Pacini F, Perri G, Bagnolesi P, Cilotti A, Pinchera A
Istituto di Metodologia Clinica e Medicina del Lavoro, University of Pisa, Italy.
J Endocrinol Invest. 1987 Aug;10(4):417-20. doi: 10.1007/BF03348161.
We describe the case of a 38-year-old man with typical Mc Cune-Albright syndrome and the unusual combination of both growth-hormone and prolactin hypersecretion. The patient was extremely tall, which is unusual in Mc Cune-Albright syndrome, suggesting that he did not have precocious fusion of the epiphysis, a common finding in this syndrome. Unfortunately the patient refused any treatment for his disease. A similar case has been previously described only in a 14-year-old boy.
我们描述了一名38岁男性患者的病例，他患有典型的McCune-Albright综合征，同时存在生长激素和催乳素分泌过多的不寻常组合。该患者身材极高，这在McCune-Albright综合征中并不常见，提示他没有骨骺早熟融合，而这是该综合征的常见表现。不幸的是，患者拒绝接受任何针对其疾病的治疗。此前仅在一名14岁男孩中描述过类似病例。
