Chronic interstitial lung disease with lung fibrosis in a girl: Uncommon sequelae of Epstein-Barr virus infection

被引:14
作者
Ankermann, T
Claviez, A
Wagner, HJ
Krams, M
Riedel, F
机构
[1] Univ Kiel, Dept Pediat, D-24105 Kiel, Germany
[2] Med Univ Lubeck, Dept Pediat, D-23538 Lubeck, Germany
[3] Univ Kiel, Dept Pediat Pathol, D-24105 Kiel, Germany
[4] Childrens Hosp, Hamburg, Germany
关键词
interstitial lung disease; Epstein-Barr virus infection; fibrosis;
D O I
10.1002/ppul.10244
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
A 12-month-old immunocompetent girl presented with tachypnea, inspiratory crackles, mild hypoxemia, and failure to thrive after an acute Epstein-Barr virus (EBV) infection. The course of acute EBV infection was demonstrated by viral load measurement in plasma and peripheral blood mononuclear cells (PBMC) by using real-time polymerase chain reaction (PCR). EBV DNA was further detected by PCR in bronchoalveolar lavage (BAL) fluid and from a lung-tissue specimen obtained by open-lung biopsy, which indicates the pulmonary involvement of active EBV infection. Histology revealed an uncharacteristic interstitial infiltration and fibrosis. Following topic and systemic treatment with corticosteroids, the child became asymptomatic and showed normal weight gain as well as mental and physical development. Pulmonary parenchymal involvement during the course of primary EBV infection may result in interstitial lung disease and fibrosis not only in immunodeficient, but in immunocompetent children as well. Treatment with combined inhaled and oral steroids seems to be a treatment option in these patients. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:234 / 238
页数:5
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