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伴有角质囊肿形成的同步性皮质内成釉细胞瘤

Synchronous intracortical adamantinomas with keratin cyst formation.

作者信息

Park Yong-Koo, Ryu Kyung Nam, Han Chung Soo

机构信息

Department of Pathology, College of Medicine, Kyung Hee University Hospital, 1 Hoeki-dong, Dongdaemoon-gu, Seoul, South Korea.

出版信息

Skeletal Radiol. 2006 Mar;35(3):185-9. doi: 10.1007/s00256-005-0005-0. Epub 2005 Oct 11.

Abstract

Adamantinoma of the long bones is a rare primary bone tumor of uncertain embryogenesis. It tends to involve the tibia almost exclusively. We report on adamantinomas occurring in a 16-year-old male patient, with synchronous tibial and fibular lesions. Histologically, there were characteristic clusters of epithelial cells in a fibrous background, forming a keratin cyst. Immunohistochemically, these cells were strongly positive for cytokeratin. This keratin cyst formation is quite an unusual finding in classic adamantinoma.

摘要

长骨造釉细胞瘤是一种胚胎发生尚不明确的罕见原发性骨肿瘤。它几乎只累及胫骨。我们报告了一名16岁男性患者发生的造釉细胞瘤,同时存在胫骨和腓骨病变。组织学上,在纤维背景中有特征性的上皮细胞簇,形成角质囊肿。免疫组化显示,这些细胞细胞角蛋白呈强阳性。这种角质囊肿的形成在经典造釉细胞瘤中是相当不寻常的发现。

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