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具有甲状腺髓样癌特征的食管转移性神经内分泌肿瘤。

Metastatic neuroendocrine tumor of the esophagus with features of medullary thyroid carcinoma.

作者信息

Fertig Raymond M, Alperstein Adam, Diaz Carlos, Klingbeil Kyle D, Vangara Sameera S, Misawa Ryosuke, Reed Jennifer, Gaudi Sudeep

机构信息

University of Miami, Miller School of Medicine, Miami, FL, USA.

Oak Hill Hospital, Graduate Medical Education, Department of Internal Medicine, FL, USA.

出版信息

Intractable Rare Dis Res. 2017 Aug;6(3):224-229. doi: 10.5582/irdr.2017.01035.

Abstract

A 41-year-old female presented with a pedunculated mass in the upper esophagus and bilateral lymphadenopathy. Biopsies suggested a neuroendocrine tumor, possibly carcinoid, and ensuing imaging revealed cervical lymph node metastases. The esophageal mass was removed endoscopically and discovered by pathologists to closely resemble medullary thyroid carcinoma (MTC) on immunohistochemistry staining. Following surgery, further work up demonstrated very high serum calcitonin levels, suggestive of medullary thyroid carcinoma, however the thyroid gland was normal on ultrasound. The patient underwent a neck dissection to remove the lymph node metastases and subsequently her calcitonin levels dropped to 0 ng/mL, indicating remission. It appears that the primary tumor was not in the thyroid, but in the cervical esophagus. The thyroid has appeared normal on multiple ultrasounds without any detectable nodules or masses. This is quite a unique case because this patient presented with a tumor resembling medullary carcinoma of the thyroid that presented as a pedunculated mass in the cervical esophagus. The actual final diagnosis of this mass in the cervical esophagus was neuroendocrine tumor (NET), consistent with a carcinoid tumor, not ectopic MTC. This case report highlights that calcitonin-secreting tumors outside the thyroid should not lead to erroneous recommendations for thyroidectomy.

摘要

一名41岁女性因食管上段有一有蒂肿物及双侧淋巴结肿大就诊。活检提示为神经内分泌肿瘤,可能为类癌,随后的影像学检查显示有颈部淋巴结转移。经内镜切除食管肿物,病理学家在免疫组化染色时发现其与甲状腺髓样癌(MTC)极为相似。手术后,进一步检查显示血清降钙素水平非常高,提示甲状腺髓样癌,但甲状腺超声检查正常。患者接受了颈部淋巴结清扫术以清除淋巴结转移灶,随后其降钙素水平降至0 ng/mL,表明病情缓解。看来原发肿瘤不在甲状腺,而在颈段食管。多次超声检查显示甲状腺正常,未发现任何可检测到的结节或肿物。这是一个相当独特的病例,因为该患者表现为类似甲状腺髓样癌的肿瘤,却呈现为颈段食管的有蒂肿物。该颈段食管肿物的最终实际诊断为神经内分泌肿瘤(NET),符合类癌肿瘤,而非异位MTC。本病例报告强调,甲状腺外分泌降钙素的肿瘤不应导致错误的甲状腺切除术建议。

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Medullary thyroid cancer with undetectable serum calcitonin.血清降钙素检测不到的甲状腺髓样癌
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本文引用的文献

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Neuroendocrine tumors, version 1.2015.神经内分泌肿瘤,第 1.2015 版。
J Natl Compr Canc Netw. 2015 Jan;13(1):78-108. doi: 10.6004/jnccn.2015.0011.
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Endoscopic treatment for early foregut neuroendocrine tumors.早期前肠神经内分泌肿瘤的内镜治疗
Clin Endosc. 2013 Sep;46(5):450-5. doi: 10.5946/ce.2013.46.5.450. Epub 2013 Sep 30.
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Epidemiology of gastroenteropancreatic neuroendocrine tumours.胃肠胰神经内分泌肿瘤的流行病学。
Best Pract Res Clin Gastroenterol. 2012 Dec;26(6):691-703. doi: 10.1016/j.bpg.2013.01.006.

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