血管性水肿

{{Infobox medical condition (new)
| name = 血管神经性水肿
| synonyms = 血管性水肿，Angiooedema, Quincke's edema, angioneurotic edema
| image = Angioedema2010.JPG
| caption = 血管神经性水肿: 患儿由于眼皮肿胀不能睁眼
| field = 免疫学
| symptoms = 局部肿胀
| differential = 全身型過敏性反應, 膿瘍, 接触性皮炎可发生于面部、舌头、喉、腹部、四肢。

为保护呼吸道通畅，对呼吸道特别是喉部发作水肿，必要时应进行气管插管或环甲膜切开术。 There is usually no associated itch or urticaria, as it is not an allergic response. Patients with HAE can also have recurrent episodes (often called "attacks") of abdominal pain, usually accompanied by intense vomiting, weakness, and in some cases, watery diarrhea, and an unraised, nonitchy splotchy/swirly rash. These stomach attacks can last one to five days on average, and can require hospitalization for aggressive pain management and hydration. Abdominal attacks have also been known to cause a significant increase in the patient's white blood cell count, usually in the vicinity of 13,000 to 30,000. As the symptoms begin to diminish, the white count slowly begins to decrease, returning to normal when the attack subsides. As the symptoms and diagnostic tests are almost indistinguishable from an acute abdomen (e.g. perforated appendicitis) it is possible for undiagnosed HAE patients to undergo laparotomy (operations on the abdomen) or laparoscopy (keyhole surgery) that turns out to have been unnecessary.

HAE may also cause swelling in a variety of other locations, most commonly the limbs, genitals, neck, throat and face. The pain associated with these swellings varies from mildly uncomfortable to agonizing pain, depending on its location and severity. Predicting where and when the next episode of edema will occur is impossible. Most patients have an average of one episode per month, but there are also patients who have weekly episodes or only one or two episodes per year. The triggers can vary and include infections, minor injuries, mechanical irritation, operations or stress. In most cases, edema develops over a period of 12–36 hours and then subsides within 2–5 days.

诊断
The diagnosis is made on the clinical picture. Routine blood tests (complete blood count, electrolytes, renal function, liver enzymes) are typically performed. Mast cell tryptase levels may be elevated if the attack was due to an acute allergic (anaphylactic) reaction. When the patient has been stabilized, particular investigations may clarify the exact cause; complement levels, especially depletion of complement factors 2 and 4, may indicate deficiency of C1-inhibitor. HAE type III is a diagnosis of exclusion consisting of observed angioedema along with normal C1 levels and function.

The hereditary form (HAE) often goes undetected for a long time, as its symptoms resemble those of more common disorders, such as allergy or intestinal colic. An important clue is the failure of hereditary angioedema to respond to antihistamines or steroids, a characteristic that distinguishes it from allergic reactions. It is particularly difficult to diagnose HAE in patients whose episodes are confined to the gastrointestinal tract. Besides a family history of the disease, only a laboratory analysis can provide final confirmation. In this analysis, it is usually a reduced complement factor C4, rather than the C1-INH deficiency itself, that is detected. The former is used during the reaction cascade in the complement system of immune defense, which is permanently overactive due to the lack of regulation by C1-INH.

Angioedema is classified as either hereditary or acquired.

获得性血管性水肿
Acquired angioedema (AAE) can be immunologic, nonimmunologic, or idiopathic. It is usually caused by allergy and occurs together with other allergic symptoms and urticaria. It can also occur as a side effect to certain medications, particularly ACE inhibitors. It is characterized by repetitive episodes of swelling, frequently of the face, lips, tongue, limbs, and genitals. Edema of the gastrointestinal mucosa typically leads to severe abdominal pain; in the upper respiratory tract, it can be life-threatening.

遗传型血管性水肿
Hereditary angioedema (HAE) exists in three forms, all of which are caused by a genetic mutation inherited in an autosomal dominant form. They are distinguished by the underlying genetic abnormality. Types I and II are caused by mutations in the SERPING1 gene, which result in either diminished levels of the C1-inhibitor protein (type I HAE) or dysfunctional forms of the same protein (type II HAE). Type III HAE has been linked with mutations in the F12 gene, which encodes the coagulation protein factor XII. All forms of HAE lead to abnormal activation of the complement system, and all forms can cause swelling elsewhere in the body, such as the digestive tract. If HAE involves the larynx, it can cause life-threatening asphyxiation. The pathogenesis of this disorder is suspected to be related to unopposed activation of the contact pathway by the initial generation of kallikrein and/or clotting factor XII by damaged endothelial cells. The end product of this cascade, bradykinin, is produced in large amounts and is believed to be the predominant mediator leading to increased vascular permeability and vasodilation that induces typical angioedema "attacks".

