Shabalin A Ia, Rabkin I Kh, Natsvlishvili Z G, Germashev V G
Khirurgiia (Mosk). 1989 Dec(12):24-9.
The presence of multiple renal arteries (MRA) as a congenital developmental anomaly encountered in 13% angiographic examinations is not the cause of vasorenal hypertension. Sustained hypertension develops in affection of one or several of the MRA. The authors analyse 55 patients with vasorenal hypertension in affection of one or more of the MRA. Interventions on the MRA restored their blood flow in 91.0% of patients. Positive results with reduction of hypertension were produced in 85.4% of patients. Complications--restenosis, thromboses--occurred in 12.7% of cases. One patient died from acute renal failure which had developed in thrombosis of the renal arteries. Patients with affection of one or several of MRA of various etiology may be cured successfully by organ-preserving reconstructive operations. Nephrectomy should be resorted to only in intraorganic affection of the renal vessels or in total loss of kidney function.
在13%的血管造影检查中发现的多条肾动脉(MRA)作为一种先天性发育异常,并非肾血管性高血压的病因。当一条或多条MRA受累时会出现持续性高血压。作者分析了55例一条或多条MRA受累的肾血管性高血压患者。对MRA进行干预后,91.0%的患者恢复了血流。85.4%的患者血压降低,取得了阳性结果。并发症——再狭窄、血栓形成——发生在12.7%的病例中。1例患者死于肾动脉血栓形成后发生的急性肾衰竭。各种病因导致的一条或多条MRA受累的患者,可通过保留器官的重建手术成功治愈。仅在肾血管的器官内受累或肾功能完全丧失时才应进行肾切除术。