Evidence map›Paper›PMID 39726845›Full record

ArticleFrontiers in endocrinology2024

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

Haremaru Kubo, Ryota Wada, Naohiro Sekikawa, Yasuhisa Nomura, Mutsuo Yamada, Minoru Inoue, Naoki Hattori, Yuto Yamazaki, Kazuhiro Sugimoto

Abstract readCase Reports
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Haremaru KuboDiabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
Ryota WadaDiabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
Naohiro SekikawaDiabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
Yasuhisa NomuraDepartment of Obstetrics and Gynecology, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
Mutsuo YamadaDepartment of Surgery, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
Minoru InoueDepartment of General Internal Medicine, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.
Naoki HattoriDepartment of Orthopedic Surgery, Kansai Medical University, Osaka, Japan.
Yuto YamazakiDepartment of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kazuhiro SugimotoDiabetes Center, Ohta Nishinouchi Hospital, Koriyama, Fukushima, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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. Case presentation: A 56-year-old female was diagnosed with MEN1 based on a macroprolactinoma (19 mm in diameter), primary hyperparathyroidism, and a cortisol-producing adrenal adenoma, without a family history. At first appearance, she had a hemoglobin A1c of 12.0% and a fasting plasma glucose level of 16.3 mmol/L (294 mg/dL). She complained of headaches and had a history of prolactinoma at 28 years of age, with concomitant elevated prolactin 1102.0 μg/L (ng/mL). Insulin therapy was initiated for glucose management following the administration of an oral hypoglycemic agent. Additionally, cabergoline was initiated for due to the prolactinoma, resulting in a normalized prolactin level. Thereafter, medication for diabetes could be withdrawn. Subsequently, surgery was performed for primary hyperparathyroidism and the cortisol-producing adrenal adenoma, which was consistent with the preoperative diagnosis. Additionally, a thyroid tumor resected with primary hyperparathyroidism revealed to be invasive papillary thyroid carcinoma (PTC). Target gene testing revealed a negative genotype for Conclusions: Genotype-negative MEN1 typically has a favorable clinical course without a third primary MEN1 manifestation. However, the present case had a symptomatic macroprolactinoma with an apparent elevated glucose level and three manifestations of tumors (pituitary, parathyroid, and adrenal) with invasive PTC, and a delayed diagnosis could have caused crucial deterioration. Clinicians should pay attention to the clinical features of MEN1 including glucose intolerance. In such cases, the treatment of endocrine disorders can lead to the normalization of the glucose level.

Indexed as

Cushing SyndromeHyperglycemiaMultiple Endocrine Neoplasia Type 1Pituitary NeoplasmsProlactinomaAdrenal Gland NeoplasmsFemaleGenotypeHumansHyperparathyroidismMiddle Agedhyperglycemiamultiple endocrine neoplasia type 1primary hyperparathyroidismprolactinomasubclinical Cushing’s syndrome

Identifiers

PMID39726845
PMCPMC11669518

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