Multiple skalp ve ekstremite yerleşimli aplasia kutis konjenita

Işıl Göğem İmren; Şeniz Duygulu; H. Meral Ekşioğlu

doi:10.31362/patd.707279

Olgu Sunumu

Aplasia kutis congenita with multiple scalp and limb locations

Yıl 2021, Cilt: 14 Sayı: 1, 267 - 270, 04.01.2021

Işıl Göğem İmren , Şeniz Duygulu , H. Meral Ekşioğlu

https://doi.org/10.31362/patd.707279

Öz

Aplasia cutis congenita is a rarely seen heterogenous group of disease characterized by the absence of a portion of skin, subdermal tissue, infrequently bone and meninges. Aplasia cutis congenita is typically sporadic; however, syndromic cases have also been reported. In this report, we present sporadic case, two-day old baby who had multiple scalp and extremity defect.
We aimed to remind the rare entity in differential diagnosis of scalp defects.

Aplazia kutis konjenita, deri, subkutan doku, seyrek olarak kemik ve meninkslerin yokluğu ile karakterize, nadir görülen heterojen bir hastalık grubudur. Tipik olarak aplasia kutis konjenita sporadik vakalar olarak görülmekle birlikte, sendromik vakalar da bildirilmiştir. Bu vaka sunumunda, 2 günlük bebekte multiple skalp derisi ve ekstremite defekti ile prezente olan sporadik bir aplasia kutis konjenita olgusu ile literatüründe seyrek rastlanan antiteyi skalp defectlerinin ayırıcı tanısında hatırlatmayı amaçladık

Anahtar Kelimeler

aplasia cutis kongenita, scalp, congenital malformation

Kaynakça

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