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手部指骨骨内高分化骨肉瘤

Phalangeal intraosseous well-differentiated osteosarcoma of the hand.

作者信息

Sugano I, Tajima Y, Ishida Y, Nagao T, Nagao K, Saga N, Ohno T, Miyakawa E

机构信息

Department of Pathology, Teikyo University Ichihara Hospital, Chiba-Ken, Japan.

出版信息

Virchows Arch. 1997 Feb;430(2):185-9. doi: 10.1007/BF01008041.

Abstract

A case of intraosseous well-differentiated osteosarcoma in one phalanx of the hand is reported. A 78-year-old man noticed swelling in the little finger of his right hand approximately 7 years before referral. Imaging disclosed a tumour with a "ground glass" appearance and irregular mottled calcification occupying almost all of the phalanx marrow and suggested slight invasion into the soft tissue. Open biopsy suggested a diagnosis of well-differentiated fibroblastic osteosarcoma. The finger and its metacarpal bone were amputated and a tumour measuring 3.5 x 2.2 x 2.0 cm and with an indistinct soft tissue margin was found in the bone marrow. Histologically, the tumour was composed of fibroblastic cells with few mitoses, and neoplastic bone formation was apparent. Although the tumour appeared to be a fibrous dysplasia, the presence of nuclear atypia, hypercellularity, and the absence of a typical woven bone pattern in addition to the soft tissue invasion indicated otherwise. Ultrastructural examination showed focal myofibroblastic differentiation, and immunohistochemistry revealed smooth muscle actin, vimentin, osteocalcin, osteonectin and MIBI in the tumour cells. This ultrastructural and immunohistochemical study is believed to be the first detailed report of an intraosseous well-differentiated osteosarcoma of phalangeal bone.

摘要

报告了1例手部1个指骨的骨内高分化骨肉瘤病例。一名78岁男性在转诊前约7年发现右手小指肿胀。影像学检查显示一个呈“磨玻璃”样外观且伴有不规则斑点状钙化的肿瘤,几乎占据了整个指骨髓腔,并提示有轻微软组织浸润。切开活检提示诊断为高分化纤维母细胞性骨肉瘤。该手指及其掌骨被截肢,在骨髓中发现一个大小为3.5×2.2×2.0 cm、软组织边缘不清的肿瘤。组织学上,肿瘤由有少量核分裂象的纤维母细胞组成,可见肿瘤性骨形成。尽管该肿瘤看似纤维结构不良,但核异型性、细胞增多以及除软组织浸润外缺乏典型编织骨模式等表现提示并非如此。超微结构检查显示局灶性肌纤维母细胞分化,免疫组化显示肿瘤细胞中有平滑肌肌动蛋白、波形蛋白、骨钙素、骨连接蛋白和MIBI。据信,这项超微结构和免疫组化研究是指骨骨内高分化骨肉瘤的首份详细报告。

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