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巨大支气管类癌肿瘤:一种多学科方法。

Giant bronchial carcinoid tumors: a multidisciplinary approach.

作者信息

Fischer S, Kruger M, McRae K, Merchant N, Tsao M S, Keshavjee S

机构信息

Department of Surgery, The Toronto General Hospital, University of Toronto, Ontario, Canada.

出版信息

Ann Thorac Surg. 2001 Jan;71(1):386-93. doi: 10.1016/s0003-4975(00)02251-7.

DOI:10.1016/s0003-4975(00)02251-7
PMID:11216797
Abstract

BACKGROUND

Bronchial carcinoid tumors account for approximately 2% of all lung tumors. Although they were considered benign lesions, they are now categorized malignant, occasionally with poor prognosis. The clinical symptoms can be highly variable and are often present for many years before diagnosis. Whereas some carcinoids are entirely asymptomatic, others are accompanied by carcinoid or paraneoplastic syndromes.

METHODS

We describe the multidisciplinary management of a 34-year-old female patient with a massive actively secreting bronchial carcinoid tumor of the right lung. Furthermore, we provide a review of the literature regarding the operative treatment and the perioperative management of pulmonary carcinoid tumors with respect to surgical, anesthetic, radiologic, and pathologic considerations.

RESULTS

In the reported case, the first symptoms were chronic watery diarrhea, skin flushing, progressive shortness of breath, and increasing right shoulder pain. When the patient initially presented at our institution, the tumor had already reached an enormous size and it involved the right and left atrium as well as the atrial septum. Using an evidence-based, multidisciplinary approach the patient was treated successfully with extended surgical resection.

CONCLUSIONS

Carcinoid tumors are potentially curable even if they reach a significant size and thus an aggressive strategy is warranted. The management of such cases requires careful investigation, planning, and treatment with collaborative expertise provided by a multidisciplinary team. We demonstrated that this approach can lead to a favorable outcome in what first appeared to be a formidable and unresectable tumor.

摘要

背景

支气管类癌肿瘤约占所有肺部肿瘤的2%。尽管它们曾被认为是良性病变,但现在被归类为恶性肿瘤,偶尔预后较差。临床症状变化很大,在诊断前往往已存在多年。有些类癌完全没有症状,而其他类癌则伴有类癌综合征或副肿瘤综合征。

方法

我们描述了一名34岁女性患者的多学科管理情况,该患者患有右肺巨大且活跃分泌的支气管类癌肿瘤。此外,我们就手术、麻醉、放射学和病理学方面的考虑,对有关肺类癌肿瘤手术治疗和围手术期管理的文献进行了综述。

结果

在该报道病例中,最初症状为慢性水样腹泻、皮肤潮红、进行性气短和右肩疼痛加剧。当患者首次到我院就诊时,肿瘤已长得非常大,累及右心房、左心房以及房间隔。采用基于循证的多学科方法,患者通过扩大手术切除获得成功治疗。

结论

即使类癌肿瘤长得很大,它们仍有可能治愈,因此需要采取积极的策略。此类病例的管理需要仔细的检查、规划,并由多学科团队提供协作性专业知识进行治疗。我们证明,这种方法可以在最初看似棘手且无法切除的肿瘤治疗中取得良好效果。

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1
Giant bronchial carcinoid tumors: a multidisciplinary approach.巨大支气管类癌肿瘤:一种多学科方法。
Ann Thorac Surg. 2001 Jan;71(1):386-93. doi: 10.1016/s0003-4975(00)02251-7.
2
Pediatric Bronchial Carcinoid Tumors: A Case Series and Review of the Literature.小儿支气管类癌肿瘤:病例系列及文献综述
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Pulmonary and thymic carcinoid tumors.肺和胸腺类癌肿瘤。
World J Surg. 1996 Feb;20(2):189-95. doi: 10.1007/s002689900029.
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Bronchial carcinoid tumors: nodal status and long-term survival after resection.支气管类癌肿瘤:切除术后的淋巴结状态及长期生存情况
Ann Thorac Surg. 2004 May;77(5):1781-5. doi: 10.1016/j.athoracsur.2003.10.089.
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Total lung preservation following mainstem-bronchial resection for carcinoid tumor.类癌肿瘤主支气管切除术后的全肺保留
J La State Med Soc. 2003 Sep-Oct;155(5):256-8.
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Bronchial carcinoid tumors: long-term outcome after surgery.支气管类癌肿瘤:手术后的长期预后
Neoplasma. 2003;50(1):60-5.
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Carcinoid crisis after biopsy of a bronchial carcinoid.支气管类癌活检后发生类癌危象。
Ann Thorac Surg. 1993 Dec;56(6):1403-5. doi: 10.1016/0003-4975(93)90696-f.
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Long-term outcome after resection for bronchial carcinoid tumors.支气管类癌肿瘤切除术后的长期预后。
Eur J Cardiothorac Surg. 2000 Aug;18(2):156-61. doi: 10.1016/s1010-7940(00)00493-0.
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Management of the ectopic ACTH syndrome due to thoracic carcinoids.由胸段类癌引起的异位促肾上腺皮质激素综合征的管理。
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