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病例报告:微小肺脑膜上皮样结节的临床病理分析:7例报告

Case Report: Clinicopathological Analysis of Minute Pulmonary Meningothelial-Like Nodules: Report of 7 Cases.

作者信息

Wang Ying-Xia, Lei Zi, Yang Man, Wang Zhi-Yuan, Zhang Xuan, Pan Guo-Qing

机构信息

Department of Pathology, The First Affiliated Hospital of Kunming Medical University, Kunming, China.

Department of Pathology, Fuyuan County People's Hospital of Qujing City, Fuyuan, China.

出版信息

Front Oncol. 2022 Jul 19;12:942517. doi: 10.3389/fonc.2022.942517. eCollection 2022.

Abstract

OBJECTIVE

To investigate the clinical manifestations, radiologic features, pathological features, and immunophenotype of minute pulmonary meningothelial-like nodules (MPMNs).

METHOD

This is a retrospective observational study. We collected the clinical data of 7 cases of MPMNs, and performed comprehensive characterization using a combination of clinical, morphological, radiologic and immunohistochemical assessments.

RESULTS

Of the 7 cases of MPMNs, 6 were female and 1 was male. The median age was 55 years. All MPMNs were multiple in lung with the size from 0,01 to 0,5cm. Chest CT examination showed ground-glass attenuation or solid nodules. Four cases were concomitant with carcinoma and/or pneumonia, and 3 cases occurred alone. Four of the 7 patients had no obvious symptoms; 3 patients had chest pain or cough or shortness of breath or hemoptysis. Multiple white nodules were found macroscopically, and the diseased cells grew along the alveolar septum, with relatively normal morphology, rich cytoplasm, unclear cell boundary, and uniform nucleus with delicate chromatin and without atypia; and the diseased cells showed nest or whorls distribution. EMA, PR, CD56 and vimentin were positive in all cases by immunohistochemistry.

CONCLUSIONS

MPMNs are rare benign lesions in the lung, often multiple, usually less than 0.5cm in diameter, most of which have no obvious clinical symptoms. MPMNs are often found by chest CT, and occur independently or concomitant with other lesions. The positive immunohistochemical staining of EMA, PR, CD56, vimentin supports the diagnosis.

摘要

目的

探讨微小肺脑膜上皮样结节(MPMNs)的临床表现、影像学特征、病理特征及免疫表型。

方法

这是一项回顾性观察研究。我们收集了7例MPMNs的临床资料,并通过临床、形态学、影像学和免疫组化评估相结合的方法进行综合特征分析。

结果

7例MPMNs中,女性6例,男性1例。中位年龄为55岁。所有MPMNs在肺内均为多发,大小为0.01至0.5厘米。胸部CT检查显示磨玻璃影或实性结节。4例合并癌和/或肺炎,3例单独发生。7例患者中4例无明显症状;3例有胸痛、咳嗽、气短或咯血。肉眼可见多个白色结节,病变细胞沿肺泡间隔生长,形态相对正常,细胞质丰富,细胞边界不清,细胞核均匀,染色质细腻,无异型性;病变细胞呈巢状或漩涡状分布。免疫组化显示所有病例中EMA、PR、CD56和波形蛋白均为阳性。

结论

MPMNs是肺部罕见的良性病变,常为多发,直径通常小于0.5厘米,大多数无明显临床症状。MPMNs常通过胸部CT发现,可独立发生或与其他病变合并存在。EMA、PR、CD56、波形蛋白免疫组化染色阳性支持诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e384/9345627/0f2d60ff0db4/fonc-12-942517-g001.jpg

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