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Multiple pilomatricomas in Rubinstein-Taybi syndrome: a case report.
- Source :
-
Pediatric dermatology [Pediatr Dermatol] 1994 Mar; Vol. 11 (1), pp. 21-5. - Publication Year :
- 1994
-
Abstract
- Rubinstein-Taybi syndrome is a multisystem developmental disorder due to an autosomal dominant mutation. It is clinically defined by the presence of peculiar facies, mental retardation, and broad thumbs and first toes. Important dermatologic findings include hirsutism, keloids, hemangiomas, and dermatoglyphic abnormalities. We report a 12-year-old girl with the typical phenotype of Rubinstein-Taybi syndrome, associated with numerous pilomatricomas. These are benign epithelial neoplasms with hair cell differentiation that may have a familial transmission. Pilomatricomas have not been reported in patients with Rubinstein-Taybi syndrome, although their association with myotonic dystrophy, another autosomal dominant disorder, is well known. Possibilities to explain the association include contiguous gene syndrome, the action of a pleiotropic gene, predisposition to malformations, and mere coincidence.
- Subjects :
- Child
Female
Follow-Up Studies
Hair Diseases pathology
Humans
Neoplasm Recurrence, Local pathology
Pilomatrixoma pathology
Rubinstein-Taybi Syndrome pathology
Skin Neoplasms pathology
Hair Diseases complications
Pilomatrixoma complications
Rubinstein-Taybi Syndrome complications
Skin Neoplasms complications
Subjects
Details
- Language :
- English
- ISSN :
- 0736-8046
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Pediatric dermatology
- Publication Type :
- Academic Journal
- Accession number :
- 8170843
- Full Text :
- https://doi.org/10.1111/j.1525-1470.1994.tb00067.x