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完全性多指畸形:1例报告及尺侧多指畸形文献复习

Complete digital duplication: a case report and review of ulnar polydactyly.

作者信息

de la Torre J, Simpson R L

机构信息

Division of Plastic Surgery, Nassau County Medical Center, East Meadow, NY 11554, USA.

出版信息

Ann Plast Surg. 1998 Jan;40(1):76-9. doi: 10.1097/00000637-199801000-00017.

Abstract

An unusual case is presented of bilateral, complete digital duplication on the hand of a 9-month-old boy. Radiographic evaluation showed duplication of intact phalanges and metacarpals. Although ulnar polydactyly has been described as one of the most common congenital anomalies of the extremities, it usually manifests itself as a rudimentary skin tag. Ulnar polydactyly can be classified on the basis of genetic, morphologic, and clinical implications. Although polydactyly is reported to occur among approximately 1 in 1000 live births, most of these malformations are rudimentary skin tags. Complete ulnar polydactyly is uncommon; it occurs among approximately 0.014% of all live births. The main goal of surgical treatment of patients with complete-duplication ulnar polydactyly is to establish adequate function. This case report describes the preoperative evaluation and management of complete bilateral duplication of the ulnar digits of the hand.

摘要

本文介绍了一例罕见病例,一名9个月大男婴手部出现双侧完全性手指重复畸形。影像学评估显示指骨和掌骨完整重复。尽管尺侧多指畸形被认为是最常见的肢体先天性畸形之一,但通常表现为发育不全的皮赘。尺侧多指畸形可根据遗传、形态学和临床意义进行分类。虽然据报道多指畸形在每1000例活产中约有1例发生,但这些畸形大多是发育不全的皮赘。完全性尺侧多指畸形并不常见,约占所有活产的0.014%。手术治疗完全性重复尺侧多指畸形患者的主要目标是建立足够的功能。本病例报告描述了手部尺侧手指完全双侧重复畸形的术前评估和处理。

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