非典型甲状旁腺瘤合并甲状腺乳头状癌2例

I. Voronkova, Воронкова Ия Александровна, A. M. Lapshina, Лапшина Анастасия Михайловна, L. Gurevich, Гуревич Лариса Евсеевна, L. Rozhinskaya, Рожинская Людмила Яковлевна, T. Britvin, Бритвин Тимур Альбертович, A. Krivosheev, Кривошеев Алексей Викторович, Ilya V. Kim, Ким Илья Викторович, S. Kuznetsov, Кузнецов Сергей Николаевич, N. Mokrysheva, Мокрышева Наталья Георгиевна
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引用次数: 2

摘要

大多数临床医生都清楚地意识到遗传性和散发性多发性内分泌瘤综合征中甲状腺髓样癌和甲状旁腺功能亢进的共存。Тhe报道原发性甲状旁腺功能亢进症(pHPT)患者的非髓样甲状腺癌发病率仅约为3%。甲状腺乳头状癌(PTC)是一种恶性上皮肿瘤。PTC占所有甲状腺癌的87%。非典型甲状旁腺腺瘤(APA)是甲状旁腺肿瘤的一个子集,表现出甲状旁腺癌的一些特征,但缺乏明确的侵袭性生长。APA约占PHPT病例的0.5-4%。作为一个群体,它们可能被认为是恶性潜能不确定的肿瘤。对于APA的临床重要性、长期结果以及适当的手术管理和监测都没有很好的定义,这可能是由于总体发病率低以及缺乏APA的标准定义。我们报告两例63岁女性和57岁男性的非典型甲状旁腺瘤和甲状腺乳头状癌同步。其中一名患者有典型的pHPT症状,包括严重的代谢性骨病和肾脏疾病,但另一名患者没有。术前平均钙为3.48和4.1 mmol/l(2.12-2.6),甲状旁腺激素(PTH)分别为1300和1533 pg/ml(15-65)。两例甲状腺超声均未见甲状腺癌特征的结节。术中翻修后怀疑为甲状腺癌。患者接受了甲状腺全切除术和甲状旁腺瘤的手术切除。手术病理显示两例患者均为乳头状微癌(第一单侧,第二双侧)和APA。对这种情况的认识将使临床医生能够评估原发性甲状旁腺功能亢进患者可能的甲状腺病理。这两种内分泌疾病都可以通过一次手术同时切除甲状腺和甲状旁腺来治疗。
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Two cases synchronous atypical parathyroid adenomas and papillary thyroid carcinoma
Most clinicians are well aware of the coexistence of medullary thyroid cancer and hyperparathyroidism in hereditary and sporadic multiple endocrine neoplasia syndromes. Тhe reported incidence of nonmedullary thyroid carcinoma in patients with primary hyperparathyroidism (pHPT) is only approximately 3%. Papillary thyroid carcinomas (PTC) is a malignant epithelial tumour. PTC represent up to 87% of all thyroid carcinomas. Atypical parathyroid adenoma (APA) are a subset of parathyroid neoplasms that exhibit some of the features of parathyroid carcinoma but lack unequivocal invasive growth. APA represents about 0.5–4% of cases of PHPT. As a group, they may be considered tumors of uncertain malignant potential. The clinical importance, and long-term outcomes as well as appropriate operative management and surveillance are not well defined for APA probably due to the overall low prevalence as well as the lack of a standard definition of APA. We report two cases of a 63-year-old woman and 57-year-old man with a synchronous atypical parathyroid adenoma and papillary thyroid carcinoma. One of this patients had a classic symptoms of pHPT, including severe metabolic bone disease and renal disease, but another didn’t have. The mean preoperative calcium was 3,48 and 4,1 (range 2.12–2.6) mmol/l and a mean parathyroid hormone (PTH) of 1300 and 1533 (range 15–65) pg/ml, respectively. Thyroid ultrasound didn’t show a nodule with features of the thyroid carcinoma in both cases. The thyroid cancer was suspected after intraoperative revision. The patients underwent a total thyroidectomy and surgical excision of the parathyroid adenoma. Surgical pathology showed papillary microcarcinoma in both cases (in the first – unilateral, in the second – bilateral) and APA. Awareness of this condition will enable clinicians to evaluate for possible thyroid pathology in patients with primary hyperparathyroidism. Both of these endocrine conditions could then be managed with a single surgery involving concomitant resection of the thyroid and parathyroid glands.
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