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Atypical Presentation of a Medullary Thyroid Carcinoma Producing Acth and Serotonin

机译:甲状腺髓样癌产生Acth和5-羟色胺的非典型表现。

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摘要

Medullary carcinoma accounts for about 5% of all thyroid malignancies. The tumor may produce other hormones in addition to calcitonin that typically occurs in the presence of distant metastases. The aim of this report is to present a case of invasive medullary thyroid carcinoma producing ACTH and serotonin. A male patient sought medical attention due to facial plethora and distal paresthesia. On thyroid ultrasound, he presented a hypoechoic nodule measuring 6.7 × 3.2 × 3.5 cm, with punctate calcifications and central vascular pattern. The chest computed tomography showed an extensive solid lesion with epicenter in the superior mediastinum and absence of a cleavage plane with the left thyroid lobe. The lesion extended from the glottic area to the lower portion of the trachea and invaded esophagus, posterior tracheal wall, and left jugular. The patient presented hyperglycemia, hypokalemia, increased free urinary cortisol, calcitonin, ACTH and 5-hydroxyindoleacetic acid levels. The nodule cytological examination obtained by fine-needle aspiration was inconclusive, and the open biopsy confirmed the diagnosis of medullary thyroid carcinoma. Due to the advanced disease stage and increased risk of large caliber vessels injury in case of surgery, local chemotherapy and radiotherapy were recommended. With this report, we want to draw attention to an unusual association between advanced medullary thyroid carcinoma with an aggressive course and ectopic production of ACTH and serotonin.
机译:髓样癌约占所有甲状腺恶性肿瘤的5%。除降钙素外,肿瘤还可能产生其他激素,通常在远处转移的情况下会发生。本报告的目的是介绍一例产生ACTH和5-羟色胺的浸润性甲状腺髓样癌。一名男性患者因面部胸膜炎和远端感觉异常而寻求医疗救助。在甲状腺超声检查中,他表现出大小为6.7×3.2×3.5 cm的低回声结节,有点状钙化和中心血管图案。胸部计算机断层扫描显示上纵隔有广泛的实心病灶,震中在中心,左甲状腺叶不存在分裂平面。病变从声门区延伸至气管下部,并侵入食道,气管后壁和左颈。该患者出现高血糖,低钾血症,游离尿皮质醇,降钙素,ACTH和5-羟基吲哚乙酸水平升高。细针穿刺术所获得的结节细胞学检查尚无定论,开放式活检证实了甲状腺髓样癌的诊断。由于疾病处于晚期,并且手术时大口径血管受伤的风险增加,因此建议进行局部化疗和放疗。通过本报告,我们想提请注意甲状腺髓样癌的侵袭性病程与异位产生ACTH和5-羟色胺之间的异常关联。

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