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甲状旁腺癌合并多发性甲状旁腺腺瘤:病例报告。

Parathyroid carcinoma coexisting with multiple parathyroid adenomas: a case report.

机构信息

Kusatsu General Hosipital, Otolaryngology Head and Neck Thyroid Surgery, Shiga 525-8585, Japan.

出版信息

Endocr J. 2020 Sep 28;67(9):963-967. doi: 10.1507/endocrj.EJ20-0139. Epub 2020 May 30.

Abstract

Primary hyperparathyroidism is usually caused by parathyroid adenoma; however, parathyroid carcinoma is a rare cause. We report a rare case of 74-year-old female of primary hyperparathyroidism caused by parathyroid carcinoma (PC) and coexisting multiple parathyroid adenomas. She was referred to our hospital for primary hyperparathyroidism and a suspected thyroid tumor. She had no family history of malignant tumor. Computed tomography (CT) and ultrasonography of the neck revealed some masses posterior to both thyroid lobes. Those masses were believed to be parathyroid lesions. However, another mass located posterior to the right upper thyroid lobe seemed to be heterogeneous, which indicated a malignant thyroid tumor as well as parathyroid tumor. The preoperative diagnosis was multiple parathyroid adenoma and suspicious incidental thyroid carcinoma. Therefore, the patient underwent total parathyroidectomy and thyroidectomy. The histopathological diagnosis was parathyroid carcinoma coexisting with multiple parathyroid adenomas. There was no evidence of recurrence at 1 year after the surgery. It was difficult to diagnose PC preoperatively. Few rare cases of PC coexisting with parathyroid adenoma in multiple endocrine neoplasia type 1 (MEN1) have been reported. Therefore, careful follow-up was necessary considering the possibility of MEN1, though she did not wish for a genetic examination.

摘要

原发性甲状旁腺功能亢进症通常由甲状旁腺瘤引起;然而,甲状旁腺癌是一种罕见的病因。我们报告了一例罕见的 74 岁女性原发性甲状旁腺功能亢进症由甲状旁腺癌(PC)和共存的多发性甲状旁腺腺瘤引起。她因原发性甲状旁腺功能亢进症和疑似甲状腺肿瘤被转介到我们医院。她没有恶性肿瘤的家族史。颈部 CT 和超声检查发现双侧甲状腺叶后方有一些肿块。这些肿块被认为是甲状旁腺病变。然而,另一个位于右甲状腺上叶后方的肿块似乎不均匀,这表明不仅是甲状旁腺肿瘤,也是甲状腺肿瘤。术前诊断为多发性甲状旁腺腺瘤和可疑偶然甲状腺癌。因此,患者接受了甲状旁腺全切除和甲状腺切除术。组织病理学诊断为甲状旁腺癌伴多发性甲状旁腺腺瘤。术后 1 年无复发证据。PC 术前诊断困难。在多发性内分泌肿瘤 1 型(MEN1)中,PC 伴多发性甲状旁腺腺瘤的罕见病例很少报道。因此,虽然她不希望进行基因检查,但考虑到 MEN1 的可能性,仍有必要进行仔细的随访。

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