Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report

Abstract Background SLCO2A1 was recently reported to cause nonspecific ulcers at small bowel, it was named as chronic enteropathy associated with SLCO2A1 (CEAS). It was rarely reported beyond the Japanese population. Case presentation A 4-year-5-month old girl presented with intractable anemia since...

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Main Authors: Youhong Fang, Weizhong Gu, Youyou Luo, Jie Chen
Format: Article
Language:English
Published: BMC 2020-09-01
Series:BMC Pediatrics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12887-020-02333-0
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author Youhong Fang
Weizhong Gu
Youyou Luo
Jie Chen
author_facet Youhong Fang
Weizhong Gu
Youyou Luo
Jie Chen
author_sort Youhong Fang
collection DOAJ
description Abstract Background SLCO2A1 was recently reported to cause nonspecific ulcers at small bowel, it was named as chronic enteropathy associated with SLCO2A1 (CEAS). It was rarely reported beyond the Japanese population. Case presentation A 4-year-5-month old girl presented with intractable anemia since 1-year-3-month. Her stool occult blood test was positive and the result of esophagogastroduodenoscopy and colonoscopy were normal. She was considered as obscure gastrointestinal bleeding. The magnetic resonance enterography and ultrasound of small intestinal revealed segmental thickening of small bowel. The capsule endoscopy detected ulcers, erosion and slightly stenosis near the site of junction of jejunum and ileum. She was considered chronic non-specific multiple ulcers of the small intestine and was advised to have whole exon sequencing. She was treated with exclusive enteral nutrition and iron supplement for two months. However, she was not responsive to this treatment, then she had three doses of infliximab. At the same time, the next-generation sequencing of this patient revealed two novel compound heterozygous mutations in SLCO2A1. She was diagnosed with CEAS and was treated with oral mercaptopurine. Her hemoglobin level was stable and the serum albumin level was slightly decreased during the follow up. Conclusion CEAS may present as nonspecific small bowel ulcers, and misinterpret as small bowel Crohn’s disease. Genetic tests may help with the precise diagnosis of small bowel ulcers.
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spelling doaj.art-f8e0805238bc4ac7a3cbc7e2f814f6372022-12-22T00:41:46ZengBMCBMC Pediatrics1471-24312020-09-012011510.1186/s12887-020-02333-0Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case reportYouhong Fang0Weizhong Gu1Youyou Luo2Jie Chen3Department of Gastroenterology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child HealthDepartment of Pathology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child HealthDepartment of Gastroenterology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child HealthDepartment of Gastroenterology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child HealthAbstract Background SLCO2A1 was recently reported to cause nonspecific ulcers at small bowel, it was named as chronic enteropathy associated with SLCO2A1 (CEAS). It was rarely reported beyond the Japanese population. Case presentation A 4-year-5-month old girl presented with intractable anemia since 1-year-3-month. Her stool occult blood test was positive and the result of esophagogastroduodenoscopy and colonoscopy were normal. She was considered as obscure gastrointestinal bleeding. The magnetic resonance enterography and ultrasound of small intestinal revealed segmental thickening of small bowel. The capsule endoscopy detected ulcers, erosion and slightly stenosis near the site of junction of jejunum and ileum. She was considered chronic non-specific multiple ulcers of the small intestine and was advised to have whole exon sequencing. She was treated with exclusive enteral nutrition and iron supplement for two months. However, she was not responsive to this treatment, then she had three doses of infliximab. At the same time, the next-generation sequencing of this patient revealed two novel compound heterozygous mutations in SLCO2A1. She was diagnosed with CEAS and was treated with oral mercaptopurine. Her hemoglobin level was stable and the serum albumin level was slightly decreased during the follow up. Conclusion CEAS may present as nonspecific small bowel ulcers, and misinterpret as small bowel Crohn’s disease. Genetic tests may help with the precise diagnosis of small bowel ulcers.http://link.springer.com/article/10.1186/s12887-020-02333-0AnemiaSLCO2A1CEASObscure gastrointestinal bleedingSmall bowel ulcer
spellingShingle Youhong Fang
Weizhong Gu
Youyou Luo
Jie Chen
Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report
BMC Pediatrics
Anemia
SLCO2A1
CEAS
Obscure gastrointestinal bleeding
Small bowel ulcer
title Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report
title_full Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report
title_fullStr Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report
title_full_unstemmed Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report
title_short Obscure gastrointestinal bleeding caused by congenital enteropathy in a Chinese young child-a case report
title_sort obscure gastrointestinal bleeding caused by congenital enteropathy in a chinese young child a case report
topic Anemia
SLCO2A1
CEAS
Obscure gastrointestinal bleeding
Small bowel ulcer
url http://link.springer.com/article/10.1186/s12887-020-02333-0
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AT youyouluo obscuregastrointestinalbleedingcausedbycongenitalenteropathyinachineseyoungchildacasereport
AT jiechen obscuregastrointestinalbleedingcausedbycongenitalenteropathyinachineseyoungchildacasereport