结肠息肉并发成人郎格罕细胞组织细胞增多症一例报告及文献复习

Q4 Medicine
Feras Zaiem MD, Rafic Beydoun MD
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引用次数: 3

摘要

朗格汉斯细胞组织细胞增多症(LCH)是一种罕见的疾病,其特征是单灶性或多灶性单系统或播散性/多系统疾病,通常累及骨骼、皮肤和肺部。成人LCH累及胃肠道(GI)是罕见的,它很少涉及结肠息肉,文献中只有少数病例报道。在这个报告中,我们提出一个病例的成年女性谁被发现有盲肠息肉的常规筛查结肠镜检查。组织病理学检查和免疫组织化学检查证实了LCH的诊断。我们也回顾了成人LCH在胃肠道表现的文献,主要是结肠息肉。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adult Langerhans cell histiocytosis arising in colonic polyp: A case report and literature review

Langerhans cell histiocytosis (LCH) is a rare disease characterized by unifocal, or multifocal unisystem, or disseminated/multisystem disease that commonly involves the bone, skin and lung. LCH involvement of the gastrointestinal tract (GI) in adults is uncommon and it rarely involves colon polyps with only few case reports in the literature. In this report, we present a case of an adult female who was found to have a cecal polyp on a routine screening colonoscopy. The histopathological examination and immunohistochemical studies confirmed the diagnosis of LCH. We also review the literature of adults LCH manifested in GI mostly colonic polyps.

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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
自引率
0.00%
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0
审稿时长
16 weeks
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