探讨小肠毛细血管扩张症的诊断和治疗方法。
To explore the diagnosis and therapeutic methods of small intestinal telangiectasis.
目的探讨共济失调毛细血管扩张症的细胞遗传学异常特点。
Objective to investigate the characteristics of the cytogenetic anomalies of ataxia telangiectasia.
胃窦血管扩张症是引起严重的上消化道出血的一种少见疾病。
Gastric antral vascular ectasia (GAVE) is a rare clinical disease which can cause severe upper gastrointestinal tract bleeding.
方法：回顾分析一例颅内（广泛）毛细血管扩张症的DSA表现。
Method Retrospective study and analysis of DSA presentations of cerebral extensive telangiectasis in 1 case.
半数病人可并发遗传性毛细血管扩张症，还可并发脑梗塞和脑脓肿。
About half of the patients supervene telangiectasis, and also associated with cerebral infarction and brain abscess.
目的：探讨遗传性出血性毛细血管扩张症所引起鼻出血的治疗方法。
Objective: To study the treatment of nosebleed caused by hereditary hemorrhagic telangiectasia (HHT).
方法对9例结肠血管扩张症所致下消化道出血的诊断和治疗情况进行分析。
Methods The diagnosis and treatment of 9 patients with lower gastrointestinal tract bleeding caused by colon vascular ectasias were analyzed.
方法结合我院近期收治的3例小肠毛细血管扩张症患者的临床资料进行分析。
Methods Clinical data of 3 cases with intestinal telangiectasis treated recently in our hospital were reviewed.
AT M基因突变可导致共济失调毛细血管扩张症(AT)，一种常染色体隐性遗传病，该病特点是不协调的肌肉运动和神经退化。
Mutations in the corresponding ATM gene result in ataxia telangiectasia (at), an autosomal recessive disease characterized by uncoordinated muscle movement and neurodegeneration.
其中，蜘蛛状毛细血管扩张症23例，酒渣鼻6例，外用激素或化妆品后毛细血管扩张症34例以及局限性特发性毛细血管扩张症5例。
Out of 68 cases, 23 cases were spider telangiectasis, 6 cases were Rosacea, 34 cases were telangiectasis caused by steroids or cosmetics, and 5 cases were localized essential telangiectasis.
遗传出血性毛细血管扩张症为常染色体显性遗传病，临床少见，本文就其病理变化、临床特点进行讨论，探讨其治疗方法。附一家系25例分析。
Hereditary hemorrhagic telangiectasia is an uncommon autosomal dominant inheritance disease. 25 cases from a family were reported. The pathology, clinical presentation and treatment were discussed.
根据我们的经验，对有症状的HHT相关毛细血管扩张症者，使用微粒进行的栓塞治疗提供了令人满意的即时止血效果，其疗效可维持3周到两年。
In symptomatic HHT-related telangiectasias, embolization with particles gives a satisfactory immediate result with immediate hemostasis, lasting from 3 weeks to 2 years in our experience.
遗传性毛细血管扩张症(HHT)或Rendu - Osler - Weberdisease (ROW)是一种表现为反复出血发作的障碍。
Hereditary hemorrhagic telangiectasia (HHT) or Rendu-Osler-Weber disease (ROW) is a disorder that presents with recurrent episodes of EPX.
目的：已有事实表明高血糖症可通过减弱血管扩张，提高组织酸度，释放刺激性产物导致脊髓的缺血损伤。
Hyperglycemia has been shown to potentiate ischemic injury of the spinal cord by quenching vasodilators and potentiating tissue acidosis and free radical production.
结论吸烟患者冠脉病变特点为冠脉瘤样扩张或冠脉扩张症多发。吸烟患者PT CA术中相关血管慢血流现象的发生率较高。
Conclusions There are the characters of more coronary artery ectasia, and more slow reflow phenomenon in PTCA related vessel in smoking patients.
用于治疗高血脂症，可以降低血清中胆固醇、甘油三酯和B-酯蛋白的不同程度的含量，扩张血管，抑制血栓形成。
Used in the treatment of hyperlipidemia, can reduce serum cholesterol, triglyceride and B - ester protein content of different level, the dilation of blood vessels, inhibit thrombosis.
大动脉扩张性降低表明动脉硬度增加，易出现各种心血管病并发症。
The lower distensibility of large arteries is related to increasing arterial stiffness, and these patients may be prone to get more cardiovascular complications.
调理和收敛血管，减轻微血管扩张造成的脸颊发红症。
Improve and contract blood vessels. Alleviate skin flushing caused by dilated blood vessels.
纵向缩缝加血管包裹法治疗小儿颈内静脉扩张症。
Longitudinal Constriction Venoplasty Plus Encapsulation Applied to Treat Internal Jugular Phlebectasia in Children.
急性高碳酸血症可因其导致脑血管扩张和增加脑血流量而加重已经存在的脑水肿。
Acute hypercarbia aggravates existing cerebral edema because it causes cerebral vasodilatation and increased cerebral blood flow.
急性高碳酸血症可因其导致脑血管扩张和增加脑血流量而加重已经存在的脑水肿。
Acute hypercarbia aggravates existing cerebral edema because it causes cerebral vasodilatation and increased cerebral blood flow.
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