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婴儿急性出血性水肿——真的是一种轻度、良性疾病吗?

Acute hemorrhagic edema of infancy - is it really a mild, benign disease?

出版信息

Turk J Pediatr. 2021;63(1):141-148. doi: 10.24953/turkjped.2021.01.017.

Abstract

BACKGROUND

Acute hemorrhagic edema of infancy (AHEI) is a rare vasculitis, which presents dramatically as palpable purpuric skin lesions on the limb, face and auricles, with swelling of these parts and low-grade fever, in children up to 2 years of age. To date, approximately 400 cases have been described in the literature. The etiology remains mostly unknown. With or without treatment, AHEI goes to spontaneous recovery within 1-3 weeks, usually without any complications. To our knowledge, compartment syndrome as complication of AHEI has only been reported in one case. We present an unusual case of AHEI with serious complications due to compartment syndrome of the right-hand fingers.

CASE

A 16-month-old male child presented with fever and sudden appearance and rapid spread of palpable, painless, non-itching ecchymotic hematomas on the thigh, cheeks, earlobes, forearms, dorsum of hands and feet, with mild edema of these regions. Complete systemic examination and all vital parameters were normal for age. There was no history of bleeding disorders in the family. Except low hemoglobin on complete blood count and increased D-dimer values, all other laboratory investigations were in the normal range. Changes on the right forearm and hand expanded on almost the entire dorsal side and all surfaces of the fingers, with pronounced swelling and formation of bullous lesions, which were spreading and cracking. Skin biopsy confirmed nonspecific small-vessel vasculitis. That required the use of Methylprednisolone, low-molecularweight heparin, antibiotics and debridement of necrotic eschar, with necrectomy of the affected fingers.

CONCLUSIONS

Early recognition of AHEI is important to avoid unnecessary investigation and therapy. On the other hand, our reported case warns that unexpected complications may occur.

摘要

背景

婴儿急性出血性水肿(AHEI)是一种罕见的血管炎,主要表现为 2 岁以下儿童四肢、面部和耳廓出现可触及的紫癜性皮肤病变,这些部位出现肿胀和低热。迄今为止,文献中大约描述了 400 例病例。病因大多未知。无论是否治疗,AHEI 在 1-3 周内自发恢复,通常没有任何并发症。据我们所知,AHEI 的并发症作为并发症仅在一例中报告。我们报告了一例不常见的 AHEI 病例,由于手部手指的间隔综合征导致严重并发症。

病例

一名 16 个月大的男性儿童出现发热,大腿、脸颊、耳垂、前臂、手和脚的背部突然出现并迅速扩散可触及的、无痛的、非瘙痒性瘀斑血肿,这些部位有轻度肿胀。全身检查和所有生命体征均与年龄相符。家族中无出血性疾病史。除全血细胞计数低血红蛋白和 D-二聚体值增加外,所有其他实验室检查均在正常范围内。右前臂和手部的变化几乎扩展到整个背面和手指的所有表面,出现明显肿胀和形成大疱性病变,这些病变正在扩散和破裂。皮肤活检证实为非特异性小血管血管炎。需要使用甲基强的松龙、低分子量肝素、抗生素和坏死焦痂清创术,以及受影响手指的坏死切除术。

结论

早期识别 AHEI 很重要,以避免不必要的检查和治疗。另一方面,我们报告的病例警告可能会出现意外并发症。

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