Challenges in the Histopathologic Diagnosis of Histiocytic Neoplasms.

IF 16.4
Karen L Rech, Rong He
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引用次数: 8

Abstract

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.

组织细胞肿瘤组织病理学诊断的挑战。
组织细胞性肿瘤,包括朗格汉斯细胞组织细胞增生症(LCH)、Erdheim-Chester病(ECD)和Rosai-Dorfman病(RDD),由于非特异性纤维炎症浸润和不同的临床表现,给诊断带来了挑战。病理学家可以在这些疾病的分类中发挥关键作用,通过多学科合作和病理特征与临床和放射学发现的相关性。组织病理学鉴别诊断是广泛的,需要了解每个特定解剖部位的可能诊断,并仔细评估以排除其他炎症和肿瘤疾病。包括CD163、CD1a、langerin、S100、Factor XIIIa、OCT2和BRAF V600E在内的免疫组化检测可以为LCH和RDD提供明确的诊断,而ECD则需要经典的临床特征以及通过遗传学研究确认激活MAPK通路突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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