Literature DB >> 26724883

Aplasia Cutis Congenita in a Newborn Child Associated with Two Fetus Papyraceous.

Dubravka Šimić1, Asja Prohić, Neira Puizina Ivić, Jasna Zeljko Penavić, Teo Tomić.   

Abstract

Aplasia cutis congenita (ACC) is a rare inborn lesion, presenting with absence of skin. The etiology is unknown and is probably not attributable to a single cause but to a combination of genetic factors. Multiple causes have been suggested for ACC: syndromes and teratogens, intrauterine infection--varicella zoster virus, herpes simplex virus--fetal exposure to cocaine, heroin, alcohol, or antithyroid drugs. The most common site is the scalp. We report a case with multiple lesions on the trunk, resembling an instance with ACC group 5. This form of ACC occurs in association with the in utero death of a twin or more (in this case triple) fetus. Histological findings are available in very few reports. Therapy options depend on the characteristics of the lesion, but conservative treatment is usually chosen.

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Year:  2015        PMID: 26724883

Source DB:  PubMed          Journal:  Acta Dermatovenerol Croat        ISSN: 1330-027X            Impact factor:   1.256


  2 in total

1.  Aplasia cutis congenita: Two case reports and discussion of the literature.

Authors:  Alexandros Blionas; Dimitrios Giakoumettis; Elias Antoniades; Evangelos Drosos; Andreas Mitsios; Sotirios Plakas; Georgios Sfakianos; Marios S Themistocleous
Journal:  Surg Neurol Int       Date:  2017-11-09

Review 2.  Multiple aplasia cutis congenita type V and fetus papyraceous: a case report and review of the literature.

Authors:  V Thadchanamoorthy; Kavinda Dayasiri; M Thirukumar; N Thamilvannan; S H Chandraratne
Journal:  J Med Case Rep       Date:  2021-03-04
  2 in total

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