Kota Sunil Kumar, Kota Siva Krishna, Meher Lalit Kumar, Jammula Sruti, Panda Sandip, Modi Kirtikumar D
Department of Endocrinology, Medwin Hospital, Hyderabad, Andhra Pradesh, India.
Indian J Endocrinol Metab. 2012 Nov;16(6):962-71. doi: 10.4103/2230-8210.103000.
Pheochromocytoma/paragangliomas have been described to be associated with rare vascular abnormalities like renal artery stenosis. Coexistence of physiologically significant renal artery lesions is a compounding factor that alters management and prognosis of pheochromocytoma patients. Apart from individual case reports, data on such association in Indian population is not available. The aim of this study is to find the nature and prevalence of associated vascular abnormalities.
From 1990 to 2010, a total of 50 patients were diagnosed with pheochromocytoma/paragangliomas. Hospital charts of these patients were reviewed retrospectively to identify those with unusual vascular abnormalities. Available literature was also reviewed.
Of the 50 patients with pheochromocytoma, 7 (14%) had coexisting vascular lesions including renal artery stenosis in 4, aortoarteritis in 1, aortic aneurysm in 1 and inferior vena cava thrombosis in 1. Pheochromocytoma was adrenal in 42 and extra adrenal in 8. Laparoscopic adrenalectomy was done in the patients. One patient with renal artery stenosis due to intimal fibrosis was subjected to percutaneous balloon angioplasty; the other three improved after adrenalectomy and lysis of fibrous adhesive bands. The patient with aortoarteritos was treated with oral steroids. Inferior vena cava thrombosis was reversed with anticoagulants. The patient with abdominal aortic aneurysm was advised for annual follow-up on account of its size of 4.5 cm and asymptomatic presentation.
There are multiple mechanisms that can lead to renal artery stenosis and other vascular abnormalities in a case of pheochromocytoma. A high index of suspicion is necessary to enable both entities to be diagnosed preoperatively and allow proper planning of surgical therapy. Incomplete diagnosis may lead to persistent hypertension postoperatively in a case of associated renal artery stenosis.
嗜铬细胞瘤/副神经节瘤已被描述与诸如肾动脉狭窄等罕见血管异常有关。具有生理意义的肾动脉病变的共存是一个复杂因素,它会改变嗜铬细胞瘤患者的治疗和预后。除了个别病例报告外,印度人群中关于这种关联的数据并不存在。本研究的目的是找出相关血管异常的性质和患病率。
从1990年到2010年,共有50例患者被诊断为嗜铬细胞瘤/副神经节瘤。对这些患者的医院病历进行回顾性审查,以确定那些有异常血管异常的患者。还对现有文献进行了回顾。
在50例嗜铬细胞瘤患者中,7例(14%)存在共存的血管病变,其中4例为肾动脉狭窄,1例为大动脉炎,1例为主动脉瘤,1例为下腔静脉血栓形成。嗜铬细胞瘤位于肾上腺的有42例,位于肾上腺外的有8例。对患者进行了腹腔镜肾上腺切除术。1例因内膜纤维化导致肾动脉狭窄的患者接受了经皮球囊血管成形术;另外3例在肾上腺切除和纤维粘连带松解后病情改善。大动脉炎患者接受口服类固醇治疗。下腔静脉血栓形成通过抗凝治疗得到缓解。腹主动脉瘤患者因其瘤体大小为4.5 cm且无症状表现,建议每年进行随访。
在嗜铬细胞瘤病例中,有多种机制可导致肾动脉狭窄和其他血管异常。需要高度的怀疑指数,以便在术前诊断这两种疾病,并允许对手术治疗进行适当规划。在伴有肾动脉狭窄的情况下,诊断不完整可能导致术后持续高血压。