Solitary calcifying fibrous tumour of the pleura: A case report and literature review

Harry James Gaffney , Sonja Klebe , Kais Kasem , Sarita Prabhakaran
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引用次数: 0

Abstract

Calcifying fibrous tumours of the pleura (CFTPs) are extremely rare benign tumours with uncertain aetiology, with only 34 cases, including this one, reported worldwide to date. CFTPs commonly originate from subcutaneous and deep soft tissues of the gastrointestinal tract and pleura. It is essential to differentiate CFTP from other pleural intrathoracic masses that present similarly but are challenging with radiological imaging alone. As a result, excision via surgical intervention alongside immunohistological and histological assessment is the current best method for definitive diagnosis. Due to the significantly low incidence of CFTP, extensive sample studies for further research are currently not possible. As a result, all cases of CFTP should be reported to help improve future research in diagnostic accuracy and understanding of pathogenicity and aetiology. We are reporting a case of an incidentally detected CFTP on CT in a 30-year-old female.

胸膜孤立性钙化纤维瘤1例报告及文献复习
胸膜钙化纤维瘤(CFTP)是一种极为罕见的良性肿瘤,病因不确定,迄今为止,全球仅报告了34例,包括这一例。CFTP通常起源于胃肠道和胸膜的皮下和深层软组织。将CFTP与其他胸内胸膜肿块区分开来是至关重要的,这些肿块表现相似,但仅凭放射学成像具有挑战性。因此,通过手术干预以及免疫组织学和组织学评估进行切除是目前确定诊断的最佳方法。由于CFTP的发病率极低,目前尚不可能进行广泛的样本研究以进行进一步研究。因此,应报告所有CFTP病例,以帮助提高未来诊断准确性的研究以及对致病性和病因的理解。我们报告了一例30岁女性的CT上偶然检测到的CFTP。
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