Colonic Pseudo-obstruction With Transition Zone: A Peculiar Eastern Severe Dysmotility.

BACKGROUND/AIMS: Previous studies from Korea have described chronic intestinal pseudo-obstruction (CIPO) patients with transition zone (TZ) in the colon. In this study, we evaluated the pathological characteristics and their association with long-term outcomes in Korean colonic pseudo-obstruction (CPO) patients with TZ.
METHODS: We enrolled 39 CPO patients who were refractory to medical treatment and underwent colectomy between November 1989 and April 2016 (median age at symptoms onset: 45 [interquartile range, 29-57] years, males 46.2%). The TZ was defined as a colonic segment connecting a proximally dilated and distally non-dilated segment. Detailed pathologic analysis was performed.
RESULTS: Among the 39 patients, 37 (94.9%) presented with TZ and 2 (5.1%) showed no definitive TZ. Median ganglion cell density in the TZ adjusted for the colonic circumference was significantly decreased compared to that in proximal dilated and distal non-dilated segments in TZ (+) patients (9.2 vs 254.3 and 150.5, P ＜ 0.001). Among the TZ (+) patients, 6 showed additional pathologic findings including eosinophilic ganglionitis (n = 2), ulcers with combined cytomegalovirus infection (n = 2), diffuse ischemic changes (n = 1), and heterotropic myenteric plexus (n = 1). During follow-up (median, 61 months), 32 (82.1%) TZ (+) patients recovered without symptom recurrence after surgery. The presence of pathological features other than hypoganglionosis was an independent predictor of symptom recurrence after surgery (P = 0.046).
CONCLUSIONS: Hypoganglionosis can be identified in the TZ of most Korean CPO patients. Detection of other pathological features in addition to TZ-associated hypoganglionosis was associated with poor post-operative outcomes.

Introduction

Chronic intestinal pseudo-obstruction (CIPO) is a rare, intractable disease characterized by recurrent symptoms of bowel obstruction without demonstrable occluding lesions. Previously, studies evaluating adult CIPO patients have mainly been reported from Western countries.1–4 Most patients described were first diagnosed as having CIPO in their late teens and early 20s, requiring over 5 years from symptom onset to establish a diagnosis. The clinical course of Western CIPO patients is invariably severe2,3 with 80–90% of patients requiring surgery, one-third of patients needing long-term home total parenteral nutrition, and a significant proportion becoming opioid-dependent due to long-standing, severe abdominal pain.1,3,5 The pathology underlying CIPO involves heterogeneous changes including neuropathies, myopathies, and mesenchymopathies (interstitial cells of Cajal [ICC] abnormalities).6,7 Few studies have examined the clinical and pathological characteristics of CIPO in Eastern countries.8

Studies from Korea have reported on a specific group of patients characterized by features of colonic type CIPO with a distinct transition zone (TZ) on macroscopic and microscopic evaluation.9–14 The TZ refers to a focally narrowed colonic segment connecting proximally dilated and distally non-dilated segments. Previous studies from referral centers in Korea indicated 74–79% of patients with colonic pseudo-obstruction (CPO) showed TZ on radiologic studies.13–15 Clinical symptoms of Korean CPO patients with TZ were similar to those of Western CIPO patients. Recurrent sub-occlusive events with abdominal pain, distension, nausea, and vomiting were present and marked dilations of the bowel visualized by computed tomography (CT) scan or radiography were also observed.13,14 However, Korean CPO patients with TZ showed less small bowel involvement14 and favorable clinical course, unlike Western CIPO patients.13–15

Few studies have reported pathological analysis of TZ,9,11,13 in which a significant reduction of ganglion cells defined as segmental hypoganglionosis was found. The number of ICC also decreased in 32.2–60.0% of patients.11,13 Moreover, functional and molecular analysis showed a reduced response to depolarization and a decreased number of neural nitric oxide synthase (nNOS)-positive cells in the TZ.10 However, even in these studies, evaluation was limited to only focal colonic segments, and not to the whole resected colon including the proximally dilated and distally non-dilated segments.11,13

Therefore, our objective was to evaluate Korean CPO patients with radiologically confirmed TZ by detailed pathologic analysis of the resected colon specimen. Next, we assessed the long-term outcomes of TZ-associated CPO patients according to the underlying pathologic characteristics.

