肺大细胞神经内分泌癌伴兰伯特-伊顿综合征。

IF 1.9 Q3 PATHOLOGY
Clinical Pathology Pub Date : 2021-10-11 eCollection Date: 2021-01-01 DOI:10.1177/2632010X211051741
Pamela Hernandez-Arriaga, Mauricio Gonzalez-Urquijo, Daniel Fernando López Altamirano, Bryan Vaca-Cartagena, Andres Vergil-Vargas, Silviano Rios-Pascual, Jose Eduardo Perez-Saucedo, Ricardo Sepúlveda-Malec
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引用次数: 1

摘要

兰伯特-伊顿综合征是一种罕见的神经肌肉交界处的副肿瘤疾病,其特征是乙酰胆碱释放受损,导致近端肌肉无力,肌腱反射抑制和自主神经改变。大多数兰伯特-伊顿综合征出现在小细胞肺癌,只有少数病例报道在其他肺亚型。在此,我们报告一例69岁男性Lambert-Eaton综合征罕见合并肺大细胞神经内分泌癌的病例,该病例在肿瘤诊断前5个月出现。我们顺利地进行了肺叶切除术。文献综述也提出。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pulmonary Large Cell Neuroendocrine Carcinoma Associated With Lambert-Eaton Syndrome.

Pulmonary Large Cell Neuroendocrine Carcinoma Associated With Lambert-Eaton Syndrome.

Pulmonary Large Cell Neuroendocrine Carcinoma Associated With Lambert-Eaton Syndrome.

Pulmonary Large Cell Neuroendocrine Carcinoma Associated With Lambert-Eaton Syndrome.

Lambert-Eaton syndrome is a rare paraneoplastic disorder of the neuromuscular junction, characterized by impaired release of acetylcholine, which causes proximal muscle weakness, depressed tendon reflexes, and autonomic changes. Most cases of Lambert-Eaton syndrome present in small-cell lung carcinoma, and only a few cases have been reported in other lung subtypes. Herein, we report a case of 69 years old male patient with Lambert-Eaton syndrome as a rare association with a pulmonary large-cell neuroendocrine carcinoma, which presented 5 months before neoplasm diagnosis. A lobectomy was auspiciously performed. A review of the literature is also presented.

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来源期刊
Clinical Pathology
Clinical Pathology PATHOLOGY-
CiteScore
2.20
自引率
7.70%
发文量
66
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