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肺黏膜相关淋巴组织淋巴瘤合并肺癌的临床分析

Clinical analysis of pulmonary mucosa-associated lymphoid tissue lymphoma coexisting with lung cancer.

作者信息

Yang Heng, Li Man-Hui, Li Qiu-Hong, Cheng Ke-Bin, Cao Wei-Jun

机构信息

Department of Pulmonary and Critical Care Medicine, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.

出版信息

BMC Cancer. 2025 Jan 22;25(1):120. doi: 10.1186/s12885-025-13441-4.

Abstract

BACKGROUND

Primary pulmonary Mucosa-associated lymphoid tissue (MALT) lymphoma is a sporadic disease with a favorable prognosis. Particularly, pulmonary MALT lymphoma coexisting with lung cancer is not only rare but also prone to misdiagnosis. The clinical characteristics and prognostic factors of this co-occurrence, however, remain poorly understood.

METHODS

We retrospectively analyzed the clinical, imaging, genetic mutations and pathological data among adult patients with pulmonary MALT lymphoma coexisting with lung cancer who were confirmed by pathological examinations after operation at Shanghai Pulmonary Hospital between 1st January 2013 and 31st May 2024.

RESULTS

After exclusions, a total of 14 patients were included in the study, of which eleven patients were women and only 3 were men, with a median age of 57 [IQR: 53-67] years. Pulmonary MALT lymphoma presented a median diameter of 14 mm (IQR: 6-23). Nodule was the most frequent CT feature and existing pattern of pulmonary lesions (n = 8). The lung cancer was with a median diameter of 10.7 [IQR:6,20] mm, with nodules as the predominant CT feature (n = 12). Six patients manifested dual primary malignancies within the same lung lobe, termed collision tumors, whereas the remaining eight had lesions in different lobes. Five cases exhibited EGFR mutant, and one case showed no mutation. 13 patients were pathological confirmed with lung adenocarcinoma and one with microcarcinoma. Postoperatively, all-cause mortality rate was low, indicating a positive prognosis. One patient died 41 months after surgery due to a pulmonary infection, while the remaining 13 patients were in good condition with an average follow-up of 37.92 months.

CONCLUSIONS

In patients with pulmonary lesions, particularly multiple lesions, comprehensive preoperative evaluation is crucial to prevent misdiagnosis or missed diagnoses. Besides, surgical resection is desirable when both lung cancer and MALT are at an early stage and can be resected with minimally invasive surgery (minimally lung resection).

摘要

背景

原发性肺黏膜相关淋巴组织(MALT)淋巴瘤是一种散发性疾病,预后良好。特别是,肺MALT淋巴瘤与肺癌共存不仅罕见,而且容易误诊。然而,这种共存情况的临床特征和预后因素仍知之甚少。

方法

我们回顾性分析了2013年1月1日至2024年5月31日在上海肺科医院接受手术后经病理检查确诊的成年肺MALT淋巴瘤合并肺癌患者的临床、影像、基因突变和病理数据。

结果

排除后,共有14例患者纳入研究,其中11例为女性,仅3例为男性,中位年龄为57岁[四分位间距:53 - 67岁]。肺MALT淋巴瘤的中位直径为14毫米(四分位间距:6 - 23)。结节是最常见的CT特征和肺部病变的现存模式(n = 8)。肺癌的中位直径为10.7[四分位间距:6,20]毫米,以结节为主要CT特征(n = 12)。6例患者在同一肺叶内表现为双原发性恶性肿瘤,称为碰撞瘤,而其余8例在不同肺叶有病变。5例表现为表皮生长因子受体(EGFR)突变,1例未显示突变。13例经病理确诊为肺腺癌,1例为微癌。术后全因死亡率较低,提示预后良好。1例患者术后41个月因肺部感染死亡,其余13例患者情况良好,平均随访37.92个月。

结论

对于肺部病变患者,尤其是多发病变患者,术前全面评估对于防止误诊或漏诊至关重要。此外,当肺癌和MALT均处于早期且可通过微创手术(肺叶微创切除)切除时,手术切除是可取的。

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