Materials and Methods

Study Population

This was a retrospective study performed in a tertiary referral center in Seoul, South Korea. Overall, 129 patients were referred with a suspicion of CPO to our center between November 1989 and April 2016. CPO diagnosis was made when patients fulfilled the following criteria: (1) recurrent episodes with symptoms mimicking mechanical obstruction including abdominal pain and abdominal bloating; (2) bowel dilatation and/or intestinal air-fluid levels on abdomen X-ray and/or CT scan; and (3) no evidence of structural disease causing obstruction on upper and lower endoscopy, CT scan, small bowel series, and barium enema.8 Among the 84 CPO-confirmed patients, 38 were managed conservatively, while the remaining 46 underwent colectomy, and of these, 7 patients were excluded because the pathologic specimen was insufficient. Thirty-nine patients were finally enrolled in this study (Supplementary Fig. 1). The Institutional Review Board of Asan Medical Center approved the protocol of this study (No. 2016-1145).

Pathological Examination

All resected specimens were opened, photographed, and fixed with 10% neutral buffered formalin on corkboard. Dilated and apparently normal segments were identified, and maximum and minimum internal circumferences were measured. Segments, which connected dilated and non-dilated areas, were considered TZ. Longitudinal sections for microscopic examination were taken every 10 cm from the proximal to the distal part of the resected specimen. For the TZ, sections were taken contiguously along the long axis of the pathological segment.

Myenteric cell bodies, identified by their characteristic microscopic morphology, such as Nissl substance, large vesicular nuclei, and single prominent nucleoli, were counted per ganglion (Supplementary Fig. 2A). Calretinin immunostaining was used only when no unequivocal ganglion cells were identifiable with hematoxylin and eosin (H&E) staining (Supplementary Fig. 2B). The number of ganglion cells in the myenteric plexus was counted per centimeter.16 Since luminal dilatation might decrease ganglion cell number in proportion to the luminal circumference, we multiplied the ganglion cell number per centimeter by the mean internal circumference in a given intestinal segment and chose the product as a ganglion cell density. To evaluate the potential contribution of ICCs to intestinal motility disturbances, we counted the number of CD117-positive ICC in 10 high magnification fields (×40 objective lens) (Supplementary Fig. 2C). Since mast cells also express CD117 (Supplementary Fig. 2D), we only counted CD117-positive cells that showed unequivocal dendritic cell processes.

In addition, we counted the number of eosinophils per high power field. Eosinophilic ganglionitis was defined as prominent eosinophilic infiltration in and around the myenteric plexus, the number of which is no less than 10/high power field based on previous case reports.17,18

Immunohistochemistry

To identify ganglion cells and ICC, formalin-fixed paraffin-embedded tissue sections were stained with anti-Calretinin antibodies (rabbit monoclonal, clone DC8, Catalog No. 18-0211; dilution 1:400; Zymed, Camarillo; CA, USA,) and anti-CD117 antibodies (rabbit polyclonal, Catalog No. A4502; dilution 1:400; DAKO, Glostrup, Denmark,), respectively. All immunostaining studies were performed using a BenchMark XT automatic immunostaining device with OptiView 3,3′-Diaminobenzidine Immunohistochemistry Detection Kit (Ventana Medical Systems, Tuscon, AZ, USA) according to the manufacturer’s instructions.

Data Collection and Disease Outcome Measurement

We compared the baseline characteristics of CPO patients according to pathological characteristics including the presence of TZ and additional pathologic features. Data including patient demographics, symptoms, results of radiologic studies (abdomen simple X-ray and CT scan), results of endoscopy (upper and lower endoscopy), and laboratory findings were collected by reviewing the medical records. Symptom patterns of patients were classified as follows: (1) acute onset (patients who had symptoms that started within 6 months from CPO diagnosis), (2) acute exacerbation of chronic symptoms (patients whose symptoms were suddenly aggravated and long-standing), and (3) chronic intractable symptoms (patients who had progressive and uncontrolled symptoms lasting more than 6 months).9

The clinical outcomes including disease recurrence, which was defined as re-hospitalization and/or re-operation for treating symptoms and complications of CPO were compared according to the pathologic characteristics. In addition, we evaluated the factors associated with disease recurrence. For patients who had not visited the outpatient department for an extended period, we collected data by telephone interview.

