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肾上腺转移作为同步性乳头状和滤泡状甲状腺癌的初始诊断

Adrenal metastasis as the initial diagnosis of synchronous papillary and follicular thyroid cancer.

作者信息

He Xin, Soleimanpour Scott A, Clines Gregory A

机构信息

Department of Internal MedicineDivision of MetabolismEndocrinology & Diabetes, University of Michigan, 1500 East Medical Center Drive, Ann Arbor, MI, 48109, USA.

Veterans Affairs Ann Arbor Healthcare System, 2215 Fuller Road, Ann Arbor, MI, 48105, USA.

出版信息

Clin Diabetes Endocrinol. 2020 Nov 4;6(1):19. doi: 10.1186/s40842-020-00109-0.

Abstract

BACKGROUND

Differentiated thyroid cancer uncommonly presents with distant metastases. Adrenal metastasis from differentiated thyroid cancer presenting as the initial finding is even less common.

CASE PRESENTATION

A 71-year-old male was incidentally found on chest CT to have bilateral thyroid nodules, which were confirmed on ultrasound. Fine needle aspiration of the dominant right 3.3 cm nodule contained histologic features most consistent with Bethesda classification III, and repeat fine needle aspiration revealed pathology consistent with Bethesda classification II. Follow-up thyroid ultrasound showed 1% increase and 14% increase in nodule volume at one and two years, respectively, compared to baseline. Prior to the second annual thyroid ultrasound, the patient was incidentally found to have a 4.1 cm heterogeneously enhancing mass in the right adrenal gland on CT of the abdomen and pelvis. Biochemical evaluation was unremarkable with the exception of morning cortisol of 3.2 µg/dL after dexamethasone suppression. The patient then underwent laparoscopic right adrenal gland excision, which revealed metastatic follicular thyroid carcinoma. Total thyroidectomy was then performed, with pathology showing a 4.8 cm well-differentiated follicular thyroid carcinoma of the right lobe, a 0.5 cm noninvasive follicular thyroid neoplasm with papillary-like nuclear features of the left lobe, and a 0.1 cm papillary microcarcinoma of the left lobe. Thyrotropin-stimulated whole body scan showed normal physiologic uptake of the remnant thyroid tissue without evidence of other iodine avid disease. The patient then received radioactive iodine. At follow-up 14 months after total thyroidectomy, he remains free of recurrent disease.

CONCLUSION

Despite following the recommended protocol for evaluation and surveillance of thyroid nodules, thyroid cancer can be challenging to diagnose, and may not be diagnosed until distant metastases are identified.

摘要

背景

分化型甲状腺癌很少出现远处转移。以肾上腺转移作为首发表现的分化型甲状腺癌更为罕见。

病例介绍

一名71岁男性在胸部CT检查时偶然发现双侧甲状腺结节,超声检查予以证实。对右侧3.3厘米的优势结节进行细针穿刺活检,组织学特征最符合贝塞斯达分类III级,再次细针穿刺活检显示病理结果符合贝塞斯达分类II级。后续甲状腺超声检查显示,与基线相比,结节体积在1年和2年时分别增加了1%和14%。在第二次年度甲状腺超声检查前,患者在腹部和盆腔CT检查时偶然发现右侧肾上腺有一个4.1厘米的不均匀强化肿块。除地塞米松抑制后晨皮质醇为3.2微克/分升外,生化检查无异常。患者随后接受了腹腔镜右侧肾上腺切除术,术后病理显示为转移性滤泡状甲状腺癌。随后进行了全甲状腺切除术,病理显示右叶有一个4.8厘米的高分化滤泡状甲状腺癌,左叶有一个0.5厘米的具有乳头状核特征的非侵袭性滤泡状甲状腺肿瘤,左叶还有一个0.1厘米的乳头状微小癌。促甲状腺素刺激的全身扫描显示残余甲状腺组织有正常的生理性摄取,未发现其他摄碘性疾病迹象。患者随后接受了放射性碘治疗。在全甲状腺切除术后14个月的随访中,他未出现疾病复发。

结论

尽管遵循了甲状腺结节评估和监测的推荐方案,但甲状腺癌的诊断仍具有挑战性,可能直到发现远处转移时才得以诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f3/7640618/cbbac21e7c73/40842_2020_109_Fig1_HTML.jpg

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