A case report of McCune–Albright syndrome with hepatic manifestations

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...

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Detalles Bibliográficos
Autores principales: Haddadi, Mohammad, Lal Kheirkhah, Elahe, Ansari, Mojgan, Ahmadzade, Samieh, Taraz, Zeinab, Yazdi, Saeid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9295684/
https://www.ncbi.nlm.nih.gov/pubmed/35865771
http://dx.doi.org/10.1002/ccr3.6077
Descripción
Sumario: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.

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