Statistical Methods

Continuous variables are expressed as medians with inter-quartile ranges (IQRs) and categorical variables as numbers with percentages (%). The chi-squared or Fisher’s exact test was used to compare categorical variables, and the Mann-Whitney U test for continuous variables between groups. The cumulative probability of disease recurrence after surgery was calculated using the Kaplan-Meier method and comparisons between the groups was performed using the log-rank test. To evaluate factors associated with disease recurrence, a logistic regression model was used. All variables with P-values < 0.1 in univariate analysis were included in the multivariate model. P-value of < 0.05 was considered statistically significant. All statistical analyses were performed with the aid of SPSS version 21.0 software for Windows (IBM SPSS; IBM Co, Armonk, NY, USA).

Results

Clinical Characteristics

Table 1 shows the clinical characteristics of patients. The median age of symptom onset of the 39 patients enrolled in this study was 45 years (IQR, 29–57 years). The median duration from the symptom onset to CPO diagnosis was 2.0 years (IQR, 1.0–5.3 years). The most common presenting symptom was abdominal distension (92.3%), followed by abdominal pain (79.5%), constipation (76.9%), and nausea/vomiting (35.9%). Among 39 patients, 10 patients (25.6%) had diabetes mellitus and 2 patients (5.1%) had thyroid disease. Sixteen patients (41.0%) had previous history of abdominal surgery. In the abdomen CT scan, small bowel dilation was demonstrated in 23 (59.0%) patients. Among 39 patients, 13 (33.3%) underwent emergency surgery due to intractable gastrointestinal symptoms, particularly when accompanied by signs suggesting septic conditions. Twenty-six patients (66.7%) underwent elective surgery due to symptoms refractory to medical treatment.

Table 1

Baseline Characteristics

Variables	All patients (n = 39)	TZ (+) group		TZ (−) group (n = 2)	P-valuea
		Classic TZ group (n = 31)	Atypical TZ group (n = 6)
Age at symptom onset (yr)	45 (29–57)	41 (29–62)	50 (15.3–57.8)	31.5 (13.0–31.5)	0.843
Age at surgery (yr)	49 (34–65)	45 (34–65)	57 (47.8–66.0)	36.0 (20.0–36.0)	0.435
Male sex	18 (46.2)	13 (41.9)	4 (66.7)	1 (50.0)	0.383
Duration from onset to diagnosis (yr)	2.0 (1.0–5.25)	2.0 (1.0–4.5)	1.5 (1.0–16.3)	3.5 (1.0–3.5)	0.141
Symptom pattern					0.140
Acute onset	9 (23.1)	8 (35.8)	1 (16.7)	0 (0.0)
Acute exacerbation of chronic symptoms	16 (41.0)	15 (48.4)	1 (16.7)	0 (0.0)
Chronic intractable symptoms	14 (35.9)	8 (25.8)	4 (66.7)	2 (100.0)
BMI	20.3 (17.9–22.6)	20.3 (17.6–22.3)	21.4 (19.5–24.2)	20.7 (17.9–20.7)	0.248
Dilatation of small bowel	23 (59.0)	12 (61.3)	2 (33.3)	2 (100.0)	0.213
TZ on abdominal CT	36 (92.3)	30 (96.8)	6 (100)	0 (0.0)	> 0.999
Location of TZ					0.068
Transverse-descending colon	30 (76.9)	27 (87.1)	3 (50.0)	–
Sigmoid colon-rectum	7 (17.9)	4 (12.9)	3 (50.0)	–

P-value: classic transition zone (TZ) group vs atypical TZ group.

BMI, body mass index; DM, diabetes mellitus; CT, computed tomography.

Values are expressed as n (%) or median (interquartile range).

