Open AccessA case report of McCune –Albright syndrome with hepatic manifestations
Author(s) -
Haddadi Mohammad,
Lal Kheirkhah Elahe,
Ansari Mojgan,
Ahmadzade Samieh,
Taraz Zeinab,
Yazdi Saeid
Publication year - 2022
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.6077
Subject(s) - medicine , mccune–albright syndrome , fibrous dysplasia , café au lait spot , family history , jaundice , cholestatic jaundice , pediatrics , dermatology , surgery , pathology , precocious puberty , hormone , neurofibromatosis
McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture. During the follow‐up, liver function tests were abnormal. Considering the clinical and paraclinical findings, the patient was diagnosed with McCune–Albright syndrome.