Murphy Alexandra N, Byrne Danielle, Salati Umer, Lawler Leo
Department of Radiology, Mater Misericordiae University Hospital, Dublin, Ireland.
BMJ Case Rep. 2019 Mar 20;12(3):e228267. doi: 10.1136/bcr-2018-228267.
A 51-year-old, otherwise well woman, presented with progressive severe dyspnoea. CT pulmonary angiogram (CTPA) demonstrated a large filling defect within the right main pulmonary artery with evidence of right heart strain. She was anticoagulated and discharged home; however, was readmitted with progression of symptoms and hypotension within 1 month. Repeat CTPA demonstrated progression of the filling defect. Formal surgical thrombectomy was performed with removal of an unusual cream-coloured, rubber-like material. Histological analysis revealed intravenous leiomyomatosis (IVL). IVL is a rare benign neoplasm, characterised by smooth muscle cell proliferation in vascular structures that can act aggressively. This case describes the workup, recognition and management of IVL.
一名51岁、其他方面健康的女性,出现进行性严重呼吸困难。胸部CT血管造影(CTPA)显示右主肺动脉内有一个大的充盈缺损,并伴有右心劳损的迹象。她接受了抗凝治疗后出院回家;然而,在1个月内因症状进展和低血压再次入院。重复CTPA显示充盈缺损有进展。进行了正式的手术血栓切除术,切除了一种不寻常的奶油色、橡胶样物质。组织学分析显示为静脉内平滑肌瘤病(IVL)。IVL是一种罕见的良性肿瘤,其特征是血管结构中的平滑肌细胞增殖,可具有侵袭性。本病例描述了IVL的检查、识别和管理。