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以纤维发育异常为主要特征的胫骨造釉细胞瘤——病例报告

Adamantinoma of tibia with predominant features of fibrous dysplasia--a case report.

作者信息

Kim J Y, Kang G H, Chi J G

机构信息

Department of Pathology, Seoul National University, College of Medicine, Seoul, Korea.

出版信息

J Korean Med Sci. 1996 Oct;11(5):444-8. doi: 10.3346/jkms.1996.11.5.444.

Abstract

We report a case of adamantinoma of the tibia resembling fibrous dysplasia. The patient was a 55-year-old male, and complained of pain in the right lower leg. Roentgenographs showed a well demarcated osteolytic lesion with small foci of calcification and septation within the diaphysis of the distal tibia. The cortex was partially disrupted. Histologically, initial biopsy specimen showed fibrous connective tissue and trabeculae of immature woven bone, strongly suggestive of fibrous dysplasia. The lesion recurred and the second biopsy revealed nests of spindle cells and tubular epithelial structures embedded in granulation type-fibrous tissue. Immunohistochemically, both the nests of spindle cells and the tubular structures gave a positive reaction for cytokeratin. The present case emphasizes once again that histological diagnosis of fibrous dysplasia of the tibia should be made carefully with exclusion of the possibility of adamantinoma.

摘要

我们报告一例胫骨造釉细胞瘤,其表现类似骨纤维异常增殖症。患者为一名55岁男性,主诉右小腿疼痛。X线片显示在胫骨远端骨干有一个边界清晰的溶骨性病变,伴有小的钙化灶和骨小梁分隔。皮质部分中断。组织学上,最初的活检标本显示为纤维结缔组织和未成熟编织骨的骨小梁,强烈提示骨纤维异常增殖症。病变复发,第二次活检显示在肉芽组织样纤维组织中存在梭形细胞巢和管状上皮结构。免疫组织化学检查显示,梭形细胞巢和管状结构均对细胞角蛋白呈阳性反应。本例再次强调,对于胫骨骨纤维异常增殖症的组织学诊断应谨慎进行,排除造釉细胞瘤的可能性。

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Dedifferentiated adamantinoma associated with fibrous dysplasia.骨化性纤维瘤伴去分化的骨样骨瘤。
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