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特发性塞德迈尔紫癜:一例报告

Idiopathic Seidlmayer's Purpura: A Case Report.

作者信息

Maggio Maria Cristina, Ferraro Fabrizia, Ragusa Saveria Sabrina, Corpora Umberto, Corsello Giovanni

机构信息

Department Pro.S.A.M.I., Ospedale dei Bambini 'G. Di Cristina', ARNAS Palermo, Palermo, Italy.

出版信息

Case Rep Dermatol. 2014 May 17;6(2):150-3. doi: 10.1159/000362754. eCollection 2014 May.

Abstract

Acute hemorrhagic edema of infancy (AHEI) was considered a rare form of Henoch-Schönlein purpura; however, it is now regarded as an independent disease typically involving patients aged 4-24 months. The authors describe the clinical case of a toddler aged 8 months, with skin erythematous pomphoid lesions, treated at home with topical steroids without benefits. The appearance of new lesions and the worsening of the previous skin signs induced the parents to drive the child to the hospital. The medical history revealed the administration of a vaccine dose 2 months before.

摘要

婴儿急性出血性水肿(AHEI)曾被认为是过敏性紫癜的一种罕见形式;然而,现在它被视为一种独立的疾病,通常累及4至24个月大的患者。作者描述了一名8个月大幼儿的临床病例,该患儿有皮肤红斑性水疱样病变,在家中使用外用类固醇治疗但无效果。新病变的出现以及先前皮肤症状的恶化促使家长带孩子前往医院。病史显示2个月前接种过一剂疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d6a/4049020/8bd7469baeb0/cde-0006-0150-g01.jpg

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