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A Case of Histiocytic Sarcoma Presenting with Primary Bone Marrow Involvement

机译:伴原发性骨髓侵犯的组织细胞肉瘤1例

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摘要

Histiocytic sarcoma (HS) is a very rare neoplasm that often shows an aggressive clinical course and systemic symptoms, such as fever, weight loss, adenopathy, hepatosplenomegaly and pancytopenia. It may present as localized or disseminated disease. We describe here a 63-yr-old male who manifested systemic symptoms, including fever, weight loss and generalized weakness. Abdominal and chest computed tomography failed to show specific findings, but there was suspicion of multiple bony changes at the lumbar spine. Fusion whole body positron emission tomography, bone scan and lumbar spine magnetic resonance imaging showed multiple bone lesions, suggesting a malignancy involving the bone marrow (BM). Several BM and bone biopsies were inconclusive for diagnosis. Necropsy showed replacement of the BM by a diffuse proliferation of neoplastic cells with markedly increased cellularity (95%). The neoplastic cells were positive for lysozyme and CD68, but negative for T- and B-cell lineage markers, and megakaryocytic, epithelial, muscular and melanocytic markers. Morphologic findings also distinguished it from other dendritic cell neoplasms.
机译:组织细胞肉瘤(HS)是一种非常罕见的肿瘤,通常表现出侵袭性的临床病程和全身症状,例如发烧,体重减轻,腺病,肝脾肿大和全血细胞减少症。它可能表现为局部或传播性疾病。我们在这里描述了一个63岁的男性,他表现出全身症状,包括发烧,体重减轻和全身无力。腹部和胸部计算机断层扫描未能显示出特定的发现,但怀疑腰椎有多个骨质改变。融合全身正电子发射断层扫描,骨扫描和腰椎磁共振成像显示多处骨病变,提示恶性肿瘤累及骨髓(BM)。几项BM和骨活检无法确定诊断。尸检显示肿瘤细胞扩散增生(95%),从而代替了BM。肿瘤细胞对溶菌酶和CD68呈阳性,但对T和B细胞谱系标记以及巨核细胞,上皮,肌肉和黑素细胞标记呈阴性。形态学发现也将其与其他树突状细胞肿瘤区分开。

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