1型多发性内分泌腺瘤病的多模态表现：一例报告

Monge John, Homuth Daniel, Zuiderveld Loren

Advocate Illinois Masonic Medical Center, 836 W Wellington Ave, Chicago, IL 60657, USA.

Radiol Case Rep. 2019 Jan 23;14(4):439-443. doi: 10.1016/j.radcr.2019.01.007. eCollection 2019 Apr.

Multiple endocrine neoplasia type 1 is a rare autosomal dominant disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary, and enteropancreatic endocrine cells. We present the clinical details of a patient with diarrhea, nephrolithiasis, erectile dysfunction, and new onset abdominal pain, as well as a discussion of the etiology, pathophysiology, and classical imaging findings of this condition.

1型多发性内分泌腺瘤病是一种罕见的常染色体显性疾病，典型特征是易患甲状旁腺、垂体前叶和肠胰腺内分泌细胞肿瘤。我们介绍了一名患有腹泻、肾结石、勃起功能障碍和新发腹痛患者的临床细节，并对该疾病的病因、病理生理学和经典影像学表现进行了讨论。