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Pediatr Dermatol ; 29(5): 665-6, 2012.
Article in English | MEDLINE | ID: mdl-22329457

ABSTRACT

We report a large infiltrating atypical granular cell tumor in a child with Noonan syndrome. Even though granular cell tumors are rare in childhood, five cases have been reported in children with Noonan syndrome. This study compares these different cases and explores the possibility of activation of the granular cell by the Ras pathway.


Subject(s)
Granular Cell Tumor/diagnosis , Human Growth Hormone/therapeutic use , Noonan Syndrome/drug therapy , Child , Female , Granular Cell Tumor/genetics , Granular Cell Tumor/pathology , Granular Cell Tumor/surgery , Humans , Mutation , Noonan Syndrome/genetics , Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics , Treatment Outcome
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