医学
兰格林
埃尔德海姆-切斯特病
组织细胞
朗格汉斯细胞组织细胞增多症
病理
组织细胞增多症
罗赛-多夫曼病
鉴别诊断
分子病理学
疾病
皮肤病理学
皮肤病科
免疫学
免疫系统
树突状细胞
化学
基因
生物化学
出处
期刊:Journal of The National Comprehensive Cancer Network
日期:2021-11-01
卷期号:19 (11): 1305-1311
被引量:14
标识
DOI:10.6004/jnccn.2021.7098
摘要
Histiocytic neoplasms, including Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), and Rosai-Dorfman disease (RDD), present a diagnostic challenge due to nonspecific fibroinflammatory infiltrates and a diverse clinical presentation. The pathologist can play a key role in classification of these disorders through multidisciplinary collaboration and correlation of pathologic features with clinical and radiologic findings. The histopathologic differential diagnosis is broad, requiring knowledge of the possible diagnoses at each specific anatomic site, and a careful assessment to exclude other inflammatory and neoplastic disorders. An immunohistochemistry panel including CD163, CD1a, langerin, S100, Factor XIIIa, OCT2, and BRAF V600E can provide definitive diagnosis in LCH and RDD, whereas ECD requires classic clinical features as well as confirmation of an activating MAPK pathway mutation by genetic studies.
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