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Severe candida sepsis in a preterm infant with congenital ichthyosis

Yıl 2020, , 405 - 406, 25.06.2020
https://doi.org/10.38136/jgon.666958

Öz

Ichthyosis which is an inherited keratinisation disorder of the skin, is heterogeneous as clinically. This disease’s clinic is considerably variable from widespread skin dryness to hyperkeratosis. While the prevention of complications such as dehydration, sepsis and electrolyte imbalance, is very important in respect to survival, in premature neonates, more severe complications may be seen. In this case, we reported that a premature infant who developed catastrophic candida sepsis with congenital ichthyosis.

Kaynakça

  • Referans1. Oji V, Tadini G, Akiyama M, et al. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. J Am Acad Dermatol 2010; 63(4): 607-41.
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  • Referans6. Leibovitz E. Neonatal candidosis:clinical Picture, management controversies and consensus, and new therapeutic options. J Antimicrob Chemother 2002; 49: 69-73.
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  • Referans9.Odio CM, Araya R, Pinto LE et al. Caspofungin therapy of neonates with invasive candidiasis.Pediatr İnfect Dis J 2004; 23 (12):1093-7.
  • Referans10. Haase R, Kreft B, Foell J, Kekulé AS, Merkel N. Successful treatment of Candida albicans septicemia in a preterm infant with severe congenital ichthyosis (Harlequin baby). Pediatr Dermatol. 2009; 26 (5): 575-8.
Toplam 10 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Çocuk Sağlığı ve Hastalıkları
Bölüm Olgu Sunumu
Yazarlar

Şebnem Özmen 0000-0002-4428-3693

Fuat Baştürk 0000-0003-4630-8417

Serkan Kırık 0000-0002-8658-2448

Mehmet Yaşar Özkars 0000-0003-1290-8318

Sadık Yurttutan 0000-0003-1607-8980

Can Acıpayam 0000-0002-6379-224X

Yayımlanma Tarihi 25 Haziran 2020
Gönderilme Tarihi 30 Aralık 2019
Kabul Tarihi 23 Şubat 2020
Yayımlandığı Sayı Yıl 2020

Kaynak Göster

Vancouver Özmen Ş, Baştürk F, Kırık S, Özkars MY, Yurttutan S, Acıpayam C. Severe candida sepsis in a preterm infant with congenital ichthyosis. JGON. 2020;17(2):405-6.