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毛发石:蛋白丢失性肠病的罕见病因。

Trichobezoar: A Rare Cause of Protein-losing Enteropathy.

作者信息

Bashir Anam, Tejada Andrea Gosalvez, Oldham Keith T, Thakrar Pooja D, Lerner Diana G

机构信息

From the Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI.

Division of Pediatric Surgery, Department of Surgery, Medical College of Wisconsin, Milwaukee, WI.

出版信息

JPGN Rep. 2023 Apr 18;4(2):e310. doi: 10.1097/PG9.0000000000000310. eCollection 2023 May.

DOI:10.1097/PG9.0000000000000310
PMID:37200722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10187844/
Abstract

Protein-losing enteropathy (PLE) is caused by protein loss through the gastrointestinal tract which results in hypoalbuminemia. The most common causes of PLE in children include cow milk protein allergy, celiac disease, inflammatory bowel disease, hypertrophic gastritis, intestinal lymphangiectasia, and right-sided heart dysfunction. We present a case of a 12-year-old male with bilateral lower extremity edema, hypoalbuminemia, elevated stool alpha-1-antitrypsin, and microcytic anemia. He was found to have a trichobezoar in the stomach extending to the jejunum, an unusual cause of PLE. The patient underwent an open laparotomy and gastrostomy to remove the bezoar. Follow-up confirmed resolution of hypoalbuminemia.

摘要

蛋白丢失性肠病(PLE)是由蛋白质通过胃肠道丢失引起的,这会导致低白蛋白血症。儿童PLE最常见的病因包括牛奶蛋白过敏、乳糜泻、炎症性肠病、肥厚性胃炎、肠淋巴管扩张症和右心功能不全。我们报告一例12岁男性患者,有双侧下肢水肿、低白蛋白血症、粪便α-1抗胰蛋白酶升高和小细胞贫血。他被发现胃内有一个毛粪石延伸至空肠,这是PLE的一个不寻常病因。患者接受了剖腹探查术和胃造口术以取出粪石。随访证实低白蛋白血症已得到缓解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/635d/10187844/892615b3b2ca/pg9-4-e310-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/635d/10187844/892615b3b2ca/pg9-4-e310-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/635d/10187844/892615b3b2ca/pg9-4-e310-g001.jpg

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本文引用的文献

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Endoscopic removal of a massive trichobezoar in a pediatric patient by using a variceal ligator cap: A case report and literature review.使用静脉曲张套扎帽内镜下切除小儿巨大毛粪石:病例报告及文献复习
Front Med (Lausanne). 2022 Nov 4;9:1020648. doi: 10.3389/fmed.2022.1020648. eCollection 2022.
2
Rapunzel Syndrome.长发公主综合征
J Gastrointest Surg. 2022 May;26(5):1111-1112. doi: 10.1007/s11605-021-05239-z. Epub 2022 Jan 7.
3
Endoscopic retrieval of a huge gastric trichobezoar using a polypectomy snare and an electrosurgical knife: A case report.
使用息肉切除圈套器和电刀经内镜取出巨大胃毛石:一例报告
J Dig Dis. 2022 Jan;23(1):54-56. doi: 10.1111/1751-2980.13073.
4
A Novel Method of Endoscopic Retrieval of Massive Gastric Trichobezoar.
Am J Gastroenterol. 2021 Jul 1;116(7):1376. doi: 10.14309/ajg.0000000000001115.
5
An Unusual Case of Hypoproteinemia in Childhood: Keep in Mind Trichobezoar.儿童低蛋白血症的罕见病例:警惕毛发石。
Front Pediatr. 2020 Mar 4;8:82. doi: 10.3389/fped.2020.00082. eCollection 2020.
6
Pathophysiological and clinical aspects of the diagnosis and treatment of bezoars.胃石症诊断与治疗的病理生理及临床方面
Ann Gastroenterol. 2019 May-Jun;32(3):224-232. doi: 10.20524/aog.2019.0370. Epub 2019 Mar 15.
7
Rapunzel syndrome (gastric trichobezoar), a rare presentation with generalised oedema: case report and review of the literature.长发公主综合征(胃内毛粪石),一种伴有全身性水肿的罕见表现:病例报告及文献复习
Paediatr Int Child Health. 2019 Feb;39(1):76-78. doi: 10.1080/20469047.2017.1389809. Epub 2017 Oct 23.
8
Endoscopic retrieval of gastric trichophytobezoar: Case report of a 12-year-old girl with trichophagia.内镜下取出胃毛植物性胃石:一名患食毛癖的12岁女孩的病例报告
Medicine (Baltimore). 2017 Jan;96(3):e5969. doi: 10.1097/MD.0000000000005969.
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