患者患有典型类癌,最初被诊断为高级别神经内分泌癌。

Pub Date : 2017-11-01 Epub Date: 2017-10-26 DOI:10.2217/lmt-2017-0010
Sean Warsch, Mohammad Jahanzeb
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引用次数: 0

摘要

我们报告了一例最初被诊断为高级别神经内分泌癌的患者,5 年后被确定为低级别典型类癌。患者接受了放射治疗和多种化疗方案,以治疗高级别转移性大、小细胞混合型神经内分泌癌,但对任何治疗均无明显反应。随后的影像学检查发现了广泛的转移性疾病,计算机断层扫描引导下的活组织检查显示患者患有类癌,但没有坏死。患者开始接受替莫唑胺+卡培他滨、长效奥曲肽和地诺单抗治疗,并计划在疾病进展后接受依维莫司治疗。本病例的研究结果凸显了在诊断时对胸部神经内分泌肿瘤进行准确组织病理学分类的重要性,以避免对低分级肿瘤患者进行不必要的侵袭性化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Patient with typical carcinoid initially diagnosed as high-grade neuroendocrine carcinoma.

We report the case of a patient initially diagnosed with a high-grade neuroendocrine carcinoma, which 5 years later was determined to have a low-grade typical carcinoid. The patient received radiotherapy and numerous chemotherapy regimens for treatment of a high-grade metastatic mixed large and small cell neuroendocrine carcinoma, without a significant response to any treatment. Subsequent imaging revealed widely metastatic disease and computed tomography-guided biopsy demonstrated a carcinoid tumor with no necrosis. The patient was started on temozolomide + capecitabine, long-acting octreotide and denosumab, with everolimus planned upon disease progression. Findings from this case study highlight the importance of accurate histopathologic classification of thoracic neuroendocrine tumors at diagnosis, to avoid the unnecessary administration of aggressive chemotherapy to patients with low-grade tumors.

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