Suppr超能文献

病例报告:1例采用多模式联合治疗的原发性心包间皮瘤病例。

Case Report: A case of primary pericardial mesothelioma treated with multimodal combined therapy.

作者信息

Gong Jinlan, Wu Xiaofeng, Wang Jiehua

机构信息

Department of Radiation Oncology, Shidong Hospital, Yangpu District, Shanghai, China.

出版信息

Front Cardiovasc Med. 2024 Oct 7;11:1433668. doi: 10.3389/fcvm.2024.1433668. eCollection 2024.

Abstract

BACKGROUND

Primary pericardial mesothelioma (PMPM) is a rare, aggressive, and lethal form of cancer. Due to its rarity, low incidence and poor prognosis, PMPM has no accepted standard-of-care treatment options with management and outcomes often extrapolated from diffuse pleural mesothelioma. Disease-specific studies are needed to better define PMPM. We report a case of PMPM highlighting the potential role for multimodal combined therapy.

CASE REPORT

The patient is a 62 years old female who had nonspecific syndromes and inconclusive image findings in May 2023. Then monthly follow-up echocardiography was performed. Two months later, cardiac ultrasound showed pericardial fluid. Pericardiocentesis with pericardial drain was performed. The fluid was bloody, cultivations for tuberculosis were negative and cytological analysis of the fluid showed no malignant cells. Positron emission tomography-computed tomography revealed that the lesion was localized at the anterior and left part of the mediastinum without distant metastasis. Followed up a pericardiectomy was operated. The diagnosis of PMPM is determined by pathological and immunohistochemical evaluation of tissue specimens. Postoperative patient experienced chest pain, right shoulder and upper limb swelling and pain. Pain management and anticoagulant therapy were administered. The patient underwent multimodal therapy consisting of surgical resection, six cycles of chemotherapy (carboplatin plus pemetrexed) in combination with pembrolizumab, and sequential adjuvant intensity-modulated radiation therapy, totaling 50 Gy in 25 fractions, as the first-line treatment, resulting in complete relief of symptoms and satisfactory outcomes with no complications. Presently, the tumor is under local control, with no signs of distant metastasis, and maintenance immunotherapy is scheduled. Continued observation is necessary for monitoring subsequent disease progression.

CONCLUSION

PMPM represents a distinct disease with no universally accepted treatment options. The case suggests that multimodal treatment may improve outcomes in selected patients with PMPM.

摘要

背景

原发性心包间皮瘤(PMPM)是一种罕见、侵袭性且致命的癌症形式。由于其罕见性、低发病率和不良预后,PMPM没有被广泛接受的标准治疗方案,其管理和治疗结果通常是从弥漫性胸膜间皮瘤推断而来。需要开展针对该疾病的研究以更好地明确PMPM。我们报告一例PMPM病例,突出多模式联合治疗的潜在作用。

病例报告

患者为一名62岁女性,2023年5月出现非特异性症状且影像检查结果不明确。随后每月进行超声心动图随访。两个月后,心脏超声显示心包积液。进行了心包穿刺置管引流。引流液为血性,结核培养阴性,引流液细胞学分析未发现恶性细胞。正电子发射断层扫描 - 计算机断层扫描显示病变位于纵隔前部和左侧,无远处转移。随后进行了心包切除术。PMPM的诊断通过组织标本的病理和免疫组化评估确定。术后患者出现胸痛、右肩及上肢肿胀疼痛。给予了疼痛管理和抗凝治疗。患者接受了多模式治疗,作为一线治疗包括手术切除、六个周期的化疗(卡铂联合培美曲塞)联合帕博利珠单抗,以及序贯辅助调强放疗,共25次分割,总量50 Gy,症状完全缓解,结果令人满意,无并发症。目前,肿瘤处于局部控制状态,无远处转移迹象,计划进行维持免疫治疗。持续观察对于监测后续疾病进展很有必要。

结论

PMPM是一种独特的疾病,没有普遍接受的治疗方案。该病例表明多模式治疗可能改善部分PMPM患者的治疗结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a0b/11491337/52d3f2ec6d2a/fcvm-11-1433668-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验