Myers J H, Eversman J J
Arch Intern Med. 1981 Oct;141(11):1521-2.
In the course of follow-up of a patient with primary hyperparathyroidism, signs and symptoms of acromegaly developed. The patient subsequently was found to have recurrent primary hyperparathyroidism and, later, pheochromocytoma was discovered. The patient seems to have an overlap of features found in the multiple endocrine neoplasia syndromes, type 1 and type 2 as previously classified.
在对一名原发性甲状旁腺功能亢进患者的随访过程中，出现了肢端肥大症的体征和症状。该患者随后被发现患有复发性原发性甲状旁腺功能亢进，后来又发现了嗜铬细胞瘤。该患者似乎具有先前分类的1型和2型多发性内分泌肿瘤综合征中所发现的特征重叠。
