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前连合钙化性脂肪瘤合并皮下脂肪瘤和胼胝体发育不全:一种罕见的中线颅面发育不良表现。

Anterior interhemispheric calcified lipoma together with subcutaneous lipoma and agenesis of corpus callosum: a rare manifestation of midline craniofacial dysraphism.

机构信息

Department of Radiology, Faculty of Medicine, Harran University, 63300, Sanliurfa, Turkey.

出版信息

Jpn J Radiol. 2013 Jul;31(7):496-9. doi: 10.1007/s11604-013-0200-1. Epub 2013 Mar 17.

Abstract

Frontonasal dysplasia (FND) or craniofacial dysraphism includes a variety of craniofacial defects. FNDs are rarely associated with intracranial lipoma. The majority of intracranial lipomas are incidentally identified on radiological examinations. They are commonly accompanied by other congenital intracranial malformations. Moreover, they are rarely associated with subcutaneous lipoma. We present a rare case of midline craniofacial dysraphism with interhemispheric calcified lipoma together with subcutaneous lipoma and agenesis of the corpus callosum.

摘要

额鼻发育不全(FND)或颅面发育不良包括各种颅面缺陷。FND 很少与颅内脂肪瘤相关。大多数颅内脂肪瘤是在影像学检查中偶然发现的。它们通常伴有其他先天性颅内畸形。此外,它们很少与皮下脂肪瘤相关。我们报告了一例罕见的中线颅面发育不良病例,该病例伴有半球间钙化脂肪瘤,以及皮下脂肪瘤和胼胝体发育不全。

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