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一种不寻常的皮肤病变作为早产儿脊柱裂的首发体征。

An unusual cutaneous lesion as the presenting sign of spinal dysraphism in a preterm infant.

作者信息

Tatli M Mansur, Kumral Abdullah, Duman Nuray, Ozkan Sebnem, Ozkan Hasan

机构信息

Department of Pediatrics, Faculty of Medicine, Dokuz Eylul University, 35340 Inciralti/Izmir, Turkey.

出版信息

Pediatr Dermatol. 2004 Nov-Dec;21(6):664-6. doi: 10.1111/j.0736-8046.2004.21611.x.

Abstract

We present a preterm female infant with an unusual vascular nevus on the lumbosacral and gluteal regions. Our clinical diagnosis was probable twin nevus, with a blanched nevus adjacent to a telangiectatic nevus, later complicated by ulceration. Ultrasonography and magnetic resonance imaging of the lumbosacral region revealed that her conus medullaris level was at L4 and the spinal cord was tethered by an intraspinal lipoma, without evidence of a hemangioma. We could not find any literature reporting the association of twin nevus with spinal dysraphism.

摘要

我们报告一例早产女婴,其腰骶部和臀部有一处不寻常的血管痣。我们的临床诊断可能为双痣,表现为一处苍白痣毗邻一处毛细血管扩张痣,后来出现了溃疡。腰骶部区域的超声检查和磁共振成像显示,她的脊髓圆锥水平位于L4,脊髓被椎管内脂肪瘤牵拉,未发现血管瘤迹象。我们未找到任何关于双痣与脊柱裂相关联的文献报道。

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