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Neonatal Sweet’s Syndrome Associated with Rectovestibular Fistula with Normal Anus

机译:肛门前庭瘘与新生儿肛门甜美综合征

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摘要

Sweet’s syndrome, characterized by fever and a painful erythematous rash with a dermal neutrophilic infiltrate, develops primarily due to paraneoplastic phenomena in adults. Sweet’s syndrome is very rare in neonates. We report a Japanese female neonate (age <2 months), who developed Sweet’s syndrome with episodes of perineal infection in association with congenital rectovestibular fistula with normal anus. Sweet’s syndrome was diagnosed basing on clinical features and histopathology of biopsied skin tissues. Rectovestibular fistula was confirmed after the signs of inflammation subsided and the rash disappeared. In the literature, we found another case of neonatal Sweet’s syndrome associated with rectovestibular fistula in a Japanese female neonate. The perineal region should be screened for anomalies following diagnosis of Sweet’s syndrome in neonates.
机译:Sweet氏综合症的特征是发烧和皮肤中性粒细胞浸润引起的疼痛性红斑皮疹,主要是由于成年人的副肿瘤现象引起的。甜氏综合症在新生儿中非常罕见。我们报道了一名日本女性新生儿(年龄小于2个月),该患者发展成Sweet综合征并伴有会阴部感染,并伴有先天性直肠前庭瘘和正常肛门。根据活检皮肤组织的临床特征和组织病理学诊断出Sweet综合征。炎症体征消退,皮疹消失后,可确认前庭瘘。在文献中,我们在日本女性新生儿中发现了另一例与直肠前庭瘘相关的新生儿甜综合征。在诊断出新生儿的Sweet's综合征后,应检查会阴区域是否存在异常。

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