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一名3岁儿童的经典型造釉细胞瘤。

Classic adamantinoma in a 3-year-old.

作者信息

Kumar D, Mulligan M E, Levine A M, Dorfman H D

机构信息

Department of Pathology, University of Maryland School of Medicine, Baltimore 21201, USA.

出版信息

Skeletal Radiol. 1998 Jul;27(7):406-9. doi: 10.1007/s002560050409.

Abstract

Classic adamantinoma of the long bones is a rare, low-grade malignant neoplasm arising most often in the tibia and usually in patients during the second to fifth decades. Although adamantinomas have been described in children, the histologic pattern in this age group is different from that seen in adults and resembles osteofibrous dysplasia. The usual pattern of adamantinoma in children has been termed "differentiated adamantinoma" and follows a benign course. We report a case of adamantinoma in the proximal tibia of a 3-year-old patient. The lesion had abundant epithelial component with formation of keratin pearls, a pattern that has been described only in classic adamantinoma occurring in adults. Since differentiated adamantinomas are essentially benign and classic adamantinomas are low-grade malignancies, the finding of a classic variant at this young age raised important therapeutic and prognostic issues.

摘要

长骨经典型造釉细胞瘤是一种罕见的低级别恶性肿瘤,最常发生于胫骨,患者通常为二三十岁至四五十岁。虽然儿童中也有造釉细胞瘤的报道,但该年龄组的组织学模式与成人不同,类似于骨纤维发育不良。儿童造釉细胞瘤的常见模式被称为“分化型造釉细胞瘤”,病程呈良性。我们报告一例3岁患者胫骨近端造釉细胞瘤。病变有丰富的上皮成分并形成角化珠,这种模式仅在成人的经典型造釉细胞瘤中被描述过。由于分化型造釉细胞瘤本质上是良性的,而经典型造釉细胞瘤是低级别恶性肿瘤,在这个年幼患者中发现经典型变异提出了重要的治疗和预后问题。

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