Vantyghem Marie-Christine, Douillard Claire, Balavoine Anne-Sophie
Centre hospitalier régional universitaire de Lille, hôpital Huriez, service d'endocrinologie et maladies métaboliques, 59000 Lille, France.
Presse Med. 2012 Nov;41(11):1137-50. doi: 10.1016/j.lpm.2012.03.023. Epub 2012 Sep 10.
Hypotension is defined by a low blood pressure either permanently or only in upright posture (orthostatic hypotension). In contrast to hypertension, there is no threshold defining hypotension. The occurrence of symptoms for systolic and diastolic measurements respectively below 90 and 60 mm Hg establishes the diagnosis. Every acute hypotensive event should suggest shock, adrenal failure or an iatrogenic cause. Chronic hypotension from endocrine origin may be linked to adrenal failure from adrenal or central origin, isolated hypoaldosteronism, pseudohypoaldosteronism, pheochromocytoma, neuro-endocrine tumors (carcinoïd syndrome) or diabetic dysautonomia. Hypotension related to hypoaldosteronism associates low blood sodium and above all high blood potassium levels. They are generally classified according to their primary (hyperreninism) or secondary (hyporeninism) adrenal origin. Isolated primary hypoaldosteronisms are rare in adults (intensive care unit, selective injury of the glomerulosa area) and in children (aldosterone synthase deficiency). Isolated secondary hypoaldosteronism is related to mellitus diabetes complicated with dysautonomia, kidney failure, age, iatrogenic factors, and HIV infections. In both cases, they can be associated to glucocorticoid insufficiency from primary adrenal origin (adrenal failure of various origins with hyperreninism, among which congenital 21 hydroxylase deficiency with salt loss) or from central origin (hypopituitarism with hypo-reninism). Pseudohypoaldosteronisms are linked to congenital (type 1 pseudohypoaldosteronism) or acquired states of resistance to aldosterone. Acquired salt losses from enteric (total colectomy with ileostomy) or renal (interstitial nephropathy, Bartter and Gitelman syndromes…) origin might be responsible for hypotension and are associated with hyperreninism-hyperaldosteronism. Hypotension is a rare manifestation of pheochromocytomas, especially during surgical removal when the patient has not been prepared with calcium inhibitors. Every flush with hypotension should suggest a carcinoid crisis, which is very sensitive to subcutaneous somatostatin analog. An accurate etiological diagnosis should allow treat efficiently endocrine hypotension without inducing hypertension in supine posture.
低血压的定义是血压持续偏低或仅在直立姿势时出现低血压(体位性低血压)。与高血压不同,低血压没有明确的界定阈值。收缩压和舒张压分别低于90毫米汞柱和60毫米汞柱且出现症状时可确立诊断。每一次急性低血压事件都应怀疑休克、肾上腺功能衰竭或医源性原因。内分泌源性慢性低血压可能与肾上腺或中枢性肾上腺功能衰竭、孤立性醛固酮减少症、假性醛固酮减少症、嗜铬细胞瘤、神经内分泌肿瘤(类癌综合征)或糖尿病自主神经病变有关。与醛固酮减少症相关的低血压伴有低血钠,尤其是高血钾水平。它们通常根据原发性(高肾素血症)或继发性(低肾素血症)肾上腺起源进行分类。孤立性原发性醛固酮减少症在成人(重症监护病房、球状带区域选择性损伤)和儿童(醛固酮合成酶缺乏)中较为罕见。孤立性继发性醛固酮减少症与合并自主神经病变的糖尿病、肾衰竭、年龄、医源性因素及HIV感染有关。在这两种情况下,它们都可能与原发性肾上腺源性糖皮质激素不足(各种原因导致的肾上腺功能衰竭伴高肾素血症,其中包括先天性21羟化酶缺乏伴失盐)或中枢性肾上腺源性糖皮质激素不足(垂体功能减退伴低肾素血症)有关。假性醛固酮减少症与先天性(1型假性醛固酮减少症)或获得性醛固酮抵抗状态有关。肠道(全结肠切除加回肠造口术)或肾脏(间质性肾病、巴特综合征和吉特曼综合征等)源性的获得性失盐可能导致低血压,并伴有高肾素血症 - 高醛固酮血症。低血压在嗜铬细胞瘤中是一种罕见表现,尤其是在手术切除时患者未用钙拮抗剂进行预处理的情况下。每次伴有低血压的潮红都应怀疑类癌危象,类癌危象对皮下注射生长抑素类似物非常敏感。准确的病因诊断应能有效治疗内分泌性低血压,同时不会在仰卧位时诱发高血压。