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地方性甲状腺肿地区原发性甲状旁腺功能亢进患者合并甲状腺癌

Concomitant thyroid cancer in patients with primary hyperparathyroidism in an endemic goitre region.

作者信息

Simsek Besir, Guldogan Cem Emir, Ozden Sabri, Saylam Baris, Karabeyoglu Serif Melih, Tez Mesut

出版信息

Ann Ital Chir. 2017;88:15-19.

Abstract

OBJECTIVE

Primary hyperparathyroidism (pHPT) is often accompanied by underlying thyroid pathology and 1 to 36% of these thyroid pathologies are malignant. How the identification of these lesions affects patient management is unclear. We present a single-center experience with the prevalence of concomitant thyroid cancer in patients who underwent parathyroidectomy for pHPT.

MATERIALS AND METHODS

This was a retrospective cohort study. Two hundred-two patients with primary hyperparathyroidism included study. Demographic data, clinical findings, and final histopathological diagnosis were recorded retrospectively.

RESULTS

Preoperative cervical ultrasound examination revealed co-existent thyroid abnormalities in 117 (57.9%) patients. Mean age of these patients was 57.8 ± 12.2 years and 88% were female. Sixty-three (53.9%) of the patients with thyroid abnormalities, underwent preoperative fine needle aspiration biopsy (FNAB). Cytology result was malignant in one (1.6%) patient, benign in 47(85.7%) patients, indeterminate in six (9.5%) patients and Hurthle cell neoplasm in two (3.2%) patients. Ninety-four (80.3%) of the patients underwent simultaneous thyroid surgery. Final pathology of the thyroid specimen was malignant in 26 (12.9%) patients. Sixteen of the malignant patients had preoperative FNAB. Preoperative FNAB result of these patients was malignant in one patient, indeterminate in two patients and benign in 13 patients.

CONCLUSION

By implementing a comprehensive approach to patients with pHPT who present with thyroid disease, concomitant pathology may be elucidated preoperatively. But, this approach will not facilitate the detection of otherwise unsuspected thyroid cancer in an endemic goitre region.

KEY WORDS

Cancer, Parathyroid adenoma, Parathyroidectomy, Thyroid, Thyroidectomy.

摘要

目的

原发性甲状旁腺功能亢进症(pHPT)常伴有潜在的甲状腺病变,其中1%至36%的甲状腺病变为恶性。这些病变的识别如何影响患者管理尚不清楚。我们展示了在因pHPT接受甲状旁腺切除术的患者中,同时存在甲状腺癌的单中心经验。

材料与方法

这是一项回顾性队列研究。纳入202例原发性甲状旁腺功能亢进症患者进行研究。回顾性记录人口统计学数据、临床发现和最终组织病理学诊断。

结果

术前颈部超声检查发现117例(57.9%)患者存在甲状腺异常。这些患者的平均年龄为57.8±12.2岁,88%为女性。63例(53.9%)甲状腺异常患者接受了术前细针穿刺活检(FNAB)。细胞学结果为恶性1例(1.6%),良性47例(85.7%),不确定6例(9.5%),许特氏细胞瘤2例(3.2%)。94例(80.3%)患者同时进行了甲状腺手术。甲状腺标本的最终病理结果显示26例(12.9%)患者为恶性。16例恶性患者术前进行了FNAB。这些患者术前FNAB结果为恶性1例,不确定2例,良性13例。

结论

通过对患有甲状腺疾病的pHPT患者采用综合方法,可在术前阐明合并的病变。但是,这种方法在地方性甲状腺肿地区无法促进发现原本未被怀疑的甲状腺癌。

关键词

癌;甲状旁腺腺瘤;甲状旁腺切除术;甲状腺;甲状腺切除术

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