Cytomegalovirus pneumonia as cause of persistently wheezing in an infant with cystic fibrosis
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Çiğdem Aliosmanoğlu 1 * , Zehra Şule Haskaloğlu, Ömer Cevit
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1 Siverek Devlet Hastanesi Çocuk Sağlığı ve Hastalıkları Bölümü, S.Urfa, Turkey* Corresponding Author

Abstract

Cystic fibrosis, presenting in childhood, is a hereditary disease that proceeds with the dysfunction of all exocrine glands. Two months infant who was born premature admitted with respiratory distress. The infant's oxygen saturation was 80% and white sphere was 23.000/mm3. Clor levels were found as 88 mEq/l and 103 mEq/l by sweat chloride test. Cystic fibrosis was diagnosed. The patient not responded to treatment and was positive CMV-DNA was detected. The patient responded well to ganciclovir treatment. When a case with cystic fibrosis does not respond to treatment, another underlying causes should be considered.

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Article Type: Case Report

J Clin Exp Invest, Volume 2, Issue 2, June 2011, 235-237

https://doi.org/10.5799/ahinjs.01.2011.02.0248

Publication date: 14 Jun 2011

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