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原发性肺淋巴瘤的临床特征与外科治疗:一项回顾性研究

Clinical Features and Surgical Treatment of Primary Pulmonary Lymphoma: A Retrospective Study.

作者信息

Shen Hui, Zhou Yaodong

机构信息

Department of Thoracic Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.

出版信息

Front Oncol. 2022 Feb 3;12:779395. doi: 10.3389/fonc.2022.779395. eCollection 2022.

Abstract

BACKGROUND

Primary pulmonary lymphoma (PPL) is a rare clonal lymphoproliferative lung disease. The present study analyzes the clinical features, imaging data, pathologic characteristics, treatment, and prognosis of PPL patients, with the aim to discuss the appropriate diagnosis and therapy of PPL patients in thoracic surgery.

METHODS

We performed a retrospective analysis on 36 patients with PPL confirmed by postoperative pathology between 2006 and 2020. We divided the patients into low-stage (IE) and high-stage (IIE) groups using modified Ann Arbor staging. The clinical manifestations, imaging findings, treatment modalities, and outcomes were evaluated.

RESULTS

The female to male ratio was 1.57:1 and the median age was 55 (31-69) years old. The majority of the patients had stage IE disease (75%; 27 of 36) and 9 patients had stage IIE disease. Patients with advancing stage were more likely to have respiratory symptoms. The imaging findings presented solid nodule or mass, pneumonia-like consolidative pattern, ground-glass opacity, and mixed pattern. There were 31 cases of mucosa-associated lymphoid tissue lymphoma (MALT), 2 diffuse large B-cell lymphoma (DLBCL), 2 nodular sclerosing Hodgkin's lymphoma, and 1 marginal zone B-cell lymphoma. Two patients were diagnosed with PPL and non-small cell lung cancer (NSCLC) synchronously (one AIS and MIS and one lung adenocarcinoma). All the patients received surgery. Nine patients received adjuvant therapy after surgery (five radiotherapy, two chemotherapy, and two chemoradiotherapy). Thirty-four patients had a median follow-up time of 31 months (follow-up range: 7-152 months). Of the 34 patients, 1 patient died of liver metastases and 1 patient died of intestinal metastases.

CONCLUSIONS

Our retrospective analysis suggested that most PPLs were indolent and had favorable prognosis, but the discrimination of PPL with other lung diseases was difficult. Preoperative biopsy and intraoperative frozen section examination might help in the surgical choice. Limited lung resection was enough for peripherally localized PPL.

摘要

背景

原发性肺淋巴瘤(PPL)是一种罕见的克隆性淋巴细胞增殖性肺部疾病。本研究分析PPL患者的临床特征、影像学数据、病理特征、治疗及预后,旨在探讨胸外科中PPL患者的合适诊断及治疗方法。

方法

我们对2006年至2020年间36例经术后病理确诊为PPL的患者进行回顾性分析。采用改良的Ann Arbor分期将患者分为低分期(IE)组和高分期(IIE)组。评估临床表现、影像学表现、治疗方式及结果。

结果

男女比例为1.57:1,中位年龄为55(31 - 69)岁。大多数患者为IE期疾病(75%;36例中的27例),9例为IIE期疾病。分期较晚患者更易出现呼吸道症状。影像学表现为实性结节或肿块、肺炎样实变影、磨玻璃影及混合影。有31例黏膜相关淋巴组织淋巴瘤(MALT)、2例弥漫性大B细胞淋巴瘤(DLBCL)、2例结节硬化型霍奇金淋巴瘤及1例边缘区B细胞淋巴瘤。2例患者同时诊断为PPL和非小细胞肺癌(NSCLC)(1例为原位腺癌和微浸润腺癌,1例为肺腺癌)。所有患者均接受了手术。9例患者术后接受了辅助治疗(5例放疗、2例化疗、2例放化疗)。34例患者的中位随访时间为31个月(随访范围:7 - 152个月)。34例患者中,1例死于肝转移,1例死于肠转移。

结论

我们的回顾性分析表明,大多数PPL进展缓慢且预后良好,但PPL与其他肺部疾病的鉴别困难。术前活检及术中冰冻切片检查可能有助于手术选择。对于周围型局限性PPL,有限的肺切除就足够了。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e851/8850835/2313b92d88c5/fonc-12-779395-g001.jpg

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