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浆膜腔局限性纤维瘤。免疫组织化学、电子显微镜及流式细胞术DNA研究

Localized fibrous tumor of the serosal cavities. Immunohistochemical, electron-microscopic, and flow-cytometric DNA study.

作者信息

el-Naggar A K, Ro J Y, Ayala A G, Ward R, Ordóñez N G

机构信息

Department of Pathology, University of Texas M. D. Anderson Cancer Center, Houston 77030.

出版信息

Am J Clin Pathol. 1989 Nov;92(5):561-5. doi: 10.1093/ajcp/92.5.561.

Abstract

Localized fibrous tumor of the serosal cavities (localized fibrous mesothelioma) is a generally benign spindle cell neoplasm of uncertain histogenesis. Fourteen histologically similar primary tumors from different mesothelium-lined sites (11 pleural and 1 each in the pericardium, peritoneal cavity, and pouch of Douglas) and 2 recurrences of those tumors (pericardium and pouch of Douglas) were examined histopathologically and by flow cytometry to relate histologic features and DNA ploidy to biologic behavior (follow-up, 48-255 months among 13 patients). All 16 tumors (14 primaries and 2 recurrences) displayed diploid DNA pattern, and none of 13 patients died of disease (1 patient was lost to follow-up). To elucidate the histogenesis, seven primary tumors were examined for vimentin and keratin immunostaining and six primary tumors were assessed by electron microscopy. All cases exhibited spindle-fibroblastic cell proliferation with a prominent hemangiopericytic pattern. All cases so examined had positive results for vimentin and negative results for keratin. Ultrastructurally, the tumor cells showed mesenchymal-fibroblastic features. These results support a mesenchymal origin, most likely from submesothelial fibroblasts. Further, this neoplasm may recur but retain its basic histologic features, diploidy, and benign outcome.

摘要

浆膜腔局限性纤维瘤(局限性纤维性间皮瘤)是一种组织发生不明的一般为良性的梭形细胞肿瘤。对来自不同间皮衬里部位的14例组织学相似的原发性肿瘤(11例胸膜肿瘤,心包、腹腔和Douglas陷凹各1例)以及其中2例肿瘤的复发灶(心包和Douglas陷凹)进行了组织病理学检查和流式细胞术检测,以将组织学特征和DNA倍性与生物学行为相关联(13例患者的随访时间为48 - 255个月)。所有16例肿瘤(14例原发性肿瘤和2例复发灶)均显示二倍体DNA模式,13例患者中无1例死于该疾病(1例患者失访)。为阐明组织发生,对7例原发性肿瘤进行了波形蛋白和角蛋白免疫染色检查,并通过电子显微镜对6例原发性肿瘤进行了评估。所有病例均表现为梭形纤维母细胞增殖,具有明显的血管外皮细胞瘤模式。所有接受检查的病例波形蛋白呈阳性,角蛋白呈阴性。超微结构上,肿瘤细胞表现出间充质 - 纤维母细胞特征。这些结果支持间充质起源,最可能来自间皮下成纤维细胞。此外,该肿瘤可能复发,但保留其基本组织学特征、二倍体状态和良性转归。

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