Congenital candidiasis – a diagnostic challenge

Sara Rolim, Joana Figueirinha, C. Miguel, S. Lopes, Felisbela Rocha, Cecília Martins, S. Carvalho
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Abstract

Introduction: Congenital candidiasis is a rare intrauterine infection characterized by vesicular and pustular skin lesions appearing in the first six days of life. Clinical case: The authors describe the case of a full-term infant presenting erythematous macules, vesicles and pustules involving the trunk and extremities and cervical burn-like dermatitis at birth. Mycological skin lesion culture was positive for Candida albicans. Blood culture was positive for methicillin-sensitive Staphylococcus aureus. After systemic antifungal and antibiotic therapy was started, the newborn remained asymptomatic with lesion improvement. Discussion/ Conclusion: Herein is reported a case of congenital candidiasis in a full-term infant, with a successful recovery. The rarity of congenital candidiasis can lead to delayed diagnosis and unnecessary treatment. This case shows that fungal infection should be considered in the differential diagnosis of vesiculopustular skin lesions in neonates. Systemic therapy should be initiated if invasive candidiasis is suspected.
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先天性念珠菌病-诊断的挑战
简介:先天性念珠菌病是一种罕见的宫内感染,其特征是在生命的前6天出现水泡和脓疱性皮肤病变。临床病例:作者描述了一个足月婴儿的情况下表现为红斑,囊泡和脓疱累及躯干和四肢和颈部烧伤样皮炎出生。真菌学皮肤病变培养白色念珠菌阳性。血培养甲氧西林敏感金黄色葡萄球菌阳性。在开始全身抗真菌和抗生素治疗后,新生儿无症状,病变有所改善。讨论/结论:本文报告一例先天性念珠菌病在足月婴儿,成功恢复。先天性念珠菌病的罕见性可能导致诊断延误和不必要的治疗。本病例表明,真菌感染应考虑在鉴别诊断的膀胱脓疱性皮肤病变的新生儿。如果怀疑有侵袭性念珠菌病,应开始全身治疗。
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