Pathologic Analyses

The pathologic characteristics of each patient are summarized in Table 2. Overall, 37/39 (94.9%) patients showed pathologically detectable TZ. Median ganglion cell density in the TZ adjusted for the colonic circumference was significantly decreased compared to that in proximal dilated and distal non-dilated segments (9.2 vs 254.3 and 150.5, P < 0.001) (Fig. 1). Generally, ganglion cell densities in colonic segments just distal to TZ were lower by more than 50% of those in adjacent normal ganglionated segments. In 3 patients (patients No. 29, 30, and 31), however, only mild decrease of ganglion cell density (decrease between 15% and 50% of the ganglion cell density in adjacent normal ganglionated segments) was observed. Locations of the TZs were the descending colon (n = 16 [41.0%]), transverse colon (n = 14 [35.9%]), rectum (n = 4 [10.3%]), and sigmoid colon (n = 3 [7.7%]). Based on pathological analysis, patients were classified as those (1) with pathologically identified TZ (TZ [+] group, n = 37 [94.9%]) and (2) without definable TZ (TZ [−] group, n = 2 [5.1%]). The TZ (+) group was subdivided into subsets (i) cases with typical hypoganglionosis (classic TZ group, n = 31 [79.5%]); and (ii) cases with hypoganglionic TZ and additional pathologic features (atypical TZ group, n = 6 [15.4%]).

Table 2

Pathological Characteristics of Colonic Pseudo-obstruction Patients

No.	Ganglion cell count × mIC			TZb length (cm)	Distal RM	Comments
	Proximal dilated	TZ	Distal non-dilateda
1	122.9	3.2	79.4	50	Normal
2	251.5	18.0	252.9	30	Normal
3	236.0	8.8	150.5	50	Normal
4	182.5	14.2	201.6	20	Normal
5	402.8	37.7	327.6	30	Normal
6	320.0	23.9	278.5	30	Normal
7	237	20.3	167.9	45	Normal
8	287.5	5.4	85.9	10	Normal
9	418.2	2.2	138.7	20	Normal
10	253.1	8.3	131.8	20	Normal	Ulcers
11	281.3	8.4	163.2	22	Normal
12	199.1	22.9	112.9	6	Normal	Ischemic colitis in proximal segment
13	312.6	4.5	237.4	25	Normal
14	188.2	0.6	56.0	50	Normal
15	190.0	25.4	203.1	40	Normal
16	281.2	2.4	174.9	45	Normal	Ulcer with CMV
17	382.3	30.5	NA	120b	Hypoganglionic
18	266.1	25.7	NA	25b	Hypoganglionic
19	435.0	12.5	NA	5b	Hypoganglionic
20	200.0	0.2	NA	80b	Hypoganglionic
21	53.5	14.7	NA	5b	Hypoganglionic
22	280.6	0.0	NA	28	Hypoganglionic	Aganglionosis from the ileocecal valve
23	112.4	0.8	NA	15	Hypoganglionic	Aganglionosis in distal 12 cm
24	286.4	9.2	NA	70	Hypoganglionic	Eosinophilic ganglionitis
25	190.5	2.8	24.0	50	Slightly hypoganglionic
26	349.0	41.5	95.4	30	Slightly hypoganglionic
27	217.0	13.3	71.4	30	Slightly hypoganglionic
28	587.3	5.2	105.8	30	Slightly hypoganglionic
29	215.2	85.7	242.2	10	Normal	Mild form
30	396.7	126.2	238.0	30	Normal	Mild form
31	255.4	121.5	NA	30b	Hypoganglionic	Mild form, diverticulitis, eosinophilic ganglionitis
32	108.6	13.0	84.5	15	Normal
33	148.0	2.5	NA	2	Hypoganglionic
34	192	NA	NA	NA	Proximal to TZ
35	333	NA	NA	NA	Proximal to TZ	Ulcer with CMV
36	152	2.8	40.0	5/10	Slightly hypoganglionic	Two hypoganglionic segments
37	NA	0.7	NA	Entire	Hypoganglionic	Ischemic colitis
38	330.0	NA	286.7	NA	Normal	Heterotopic myenteric plexus in outer longitudinal muscle in TZ
39	123.8	NA	NA	NA	Myopathic changes	Loss of smooth muscle fibers with interstitial fibrosis

Segments that had apparently normal ganglion cell number, but were distal to those with decreased ganglion cells.

