Langerhans细胞组织细胞增多症的口腔粘膜病变伴短暂自愈:一例报告。

Xiaoling Zhang, Ningning Xue, Minhui Ruan, Xin Zeng
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引用次数: 0

摘要

朗格汉斯细胞组织细胞增生症(LCH)是一组无法解释的朗格汉斯细胞异常增殖和聚集。LCH可分为四种临床变异:Letter-Siwe病、Hand-Schüller-Christian病、嗜酸性肉芽肿和先天性自愈性LCH。LCH在儿童中最为普遍。病变可以局限于单个系统或多个器官,临床表现因受影响的器官而异。皮肤和粘膜皮肤组织是受影响组织的起点。本研究提出了一个以瞬时自愈为特征的LCH病例。该病例可进一步为LCH的临床诊断和治疗提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral mucosal lesions with transient self-healing of Langerhans cell histiocytosis: a case report.

Langerhans cell histiocytosis (LCH) is a group of unexplainable abnormal proliferation and aggregation of Langerhans cell. LCH can be classified into four clinical variants: Letterer-Siwe disease, Hand-Schüller-Christian disease, eosinophilic granuloma, and congenital self-healing LCH. LCH is most prevalent in children. Lesions can be localized in a single system or multiple organs, and clinical manifestations vary depending on the affected organs. The skin and mucocutaneous tissues are the starting point of the affected tissue. This study presents a LCH case characterized by transient self-healing. This case can further provide references for the clinical diagnosis and treatment of LCH.

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