Document Detail


Unusual cystic scalp lesions in Gorlin syndrome: a brief report.
MedLine Citation:
PMID:  20537080     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Nevoid basal cell carcinoma syndrome (Gorlin syndrome) is a rare, autosomal dominant syndrome that is known to have variable expressivity in multiple organ systems. We describe the case of a young male child with nevoid basal cell carcinoma syndrome and scalp lesions, including a branchial cleft cyst with respiratory epithelium and a rudimentary meningocele. These are both new, previously unreported findings, possibly associated with nevoid basal cell carcinoma syndrome.
Authors:
Alyssa B Findley; Howard Pride
Publication Detail:
Type:  Case Reports; Journal Article    
Journal Detail:
Title:  Pediatric dermatology     Volume:  27     ISSN:  1525-1470     ISO Abbreviation:  Pediatr Dermatol     Publication Date:    2010 Mar-Apr
Date Detail:
Created Date:  2010-06-11     Completed Date:  2010-09-27     Revised Date:  2011-01-11    
Medline Journal Info:
Nlm Unique ID:  8406799     Medline TA:  Pediatr Dermatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  204-7     Citation Subset:  IM    
Affiliation:
Department of Dermatology, Geisinger Medical Center, Danville, Pennsylvania, USA. agfindley@geisinger.edu
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MeSH Terms
Descriptor/Qualifier:
Basal Cell Nevus Syndrome / diagnosis*,  genetics,  pathology
Branchioma / diagnosis*,  genetics,  pathology
Child
Head and Neck Neoplasms / diagnosis*,  genetics,  pathology
Humans
Male
Scalp*
Skin Neoplasms / diagnosis*,  genetics,  pathology

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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