Length may be incorrect because hypoganglionic segment had not been completely resected.

mIC, mean internal circumference (cm); TZ, transition zone; RM, resection margin; CMV, cytomegalovirus; NA, not assessed.

Figure 1

Ganglion cell count (A) and ganglion cell density (B) differences between the transition zone (TZ) and other colonic segment. The median value of each groups are presented. *Ganglion cell count/cm × internal circumference (cm). PD, proximal dilated; DN, distal non-dilated.

Typical hypoganglionosis with transition zone (classic transition zone group)

Most resected specimens showed marked luminal dilatation in proximal segments and distinctive TZ and non-dilated distal segments. An example (patient No. 13) is shown in Figure 2A. In this specimen, while dilated proximal segments and non-dilated distal segments were present in the myenteric plexus with abundant ganglion cells (Fig. 2B), the TZ and approximately 10 cm of non-dilated segment distal to TZ showed atrophic Schwann cells with markedly decreased ganglion cells (Fig. 2C). The ganglion cell density, calculated by multiplication of the ganglion cell count per centimeter by the mean internal circumference, gradually decreased from the distal part of the TZ, reaching the nadir at the beginning of the distal non-dilated segment (Fig. 2D). The decrease continued along the 10-cm length (the hypoganglionic segment), and the ganglion cell density gradually recovered to its normal level (Fig. 2D). The degree of decrease in ganglion cell density varied from a ratio of 0.5 (hypoganglionic segment [TZ]/normal segment, patient No. 31) to total aganglionosis in affected segments (patient No. 22) (median = 0.10; IQR, 0.06–0.20) and the length of hypoganglionic segments ranged from 5 cm to 120 cm (median = 30 cm; IQR, 20–50 cm) (Table 2). Interestingly, in patient No. 36, two hypoganglionic segments were found separated by an intervening segment with normal ganglion cell density; thus, the gross TZ was located just proximal to the first hypoganglionic segment.

Figure 2

Pathologic characteristics of typical hypoganglionosis with transition zone (TZ) (patient No. 13). (A) Gross photograph shows markedly dilated proximal colonic segments, non-dilated distal segments, and TZ connecting them (arrow). Dashed line indicates hypoganglionic segment. (B) Myenteric plexus of the proximal dilated segment shows abundant ganglion cells and Schwann cells (×40 objective lens, scale bar = 50 μm). (C) Myenteric plexus in TZ shows atrophic Schwann cells without ganglion cells or inflammation (×40 objective lens, scale = 50 μm). (D) Schematic view of a novel pathologic analysis. In this particular case, sections were taken every 5-cm (intervals of vertical lines of upper panel). Numbers of ganglion cells are markedly decreased especially in the distal TZ and the decrease in ganglion cells is observed for a certain length (approximately 10 cm in this case) after TZ. Then, the number of ganglion cells recovers thereafter. The recovered ganglion cell numbers are seemingly larger than those of proximal dilated segment, but both become similar when the internal circumference (IC) is taken into account (lower panel).

Hypoganglionosis with transition zone and other additional pathologic features (atypical transition zone group)

In 6 patients, pathological features other than typical hypoganglionosis included eosinophilic ganglionitis (n = 2), ulcers with/without combined cytomegalovirus (CMV) infection (n = 2), ischemic changes (n = 1), and evidence of heterotopic myenteric plexus (n = 1) (Fig. 3). Eosinophilic ganglionitis (cases No. 24 and 31) was characterized by the infiltration of eosinophils specifically in the myenteric plexus of the distal non-dilated segment (Fig. 3A and 3B). In CMV-infected cases (cases No. 16 and 35), geographic ulcers were observed where several CMV inclusions were identified through immunohistochemistry analysis (Fig. 3C and 3D). CMV ulcers were observed in the proximal dilated segment (patients No. 16 and 35) and distal non-dilated segment (patient No. 16). Patient No. 12 showed a proximal dilated segment with reddish mucosal changes and mucosal necrosis and transmural ischemic changes were observed microscopically (Fig. 3E and 3F). In patient No. 38, the TZ was prominent, but without visible decrease in ganglion cell density (Table 2). Instead, there were several heterotopic myenteric plexuses within the outer longitudinal muscle layer (Fig. 3G and 3H).

