Klin Padiatr 2011; 223(06): 368-369
DOI: 10.1055/s-0031-1285880
Pictorial Essay
© Georg Thieme Verlag KG Stuttgart · New York

Acute Lymphoblastic Leukemia in a 10-Year-Old Boy With Cystic Fibrosis – Improvement of Pulmonary Function During Chemotherapy in spite of Intermittent Pseudomonas Aeruginosa Colonisation

Akute lymphoblastische Leukämie bei einem 10-jährigen Jungen mit zystischer Fibrose – Verbesserung der Lungenfunktion während Chemotherapie trotz intermittierender Pseudomonas-aeruginosa-Besiedlung

Authors

  • C. Dopfer

    1   Department of Pediatrics, Cystic Fibrosis Centre, Jena University Hospital, Germany
  • K. Kentouche

    2   Department of Pediatrics, Hematology and Oncology, Jena University Hospital, Germany
  • B. Gruhn

    2   Department of Pediatrics, Hematology and Oncology, Jena University Hospital, Germany
  • R. Dopfer

    3    Rehabilitation Hospital, Villingen-Schwenningen, Tannheim gGmbH, Germany
  • S. Becker

    2   Department of Pediatrics, Hematology and Oncology, Jena University Hospital, Germany
  • H.-J. Mentzel

    4   Pediatric Radiology, Institute of Diagnostic and Interventional Radiology, Jena University Hospital, Germany
  • J. F. Beck

    2   Department of Pediatrics, Hematology and Oncology, Jena University Hospital, Germany
  • J. G. Mainz

    1   Department of Pediatrics, Cystic Fibrosis Centre, Jena University Hospital, Germany
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
19. Oktober 2011 (online)

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Background

Multiorgan involvement in cystic fibrosis (CF), including chronic airway infection with pathogens like Pseudomonas aeruginosa, is a critical risk factor in patients with malignancy during aggressive immunosuppressive therapy, and was therefore formerly associated with high mortality rates. A 10 year old boy with CF and acute lymphoblastic leukemia (ALL) underwent induction and reinduction treatment without severe infectious complications whereas lung function improved.