean number of biopsies per patient
was 4.1. [Fig. 5] shows a plot of number of infiltrated eosinophils in the gastric mucosa against
endoscopic findings. There were no significant differences in the number of infiltrated
eosinophils between the endoscopic findings. The median (IQR) number of eosinophils
was 36.0 eos/hpf (30.0–70.0 eos/hpf) in ulcers, 62.5 eos/hpf (27.5–100.0 eos/hpf)
in erosions, 20.0 eos/hpf (11.5–37.5 eos/hpf) in erythemas, 22.0 eos/hpf (2.5–39.5
eos/hpf) in nodularities, 118.0 eos/hpf (70.0–141.0 eos/hpf) in discolorations, 62.5
eos/hpf (27.5–100.0 eos/hpf) in cracks, and 27.0 eos/hpf (18.5–53.8 eos/hpf) in normal
background mucosa. The positive rate of gastric eosinophilia was 88.2 % in ulcers,
100 % in erosions, 54.5 % in erythemas, 63.6 % in nodularities, 100 % in discolorations,
33 % in cracks, and 75 % in normal mucosa. Fifty-three target biopsies and 20 random
biopsies were performed, and there was no significant difference in the positive rate
of gastric eosinophilia between target biopsies (75.1 %) and random biopsies (75.0 %).
There was also no significant difference in the number of gastric eosinophils between
the biopsy sites as shown below: 27.5 eos/hpf (13.5–52.0 eos/hpf) in the antrum and
30.0 eos/hpf (20.0–70.0 eos/hpf) in the gastric body.
Fig. 5 Association between endoscopic findings and gastric eosinophilia. The peak number
of eosinophils in the gastric mucosa in each specimen was plotted against the endoscopic
findings. The green dots represent gastric eosinophilia (≥ 20 eos/hpf) and the blue
dots represent non-eosinophilia (< 20 eos/hpf).
Changes in endoscopic findings at post-treatment
Eleven patients received systemic steroid therapy (including 7 patients received both
steroid and PPIs or potassium-competitive acid blockers [P-CAB]), two topical steroid
therapy, four PPIs or P-CAB, and one food elimination therapy. Post-treatment endoscopic
examination in four patients was not performed. Of the patients with ulcer, four achieved
complete remission, two achieved remission, and one had no changes. Among the four
patients with erosions, two achieved complete remission and two had no changes. Of
the patients with erythema, eight of nine cases with patchy erythema, one of two red
streaks, one of two localized diffuse redness, and one spotty redness achieved complete
remission or remission. Patients with multiple white granular elevation achieved complete
remission; however, two patients with antral Penthorum-like appearances had no changes. Three patients with multiple patchy discoloration
achieved complete remission, whereas two patients with muskmelon-like appearances
achieved remission, but had not completely recovered. All patients with cracks had
no changes at post-treatment.
Discussion
Data on the endoscopic findings of gastric lesions in patients with EGIDs are limited,
and mostly derived from case reports. This study is the first to report the various
endoscopic findings of gastric lesions in patients with EGIDs in detail. Erythemas
were the most common finding observed (72 %), followed by ulcers (39 %), discolorations
(33 %), erosions (28 %), nodularities (28 %), and polyps (28 %). It was reported in
a Japanese study of 144 patients with non-EoE EGIDs that erosions (43 %), edema (42 %),
and erythemas (38 %) were the common endoscopic findings in the gastrointestinal tract
[3]. Zhang et al. examined 42 patients with EGE and reported that of the endoscopic
abnormalities in the gastrointestinal tract observed, including mucosal hyperemia,
area of roughening, scattered or widespread erythema, erosions, superficial ulcers,
and nodularity, erythema was the most common [18]. In a multicenter retrospective cohort study by Pesek et al., endoscopic findings
in patients with non-EoE EGIDs were analyzed. They examined 376 patients with non-EoE
EGIDs, which included 317 children, and EG was found in 142 patients and EGE in 123
patients. Gastric endoscopy performed on the 265 patients with EG or EGE revealed normal
healthy mucosa in 169 patients (64 %), erythema in 52 (22 %), nodularity in 23 (9 %),
and ulcer in 26 (10 %) [19]. The differences and similarities between our study and other studies may be due
to race (Japanese/Asians or mostly Whites), age (adults only or predominantly children),
and methodology (detailed analysis of endoscopic images or analysis of endoscopic
records).
