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本文引用的文献

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2
Nationwide incidence of sarcomas and connective tissue tumors of intermediate malignancy over four years using an expert pathology review network.利用专家病理审查网络,四年间全国范围内的中间恶性肉瘤和结缔组织肿瘤的发病率。
PLoS One. 2021 Feb 25;16(2):e0246958. doi: 10.1371/journal.pone.0246958. eCollection 2021.
3
An unusual presentation of pneumothorax associated with cystic lung metastasis from epithelioid sarcoma: A case report and review of the literature.上皮样肉瘤肺囊性转移伴气胸的罕见表现:一例报告并文献复习
Oncol Lett. 2018 Apr;15(4):4531-4534. doi: 10.3892/ol.2018.7868. Epub 2018 Jan 26.
4
Risk assessment in solitary fibrous tumors: validation and refinement of a risk stratification model.孤立性纤维瘤的风险评估:风险分层模型的验证和改进。
Mod Pathol. 2017 Oct;30(10):1433-1442. doi: 10.1038/modpathol.2017.54. Epub 2017 Jul 21.
5
Occult primary pulmonary synovial sarcoma presenting as recurrent spontaneous pneumothorax and explosive progression.以复发性自发性气胸和爆发性进展为表现的隐匿性原发性肺滑膜肉瘤。
Thorac Cancer. 2017 Mar;8(2):121-123. doi: 10.1111/1759-7714.12410. Epub 2016 Dec 20.
6
The Current Status of Solitary Fibrous Tumor: Diagnostic Features, Variants, and Genetics.孤立性纤维性肿瘤的现状:诊断特征、变异型及遗传学
Int J Surg Pathol. 2016 Jun;24(4):281-92. doi: 10.1177/1066896915627485. Epub 2016 Jan 25.
7
Spontaneous pneumothorax as the first manifestation of lung cancer: two case report.自发性气胸作为肺癌的首发表现:两例病例报告
J Thorac Dis. 2015 Aug;7(8):E252-4. doi: 10.3978/j.issn.2072-1439.2015.07.31.
8
Bronchial carcinoid tumor presenting with recurrent pneumothorax.以复发性气胸为表现的支气管类癌肿瘤。
Rev Port Pneumol. 2014 Mar-Apr;20(2):115-6. doi: 10.1016/j.rppneu.2013.08.005. Epub 2014 Jan 17.
9
Malignant solitary fibrous tumors of the pleura: retrospective review of a multicenter series.胸膜恶性孤立性纤维瘤:多中心系列回顾性研究。
J Thorac Oncol. 2012 Nov;7(11):1698-706. doi: 10.1097/JTO.0b013e3182653d64.
10
Solitary fibrous tumors of the pleura.胸膜孤立性纤维瘤。
Curr Opin Pulm Med. 2012 Jul;18(4):339-46. doi: 10.1097/MCP.0b013e328352f696.

胸膜隐匿性孤立性纤维瘤,表现为复发性自发性气胸。

Occult solitary fibrous tumour of the pleura presenting as recurrent spontaneous pneumothorax.

机构信息

Department of Pneumology, Sint-Elisabeth Hospital, Zottegem, Belgium

Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium.

出版信息

BMJ Case Rep. 2024 Mar 19;17(3):e257161. doi: 10.1136/bcr-2023-257161.

DOI:10.1136/bcr-2023-257161
PMID:38508593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10952873/
Abstract

A woman in her 30s, non-smoker, presented at the emergency department two times because of spontaneous pneumothorax. The first episode was treated with small bore catheter drainage, while during the second episode-occurring only 1 week later-thoracoscopic talcage was attempted. The postoperative course was characterised by slow clinical and radiological resolution, and recurrence 3 days after discharge. Eventually, multiportal video-assisted thoracoscopic exploration identified an interfissural solid mass. Resection and further work-up revealed the diagnosis of 'low-risk' solitary fibrous tumour (SFT) stage pT1N0M0. The interdisciplinary tumour board advised no adjuvant therapy. A CT thorax was scheduled in 1 year for follow-up. The patient was discharged without complications and has had no recurrences of pneumothorax at 6 months of follow-up. This report shows that SFT can easily be missed on initial presentation and should be considered in the differential diagnosis of pneumothorax, especially when frequently recurring.

摘要

一位 30 多岁的女性,不吸烟,因自发性气胸两次到急诊科就诊。第一次发作采用小口径导管引流治疗,而第二次发作(仅在 1 周后)则尝试了胸腔镜滑石粉固定术。术后病程表现为临床和影像学缓慢缓解,出院后 3 天复发。最终,多端口电视辅助胸腔镜探查发现了一个界面间实性肿块。切除和进一步检查显示诊断为“低风险”孤立性纤维瘤(SFT)分期 pT1N0M0。多学科肿瘤委员会建议不进行辅助治疗。计划在 1 年内进行胸部 CT 随访。患者无并发症出院,在随访 6 个月时气胸无复发。本报告表明,SFT 在初次就诊时很容易被遗漏,在气胸的鉴别诊断中应考虑到 SFT,特别是在频繁复发时。