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胸膜腔软组织肉瘤。

Soft tissue sarcoma of the pleural cavity.

作者信息

Myoui A, Aozasa K, Iuchi K, Mori T, Yamamoto S, Kuratsu S, Ohsawa M, Ono K, Matsumoto K

机构信息

Department of Pathology, Osaka University Medical School, Japan.

出版信息

Cancer. 1991 Oct 1;68(7):1550-4. doi: 10.1002/1097-0142(19911001)68:7<1550::aid-cncr2820680716>3.0.co;2-i.

DOI:10.1002/1097-0142(19911001)68:7<1550::aid-cncr2820680716>3.0.co;2-i
PMID:1893356
Abstract

Seventeen cases of soft tissue sarcoma (STS) developing in the pleural cavity were collected from Japanese hospitals, and their clinical and pathologic findings summarized. Eight of the 17 patients had a 15-year to 50-year (mean, 28.8) history of chronic pleural inflammatory disease (pleuritis, pyothorax, and pulmonary tuberculosis) before the onset of the pleural sarcoma. Histologically, malignant fibrous histiocytoma was the most common tumor type (11 cases), followed by angiosarcoma (four). The age at diagnosis of the sarcoma ranged from 15 to 74 years (mean, 58); the male-to-female ratio was 3.3:1. In the eight cases of sarcoma associated with chronic pleural inflammatory disease, male preponderance was more marked (7:1). The commonest presenting symptom was chest pain. A mass could be detected by chest roentgenograms in 13 patients and computed tomographic scans in 15 patients. No patient had distant metastases at first admission. Thirteen patients were treated by surgery, chemotherapy, and/or radiation therapy. Thirteen of the 17 patients died 1 to 87 months (mean, 14.2) after therapy for STS. The actuarial 1-year survival rate was 38.5%. These findings suggest that long-standing pleural inflammation might be an etiologic factor for development of pleural STS.

摘要

从日本医院收集了17例发生于胸腔的软组织肉瘤(STS)病例,并总结了其临床和病理特征。17例患者中有8例在胸腔肉瘤发病前有15年至50年(平均28.8年)的慢性胸膜炎性疾病(胸膜炎、脓胸和肺结核)病史。组织学上,恶性纤维组织细胞瘤是最常见的肿瘤类型(11例),其次是血管肉瘤(4例)。肉瘤诊断时的年龄为15岁至74岁(平均58岁);男女比例为3.3:1。在8例与慢性胸膜炎性疾病相关的肉瘤病例中,男性优势更为明显(7:1)。最常见的症状是胸痛。13例患者胸部X线片可检测到肿块,15例患者计算机断层扫描可检测到肿块。首次入院时无患者有远处转移。13例患者接受了手术、化疗和/或放疗。17例患者中有13例在接受STS治疗后1至87个月(平均14.2个月)死亡。精算1年生存率为38.5%。这些发现表明,长期的胸膜炎可能是胸腔STS发生的一个病因。

相似文献

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Soft tissue sarcoma of the pleural cavity.胸膜腔软组织肉瘤。
Cancer. 1991 Oct 1;68(7):1550-4. doi: 10.1002/1097-0142(19911001)68:7<1550::aid-cncr2820680716>3.0.co;2-i.
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Non-Hodgkin's lymphoma of the pleural cavity developing from long-standing pyothorax. Summary of clinical and pathological findings in thirty-seven cases.由长期脓胸发展而来的胸腔非霍奇金淋巴瘤。37例临床及病理结果总结
Jpn J Clin Oncol. 1989 Sep;19(3):249-57.
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[A clinical study of six surgically treated patients with malignant tumors arising from chronic pleuritis and pyothorax].6例慢性胸膜炎和脓胸所致恶性肿瘤手术治疗患者的临床研究
Nihon Kyobu Geka Gakkai Zasshi. 1989 Feb;37(2):281-6.
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[Non-Hodgkin's lymphoma of the pleural cavity developing from long-standing pyothorax].[源于长期脓胸的胸腔非霍奇金淋巴瘤]
Rinsho Ketsueki. 1990 May;31(5):547-53.
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[Two cases of sarcoma arising from the chest wall in chronic pleuritis or pyothorax].[两例源于慢性胸膜炎或脓胸胸壁的肉瘤]
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Angiosarcoma developing from chronic pyothorax.源于慢性脓胸的血管肉瘤。
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Epithelioid angiosarcoma arising in the tuberculous pyothorax: report of an autopsy case.结核性脓胸并发上皮样血管肉瘤:一例尸检病例报告
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引用本文的文献

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Primary pleural angiosarcoma as a mimicker of mesothelioma: a case report **VS**.原发性胸膜血管肉瘤酷似间皮瘤:病例报告**VS**。
Diagn Pathol. 2011 Dec 30;6:130. doi: 10.1186/1746-1596-6-130.
2
Primary intracranial leiomyosarcoma: a case report and review of the literature.原发性颅内平滑肌肉瘤:一例病例报告并文献复习
Childs Nerv Syst. 2009 Aug;25(8):1013-7. doi: 10.1007/s00381-009-0845-3. Epub 2009 Mar 24.
3
Commentary: pleural empyema and malignancy--another dimension.评论:胸膜脓胸与恶性肿瘤——另一个层面
Thorax. 1996 Jan;51(1):107-8. doi: 10.1136/thx.51.1.107.
4
Pleural non-Hodgkin's lymphoma arising in a patient with a chronic pyothorax.一名慢性脓胸患者发生的胸膜非霍奇金淋巴瘤。
Thorax. 1996 Jan;51(1):103-4. doi: 10.1136/thx.51.1.103.
5
Artificial pneumothorax as a risk factor for development of pleural lymphoma.人工气胸作为胸膜淋巴瘤发生的一个危险因素。
Jpn J Cancer Res. 1993 Jan;84(1):55-7. doi: 10.1111/j.1349-7006.1993.tb02784.x.