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家族性地中海热中的血管炎

Vasculitis in familial Mediterranean fever.

作者信息

Ozdogan H, Arisoy N, Kasapçapur O, Sever L, Calişkan S, Tuzuner N, Mat C, Yazici H

机构信息

Department of Rheumatology, Cerrahpaşa Medical Faculty, University of Istanbul, Turkey.

出版信息

J Rheumatol. 1997 Feb;24(2):323-7.

PMID:9034991
Abstract

OBJECTIVE

To evaluate the frequency of vasculitis, mainly in the forms of Henoch-Schönlein purpura and polyarteritis nodosa (PAN), and to investigate the presence of occult blood in the first stool specimens after an abdominal attack in Turkish patients with familial Mediterranean fever (FMF).

METHODS

Review of the charts of 207 patients with FMF seen between 1983 and 1993 with respect to clinical vasculitis. A prospective study designed to test the presence of occult blood in the first stool specimens obtained after abdominal attack and at least one week later in 36 patients with FMF compared with healthy and diseased controls.

RESULTS

There were 15 patients with Henoch-Schönlein purpura (7%), 2 with definite and one with probable PAN (1%), one of whom developed perirenal hematoma. The diagnosis of FMF was made after the onset of Henoch-Schönlein purpura in 9 and subsequent to the development of PAN in one patient. Occult blood was positive in the first stool specimens obtained after an attack in 17 of the 36 patients with FMF (47%), a finding not reported previously.

CONCLUSION

Vasculitis seems to be an important but not a widely recognized feature of FMF.

摘要

目的

评估血管炎的发生频率,主要是过敏性紫癜和结节性多动脉炎(PAN)的形式,并调查土耳其家族性地中海热(FMF)患者腹部发作后首次粪便标本中潜血的情况。

方法

回顾1983年至1993年间就诊的207例FMF患者的病历,了解临床血管炎情况。一项前瞻性研究旨在检测36例FMF患者腹部发作后首次粪便标本及至少一周后粪便标本中潜血的情况,并与健康对照和疾病对照进行比较。

结果

有15例过敏性紫癜患者(7%),2例确诊PAN和1例可能为PAN患者(1%),其中1例发生肾周血肿。9例患者在过敏性紫癜发作后确诊为FMF,1例在PAN发生后确诊。36例FMF患者中,17例(47%)发作后首次粪便标本潜血呈阳性,这一发现此前未见报道。

结论

血管炎似乎是FMF的一个重要但未被广泛认识的特征。

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