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淋巴结的网状细胞肿瘤:11例临床病理研究,其中识别出一种源自成纤维网状细胞的新亚型。

Reticulum cell neoplasms of lymph nodes: a clinicopathologic study of 11 cases with recognition of a new subtype derived from fibroblastic reticular cells.

作者信息

Andriko J W, Kaldjian E P, Tsokos M, Abbondanzo S L, Jaffe E S

机构信息

Department of Hematatologic and Lymphatic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.

出版信息

Am J Surg Pathol. 1998 Sep;22(9):1048-58. doi: 10.1097/00000478-199809000-00002.

Abstract

Lymph nodes contain nonlymphoid accessory cells including follicular dendritic cells (FDCs), interdigitating dendritic cells (IDCs) and fibroblastic reticular cells (FBRCs). Neoplasms derived from FDCs are uncommon, and those of IDC origin are even more rare. We report the clinicopathologic features of 11 reticulum cell neoplasms, including 2 of FBRC origin. There were seven male patients and four female patients ranging in age from 13 to 73 years. All cases involved lymph nodes (cervical or supraclavicular-6 cases), (abdominal--2 cases), epitrochlear (1 case); two had more than one site of involvement (cervical lymph node and mediastinum--1 case, cervical and abdominal lymph nodes--1 case). One case of FDC tumor had concomitant Castleman's disease, plasma cell variant. Each neoplasm showed similar histology with oval-to-spindle-shaped cells in a storiform or fascicular pattern. Based on immunophenotypic findings, the neoplasms were classified as FDC (five cases), IDC (two cases), FBRC (three cases), and reticulum cell neoplasm, not otherwise specified (one case). The FDC tumors showed immunoreactivity for CD21 or CD35, vimentin, and CD68. The IDC tumors showed strong positivity for S-100 protein and variable positivity for CD68 and CD1a. The cases derived from FBRCs were positive for vimentin, desmin, and smooth-muscle actin. The neoplasm classified as reticulum cell neoplasm, not otherwise specified had similar morphologic features but showed only equivocal positivity for CD68 and vimentin. Follow-up was available for 9 of 11 (82%) cases with a mean of 3.5 years. Four of five patients with FDC tumors were alive with disease when last seen; the fifth is alive and well with no evidence of disease at 4-year follow-up. One patient with IDC tumor had a recurrence in a different nodal site. Two patients with FBRC tumor were disease free at follow-up of 2 years and 8 years, respectively. The patient with reticulum cell neoplasm, not otherwise specified, was alive and disease free 8 years after diagnosis.

摘要

淋巴结包含非淋巴细胞辅助细胞,包括滤泡树突状细胞(FDC)、交错突细胞(IDC)和成纤维网状细胞(FBRC)。源自FDC的肿瘤并不常见,源自IDC的肿瘤则更为罕见。我们报告了11例网状细胞肿瘤的临床病理特征,其中包括2例源自FBRC的肿瘤。患者有7名男性和4名女性,年龄在13岁至73岁之间。所有病例均累及淋巴结(颈部或锁骨上淋巴结6例)、(腹部淋巴结2例)、滑车上淋巴结(1例);2例有多个受累部位(颈部淋巴结和纵隔1例、颈部和腹部淋巴结1例)。1例FDC肿瘤合并有浆细胞型Castleman病。每个肿瘤均显示出相似的组织学特征,细胞呈椭圆形至梭形,呈车辐状或束状排列。根据免疫表型结果,这些肿瘤被分类为FDC肿瘤(5例)、IDC肿瘤(2例)、FBRC肿瘤(3例)和未另行指定的网状细胞肿瘤(1例)。FDC肿瘤对CD21或CD35、波形蛋白和CD68呈免疫反应性。IDC肿瘤对S-100蛋白呈强阳性,对CD68和CD1a呈可变阳性。源自FBRC的病例对波形蛋白、结蛋白和平滑肌肌动蛋白呈阳性。分类为未另行指定的网状细胞肿瘤的肿瘤具有相似的形态学特征,但仅对CD68和波形蛋白呈可疑阳性。11例患者中有9例(82%)获得随访,平均随访时间为3.5年。5例FDC肿瘤患者中,4例在最后一次就诊时仍患有疾病存活;第5例在4年随访时存活且状况良好,无疾病证据。1例IDC肿瘤患者在不同的淋巴结部位复发。2例FBRC肿瘤患者在分别随访2年和8年时无疾病。未另行指定的网状细胞肿瘤患者在诊断后存活8年且无疾病。

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