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Littoral cell angioma of the spleen in a patient with previous pulmonary sarcoidosis: a TNF-α related pathogenesis?

机译:先前患有肺结节病患者的脾脏沿海细胞血管瘤:与TNF-α相关的发病机制?

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Background Littoral cell angioma (LCA) is a rare vascular tumor of the spleen. Generally thought to be benign, additional cases of LCA with malignant features have been described. Thus, its malignant potential seems to vary and must be considered uncertain. The etiology remains unclear, but an immune dysregulation for the apparent association with malignancies of visceral organs or immune-mediated diseases has been proposed. Case Presentation We report a case of LCA in a 43-year old male patient who presented with a loss of appetite and intermittent upper abdominal pain. Computed tomography showed multiple hypoattenuating splenic lesions which were hyperechogenic on abdominal ultrasound. Lymphoma was presumed and splenectomy was performed. Pathological evaluation revealed LCA. Conclusions LCA is a rare, primary vascular neoplasm of the spleen that might etiologically be associated with immune dysregulation. In addition, it shows a striking association with synchronous or prior malignancies. With about one-third of the reported cases to date being co-existent with malignancies of visceral organs or immune-mediated diseases, this advocates for close follow-ups in all patients diagnosed with LCA. To our knowledge, this report is the first one of LCA associated with previous pulmonary sarcoidosis and hypothesizes a TNF-α related pathogenesis of this splenic tumor.
机译:背景技术沿海细胞血管瘤(LCA)是一种罕见的脾脏血管瘤。通常认为是良性的,已经描述了具有恶性特征的LCA的其他情况。因此,其恶性潜能似乎是变化的,必须被认为是不确定的。病因尚不清楚,但是已经提出了针对内脏器官恶性肿瘤或免疫介导的疾病的明显免疫关联失调。病例介绍我们报告了一位43岁的男性患者的LCA病例,该患者表现为食欲不振和间歇性上腹部疼痛。计算机体层摄影术显示出多个低衰减的脾脏病变,在腹部超声检查中具有高回声性。推测为淋巴瘤并行脾切除术。病理评估显示LCA。结论LCA是一种罕见的脾脏原发性血管肿瘤,其病因可能与免疫功能异常有关。此外,它显示出与同步或先前恶性肿瘤的惊人关联。迄今为止,约三分之一的报告病例与内脏器官的恶性肿瘤或免疫介导的疾病并存,因此主张对所有诊断为LCA的患者进行密切随访。据我们所知,该报告是与先前的肺结节病相关的LCA的第一个报告,并假设该脾脏肿瘤的TNF-α相关发病机理。

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