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Case Report: Solitary fibrous tumour of the pleura masquerading as catecholamine-secreting paraganglioma

机译:病例报告:伪装儿茶酚胺分泌性神经节瘤的胸膜孤立性纤维性肿瘤

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摘要

A 33-year-old African-American woman presented with left-sided chest pain for 2 months before admission. Physical examination revealed no breath sound in the left chest and CT scan of the chest showed total obliteration of the left pleural cavity. The patient also had hypertension and elevated urinary metanephrines, leading to a tentative diagnosis of a catecholamine-secreting paraganglioma. MRI revealed a large, heterogeneous soft tissue mass that occupied the entire left chest cavity, causing displacement of the heart and mediastinal structures to the right. Through a left thoracotomy incision, a tumour weighing 2790 g was removed along with a small portion of adherent lung. The tumour was positive for CD34 but negative for S-100, keratin, desmin and progesterone-receptor, which is consistent with pathological diagnosis of a solitary fibrous tumour of the pleura. The patient remains symptom free 4 years after the operation.
机译:一名33岁的非洲裔美国妇女在入院前出现左侧胸痛2个月。体格检查显示左胸无呼吸音,胸部CT扫描显示左胸膜腔完全闭塞。该患者还患有高血压和尿中肾上腺素升高,导致初步诊断为分泌儿茶酚胺的副神经节瘤。 MRI显示,巨大的异质性软组织肿块占据了整个左胸腔,从而导致心脏和右侧的纵隔结构移位。通过左胸切开术切口,切除了重2790μg的肿瘤以及一小部分附着的肺。肿瘤对CD34呈阳性,但对S-100,角蛋白,结蛋白和孕激素受体呈阴性,这与胸膜孤立性纤维性肿瘤的病理诊断是一致的。手术后4年无症状。

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