Figure 3

Representative photomicrographs for segmental hypoganglionosis cases with other specific features. (A, B) A segmental hypoganglionosis case with eosinophilic ganglionitis (patient No. 24). Colonic segment distal to the transition zone shows reddish discoloration (arrow) (A). Several eosinophils are observed along the hypoganglionic myenteric plexus (arrow) (B) (H&E, ×20 objective lens, scale bar = 100 μm). (C, D) A segmental hypoganglionosis case with cytomegalovirus (CMV) infection (patient No. 16). Several geographic ulcers (arrow) are observed in distal ganglionated segment (arrow) (C). CMV immunostaining reveals several CMV inclusions (brown dots) (D) (CMV immunohistochemistry, ×20 objective lens, scale bar = 100 μm). (E, F) A segmental hypoganglionosis case with ischemia (patient No. 12). Proximal dilated segment shows reddish mucosal discoloration and loss of semilunar folds (E). Transmural ischemic changes are seen (F) (H&E, ×4 objective lens, scale bar = 500 μm). (G, H) An intestinal pseudo-obstruction case with transition zone without hypoganglionosis (patient No. 38). Marked dilatation of proximal colon with prominent transition zone (G). Heterotopic ganglions are observed in outer longitudinal muscle layer (arrows) (H) (H&E, ×4 objective lens, scale bar = 500 μm).

Colonic pseudo-obstruction without definable transition zone (transition zone [−] group)

Of 39 patients, 2 (5.4%) showed no identifiable TZ (Table 3). In patient No. 37, diffuse hypoganglionosis with ischemic changes was observed (Fig. 4A and 4B). In patient No. 39, there was a severe loss of smooth muscle fibers and interstitial fibrosis, suggesting degenerative myopathy (Fig. 4C and 4D). In cases of the TZ (−) group and atypical TZ without hypoganglionosis (patient No. 38 with heterotopic myenteric plexus), we hypothesized that the differences in ICC number might explain the CPO symptoms. However, the ICC number was not decreased in the TZ of the resected specimen of patient No. 38 and was not significantly decreased in a patient in the TZ (−) group (patient No. 40) compared to normal segments present in the typical TZ group (Supplementary Table 1).

Table 3

Pathologic Classification of Colonic Pseudo-obstruction Patients With and Without Transition Zone

Classification	TZ	Hypoganglionosis	Disease recurrence after surgery (n [%])	Comment
TZ (+) group (n = 37)			5 (15.6)
Classic TZ group (n = 31)	+	+	2 (6.5)
Atypical TZ group (n = 6)	+	+	3 (50.0)	Eosinophilic ganglionitis (n = 2)
				Ulcers with combined CMV infection (n = 2)
				Ischemic change (n = 1)
				Heterotopic myenteric plexus (n = 1)
TZ (−) group (n = 2)			2 (100.0)
Diffuse hypoganglionosis (n = 1)	−	+	1 (100.0)
Degenerative myopathy (n = 1)	−	−	1 (100.0)

TZ, transition zone; CMV, cytomegalovirus.

Figure 4

Microscopic appearance of colonic pseudo-obstruction without transition zone. (A, B) Diffuse hypoganglionosis with ischemia (patient No. 37). Transmural ischemic necrosis is seen (A) (H&E, ×4 objective lens, scale bar = 500 μm). Note that ganglion cell is absent in the myenteric plexus (arrow) (B) (hematoxylin and eosin [H&E], ×400 objective lens, scale bar = 50 μm), (C, D) Myopathic changes without hypoganglionosis (patient No. 39). Proper muscle layer shows severe loss of smooth muscle fibers and marked interstitial fibrosis (C) (Masson’s Trichrome, ×10 objective lens, scale bar = 200 μm). Ganglion cells are present in the myenteric plexus (arrow) (D) (H&E, ×20 objective lens, scale bar = 100 μm).

