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Recurrent ectopic calcification involving the maxillofacial skeleton: A potential harbinger of Albright's osteodystrophy.
J Craniofac Surg. 2006 Jan; 17(1):21-7.JC

Abstract

We present a case of osteoma cutis as the initial presenting sign of Albright's osteodystrophy. Albright's osteodystrophy represents a challenge in both diagnosis and treatment because the phenotype manifests as a broad spectrum of biochemical and physical findings. The syndrome may be overlooked, particularly in the early phases when serum calcium and phosphorous levels may be normal. Although surgery is the treatment of osteoma cutis, recurrence is common, creating frustration for the patient's family and the surgeon. In the present case, a girl 4 months and 2 years of age presented with refractory ectopic calcification emanating from the maxilla and demonstrated repeated recurrence after surgical resection. This ectopic calcification was not adequately controlled until Albright's osteodystrophy was properly diagnosed and treated. A differential diagnosis and surgical approach to deal with recurrent ectopic calcification of the facial skeleton is outlined.

Authors+Show Affiliations

Department of Plastic Surgery, The Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.No affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

16432403

Citation

Cortes, Wilberto, and Arun K. Gosain. "Recurrent Ectopic Calcification Involving the Maxillofacial Skeleton: a Potential Harbinger of Albright's Osteodystrophy." The Journal of Craniofacial Surgery, vol. 17, no. 1, 2006, pp. 21-7.
Cortes W, Gosain AK. Recurrent ectopic calcification involving the maxillofacial skeleton: A potential harbinger of Albright's osteodystrophy. J Craniofac Surg. 2006;17(1):21-7.
Cortes, W., & Gosain, A. K. (2006). Recurrent ectopic calcification involving the maxillofacial skeleton: A potential harbinger of Albright's osteodystrophy. The Journal of Craniofacial Surgery, 17(1), 21-7.
Cortes W, Gosain AK. Recurrent Ectopic Calcification Involving the Maxillofacial Skeleton: a Potential Harbinger of Albright's Osteodystrophy. J Craniofac Surg. 2006;17(1):21-7. PubMed PMID: 16432403.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Recurrent ectopic calcification involving the maxillofacial skeleton: A potential harbinger of Albright's osteodystrophy. AU - Cortes,Wilberto, AU - Gosain,Arun K, PY - 2006/1/25/pubmed PY - 2006/4/21/medline PY - 2006/1/25/entrez SP - 21 EP - 7 JF - The Journal of craniofacial surgery JO - J Craniofac Surg VL - 17 IS - 1 N2 - We present a case of osteoma cutis as the initial presenting sign of Albright's osteodystrophy. Albright's osteodystrophy represents a challenge in both diagnosis and treatment because the phenotype manifests as a broad spectrum of biochemical and physical findings. The syndrome may be overlooked, particularly in the early phases when serum calcium and phosphorous levels may be normal. Although surgery is the treatment of osteoma cutis, recurrence is common, creating frustration for the patient's family and the surgeon. In the present case, a girl 4 months and 2 years of age presented with refractory ectopic calcification emanating from the maxilla and demonstrated repeated recurrence after surgical resection. This ectopic calcification was not adequately controlled until Albright's osteodystrophy was properly diagnosed and treated. A differential diagnosis and surgical approach to deal with recurrent ectopic calcification of the facial skeleton is outlined. SN - 1049-2275 UR - https://www.unboundmedicine.com/medline/citation/16432403/Recurrent_ectopic_calcification_involving_the_maxillofacial_skeleton:_A_potential_harbinger_of_Albright's_osteodystrophy_ L2 - http://dx.doi.org/10.1097/01.scs.0000188906.42225.39 DB - PRIME DP - Unbound Medicine ER -