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同时性髓样癌、乳头状癌和滤泡状甲状腺癌与库欣综合征

Concurrent Medullary, Papillary, and Follicular Thyroid Carcinomas and Simultaneous Cushing's Syndrome.

作者信息

Mazeh Haggi, Orlev Amir, Mizrahi Ido, Gross David J, Freund Herbert R

机构信息

Department of SurgeryEndocrinology and Metabolism Service Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

Endocrinology and Metabolism Service Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

出版信息

Eur Thyroid J. 2015 Mar;4(1):65-8. doi: 10.1159/000368750. Epub 2014 Nov 22.

Abstract

BACKGROUND

Papillary thyroid carcinoma is the most common thyroid cancer (85%). Follicular thyroid carcinoma is the second most common type of thyroid cancer, accounting for up to 10% of all thyroid cancers. Medullary thyroid carcinoma accounts for only 5-8% of thyroid cancers. Concurrent medullary, follicular, and papillary carcinomas of the thyroid gland are extremely rare and reported scarcely.

CASE REPORT

A 72-year-old male presented with nonspecific neck pain. The workup revealed a nodular thyroid gland with a follicular lesion on fine-needle aspiration. Total thyroidectomy was performed and pathological examination identified a 25-mm follicular carcinoma, two papillary microcarcinomas, and two medullary microcarcinomas. The genetic workup was negative and no other family members were diagnosed with any endocrinopathy. Two months after surgery, the patient was diagnosed with Cushing's syndrome that was treated with laparoscopic left adrenalectomy. On 3-year follow-up, the patient is asymptomatic with no evidence of recurrent disease.

CONCLUSION

We present a rare case of a patient with follicular, papillary, and medullary thyroid carcinoma, and Cushing's syndrome. To date, no known genetic mutation or syndrome can account for this combination of neoplastic thyroid and adrenal pathologies, although future research may prove differently.

摘要

背景

乳头状甲状腺癌是最常见的甲状腺癌(占85%)。滤泡状甲状腺癌是第二常见的甲状腺癌类型,占所有甲状腺癌的比例高达10%。髓样甲状腺癌仅占甲状腺癌的5 - 8%。甲状腺同时发生髓样、滤泡状和乳头状癌极为罕见,报道甚少。

病例报告

一名72岁男性因非特异性颈部疼痛就诊。检查发现甲状腺有结节,细针穿刺显示有滤泡性病变。行甲状腺全切除术,病理检查发现一个25毫米的滤泡状癌、两个乳头状微癌和两个髓样微癌。基因检查结果为阴性,且未发现其他家庭成员患有任何内分泌疾病。术后两个月,患者被诊断为库欣综合征,接受了腹腔镜左肾上腺切除术。在3年的随访中,患者无症状,无疾病复发迹象。

结论

我们报告了一例罕见的同时患有滤泡状、乳头状和髓样甲状腺癌以及库欣综合征的患者。迄今为止,尚无已知的基因突变或综合征能够解释这种甲状腺和肾上腺肿瘤病变的组合,不过未来的研究可能会有不同结果。

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