Cutaneous and superficial soft tissue lesions associated with Albright hereditary osteodystrophy: clinicopathological and molecular genetic study of 4 cases, including a novel mutation of the GNAS gene.

Abstract

Albright hereditary osteodystrophy is a rare syndrome, in which cutaneous and superficial soft tissue lesions traditionally include osteomas and calcifications. We report 4 patients from 2 families affected with Albright hereditary osteodystrophy and demonstrate that the spectrum of these cutaneous and soft tissue lesions is broader than is usually defined in the literature. In addition to osteomas in the dermis and subcutis, including so-called plaque-like osteoma, we identified the following lesions: calcifying aponeurotic fibroma-like lesion, calcinosis circumscripta-like lesion, and unusual nevi with osteoid and/or peculiar intranuclear pseudoinclusions. One osteoma and the calcifying aponeurotic fibroma-like lesion were analyzed by HUMARA and proved to be clonal. In a family, a novel mutation in the GNAS gene was also identified.

• Authors: Denisa Kacerovska, Jana Nemcova, Renata Pomahacova, Michal Michal, Dmitry V Kazakov
• Journal: The American Journal of dermatopathology (Am J Dermatopathol) Vol. 30 Issue 5 Pg. 417-24 (Oct 2008) ISSN: 1533-0311 [Electronic] United States
• PMID: 18806481 (Publication Type: Case Reports, Journal Article)

Chemical References

• Chromogranins
• GNAS protein, human
• GTP-Binding Protein alpha Subunits, Gs

Topics

• Adult
• Bone Neoplasms (diagnosis, genetics, pathology)
• Calcinosis (diagnosis, genetics, pathology)
• Child
• Child, Preschool
• Chromogranins
• Female
• Fibroma (diagnosis, genetics, pathology)
• Fibrous Dysplasia, Polyostotic (diagnosis, genetics, pathology)
• GTP-Binding Protein alpha Subunits, Gs (genetics)
• Humans
• Male
• Mutation (genetics)
• Nevus (diagnosis, genetics, pathology)
• Osteoma (diagnosis, genetics, pathology)
• Skin Neoplasms (diagnosis, genetics, pathology)