Article
Genotype-negative multiple endocrine neoplasia type 1 with prolactinoma, hyperparathyroidism, and subclinical Cushing's syndrome accompanied by hyperglycemia: a case report.
Frontiers in endocrinology - 1 Jan 2024
Kubo Haremaru, Wada Ryota, Sekikawa Naohiro, Nomura Yasuhisa, Yamada Mutsuo, Inoue Minoru, Hattori Naoki, Yamazaki Yuto, Sugimoto Kazuhiro
Abstract excerpt
Background: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant disorder, accompanied by multiple endocrine neoplasms of the parathyroid, pancreas, pituitary, and other neoplasms in the adrenal glands. However, in some cases, patients clinically diagnosed with MEN1 may be genotype-negative. Case presentation: A 56-year-old female was diagnosed with MEN1 based on a macroprolactinoma (19 mm in...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
