Osteoma cutis as the presenting feature of albright hereditary osteodystrophy associated with pseudopseudohypoparathyroidism

Annals of Dermatology

Volumn 21, Issue 2, 2009, Pages 154-158

  Jeong, Ki Heon ^a   Lew, Bark Lynn ^a   Sim, Woo Young ^a  

^a Kyung Hee University Hospital   (South Korea)

Author keywords

Albright hereditary osteodystrophy; Osteoma cutis; Pseudohypoparathyroidism; Pseudopseudohypoparathyroidism

Indexed keywords

EID: 73449147988     PISSN: 10139087     EISSN: None     Source Type: Journal    
DOI: 10.5021/ad.2009.21.2.154     Document Type: Article

References (15)

1. Albright F, Burnett CH, Smith PH, Parson W. Pseudohypoparathyroidism: an example of Seabright-Bantam syndrome. Endocrinology 1942;30:922-932.
2. Novak C, Siller G, Wood D. Idiopathic multiple miliary osteomas of the face. Australas J Dermatol 1998;39:109-111.
3. Roth SI, Stowell RE, Helwig EB. Cutaneous ossification. Report of 120 cases and review of the literature. Arch Pathol 1963;76:44-54.
4. Sethuraman G, Malhotra AK, Khaitan BK, Kumar R, Sharma VK, Kabra M, et al. Osteoma cutis in pseudohypoparathyroidism. Clin Exp Dermatol 2006;31:225-227.
5. Walsh JS, Fairley JA. Cutaneous mineralization and ossification. In: Wolff K, Goldsmith LA, Katz SI, Gilchrest BA, Paller AS, Leffell DJ, editors. Fitzpatrick's dermatology in general medicine. 7th ed. New York: McGraw-Hill, 2008:1296-1297.
6. Kapoor S, Gogia S, Paul R, Banerjee S. Albright's hereditary osteodystrophy. Indian J Pediatr 2006;73:153-156.
7. Trueb RM, Panizzon RG, Burg G. Cutaneous ossification in Albright's hereditary osteodystrophy. Dermatology 1993; 186:205-209.
8. Wilson LC, Hall CM. Albright's hereditary osteodystrophy and pseudohypoparathyroidism. Semin Musculoskelet Radiol 2002;6:273-283.
9. Gelfand IM, Hub RS, Shore EM, Kaplan FS, Dimeglio LA. Progressive osseous heteroplasia-like heterotopic ossification in a male infant with pseudohypoparathyroidism type la: a case report. Bone 2007;40:1425-1428.
10. Lietman SA, Ding C, Cooke DW, Levine MA. Reduction in Gsalpha induces osteogenic differentiation in human mesenchymal stem cells. Clin Orthop Relat Res 2005;231-238.
11. Long DN, McGuire S, Levine MA, Weinstein LS, Germain-Lee EL. Body mass index differences in pseudohypoparathyroidism type 1a versus pseudopseudohypoparathyroidism may implicate paternal imprinting of Galpha(s) in the development of human obesity. J Clin Endocrinol Metab 2007;92:1073-1079.
12. Eyre WG, Reed WB. Albright's hereditary osteodystrophy with cutaneous bone formation. Arch Dermatol 1971 ;104:634-642.
13. Prendiville JS, Lucky AW, Mallory SB, Mughal Z, Mimouni F, Langman CB. Osteoma cutis as a presenting sign of pseudohypoparathyroidism. Pediatr Dermatol 1992;9:11-18.
14. Monn E, Osnes JB, Oye I, Wefring KW. Pseudohypoparathyroidism: a difficult diagnosis in early childhood. Acta Paediatr Scand 1976;65:487-493.
15. Burnstein Ml, Kottamasu SR, Pettifor JM, Sochett E, Ellis Bl, Frame B. Metabolic bone disease in pseudohypoparathyroidism: radiologic features. Radiology 1985;155:351-356.