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[川崎病。50例报告]

[Kawasaki disease. A report of 50 cases].

作者信息

González Pascual E, Villanueva Lamas J, Ros Viladoms J, Pons Odena M, Ruiz García-Diego S

机构信息

Unidad Integrada Hospital Clínico-Hospital, Sant Joan de Dèu, Servicio de Pediatría, Barcelona.

出版信息

An Esp Pediatr. 1999 Jan;50(1):39-43.

Abstract

OBJECTIVE

We present 50 cases of Kawasaki's disease (KD), diagnosed and controlled in our hospital between January 1984 and December 1997.

PATIENTS AND METHODS

Fifty patients were reviewed. In forty-six of these cases the onset was complete, according to the Research Committee of MLNS diagnosis criteria and four cases had incomplete onset.

RESULTS

The ration male/female was 1.9/1. Both fever and oral cavity lesions were present in all cases. In 93.4% desquamation of fingers was observed. The most frequent skin lesion was maculopapular rash. Fourteen patients had atypical onset: adenophlegmon, aseptic meningitis, symptomatic hepatitis, parotiditis, queratopathia punctata and arthritis. Blood analysis showed alterations of high ESR (88% of cases), C-reactive protein (62%), leukocytosis (82%) and thrombocytosis (96%). Fifteen patients were treated with gamma globulin (IGIV), five received a single 2 g/Kg dose and ten received 400 mg/Kg per day during four days. Eight percent of our cases produced cardiovascular complications, none that included coronary aneurysms.

CONCLUSIONS

After IGIV treatment we observed a shortening of the febrile period and amelioration of clinical symptoms. No deaths were reported.

摘要

目的

我们呈现1984年1月至1997年12月期间在我院诊断并得到控制的50例川崎病(KD)病例。

患者与方法

对50例患者进行了回顾性研究。根据MLNS诊断标准,其中46例起病完整,4例起病不完整。

结果

男女比例为1.9/1。所有病例均有发热和口腔损害。93.4%的患者出现手指脱皮。最常见的皮肤损害是斑丘疹。14例患者有非典型起病:腺性蜂窝织炎、无菌性脑膜炎、症状性肝炎、腮腺炎、点状角膜病变和关节炎。血液分析显示血沉升高(88%的病例)、C反应蛋白升高(62%)、白细胞增多(82%)和血小板增多(96%)。15例患者接受了静脉注射丙种球蛋白(IGIV)治疗,5例接受单次2g/kg剂量,10例在4天内每天接受400mg/kg剂量。我们的病例中有8%出现心血管并发症,无一例包括冠状动脉瘤。

结论

静脉注射丙种球蛋白治疗后,我们观察到发热期缩短,临床症状改善。无死亡病例报告。

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