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局限性恶性胸膜间皮瘤:一种需要积极进行局部手术的独立临床实体。

Localised malignant pleural mesothelioma: a separate clinical entity requiring aggressive local surgery.

作者信息

Nakas Apostolos, Martin-Ucar Antonio E, Edwards John G, Waller David A

机构信息

Department of Thoracic Surgery, Glenfield Hospital, Groby Road, Leicester LE3 9QP, UK.

出版信息

Eur J Cardiothorac Surg. 2008 Feb;33(2):303-6. doi: 10.1016/j.ejcts.2007.09.043. Epub 2007 Dec 21.

Abstract

OBJECTIVE

Localised malignant pleural mesotheliomas are very rare and although there are sporadic reports in the literature showing that they have a different biological behaviour compared to diffuse MPM there is no major series published demonstrating results of surgical treatment. We present our experience in treating these tumours.

METHODS

Over an 8-year period we performed radical or debulking surgery in 218 patients with MPM. Ten of these patients had localised chest wall tumours and a biopsy either highly suspicious or confirming malignant pleural mesothelioma. They were all male with an average age of 65.9 (56-80) years. Three of the tumours were epithelioid, three biphasic and three sarcomatoid. They all had chest wall resections, with limited lung resections where the tumours were infiltrating the lung and reconstruction using a double prolene mesh and orthopaedic cement. Perioperative events and long-term survival were analysed and survival was compared to survival following operations for diffuse malignant pleural mesothelioma.

RESULTS

There was no 30-day mortality with only two patients suffering from pleural collections that required ultrasound guided drainage 2 and 8 weeks after the operation. Two patients died from disease progression 3 and 10 months after the operation. Using Kaplan-Meier analysis the mean survival was 56 months.

CONCLUSION

Our results suggest that surgery is indicated in treating localised MPM even in T4 (diffuse chest wall involvement) tumours but pleuropneumonectomy is not necessary. These tumours seem to have a different biological behaviour compared to diffuse MPM but further research, including identification of possibly different biological markers is necessary.

摘要

目的

局限性恶性胸膜间皮瘤非常罕见,尽管文献中有零星报道表明它们与弥漫性恶性胸膜间皮瘤(MPM)具有不同的生物学行为,但尚无发表的大宗病例系列展示手术治疗结果。我们介绍我们治疗这些肿瘤的经验。

方法

在8年期间,我们对218例MPM患者进行了根治性手术或减瘤手术。其中10例患者有局限性胸壁肿瘤,活检高度怀疑或确诊为恶性胸膜间皮瘤。他们均为男性,平均年龄65.9(56 - 80)岁。其中3例肿瘤为上皮样,3例为双向型,3例为肉瘤样。他们均接受了胸壁切除术,当肿瘤侵犯肺时进行了有限的肺切除术,并使用双层普理灵网片和骨科骨水泥进行重建。分析围手术期情况和长期生存率,并将生存率与弥漫性恶性胸膜间皮瘤手术后的生存率进行比较。

结果

无术后30天死亡率,仅2例患者出现胸腔积液,分别在术后2周和8周需要超声引导下引流。2例患者术后3个月和10个月因疾病进展死亡。采用Kaplan - Meier分析,平均生存期为56个月。

结论

我们的结果表明,即使是T4期(弥漫性胸壁受累)肿瘤,手术治疗局限性MPM也是可行的,但不需要进行胸膜肺切除术。与弥漫性MPM相比,这些肿瘤似乎具有不同的生物学行为,但需要进一步研究,包括识别可能不同的生物学标志物。

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