Genotype-negative multiple endocrine neoplasia type 1 with prolactinoma, hyperparathyroidism, and subclinical Cushing's syndrome accompanied by hyperglycemia: a case report.

Journal: Frontiers in endocrinology
PMID: 39726845

Abstract

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.

Authors

  • Haremaru Kubo
    Diabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
  • Ryota Wada
    Diabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
  • Naohiro Sekikawa
    Diabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
  • Yasuhisa Nomura
    Department of Obstetrics and Gynecology, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
  • Mutsuo Yamada
    Department of Surgery, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
  • Minoru Inoue
    Department of General Internal Medicine, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
  • Naoki Hattori
    Department of Orthopedic Surgery, Kansai Medical University, Osaka, Japan.
  • Yuto Yamazaki
    Department of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
  • Kazuhiro Sugimoto
    Diabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.

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