Osteoma cutis in Pseudohypoparathyroidism

Pseudohypoparathyroidism (PHP) is a hereditary disorder characterized by an end-organ resistance for parathormone. PHP can be classified into different types by biochemical and phenotypic characteristics and the level of the defect in the hormone-receptor complex. PHP is described as Albright’s here...

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Veröffentlicht in:	Dermatology (Basel) 1999-01, Vol.198 (2), p.209-211
Hauptverfasser:	Goeteyn, V., de Potter, C.R., Naeyaert, J.M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Calcium - metabolism Dermatology Female Humans Medical sciences Ossification, Heterotopic - complications Ossification, Heterotopic - pathology Ossification, Heterotopic - surgery Pseudohypoparathyroidism - complications Pseudohypoparathyroidism - metabolism Skin Diseases - complications Skin Diseases - pathology Skin Diseases - surgery Tumors of the skin and soft tissue. Premalignant lesions
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Beschreibung
Zusammenfassung:	Pseudohypoparathyroidism (PHP) is a hereditary disorder characterized by an end-organ resistance for parathormone. PHP can be classified into different types by biochemical and phenotypic characteristics and the level of the defect in the hormone-receptor complex. PHP is described as Albright’s hereditary osteodystrophy (AHO) when a specific phenotype is present. We report a case of osteoma cutis in a 30-year-old woman with AHO. Successful treatment was obtained by debriding the lesion followed by split-thickness skin grafting.
ISSN:	1018-8665 1421-9832
DOI:	10.1159/000018115