Fetüs Papyraceus ile İlişkili Aplazia Kutis Konjenita

Yıl 2015, , 147 - 150, 01.09.2015

Ahmet Özdemir Osman Baştuğ Serra Alçı Levent Korkmaz Hülya Halis Sabriye Korkut Mehmet Adnan Öztürk Tamer Güneş

https://doi.org/10.4274/jcp.04274

Öz

Aplazia kutis konjenita AKK derinin lokalize veya geniş alanlar şeklinde yokluğu ile karakterize nadir bir anomalidir. Genellikle skalpta görülmekle birlikte, tek veya multipl lezyonlar şeklinde vücudun herhangi bir yerinde bulunabilir. On bin doğumda bir görülen AKK izole bir lezyon olarak ortaya çıkabildiği gibi, yarık damak/dudak, sindaktili, parmakların yokluğu, göz anomalileri ve konjenital kalp hastalıkları ile birlikte görülebilir. AKK’nin oldukça nadir görülen bir formu da intrauterin ex olan ikiz eşine bağlı gelişen formudur. Büyük lezyonlar cerrahi onarıma gerek duyarken, küçük defektler spontan re-epitelizasyon ile iyileşebilir. Bu yazıda; nadir olarak görülen, fetüs papyraceus ile ilişkili olarak gövdesinde AKK gelişen erkek olgu sunulmuştur

Anahtar Kelimeler

Aplazia kutis konjenita, re-epitelizasyon, ikiz

Aplasia Cutis Congenita Association with Fetus Papyraceus

Öz

Aplasia cutis congenita ACC is a rare malformation characterized by localized or a wide area absence of tissue. The disease may involve any site of the body, although usually seen on the scalp. Observed one in 10.000 births, it can occur as the ACC as an isolated lesion and may be associated with cleft palate/lip, syndactyly, absence of fingers, eye abnormalities and congenital heart disease. ACC’s a rare form due to intrauterine twin, which is a form of ex. Large lesions that require surgical repair small defects heal spontaneously with re-epithelialization. We present a rare case of newborn male with truncal ACC associated with fetus papyraceus

Anahtar Kelimeler

Aplasia cutis congenita, re-epithelialization, twins

Kaynakça

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