病理学
缓激肽在各种血管性水肿中扮演了关键角色。 这种肽是强力血管舒張并增加血管通透，导致组织液快速累积。这在脸部特别显著，因为脸部皮肤相对缺少结缔组织支撑，容易形成水肿。多种细胞类型在刺激下会释放缓激肽。不同的干涉缓激肽生产或降解的机制能导致血管性水肿。血管紧张素转换酶抑制剂会阻断血管紧张素转化酶（ACE）的降解缓激肽作用，可能进而导致血管性水肿。遗传性血管性水肿是导致缓激肽生成的补体系统持续活化，因为缺乏相应的抑制剂：C1酯酶（C1INH）。这种丝氨酸蛋白酶抑制剂能抑制C1r、C1s与C1q的关联，阻止了C1复合体的生成，从而激活了其他的补体系统的蛋白。此外还抑制了相应的一些凝血蛋白，虽然对出血与血栓形成的干扰效果是有限的。

有三类遗传性血管水肿：

• 第一类 - C1INH的低浓度 (85%)；
• 第二类 - C1INH浓度正常，但缺乏功能 (15%)；
• 第三类 - C1INH无异常，伴性遗传主要影响女性；怀孕与使用甾体激素者会加重 (发生频率不定) 与基因变异有关。。

血管性水肿也可能是生成了C1INH抗体，这是一种自體免疫性疾病。与淋巴瘤的发展有关。

食物消化吸收后可能带来自己的血管扩张剂，如酒精饮料或桂皮，可加重病情。菠萝蛋白酶与薑黃合用能减轻症状。中药分别称两种效果为“发货”与抗炎消肿。

布洛芬或阿司匹林可能会加重病情。对乙酰氨基酚也能加重病情。

治疗
过敏
在变应性血管性水肿中，避免过敏原和使用抗组胺药可以预防发作。西替利嗪是血管性水肿常用的抗组胺药。一些患者声称，每晚服用低剂量的西替利嗪可成功减轻发作的频率和严重程度，然后在发作时使用更高的剂量。严重的血管性水肿病例可能需要对假定的过敏原脱敏，因为可能会導致死亡。慢性病例需要类固醇治疗，这通常会导致良好的反应。如果过敏性发作正朝着气道阻塞发展，肾上腺素可能会挽救生命。

药物导致
ACE inhibitors can induce angioedema. ACE inhibitors block the enzyme ACE so it can no longer degrade bradykinin; thus, bradykinin accumulates and causes angioedema. This complication appears more common in African-Americans. In people with ACE inhibitor angioedema, the drug needs to be discontinued and an alternative treatment needs to be found, such as an angiotensin II receptor blocker (ARB) which has a similar mechanism but does not affect bradykinin. However, this is controversial, as small studies have shown some patients with ACE inhibitor angioedema can develop it with ARBs, as well.

遗传性
In hereditary angioedema, specific stimuli that have previously led to attacks may need to be avoided in the future. It does not respond to antihistamines, corticosteroids, or epinephrine. Acute treatment consists of C1-INH (C1-esterase inhibitor) concentrate from donor blood, which must be administered intravenously. In an emergency, fresh frozen blood plasma, which also contains C1-INH, can also be used. However, in most European countries, C1-INH concentrate is only available to patients who are participating in special programmes. The medications ecallantide and icatibant may be used to treat attacks.

Future attacks of hereditary angioedema can be prevented by the use of androgens such as danazol, oxandrolone or methyltestosterone. These agents increase the level of aminopeptidase P, an enzyme that inactivates kinins; kinins (especially bradykinin) are responsible for the manifestations of angioedema.
活性减弱的雄性激素如达那唑、司坦唑（康力龙）、羟甲烯龙（康复龙）等治疗先天性C1INH缺陷，可纠正其生化缺损并有预防发作的效用，但不能用于小儿和孕妇。

获得性
获得性血管神经性水肿、HAE的I型与II型、以及非组胺血管神经性水肿性，抗纤维蛋白溶酶药物如氨甲环酸或ε-氨基己酸有时可控制自然发作，也适用于小儿和孕妇。可用于抗C4活化，适用于有肝病不能使用雄性激素的患者。

历史
1882年，首次临床报告此病。虽然有些更早的临床描述。

1888年，威廉·奥斯勒认为某些是由于遗传导致的，称“遗传性血管神经性水肿”。

1963年，证实了C1酯酶抑制剂匮乏是病因。

流行病学
在美国，急诊室年度就诊患者中有80,000至112,000是血管神经性水肿，是过敏导致就医中的首位。

参见

• 药物性血管性水肿
• 格莱希综合征 (不明原因的血管性水肿伴高嗜酸性粒细胞计数)

参考文献
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