Differences in Clinical Characteristics and Outcomes According to Pathology

We compared clinical characteristics according to pathologic groups. In classic TZ group, 35.8% of patients presented with acute-onset obstructive symptoms. Whereas, only one patient of atypical TZ group had acute-onset symptoms and 66.7% of atypical TZ group complained progressive medically-refractory chronic constipation, although the difference did not reach statistical significance (P = 0.140). The specific types of presenting symptoms including abdominal distension and abdominal pain was not significantly different between the 2 groups. In addition, underlying comorbidities were not significantly different between the 2 groups as well. In the classic TZ group, the TZ was observed most frequently in the descending colon (48.4%). However, the TZ was often located in the rectosigmoid area in patients with atypical TZ compared to the classic TZ group (50.0% vs 13.0%, P = 0.065).

We evaluated clinical outcomes according to pathologic groups during the follow-up period (median 5.1 years; IQR, 1.8–8.0 years). In the classic TZ group, 29 patients (93.5%) completely recovered without any residual symptoms after colectomy. However, 3 patients (50.0%) of the atypical TZ group were treated for recurrent sub-occlusive episodes after colectomy (P < 0.001; Table 4 and Supplementary Fig. 3). Only 2 patients were in the TZ (−) group and both complained of chronic intractable constipation at diagnosis. After colectomy, recurrent obstructive symptoms occurred in these patients and both underwent additional abdominal surgery during follow-up (Table 4). One patient died from severe electrolyte imbalance despite prolonged total parenteral nutrition.

Table 4

Clinical Course of Colonic Pseudo-obstruction Patients

Variables	Overall	TZ (+) group		TZ (−) group (n = 2)	P-value
		Classic TZ group (n = 31)	Atypical TZ group (n = 6)
Duration of follow up (yr)	5.1 (1.8–8.0)	5.0 (1.5–8.8)	6.0 (3.3–7.0)	4.8 (1.1–4.8)	0.825
Number of sub-occlusive episodes before surgery	3.0 (3.0–4.0)	3.0 (3.0–4.0)	2.5 (2.0–3.3)	5.0	0.282
Post-surgical outcomes					0.022
Without disease recurrence	32 (82.1)	29 (93.5)	3 (50.0)	0 (0.0)
With disease recurrence	7 (17.9)	2 (6.5)	3 (50.0)	2 (100.0)
Re-hospitalization	7 (17.9)	2 (6.5)	3 (50.0)	2 (100.0)
Re-operation	2 (5.1)	0 (0.0)	0 (0.0)	2 (100.0)

P-value: classic transition zone (TZ) group vs atypical TZ group.

Values are expressed as median (interquartile range) or n (%).

Clinical Factors Associated With Symptom Recurrence After Surgery in the Transition Zone (+) Group

We evaluated factors associated with symptom recurrence after colectomy in the TZ (+) group (Supplementary Table 2). The presence of combined additional pathologic features other than typical hypoganglionosis was the only statistically significant associating factor of disease recurrence (OR, 14.5; 95% CI, 1.692–124.239; P = 0.015).

Discussion

In this retrospective study including 39 Korean CPO patients, we evaluated the pathologic characteristics of TZ and its relationship with patient outcomes. Overall, 37/39 (94.9%) patients showed evidence of TZ on pathological analysis and segmental hypoganglionosis was demonstrated in the TZ of these Korean CPO patients. Moreover, detection of additional specific pathologic features in association with TZ-associated hypoganglionosis was associated with poor post-surgical outcomes.

Previous reports have described differences in disease characteristics between Korean and Western CIPO patients. The age at diagnosis of Western patients was between the ages of 15 and 30, whereas in Korean CPO patients’ age ranged between 40 to 50 years.1,2 Small bowel abnormalities identified by the dilatation observed in radiologic studies was rare in Korean CPO patients. In Western patients, 36.4–100% showed abnormal findings on small bowel manometry. However, in Korean CPO patients, only 20–60% of patients showed small bowel abnormalities.14,15 The most notable difference regarded disease outcomes. In Western studies, the course of disease has been reported to be severe.1–3,19,20 However, only a limited number of studies evaluated disease outcomes, CPO patients from Korea showed relatively favorable post-operative outcomes.13,15 The TZ, a colonic segment connecting proximally dilated and distally non-dilated segments has been described in Korean CPO patients.9,10,13–15,21

