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. |
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Copyright © The Author(s), 2015. Published by Science Publishing Group |
Aplasia Cutis Congenita, Giant, Scalp
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[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. |
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
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
@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} }
TY - JOUR T1 - Giant Aplasia Cutis Congenita of the Scalp in a Newborn, Case Report AU - Albahri Z. AU - Krylová AU - K. AU - Al Mawiri A. AU - Bartoňová J. AU - Štefáčková Š. AU - Dočekalová Š. Y1 - 2015/07/23 PY - 2015 N1 - https://doi.org/10.11648/j.ajp.20150101.12 DO - 10.11648/j.ajp.20150101.12 T2 - American Journal of Pediatrics JF - American Journal of Pediatrics JO - American Journal of Pediatrics SP - 4 EP - 5 PB - Science Publishing Group SN - 2472-0909 UR - https://doi.org/10.11648/j.ajp.20150101.12 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 IS - 1 ER -