医学
组织细胞肉瘤
组织细胞
病理
病态的
恶性肿瘤
介绍(产科)
淋巴
免疫组织化学
肉瘤
放射科
作者
Madhu Rajeshwari,Vaishali Suri,Chitra Sarkar,Ajay Garg,Mehar Chand Sharma
出处
期刊:PubMed
日期:2022-07-23
卷期号:70 (3): 1254-1259
标识
DOI:10.4103/0028-3886.349657
摘要
Histiocytic sarcoma (HS) is an aggressive hematolymphoid malignancy that arises from non Langerhans histiocytes and usually involves the skin, lymph nodes, and intestine. The involvement of the central nervous system (CNS) is a rare occurrence with around 30 cases being reported in English literature. Morphological and immunohistochemical evidence of histiocytic differentiation is essential for diagnosis. Prognosis is very poor and consensus on treatment is not available mainly due to its rarity. We report two cases of HS with varied clinical presentation and pathological findings and elucidate the diagnostic challenges of this rare entity.
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