Three cases of osteoma cutis occurring in infancy. A brief overview of osteoma cutis and its association with pseudo-pseudohypoparathyroidism

Australasian Journal of Dermatology

Volumn 52, Issue 2, 2011, Pages 127-131

  Ward, Susannah ^a   Sugo, Ella ^b   Verge, Charles F ^b   Wargon, Orli ^b  

^a PRINCE OF WALES HOSPITAL   (Australia)

^b SYDNEY CHILDREN'S HOSPITAL   (Australia)

Author keywords

Albright's hereditary osteodystrophy; Osteoma cutis; Paediatric; Pseudo pseudohypoparathyroidism; Pseudohypoparathyroidism; Skin disease

Indexed keywords

CALCIUM; LIOTHYRONINE; PARATHYROID HORMONE; PHOSPHATE; THYROTROPIN; THYROXINE; VITAMIN D;

ACNE; ALBRIGHT SYNDROME; ARTICLE; CALCIUM BLOOD LEVEL; CASE REPORT; CHILD; DIET SUPPLEMENTATION; DISEASE ASSOCIATION; FAMILY HISTORY; FREE LIOTHYRONINE INDEX; FREE THYROXINE INDEX; HORMONE RESISTANCE; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; LIOTHYRONINE BLOOD LEVEL; MALE; PARATHYROID HORMONE BLOOD LEVEL; PHOSPHATE BLOOD LEVEL; PRESCHOOL CHILD; PROGNOSIS; PSEUDOPSEUDOHYPOPARATHYROIDISM; SHORT STATURE; SKIN BIOPSY; SKIN DEFECT; SKIN DISEASE; SKIN MANIFESTATION; SKIN OSTEOMA; THYROTROPIN BLOOD LEVEL; THYROXINE BLOOD LEVEL;

BONE NEOPLASMS; FEMALE; FIBROUS DYSPLASIA, POLYOSTOTIC; HUMANS; INFANT; MALE; OSSIFICATION, HETEROTOPIC; OSTEOMA; PSEUDOPSEUDOHYPOPARATHYROIDISM;

EID: 79958202432     PISSN: 00048380     EISSN: 14400960     Source Type: Journal    
DOI: 10.1111/j.1440-0960.2010.00722.x     Document Type: Article

References (17)

1. MacLean G, Anderson T, Bert P. Connective tissue ossification presenting in the skin. Arch. Dermatol. 1966; 4: 168-74.
2. Montgomery H. Dermatopathology, 1st edn. New York: Harper & Row, 1967; 1130-3.
3. Plewig G, Kligman A. Acne and Rosacea, 3rd edn. Berlin, Heidelberg and New York: Springer Verlag, 2000.
4. Farfel Z, Friedman E. Mental deficiency in pseudohypoparathyroidism type I is associated with Ns-protein deficiency. Ann. Intern. Med. 1986; 105: 197.
5. Albright F, Burnett C, Smith P et al. Pseudohypoparathyroidism- an example of Seabright-Bantam syndrome: report of three cases. Endocrinology 1942; 30: 922.
6. Albright F, Forbes A, Henneman P. Pseudopseudohypoparathyroidism. Trans. Assoc. Am. Physicians 1952; 65: 337-50.
7. Klassens M, Blom E, Schrander J et al. Unique skin changes in a case of albright hereditary osteodystrophy caused by a rare GNAS1 mutation. BJD 2010; 162: 690-4.
8. Bovin B, Walzer C, Baud C. Ultrastructural study of the longterm development of two experimental cutaneous calcinosis (topical calcyphylaxis and topical calcergy) in the rat. Cell Tissue Res. 1987; 207: 525-32. (Pubitemid 17019579)
9. Takaoka K, Nakahara H, Yoshikawa H et al. Ectopic bone induction on and in porous hydroxyapetite combined with collagen and bone morphogenetic protein. Clin. Orthop. Relat. Res. 1988; 234: 250-4.
10. Cohen A, Chetov T, Cagnano E et al. Treatment of multiple military osteoma cutis of the face with local application of tretinoin (all trans-retinoic acid): a case report and review of the literature. J. Dermatolog. Treat. 2001; 12: 171-3. (Pubitemid 33116881)
11. Smith C, Glaser D. Treatment of multiple military osteoma cutis with tretinoin gel. J. Am. Acad. Dermatol. 1999; 41: 500. (Pubitemid 29418525)
12. Wilhelmsen H, Bereston E. Treatment of osteoma cutis. Cutis 1982; 33: 481-3.
13. Fulton J. Dermabrasion-Loo-Punch-excision technique for the treatment of acne-induced osteoma cutis. J. Dermatol. Surg. Oncol. 1987; 13: 655-9.
14. Weinstein L, Yu S, Warner D et al. Endocrine manifestations of stimulatory G-protein α- subunit mutations and the role of genomic imprinting. Endocr. Rev. 2001; 22: 675-705. (Pubitemid 32955250)
15. Levine M, Downs R, Moses A. Resistance to multiple hormones in patients with pseudohypoparathyroidism. Association with deficient activity of guanine nucleotide regulatory protein. Am. J. Med. 1983; 74-545.
16. Nanclares G, Rebollo E, Santin I et al. Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy. J Clin. Endocrinol. Metab. 2007; 92: 2370-73. (Pubitemid 46997148)
17. Adegbite N, Xu M, Kaplan F et al. Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS- based heterotropic ossification. Am. J. Med. Genet. A 2008; 14: 1788-96. (Pubitemid 352000717)