一例伴有肝脏表现的McCune-Albright综合征病例报告。

Haddadi Mohammad, Lal Kheirkhah Elahe, Ansari Mojgan, Ahmadzade Samieh, Taraz Zeinab, Yazdi Saeid

Department of Nursing Tabas Branch Islamic Azad University Tabas Iran.

Department of Nursing Esfarayen University of Medical Sciences Esfarayen Iran.

Clin Case Rep. 2022 Jul 19;10(7):e6077. doi: 10.1002/ccr3.6077. eCollection 2022 Jul.

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.

McCune-Albright综合征是一种非遗传性疾病，其特征为咖啡斑、骨纤维发育不良和内分泌疾病。我们报告一名自出生起就因严重黄疸和甲状腺功能亢进多次住院的男孩。2岁时，他发生了左股骨近端骨折。随访期间，肝功能检查异常。综合临床和辅助检查结果，该患者被诊断为McCune-Albright综合征。