Literature DB >> 35088502

Cryptogenic multifocal ulcerous stenosing enteritis: a difficult diagnosis.

Chen Lew1, Anshini Jain1,2, Jonathan Chua2, Alex Wong2.   

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Year:  2022        PMID: 35088502      PMCID: PMC9541580          DOI: 10.1111/ans.17489

Source DB:  PubMed          Journal:  ANZ J Surg        ISSN: 1445-1433            Impact factor:   2.025


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Cryptogenic multifocal ulcerous stenosing enteritis (CMUSE) is chronic and recurrent stenosis from idiopathic multifocal strictures and ulcerations of small bowel. It is a rare enteropathy with just over 60 cases in literature, often misdiagnosed as Crohn's disease or NSAID‐induced enteropathy. , The ‘gold standard’ tool for this condition is capsule endoscopy or double balloon enteroscopy. We present a 59‐year‐old man with recurrent abdominal cramps and chronic iron deficiency anaemia, diagnosed with CMUSE on histology. Our patient presented acute onset bloody diarrhoea and faeculent vomiting over 1 day. He had a 10‐year history of intermittent, small‐volume bright and dark per‐rectal bleeding and iron deficiency anaemia, requiring multiple iron and blood transfusions. No pathology was evident on gastroscopy or colonoscopy, however capsule endoscopy revealed multiple circumferential ulcers with non‐obstructing stricturing distributed throughout the small bowel without active bleeding. This was attributed to NSAID‐induced enteropathy initially. He also suffered from polyarthralgia requiring long‐term NSAIDs, and symmetrical sensory neuropathy of both feet and hands with poor sensation and grip strength (Fig. 1).
Fig. 1

Pill endoscopy findings diagnostic of CMUSE (strictures shown).

Pill endoscopy findings diagnostic of CMUSE (strictures shown). Clinical examination was consistent with an acute small bowel obstruction. Oral aphthae, xerostomia, and mechanical joint pain of the ankles, hip and lower back were also observed. Pathology revealed iron deficiency anaemia (Hb:90, MCV:70) with no raised white cells and CRP of 90 (normal:0–10). No other abnormalities. His abdominal CT revealed ‘prominent mediastinal lymph nodes (up to 21 mm) with surrounding soft tissue stranding’. Several bilateral inguinal lymph nodes were also enlarged however no bowel dilation was seen. He underwent an exploratory laparotomy for a provisional diagnosis of small bowel obstruction and multiple jejunal and ileal structures were discovered intraoperatively. Multiple stricturoplasties and a 5 cm ileal resection with anastomosis were performed. Histology revealed extensive segmental chronic stenosis of small bowel tissue with inflammatory strictures with arteriovenous thickening, consistent with CMUSE (Fig. 2).
Fig. 2

Tile image of small bowel, showing superficial erosion with vascular changes in underlying stroma. Superficial ulceration, not transmural (red) abnormal blood vessels in submucosa (blue).

Tile image of small bowel, showing superficial erosion with vascular changes in underlying stroma. Superficial ulceration, not transmural (red) abnormal blood vessels in submucosa (blue). Over the following months, stricturing recurred causing per‐rectal bleeding, abdominal cramping and irregular bowel actions. Five‐months later, a second laparotomy revealed over 30 strictures from mid‐to‐distal small bowel, some with significant pre‐stenotic dilation. A 80 cm of diseased small bowel was resected with hand‐sewn end‐to‐end anastomosis. Histopathological examination again confirmed CMUSE as the diagnosis. Following this, he commenced budesonide (3 mg TDS) for 3‐months. Unfortunately, symptoms of fatigue, per‐rectal bleeding and abdominal cramping continued, and pill endoscopy revealed multiple ulcerated strictures. He had minor relief trialling exclusive enteral nutrition as he did not tolerate steroids. He has since undergone another small bowel resection performed with a cholecystectomy (due to previous ascending cholangitis) and has approximately 400 cm of small intestine remaining. Previously, CMUSE was a diagnosis of exclusion, with steroid sensitivity and extraintestinal symptoms as the leading diagnostic factors. In our case, capsule endoscopy was utilized as the primary investigative tool, however diagnosis was confirmed with histology. Due to low incidence, clinicians may have difficulty diagnosing the condition based on endoscopy unless there is a high clinical suspicion. Table 1 demonstrates that although macroscopically similar, there are some distinguishing microscopic characteristics.
Table 1