Consistent observations of the TZ in previous studies evaluating Korean CPO patients implied that the distinct clinical characteristics of these patients may be associated with the presence of TZ.9,10,13–15,21 Through detailed pathological analysis of the resected specimens, we found that the ganglion cell density, was significantly decreased in TZ compared to proximal dilated and distal non-dilated segments (P < 0.001). Interestingly, the ganglion cell density in the dilated colon located proximal to the TZ was not decreased as in the non-dilated distal colon. These results are consistent with our previous study, which suggested the TZ was the principal site of functional obstruction.10 We found that the circular muscle from the TZ was less responsive to contractile stimuli and nNOS-positive cells were depleted in the TZ.10

Previously, a group of pediatric patients, mainly from Japan, similar to Korean CPO patients with TZ has been described.11,22–24 These patients were classified as having “allied disease of Hirschsprung’s disease”23 or more commonly as having “acquired isolated hypoganglionosis (AIHG).”22 Although given a different label and patients had a different age range, similar clinical and pathological characteristics as Korean CPO patients with TZ were observed in pediatric AIHG patient group. Above all, a focal intestinal segment with a reduction in the number of ganglion cells was found.11,22,23,25,26 Second, the involved segment was mainly the colon,11,25,26 and the clinical course of this group of patients was relatively favorable.23 We think Korean CPO patients with TZ may be a late-onset form of pediatric AIHG. Taken together Korean CPO with TZ and pediatric AIHG may be a subtype of CPO with favorable outcome, which is more prevalent in Asian countries.

In some cases of pediatric AIHG, eosinophilic infiltration and ischemic changes in addition to segmental hypoganglionosis have been observed.22,25 We found specific pathologic features including, eosinophilic ganglionitis, CMV infection, ischemic changes, heterotopic myenteric plexus in addition to TZ-associated hypoganglionosis in 16.2% of the TZ (+) group. Pediatric AIHG can be ascribed to ischemia and viral infection,22 which may also contribute to ganglion cell degeneration and loss in our CPO patients. An autoimmune mechanism triggered by viral infections, such as herpes simplex virus (HSV) or CMV, may indeed result in loss of ganglion cells as also occurs in some peculiar neuropathies, such as achalasia.27 To confirm this hypothesis, we performed HSV immunostaining in selected cases. However, no HSV positive cells were identified. Further studies with larger sample sizes will be needed to evaluate the etiology and pathogenesis of CPO with TZ.

Herein, a quantitative decrease in ICC along with hypoganglionosis was identified in a subset of cases. However, the ICC decrease was much milder than that of the ganglion cell density and was neither directly proportional to the decrease of ganglion cells nor associated with post-operative outcome. Contrary to our results, there have been conflicting results about the relationship between neuropathy and ICC.11,28 Thus, the clinical impact of ICC depletion in the context of hypoganglionosis should be further evaluated.

Our study has some limitations that should be addressed. First, because we only included patients who were refractory to medical treatment and ultimately underwent surgery, the impact of TZ on the response to medical treatment in Korean CIPO patients was not evaluated. Second, only 2 patients belonged to the TZ (−) group and only one patient with visceral myopathy. This might be due to the lower prevalence of visceral myopathy in the Korean population than in Western countries (5% vs 20%).6,13,15,29 Third, we used H&E staining to detect ganglion cells and did not perform immunostaining using anti-Hu C/D antibody, which is a more precise method. However, the differences in ganglion cell density between hypoganglionic and non-hypoganglionic segments were significant; thus, the inferior precision of H&E staining may be tolerated and would not affect the analysis result as a whole.

In summary, our study determined that Korean CPO patients present distinct characteristics from Western CIPO patients, namely: (1) mainly colon involvement in Korean patients vs small bowel involvement in Western patients; (2) TZ with hypoganglionosis, commonly observed in Korean patients, but rare in Western patients; and (3) relatively good prognosis after removal of the TZ in Korean patients. Considering the decreased ganglion cell density observed in the TZ of most Korean CPO patients, the TZ could be the main site of obstructive symptoms. Mechanisms including ischemia, inflammatory (eosinophilic ganglionitis), and neurotropic virus (CMV) infection can lead to hypoganglionosis. This subset of patients was associated with poor post-operative outcomes. Further studies involving genetic evaluation are required to better elucidate the pathophysiology and specific characteristics of CPO with TZ, which manifests as a typical Eastern phenotype of severe dysmotility.