Literature DB >> 12415408

Sporadic aplasia cutis congenita.

Linda-Lynn Fagan1, Philip A Harris, Arnold G Coran, Robert Cywes.   

Abstract

Aplasia cutis congenita (ACC) is a rare group of disorders characterized by the focal absence of skin at birth. The majority of cases affect the scalp, but involvement of the trunk and extremities has been described. Proposed etiologies for ACC include infection, vascular malformations, amniogenesis, and teratogens, but no unifying theory has been identified. We present the case of a 1-day-old female with large, bilateral posterolateral trunk skin defects noted at birth. The prenatal history was significant for maternal diabetes, fetal papyraceus at 12 weeks' gestation, and a family history of limb defects. The infant was treated non-surgically with local wound care and antibiotics, as well as frequent dressing changes. The areas of absent skin developed a granulation-tissue layer followed by re-epithelialization and mild wound contracture. With early identification of the etiology of the lesions and appropriate investigation and treatment, including conservative wound management, aplastic lesions can heal successfully without affecting growth, but may require cosmetic repair at a later stage.

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Year:  2002        PMID: 12415408     DOI: 10.1007/s00383-002-0812-5

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  2 in total

Review 1.  A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents.

Authors:  Liwen Xu; Kevin X Liu; Maryanne M Senna
Journal:  Front Med (Lausanne)       Date:  2017-07-24

2.  Like Father, Like Daughter-inherited cutis aplasia occurring in a family with Marfan syndrome: a case report.

Authors:  Yasmin Florence Khodeja Islam; Charles A Williams; Jennifer Jane Schoch; Israel David Andrews
Journal:  Clin Case Rep       Date:  2016-12-20
  2 in total

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