Erythema is commonly observed in several conditions and diseases. The Kyoto classification
of gastritis [13]
[14]
[15] classifies erythema as diffuse redness, map-like redness, red streaks, patchy redness,
and spotty redness. Erythema is affected by H. pylori infection status, which can be positive, negative, or post-eradication, but red streaks
and patchy redness are observed irrespective of H. pylori infection status [13]
[14]
[15]. Although Goto et al. reported that red streaks in patients with EGE completely
disappeared after corticosteroid treatment [20], the erythema observed in this study may be non-specific as two patients were H. pylori-positive and 3 patients had post-eradication H. pylori infection status. In this study, diffuse redness and map-like redness were not observed,
but localized diffuse redness, which represent strong redness in a restricted area
and is different from the erythema described in the Kyoto classification, was observed
in two patients. It is unclear whether localized diffuse redness is associated with
EG and EGE; therefore, further accumulation of cases is necessary.
Several types of gastric ulcers were identified, and the SMT-like deep large ulcers
found in 3 patients were different from H. pylori-positive peptic ulcer disease and non-steroidal anti-inflammatory drug (NSAID)-induced
ulcers. Malignancies such as cancers and lymphomas were initially suspected in these
patients before the final diagnosis was made. Similar SMT-like deep ulcers were described
in previous case reports [21]
[22]
[23]. Multiple erosions are non-specific as they have several etiologies including stress,
alcohol, and drugs such as NSAIDs.
Endoscopy revealed relative unique findings such as antral Penthorum-like appearances, multiple white granular elevations, muskmelon-like appearances,
cracks, and antral rings. Of the three patients with antral Penthorum-like appearances, one patient had nodules of the relatively flat type in lines that
resemble the bamboo join-like appearance of Crohn’s disease [24]
[25], but their locations are different (antrum versus upper gastric body). Endoscopic
findings similar to antral Penthorum-like appearance [26] and bamboo joint-like appearance [27] have been identified in case reports. Discolorations had two patterns, namely the
multiple patchy type and muskmelon-like appearances. Discoloration and white granular
elevations may represent eosinophil accumulations like white exudates in EoE. A few
studies have reported cracked mucosa in patients with EGE [26]
[28]. Magnifying narrow-band image endoscopy showed that cracks were defects of surface
mucosal epithelium. Some patients had cracks in a linear pattern on the lesser curvature
that resemble the linear furrows in EoE [11]. In a study by Miyamoto et al. [16], cracks were more frequently observed in chronic PPI users (24.4 %) than in controls
(3.7 %). Further, 28 % of the study patients had cracks and none had received PPIs,
suggesting the high prevalence of cracks in patients with EG and EGE. In addition,
cracks in PPI users are observed in the gastric body; however, cracks in 3 of 5 patients
were located in the antrum. In one patient, the antral ring was similar to the rings
in EoE [11]. These results suggest that some endoscopic findings may be similar to those found
in EoE. However, the pathogenesis of these unique endoscopic findings is unknown.
It is unclear whether endoscopic findings observed in this study are specific for
EGIDs or associated with disease activity of EGIDs. All endoscopic findings in this
study were obtained from patients with confirmed gastric eosinophilia, suggesting
a histological active phase. Most endoscopic findings were improved by the treatment,
but some findings, especially cracks, did not. This suggests that cracks might not
be related to disease activity of EGIDs. This is further supported by the low positive
rate of gastric eosinophilia in target biopsies of craks. The difference in treatment
efficacy on improvement of endoscopic findings is discussed. First, refractory cases
were included against several treatments. Second, doses or duration of the treatment
might insufficiently improve endoscopic findings. Third, the treatment efficacy based
on endoscopic findings were categorized into complete remission, remission, and no
change/worsening. However, a detailed definition of endoscopic evaluation at post-treatment
has not yet been established. Thus, future prospective studies are necessary.
No association was observed between the endoscopic findings and gastric eosinophilic
infiltration, and positive rate of gastric eosinophilia was similar between target
and random biopsies. In this study, the mean gastric eosinophil count was 82 eos/hpf,
which is similar to that reported in the study by Peresk et al. (mean peak number:
78–87 eos/hpf) [19]. However, in the study by Peresk et al., gastric eosinophilia was reported to be
mostly found in gastric mucosa with normal appearance. The exact reasons for the common
finding of normal features on endoscopy in western countries are unclear; however,
this highlights the need for multiple biopsies when diagnosing patients refractory
to standard treatment and patients suspected of having EGIDs.
This study has some limitations. First, this study was a retrospective single-center
study with a small sample size due to the rarity of EG and EGE, but this is the first
study to perform a detailed analysis of endoscopic gastric images of patients with
EG or EGE. Second, we diagnosed EG and EGE based on guidelines from the Japanese Ministry
of Health, Labor and Welfare [12], but the diagnostic criteria are difficult to define and have not yet been established
internationally [9]
[10] since Talley first described the concept of EGE in 1990 [29].
Conclusion
In conclusion, various endoscopic findings of gastric lesions were observed in patients
with EG or EGE. Of these, SMT-like ulcers, antral Penthorum-like appearances, muskmelon-like appearances, and cracks might be associated with
EGIDs. Further studies that incorporate detailed pathological examination and image-enhanced
endoscopy should be conducted in the future.
