McCune-albright syndrome: report of a case
Iranian Journal of Nuclear Medicine. 2010; 18 (1): 57-61
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| IMEMR
| ID: emr-132096
Biblioteca responsável:
EMRO
A 29-year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. On physical examination caf au lait macular spots were noted on her neck, buttocks and left leg. Bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. Considering the presence of polyostotic fibrous dysplasia, precocious puberty and caf au lait macular spots, MacCune-Albright syndrome was confirmed in this patient
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Índice:
IMEMR
Idioma:
En
Revista:
Iran. J. Nucl. Med.
Ano de publicação:
2010