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A nonfunctioning parathyroid carcinoma misdiagnosed as a follicular thyroid nodule

机译:非功能性甲状旁腺癌被误诊为滤泡性甲状腺结节

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摘要

Parathyroid carcinoma (PC) is a rare endocrine malignancy. The tumor is mostly functioning, causing severe primary hyperparathyroidism, with high serum calcium and parathyroid hormone (PTH) levels. Nonfunctioning PC is extremely rare. We report a 50-year-old male patient who was referred to our Department for a right thyroid nodule, incidentally detected on carotid Doppler ultrasound scan, with a fine-needle aspiration cytology showing a follicular lesion. At the time of our evaluation, neck ultrasound showed a 1.3 cm right hypoechoic thyroid nodule with irregular margins and the absence of enlarged bilateral cervical lymph nodes. Thyroid function tests were normal. Serum calcium was normal and plasma PTH slightly above the upper limit of the normal range. The patients underwent right lobectomy. The intraoperative frozen-section pathological examination raised the suspicion of a PC. Definitive histology showed a markedly irregular infiltrative growth of the tumor with invasion of the thyroid tissue and cervical soft tissues. Immunostaining for thyroglobulin was negative, whereas staining for chromogranin A and PTH showed a strong reactivity. Based on the microscopic findings and the immunohistochemical profile, the tumor was diagnosed as a PC. Postoperative serum calcium and phosphate levels were in the normal range. One month after surgery, serum calcium and PTH were normal. Neck ultrasound and total body computed tomography scan were negative for local and metastatic disease. Eight months later, serum calcium was normal and plasma PTH level remained around the upper limit of normal range. Neck ultrasound did not show any pathological lesions. This is the first case of a nonfunctioning sporadic PC misdiagnosed prior of surgery as a follicular thyroid nodule. The parathyroid nature of the neck lesion could not be suspected before surgery. Fine-needle aspiration cytology (FNAC) may fail to distinguish a parathyroid tumor from a benign thyroid nodule because at FNAC, parathyroid and thyroid lesions have some morphological similarities. Histological criteria are not always sufficient for the differential diagnosis, which can definitely be established using immunohistochemistry.
机译:甲状旁腺癌(PC)是一种罕见的内分泌恶性肿瘤。肿瘤大部分在起作用,引起严重的原发性甲状旁腺功能亢进,血清钙和甲状旁腺激素(PTH)水平高。无法运行的PC极为罕见。我们报告了一名50岁的男性患者,该患者因右甲状腺结节被转诊到我们的部门,在颈动脉多普勒超声扫描中偶然发现了该患者,并有细针穿刺细胞学检查显示了滤泡性病变。在我们进行评估时,颈部超声检查显示1.3 cm的右低回声甲状腺结节,边缘不规则,且双侧颈淋巴结肿大。甲状腺功能检查正常。血清钙正常,血浆PTH略高于正常范围的上限。患者接受了右肺叶切除术。术中冰冻切片病理检查引起了对PC的怀疑。明确的组织学显示,随着甲状腺组织和宫颈软组织的浸润,肿瘤的浸润性增长明显不规则。甲状腺球蛋白的免疫染色为阴性,而嗜铬粒蛋白A和PTH染色则显示强反应性。基于显微镜下的发现和免疫组织化学特征,将肿瘤诊断为PC。术后血清钙和磷水平在正常范围内。手术一个月后,血清钙和PTH正常。颈部超声和全身计算机断层扫描对局部和转移性疾病阴性。 8个月后,血清钙恢复正常,血浆PTH水平保持在正常范围的上限附近。颈部超声未显示任何病理病变。这是在手术前误诊为散发性甲状腺结节的散发性PC无法正常工作的第一例。术前不可怀疑颈部病变的甲状旁腺性质。细针穿刺细胞学检查(FNAC)可能无法将甲状旁腺肿瘤与甲状腺良性结节区分开,因为在FNAC处,甲状旁腺和甲状腺病变具有某些形态相似性。组织学标准对于鉴别诊断并不总是足够的,可以使用免疫组织化学技术确定。

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