Alghamdi Zeead M, Othman Sharifah A, Al-Yousef Mohammed J, AlFadel Bader Z
Thoracic Surgery Division, Department of Surgery, College of Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Eastern Region, Saudi Arabia.
Department of Pathology, Imam Abdulrahman Bin Faisal University, Dammam, Eastern Region, Saudi Arabia.
Ann Thorac Med. 2020 Apr-Jun;15(2):98-101. doi: 10.4103/atm.ATM_14_20. Epub 2020 Apr 3.
Intrapulmonary solitary fibrous tumors (SFTs) are sporadic mesenchymal neoplasms that typically arise from visceral or parietal pleura. While accounting for <5% of all pleural tumors, SFTs are known to occur in nearly all bodily organs, including nasopharynx, bladder, prostate, soft tissue of neck, buttocks, extremities, and abdominal wall. Such tumors have been previously designated localized fibrous mesothelioma or pleural fibroma. SFTs have no genetic basis and are unrelated to environmental factors such as tobacco smoking or asbestos exposure. Herein, we describe a 24-year-old woman whose clinical presentation mimicked atypical carcinoid tumor. A diagnosis of intrapulmonary SFT was achieved by surgical resection.
肺内孤立性纤维瘤(SFTs)是散发性间叶性肿瘤,通常起源于脏层或壁层胸膜。虽然SFTs占所有胸膜肿瘤的比例不到5%,但已知几乎可发生于身体的所有器官,包括鼻咽、膀胱、前列腺、颈部、臀部、四肢软组织及腹壁。此类肿瘤以前被称为局限性纤维性间皮瘤或胸膜纤维瘤。SFTs没有遗传基础,与吸烟或接触石棉等环境因素无关。在此,我们描述一名24岁女性,其临床表现酷似非典型类癌肿瘤。通过手术切除确诊为肺内SFT。