Literature DB >> 17910709

Aplasia cutis congenita: a rare cutaneous sign of split cord malformations.

Yusuf Izci1, Müzeyyen Gönül, Halil Ibrahim Secer, Engin Gönül.   

Abstract

BACKGROUND: Aplasia cutis congenita (ACC) is characterized by the absence of a portion of skin in a localized or widespread area at birth. It manifests usually as a solitary defect on the scalp, but sometimes may occur on the face, trunk, or limbs. ACC is most often a benign isolated defect, but can be associated with other physical anomalies or malformation syndromes. A few cases have been reported in which patients with split cord malformation (SCM) have presented with ACC.
METHODS: Two patients with SCM are reported.
RESULTS: Both patients presented with ACC and abnormal hair growth on their backs. Type II SCM was detected in the first patient and Type I SCM in the second. No surgical treatment was performed because the patients were neurologically intact.
CONCLUSIONS: ACC may seldom manifest as a skin marker of SCM. Our patients are unique examples of SCM presenting with ACC, but not requiring surgery. It is important to recognize ACC as a cutaneous sign of SCM, and to refer these patients to radiologic evaluation as soon as possible.

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Year:  2007        PMID: 17910709     DOI: 10.1111/j.1365-4632.2007.03212.x

Source DB:  PubMed          Journal:  Int J Dermatol        ISSN: 0011-9059            Impact factor:   2.736


  3 in total

1.  Hemimyeloschisis associated with hydrocephalus.

Authors:  Yusuf Izci
Journal:  Childs Nerv Syst       Date:  2015-11-25       Impact factor: 1.475

2.  Split cord malformation types I and II: a personal series of 131 patients.

Authors:  Yusuf Erşahin
Journal:  Childs Nerv Syst       Date:  2013-09-07       Impact factor: 1.475

3.  Aplasia cutis congenita associated with type I split cord malformation: Unusual case.

Authors:  Bashar Abuzayed; Pamir Erdincler
Journal:  J Pediatr Neurosci       Date:  2014-01
  3 in total

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