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Metastatic medullary thyroid carcinoma or calcitonin‐secreting carcinoid tumor of lung? A diagnostic dilemma in a patient with lung mass and thyroid nodule

机译:转移性髓质甲状腺癌或降钙素分泌物的肺部肿瘤肿瘤? 肺部质量和甲状腺结节患者诊断困境

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摘要

Calcitonin‐secreting neuroendocrine tumors are rare and have been reported in literature as case reports or case series in various organs including lung, pancreas, larynx, bladder, and ovary. These tumors have similar cytologic features and immunohistochemical profile to medullary thyroid carcinoma and thus it is difficult to distinguish them, especially when calcitonin‐secreting neuroendocrine tumors are intermediate or higher grade and there is a mass lesion in the thyroid gland. Here, we report a rare case of calcitonin secreting atypical carcinoid tumor of the lung in a patient with thyroid nodule. However, after extensive ancillary studies on the thyroid gland, no tumor was detected and subsequent resection specimen revealed a pulmonary atypical carcinoid tumor with metastasis to level 11 lymph node. Being aware of this entity has significant clinical, diagnostic, and therapeutic implications and can prevent unnecessary thyroidectomies with subsequent possible morbidities.
机译:分析分泌的神经内分泌肿瘤是罕见的,并在文献中报道,作为各种器官的病例报告或病例系列,包括肺,胰腺,喉,膀胱和卵巢。 这些肿瘤与髓质甲状腺癌具有类似的细胞学特征和免疫组化谱,因此难以区分它们,特别是当转析素分泌神经内分泌肿瘤是中间或更高的等级时,甲状腺腺体中存在质量病变。 在这里,我们报告了含有甲状腺结节的患者中肺部的降钙素肿瘤的罕见案例。 然而,在对甲状腺的广泛辅助研究之后,未检测到肿瘤,随后的切除试样揭示了肺部非典型类癌肿瘤,转移到11级淋巴结。 意识到该实体具有显着的临床,诊断和治疗意义,可以防止不必要的甲状腺切除术与随后的可能病症。

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