儿童直肠非胃肠道朗格汉斯细胞组织细胞增多症复发1例。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL

Clinical Medicine Insights. Case Reports Pub Date : 2023-01-01 DOI:10.1177/11795476231163961

Saad Muhammad Saeed, Sundus Bilal, Asif Loya, Muhammed Aasim Yusuf

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引用次数: 0

摘要

朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的疾病，最常累及皮肤、骨骼和肺部。胃肠道(GIT)是一种罕见的疾病，只有少数病例报告存在。我们提出一个15岁的男孩与治疗LCH涉及皮肤，骨骼，中枢神经系统(CNS)和脑垂体。他表现为直肠出血，经检查发现有一个直肠息肉，经组织学和免疫学证实为LCH。进一步调查未发现其他疫源地。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Relapse of Non-Gastrointestinal Langerhans Cell Histiocytosis in the Rectum in a Child: A Case Report.

查看原文本刊更多论文

Relapse of Non-Gastrointestinal Langerhans Cell Histiocytosis in the Rectum in a Child: A Case Report.

Langerhans cell histiocytosis (LCH) is a rare disorder most commonly involving skin, bone and lung. The gastrointestinal tract (GIT) is an uncommon site of disease and only a handful of case reports exist. We present a case of a 15-year old boy with treated LCH involving the skin, bones, central nervous system (CNS) and pituitary gland. He presented with rectal bleeding and on investigation was found to have a single rectal polyp which was confirmed histologically and immunologically to be LCH. Further investigation revealed no other foci of disease.

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来源期刊

Clinical Medicine Insights. Case Reports MEDICINE, GENERAL & INTERNAL-

CiteScore

1.10

自引率

0.00%

发文量

审稿时长

8 weeks