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组织细胞肉瘤:一项包括组织细胞标志物CD163的5例病例研究。

Histiocytic sarcoma: a study of five cases including the histiocyte marker CD163.

作者信息

Vos Jeffrey A, Abbondanzo Susan L, Barekman Carol L, Andriko Joann W, Miettinen Markku, Aguilera Nadine S

机构信息

Department of Hematopathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.

出版信息

Mod Pathol. 2005 May;18(5):693-704. doi: 10.1038/modpathol.3800346.

Abstract

Histiocytic sarcoma (HS) is a rare but controversial hematopoietic neoplasm. In the past, malignancies have been misclassified as histiocytic tumors due to overlapping histologic features and inadequate phenotypic data. CD163, a recently characterized hemoglobin scavenger receptor, appears to be a 'specific' marker of histiocytic lineage and a promising diagnostic tool for evaluating histiocytic neoplasms. Five cases of HS were studied to further elucidate the clinicopathologic features of these rare tumors and to demonstrate the diagnostic utility of CD163. Criteria for diagnosis included histologic and immunohistochemical evidence of histiocytic differentiation, CD45 positivity, and exclusion of lymphoid, epithelial, melanocytic and dendritic cell phenotype. Sites of disease included the colon (two cases), palate, inguinal lymph node, and testis. The clinical course was aggressive in 4/5 patients (survival=2-15 months). One patient with localized disease of the palate, survived 17 years after diagnosis. All patients with poor survival had tumors > or =3.5 cm. Histologically, all cases showed diffuse architecture with large, discohesive polygonal cells. Spindling of cells was focally noted. Hemophagocytosis was identified in 3/5 cases. A prominent inflammatory background was present in 4/5 tumors. All cases were immunoreactive for CD45, CD163, CD68, and lysozyme. S-100 was focally positive in 4/5 cases. Antibodies for melanocytic, epithelial, lymphoid, and dendritic cell markers were negative. Molecular studies showed monoclonal IgH gene rearrangements in three cases. Our findings suggest that HS is an uncommon neoplasm frequently extranodal in presentation and aggressive in behavior, with rare exceptions. Stage of disease and possibly tumor size are significant prognostic indicators. Molecular studies remain controversial in the diagnosis. The morphologic and phenotypic features are relatively uniform; however, the diagnosis requires exclusion of more common neoplasms by extensive immunophenotypic studies. CD163 appears to be a specific histiocytic marker and is important in establishing the diagnosis of HS.

摘要

组织细胞肉瘤(HS)是一种罕见但存在争议的造血系统肿瘤。过去,由于组织学特征重叠和表型数据不足,恶性肿瘤曾被误诊为组织细胞肿瘤。CD163是一种最近被鉴定的血红蛋白清除受体,似乎是组织细胞谱系的“特异性”标志物,也是评估组织细胞肿瘤的一种有前景的诊断工具。对5例HS病例进行研究,以进一步阐明这些罕见肿瘤的临床病理特征,并证明CD163的诊断效用。诊断标准包括组织细胞分化的组织学和免疫组化证据、CD45阳性,以及排除淋巴细胞、上皮细胞、黑素细胞和树突状细胞表型。疾病部位包括结肠(2例)、腭部、腹股沟淋巴结和睾丸。4/5的患者临床病程呈侵袭性(生存期=2 - 15个月)。1例腭部局限性疾病患者诊断后存活了17年。所有生存期短的患者肿瘤直径≥3.5 cm。组织学上,所有病例均显示弥漫性结构,有大的、分散的多边形细胞。局部可见细胞呈梭形。5例中有3例发现噬血细胞现象。5例肿瘤中有4例存在明显的炎症背景。所有病例对CD45、CD163、CD68和溶菌酶均呈免疫反应阳性。4/5的病例S - 100呈局灶性阳性。黑素细胞、上皮细胞、淋巴细胞和树突状细胞标志物的抗体均为阴性。分子研究显示3例存在单克隆IgH基因重排。我们的研究结果表明,HS是一种不常见的肿瘤,表现为常发生于结外且行为侵袭性,罕见例外情况。疾病分期以及可能的肿瘤大小是重要的预后指标。分子研究在诊断中仍存在争议。形态学和表型特征相对一致;然而,诊断需要通过广泛的免疫表型研究排除更常见的肿瘤。CD163似乎是一种特异性的组织细胞标志物,在HS的诊断中很重要。

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