Suppr超能文献

川崎病合并周围及面部坏疽:病例报告及文献复习。

Kawasaki Disease with Peripheral and Facial Gangrene: A Case report and review of literature.

机构信息

Department of Pediatrics, Kalawati Saran Children's Hospital and Lady Hardinge Medical College, New Delhi, India.

Department of Dermatology, Lady Hardinge Medical College, New Delhi, India.

出版信息

Trop Doct. 2022 Jul;52(3):449-452. doi: 10.1177/00494755221081598. Epub 2022 Mar 29.

Abstract

With the onset of the SARS-CoV-2 pandemic, Kawasaki Disease (KD) has come to the fore with its many atypical manifestations. Atypical clinical neurological, ophthalmological, musculoskeletal, gastrointestinal and pulmonary manifestations in a febrile child with raised markers should prompt the clinician to think of Kawasaki disease. Peripheral gangrene is a rare atypical manifestation of KD reported in infancy. We present a three-and-a-half-year-old boy with extensive gangrene all four limbs and face along with purpura fulminans. He was successfully treated with two doses of intravenous immunoglobulin (IVIG) and infliximab, with no residual gangrene. This case highlights that very severe forms of Kawasaki disease require IVIG, pulse steroids as well as infliximab for adequate control and complete resolution of the disease.

摘要

随着 SARS-CoV-2 大流行的爆发,川崎病(KD)因其多种不典型表现而备受关注。发热患儿出现不典型的临床神经系统、眼科、肌肉骨骼、胃肠道和肺部表现,且标志物升高,应促使临床医生考虑川崎病。外周性坏疽是川崎病的一种罕见不典型表现,见于婴儿期。我们报告了一例 3 岁半的男孩,四肢和面部广泛坏疽合并紫癜性休克。他成功接受了两剂静脉注射免疫球蛋白(IVIG)和英夫利昔单抗治疗,没有残留坏疽。本例强调,非常严重的川崎病需要 IVIG、脉冲类固醇以及英夫利昔单抗来充分控制和完全解决疾病。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验