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儿童多房性和弥漫性恶性腹膜间皮瘤。

Multicystic and diffuse malignant peritoneal mesothelioma in children.

机构信息

Department of Pediatric Surgery, University Hospital of Saint-Etienne, Saint-Priest-en-Jarez, France.

Department of Pediatric Surgery, University Hospital of Rennes, Rennes, France.

出版信息

Pediatr Blood Cancer. 2020 Jun;67(6):e28286. doi: 10.1002/pbc.28286. Epub 2020 Apr 11.

Abstract

BACKGROUND

Malignant and multicystic peritoneal mesotheliomas are extremely rare tumors in children, developing from mesothelial cells. No specific guidelines are available at this age.

METHODS

We performed a retrospective analysis of all identified children (< 18-year-old) treated in France from 1987 to 2017 for a diffuse malignant peritoneal mesothelioma (DMPM) or a multicystic peritoneal mesothelioma (MCPM).

RESULTS

Fourteen patients (5 males and nine females), aged 2.2 to 17.5 years, were included. The most frequent presenting symptoms were abdominal pain, ascitis, and alteration in the general condition. Eight patients had epithelioid mesothelioma, three had biphasic mesothelioma, and three had MCPM. Eight patients with DMPM diagnosis received cytoreductive surgery (CRS) with hyperthermic intraperitoneal chemotherapy (HIPEC). Among them, six patients had neoadjuvant systemic chemotherapy, one patient, post-operative chemotherapy, and one patient CRS and HIPEC only. Three patients received only systemic chemotherapy. All patients with MCPM had only surgery. After a median follow-up of seven years (2-15), six patients (6/11; one death) with DMPM and two patients (two/three) with MCPM had a local and distant recurrences.

CONCLUSION

Peritoneal mesothelioma in children is a rare condition with difficult diagnosis and high risk of recurrence. Worldwide interdisciplinary collaboration and networking are mandatory to help diagnosis and provide harmonious treatment guidelines.

摘要

背景

恶性多房性腹膜间皮瘤是儿童中极为罕见的肿瘤,来源于间皮细胞。目前针对该年龄段尚无特定的指导原则。

方法

我们对 1987 年至 2017 年期间在法国接受治疗的所有儿童(<18 岁)的弥漫性恶性腹膜间皮瘤(DMPM)或多房性腹膜间皮瘤(MCPM)进行了回顾性分析。

结果

纳入 14 名患者(5 名男性和 9 名女性),年龄 2.2 至 17.5 岁。最常见的首发症状为腹痛、腹水和一般状况改变。8 名患者为上皮样间皮瘤,3 名患者为双相型间皮瘤,3 名患者为 MCPM。8 名 DMPM 诊断患者接受了细胞减灭术(CRS)联合腹腔内热灌注化疗(HIPEC)。其中 6 名患者接受了新辅助全身化疗,1 名患者接受了术后化疗,1 名患者仅接受了 CRS 和 HIPEC。3 名患者仅接受了全身化疗。所有 MCPM 患者仅接受了手术。中位随访 7 年(2-15 年)后,6 名(11 名中的 6 名;1 名死亡)DMPM 患者和 2 名 MCPM 患者出现局部和远处复发。

结论

儿童腹膜间皮瘤是一种罕见疾病,诊断困难,复发风险高。全球范围内的跨学科合作和网络建设是必要的,以帮助诊断并提供协调一致的治疗指南。

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