| Literature DB >> 17966106 |
Adam Nowiński1, Ewa Jabłońska-Skwiecińska, Emil Wojda, Przemysław Bieleń, Jakub Ptak, Paweł Sliwinski, Dorota Górecka.
Abstract
Severe complications of lower respiratory tract infection in a patient with hereditary glucose-6-phosphate dehydrogenase (G-6-PD) deficiency may occur. The case of a 68-year-old man with hereditary glucose-6-phosphate dehydrogenase (G6PD) deficiency who developed severe haemolysis after community-acquired pneumonia is presented. G6PD deficiency in our patient was diagnosed during childhood. We observed complications of community-acquired pneumonia: empyema, haemolytic crisis and renal failure. Videopleuroscopy and pleural drainage were successfully performed. Community-acquired streptococcal pneumonia may also lead to haemolysis in G6PD deficient patients. Acute haemolysis, severe anaemia and renal insufficiency secondary to haemoglobinuria can be observed. Severe purulent complications of pneumonia in G6PD deficient patients may suggest granulocyte function impairment.Entities:
Mesh:
Year: 2007 PMID: 17966106
Source DB: PubMed Journal: Pneumonol Alergol Pol ISSN: 0867-7077