Dermatology clinical case
DOI:
https://doi.org/10.25753/BirthGrowthMJ.v29.i2.18721Keywords:
congenital cutaneous candidiasis, newbornAbstract
Congenital cutaneous candidiasis is a rare disease acquired in utero via ascending Candida infection. Skin involvement is diffuse and often appears in the first six days of life. Diagnosis can be confirmed by microscopic examination and cutaneous lesion culture. Empiric therapy with systemic antifungal should be promptly started at the time of cutaneous manifestations, specially in preterm infants, to prevent dissemination and decrease mortality risk.
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References
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Aldana-Valenzuela C, Morales-Marquec M, Castellanos-Martinez J, DeAnda-Gomez M. Congenital candidiasis: a rare and unpredictable disease. J Perinatol. 2005; 25:680-2.
Chen KL, Chien MM, Chen CY, Chiu HC. Congenital cutaneous candidiasis. BMJ Case Rep. 2016; 2016. pii: bcr2016216037.
Kaufman DA, Coggins SA, Zanelli SA, Weitkamp JH. Congenital cutaneous candidiasis: prompt systemic treatment is associated with improved outcomes in neonates. Clinical Infectious Diseases. 2017; 64:1387-95.
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