Pathological findings of CMUSE and other differential diagnoses

CMUSENSAID‐Induced EnteropathySmall bowel Crohn's Disease
Macroscopic appearanceMultifocal ulcers and strictures restricted to the small bowel (colonic sparing), 6 resulting in chronic partial obstructive symptoms.Multiple stricture sites with semi‐circular ulcers (usually with active haemorrhage) or annular constrictions of the mucosa and submucosa leading to an obstructed lumen. 7 Skip lesions and cobblestone appearance, often in an ileocolic distribution. 8
Microscopic appearanceSuperficial ulceration, fibrosis and non‐specific inflammation of the mucosa and submucosa, vascular changes without transmural inflammation. 6 Ulceration (including diffuse loss of villi, mucosal and submucosal neutrophilic exudates) and transmural inflammation. 7 Transmural inflammation with widening of the submucosa by oedema and inflammatory infiltrate, scattered aggregations of granulomatous lymphoid tissue. 8
Pathological findings of CMUSE and other differential diagnoses Characteristic symptoms of CMUSE include abdominal cramping, gastrointestinal bleeding and anaemia, with a relapsing‐remitting course despite surgery and anti‐inflammatory treatment. Extraintestinal manifestations include peripheral neuropathy, buccal aphthae, sicca syndrome, polyarthralgia, Raynauds and arterial hypertension. Our patient had long‐standing peripheral neuropathy, oral aphthae, sicca syndrome and polyarthralgia. The incidence of gallstone‐related pathology and CMUSE is currently unknown. Chung's 2015 study identified a diagnostic delay of 50.5 months after symptom onset, and given the chronic nature of this condition, any clinical clues that aid earlier diagnosis are valuable.n. CMUSE is steroid‐sensitive in majority of cases, however up to 50–66% of patients become steroid dependent. , , Koutova (2010) suggests 20 mg of prednisolone daily should reduce steroid dependency while causing regression of disease. While higher dose regimens of steroids are likely to cause increased steroid dependence, further studies to validate this in CMUSE are required. CMUSE is a rare but important differential of benign small bowel strictures. Treatment is aimed at reducing steroid dependence and preserving small bowel length, with utilization of surgical resection for occluding strictures. This study encompasses several key clinicopathological features consistent with a diagnosis of CMUSE and aims to improve awareness to lead to earlier diagnosis.
  10 in total

1.  Cryptogenic multifocal ulcerous stenosing enteritis (CMUSE), and neuromuscular and vascular hamartoma (NMVH): two sides of the same coin?

Authors:  Lisa Setaffy; María José Martín Osuna; Wolfgang Plieschnegger; María del Pino Florez Rial; Karel Geboes; Cord Langner
Journal:  Endoscopy       Date:  2014-11-20       Impact factor: 10.093

2.  Clinical Characteristics and Treatment Outcomes of Cryptogenic Multifocal Ulcerous Stenosing Enteritis in Korea.

Authors:  Sook Hee Chung; Sang Un Park; Jae Hee Cheon; Eun Ran Kim; Jeong-Sik Byeon; Byong Duk Ye; Bora Keum; Ki-Nam Shim; Sung-Ae Jung; Jin-Oh Kim; Seong Ran Jeon; Hyun Joo Song; Jeong Seop Moon; Dong Kyung Chang
Journal:  Dig Dis Sci       Date:  2015-02-24       Impact factor: 3.199

3.  Histopathology of Crohn's disease.

Authors:  B S Morson
Journal:  Proc R Soc Med       Date:  1968-01

4.  Severe cryptogenic multifocal ulcerous stenosing enteritis. A report of three cases and review of the literature.

Authors:  Darina Kohoutová; Jan Bures; Vera Tycová; Jolana Bártová; Ilja Tachecí; Stanislav Rejchrt; Zdenek Vacek; Rudolf Repák; Marcela Kopácová
Journal:  Acta Medica (Hradec Kralove)       Date:  2010

5.  Cryptogenetic multifocal ulcerous stenosing enteritis: an atypical type of vasculitis or a disease mimicking vasculitis.

Authors:  G Perlemuter; L Guillevin; P Legman; L Weiss; D Couturier; S Chaussade
Journal:  Gut       Date:  2001-03       Impact factor: 23.059

Review 6.  Multifocal stenosing ulcerations of the small intestine revealing vasculitis associated with C2 deficiency.

Authors:  G Perlemuter; S Chaussade; O Soubrane; A Degoy; A Louvel; P Barbet; P Legman; A Kahan; L Weiss; D Couturier
Journal:  Gastroenterology       Date:  1996-05       Impact factor: 22.682

7.  Cryptogenic Multifocal Ulcerous Stenosing Enteritis (CMUSE): A Tale of Three Decades.

Authors:  Ayaskanta Singh; Manoj Kumar Sahu; Manas Kumar Panigrahi; Debasis Misra
Journal:  ACG Case Rep J       Date:  2017-03-15

Review 8.  Cryptogenic multifocal ulcerous stenosing enteritis: a review of the literature.

Authors:  Darina Kohoutová; Jolana Bártová; Ilja Tachecí; Stanislav Rejchrt; Rudolf Repák; Marcela Kopáčová; Jan Bureš
Journal:  Gastroenterol Res Pract       Date:  2013-11-24       Impact factor: 2.260

9.  Non-steroidal anti-inflammatory drug-induced enteropathy as a major risk factor for small bowel bleeding: a retrospective study.

Authors:  Doo-Ho Lim; Kyoungwon Jung; Seung Bum Lee; In Kyu Park; Hee Jeong Cha; Jae Ho Park; Byung Gyu Kim; Seok Won Jung; Jae Hyun Kim; Sung Eun Kim; Won Moon; Moo In Park; Seun Ja Park
Journal:  BMC Gastroenterol       Date:  2020-06-08       Impact factor: 3.067

10.  A case report of intestinal obstruction caused by cryptogenic multifocal ulcerous stenosing enteritis.

Authors:  Cheng Chang; Chen Jiang; Yaoyao Miao; Bin Fang; Lili Zhang
Journal:  BMC Gastroenterol       Date:  2020-09-15       Impact factor: 3.067

  10 in total

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