Yasuda Taisei, Kuba Kiyomi, Yoneyama Eijiro, Osaki Masami
Otolaryngology - Head and Neck Surgery, Ageo Central General Hospital, Ageo, JPN.
Cureus. 2024 Mar 7;16(3):e55706. doi: 10.7759/cureus.55706. eCollection 2024 Mar.
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder caused by mutations in the tumor suppressor gene and is characterized by parathyroid, pancreatic islet, and anterior pituitary tumors. Primary hyperparathyroidism is the most characteristic finding in MEN1, and intraoperative identification and accurate removal of the diseased parathyroid glands are vital since incomplete excision results in recurrence. This case report describes a 59-year-old woman who had pancreatic islet cell tumors and pituitary tumors and underwent selective transsphenoidal adenomectomy. Based on her medical history and examination, the diagnosis of primary hyperparathyroidism in MEN1 was made, and she underwent total parathyroidectomy with autotransplantation with SPY-Elite®️ Fluorescence Imaging (Stryker Corp., Kalamazoo, MI). Intraoperative identification of the parathyroid glands using autofluorescence with real-time intrinsic near-infrared (NIR) imaging made it easier to detect all of the parathyroid hyperplasia. After the surgery, she had hypoparathyroidism and continued with her oral calcium and vitamin D supplementation to maintain normal calcium levels during follow-up. Herein, we would like to advocate that the use of parathyroid gland autofluorescence with real-time intrinsic NIR imaging may be useful for identifying parathyroid tumors in patients with primary hyperparathyroidism in MEN1.
多发性内分泌腺瘤1型(MEN1)是一种由肿瘤抑制基因突变引起的常染色体显性疾病,其特征为甲状旁腺、胰岛和垂体前叶肿瘤。原发性甲状旁腺功能亢进是MEN1最典型的表现,术中识别并准确切除病变甲状旁腺至关重要,因为切除不完全会导致复发。本病例报告描述了一名59岁女性,她患有胰岛细胞瘤和垂体瘤,并接受了选择性经蝶窦腺瘤切除术。根据其病史和检查结果,诊断为MEN1相关的原发性甲状旁腺功能亢进,她接受了甲状旁腺全切术并使用SPY-Elite®荧光成像系统(史赛克公司,密歇根州卡拉马祖)进行自体移植。术中利用实时近红外(NIR)成像的自体荧光识别甲状旁腺,使得更容易检测到所有甲状旁腺增生。术后,她出现甲状旁腺功能减退,在随访期间持续口服钙剂和维生素D以维持正常血钙水平。在此,我们提倡使用实时近红外成像的甲状旁腺自体荧光技术,可能有助于识别MEN1相关原发性甲状旁腺功能亢进患者的甲状旁腺肿瘤。