Primary Pulmonary Meningioma With Associated Multiple Micronodules: A Case Report With Comprehensive Diagnostic Overview

IF 1.5 Q4 ONCOLOGY Cancer reports Pub Date : 2024-06-24 DOI:10.1002/cnr2.2123
Daoqi Zhu, Zhuan Ou, Guangning Yan, Jiawang Cao, Enwu Xu
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Abstract

Background

Primary pulmonary meningioma (PPM) is an exceedingly rare neoplasm originating in the meninges within the lung. Despite sharing similarities with its central nervous system (CNS) counterparts, PPM presents unique diagnostic challenges and therapeutic considerations owing to its infrequent occurrence.

Case

This case report describes a 73-year-old male who underwent chest computed tomography (CT), which revealed a mass in the posterior basal segment of the right lower lobe, suggestive of a low-grade malignant tumor approximately 30–40 mm in size. Single-port video-assisted thoracoscopic surgery (VATS) was performed to resect the mass via localized lesion excision (lung wedge resection). Intraoperative frozen section pathology indicated a low-grade malignant epithelial tumor, leading to a decision for maximal lung function preservation, considering the patient's advanced age. The surgical team opted for a localized excision to ensure negative margins. Histopathological analysis confirmed the diagnosis of epithelioid PPM, a rare subtype even among PPM cases (World Health Organization [WHO] Grade I). The patient was discharged 9 days after surgery without complications and resumed normal daily activities 1 month postoperatively. The rarity of PPM precludes a standardized treatment protocol, with surgical resection as the primary approach. However, the efficacy of adjunctive therapies remains uncertain due to limited evidence.

Conclusion

This case report contributes to a better understanding of PPM and emphasizes the importance of a comprehensive diagnostic evaluation and individualized treatment planning for this rare entity.

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原发性肺脑膜瘤伴多发性小结节:病例报告与综合诊断概述
背景:原发性肺脑膜瘤(PPM原发性肺脑膜瘤(PPM)是一种极为罕见的起源于肺脑膜的肿瘤。病例:本病例报告描述了一名 73 岁的男性,他接受了胸部计算机断层扫描(CT),发现右下叶后基底段有一肿块,提示为低度恶性肿瘤,大小约 30-40 毫米。患者接受了单孔视频辅助胸腔镜手术(VATS),通过局部病灶切除术(肺楔形切除术)切除了肿块。术中冰冻切片病理显示为低度恶性上皮性肿瘤,考虑到患者年事已高,决定最大限度地保留肺功能。手术团队选择了局部切除,以确保阴性边缘。组织病理分析证实了上皮样肺癌的诊断,即使在肺癌病例中也是一种罕见的亚型(世界卫生组织[WHO]I级)。患者术后 9 天出院,无并发症,术后 1 个月恢复了正常的日常活动。由于 PPM 的罕见性,因此无法制定以手术切除为主的标准化治疗方案。然而,由于证据有限,辅助疗法的疗效仍不确定:本病例报告有助于人们更好地了解 PPM,并强调了对这种罕见疾病进行全面诊断评估和制定个性化治疗方案的重要性。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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