Osteoma Cutis as a Presenting Sign of Pseudohypoparathyroidism

J. S. Prendiville, A. W. Lucky, S. B. Mallory, Z. Mughal, F. Mimouni, C. B. Langman

Research output: Contribution to journalArticlepeer-review

41 Scopus citations

Abstract

Abstract: Four unrelated children with oosteoma cutis and Albright hereditary osteodystrophy (pseudohypoparathyroidism and pseudopseudohypoparathyroidism) are described. All four patients were normocalcemic when they were first seen with cutaneous ossification. A diagnosis of Albright hereditary osteodystrophy was established on the basis of associated somatic features, radiographic abnormalities, and family history. Progression to pseudohypoparathyroidism was documented in two children who developed hypocalcemia at 2 and 3 years of age, respectively. Early recognition of the skin manifestations of this syndrome and careful follow‐up are important to prevent the deleterious effects of hypocalcemia. Osteoma cutis is a common sign of Albright hereditary osteodystrophy in infancy and childhood, and its significance should not be overlooked, even in the normocalcemic patient.

Original languageEnglish (US)
Pages (from-to)11-18
Number of pages8
JournalPediatric Dermatology
Volume9
Issue number1
DOIs
StatePublished - Jan 1 1992

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Dermatology

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