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Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report

Received: 2 July 2015    Accepted: 20 July 2015    Published: 23 July 2015
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Abstract

Aplasia cutis congenita is a rare disease of unknown etiology, usually affects the scalp, but any part of the body may be affected, full thickness loss is extremely rare. We report a case of a boy born with a large scalp and skull defect measuring 8*9 cm without associated anomalies. After 2 years follow up with conservative treatment, the patient now is without neurodeficit, with approximately healing of affected skine and small reduction of the bone defected size.

Published in American Journal of Pediatrics (Volume 1, Issue 1)
DOI 10.11648/j.ajp.20150101.12
Page(s) 4-5
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Aplasia Cutis Congenita, Giant, Scalp

References
[1] Frieden IJ. Aplasia cutis congenita: a clinical review and proposal for classification. J Am Acad Dermatol 1986;14:646-660.
[2] A Burkhead1, G Poindexter2 and D S Morrell2. A case of extensive Aplasia Cutis Congenita with underlying skull defect and central nervous system malformation: discussion of large skin defects, complications, treatment and outcome. Journal of Perinatology 2009;29:582–584.
[3] Evers ME, Steijlen PM, Hamel BC. Aplasia cutis congenita and associated disorders: an update. Clin Genet 1995;47(6): 295-301.
[4] Maillet-Declerck M, Vinchon M, Guerreschi P, Pasquesoone L, Dhellemmes P, Duquennoy-Martinot V, Pellerin P. Aplasia cutis congenita: review of 29 cases and proposal of a therapeutic strategy. Eur J Pediatr Surg. 2013;23(2):89-93.
[5] Blunk K, Quan V, Carr C. Aplasia cutis congenita: a clinical review and associated defects. Neonatal Network 1992;11:17-27.
Cite This Article
  • APA Style

    Albahri Z., Krylová, K., Al Mawiri A., Bartoňová J., et al. (2015). Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report. American Journal of Pediatrics, 1(1), 4-5. https://doi.org/10.11648/j.ajp.20150101.12

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    ACS Style

    Albahri Z.; Krylová; K.; Al Mawiri A.; Bartoňová J., et al. Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report. Am. J. Pediatr. 2015, 1(1), 4-5. doi: 10.11648/j.ajp.20150101.12

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    AMA Style

    Albahri Z., Krylová, K., Al Mawiri A., Bartoňová J., et al. Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report. Am J Pediatr. 2015;1(1):4-5. doi: 10.11648/j.ajp.20150101.12

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  • @article{10.11648/j.ajp.20150101.12,
      author = {Albahri Z. and Krylová and K. and Al Mawiri A. and Bartoňová J. and Štefáčková Š. and Dočekalová Š.},
      title = {Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report},
      journal = {American Journal of Pediatrics},
      volume = {1},
      number = {1},
      pages = {4-5},
      doi = {10.11648/j.ajp.20150101.12},
      url = {https://doi.org/10.11648/j.ajp.20150101.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajp.20150101.12},
      abstract = {Aplasia cutis congenita is a rare disease of unknown etiology, usually affects the scalp, but any part of the body may be affected, full thickness loss is extremely rare. We report a case of a boy born with a large scalp and skull defect measuring 8*9 cm without associated anomalies. After 2 years follow up with conservative treatment, the patient now is without neurodeficit, with approximately healing of affected skine and small reduction of the bone defected size.},
     year = {2015}
    }
    

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    T1  - Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report
    AU  - Albahri Z.
    AU  - Krylová
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    AU  - Dočekalová Š.
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    JO  - American Journal of Pediatrics
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    AB  - Aplasia cutis congenita is a rare disease of unknown etiology, usually affects the scalp, but any part of the body may be affected, full thickness loss is extremely rare. We report a case of a boy born with a large scalp and skull defect measuring 8*9 cm without associated anomalies. After 2 years follow up with conservative treatment, the patient now is without neurodeficit, with approximately healing of affected skine and small reduction of the bone defected size.
    VL  - 1
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Author Information
  • Department of Pediatrics, Faculty hospital, Charles University in Hradec Králové, Czech Republic

  • Department of Internal medicine, Faculty hospital, Charles University in Hradec Králové, Czech Republic

  • Pediatric Dermatology, Faculty hospital, Charles University in Hradec Králové, Czech Republic

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