Poudyal S, Pradhan M, Chapagain S, Luitel B R, Chalise P R, Sharma U K, Gyawali P R
Department of Urology and Renal Transplant Surgery, Tribhuvan University Teaching Hospital, Kathmandu, Nepal.
Case Rep Urol. 2017;2017:6270436. doi: 10.1155/2017/6270436. Epub 2017 Jun 15.
Pheochromocytoma associated with inferior vena cava (IVC) thrombosis is very rare. A 27-year-old female presented with right flank pain and hypertensive urgency. Contrast-enhanced CT abdomen and gadolinium-contrast MRI abdomen revealed right adrenal mass suspicious of malignancy with invasion and compression to the right IVC wall along with IVC thrombus extending from the level of renal veins to the level of confluence with hepatic veins. Her routine laboratory investigations including 24-hour urine fractionated metanephrines, vanillylmandelic acid, and cortisol were normal. Right adrenalectomy with IVC thrombectomy was done. Perioperative period was uneventful. Histopathology of the mass turned out to be pheochromocytoma with thrombus revealing fibroadipose tissue with fibrin. Pheochromocytoma may present with IVC thrombus as well as normal serum and urinary markers. Thus, clinical suspicion is imperative in perioperative management of adrenal mass.
嗜铬细胞瘤合并下腔静脉(IVC)血栓形成非常罕见。一名27岁女性出现右侧腰痛和高血压急症。腹部增强CT和钆增强腹部MRI显示右肾上腺肿块,怀疑为恶性,侵犯并压迫右IVC壁,同时IVC血栓从肾静脉水平延伸至与肝静脉汇合处。她的常规实验室检查,包括24小时尿分馏甲氧基肾上腺素、香草扁桃酸和皮质醇均正常。进行了右肾上腺切除术及IVC血栓切除术。围手术期顺利。肿块的组织病理学结果为嗜铬细胞瘤伴血栓,显示为含有纤维蛋白的纤维脂肪组织。嗜铬细胞瘤可能伴有IVC血栓,且血清和尿液标志物正常。因此,在肾上腺肿块的围手术期管理中,临床怀疑至关重要。