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[经典结节性多动脉炎:一个明确界定的实体。20例分析(作者译)]

[Classical panarteritis nodosa: a clearly defined entity. Analysis of 20 cases (author's transl)].

作者信息

Redondo Sánchez C, Barbado Hernández F J, Peña Sánchez de Rivera J M, Gil Aguado A, Ferrer Iturralde J, Arnalich F, García Puig J, Vázquez Rodríguez J J

出版信息

Med Clin (Barc). 1981 Jun 25;77(2):56-9.

PMID:6119404
Abstract

The clinical, biological, and immunological alterations of 20 patients with histologically confirmed classical panarteritis nodosa have been studied. Characteristic angiographic changes were present in 14 cases. There were 14 males and six females, with a mean age of 50 years. The main clinical manifestations were: fever (90%), peripheral nervous system involvement (80%), renal involvement (65%), arterial hypertension (60%), arthropathy (80%), and cutaneous lesions (45%). In most cases there was elevated VSG and alpha 2-globulin, anemia and leukocytosis. HBsAg positivity was found in five patients. The immunological study revealed a polyclonal immunoglobulin increase, changes in the complement components, and a quantitative and qualitative decrease of T lymphocytes. Steroids and immunosuppressive treatment were given to eight patients, and steroids along to 11 patients. The clinical evolution of 17 patients was followed; four patients died, all of them belonging to the group treated with steroid alone.

摘要

对20例经组织学确诊为经典结节性多动脉炎的患者的临床、生物学和免疫学改变进行了研究。14例出现特征性血管造影改变。患者中男性14例,女性6例,平均年龄50岁。主要临床表现为:发热(90%)、外周神经系统受累(80%)、肾脏受累(65%)、动脉高血压(60%)、关节病(80%)和皮肤病变(45%)。大多数病例中VSG和α2球蛋白升高、贫血和白细胞增多。5例患者HBsAg阳性。免疫学研究显示多克隆免疫球蛋白增加、补体成分改变以及T淋巴细胞数量和质量下降。8例患者接受了类固醇和免疫抑制治疗,11例仅接受类固醇治疗。对17例患者的临床病程进行了随访;4例死亡,均属于仅接受类固醇治疗的组。

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