Ha. Elsner et al., FATAL PULMONARY HEMORRHAGE IN PATIENTS WITH ACUTE-LEUKEMIA AND FULMINANT PNEUMONIA CAUSED BY STENOTROPHOMONAS-MALTOPHILIA, Annals of hematology, 74(4), 1997, pp. 155-161
Pulmonary hemorrhage is a rare cause of death in patients with acute l
eukemia. Within a 3-month period we observed three such cases, all of
which were associated with the gram-negative opportunistic pathogen St
enotrophomonas maltophilia. Since fatal lung bleeding had previously n
ot been observed in conjunction with this organism, we collected the d
ata from all patients with documented S. maltophilia infections or col
onizations of the past year and analyzed the risk factors for a lethal
outcome. A total of eight patients were identified. In the three pati
ents with fatal hemorrhage, the interval between first complaints (che
st pain, cough, fever) and death from lung bleeding was 36-72 h. A fou
rth patient with acute leukemia died of nonhemorrhagic respiratory fai
lure 9 days after developing S. maltophilia-associated pneumonia. All
four patients had received intensive chemotherapy and were severely ne
utropenic and thrombocytopenic. Such a combination of predisposing fac
tors was not observed in the four patients with nonfatal infections or
colonizations. Pulsed-field gel electrophoresis demonstrated that the
infections were unrelated. S. maltophilia was also isolated from a fa
ucet in a patient's room, but the strain isolated was genetically diff
erent from the strain causing the patient's pneumonia. Our data sugges
t that severe bone marrow aplasia and a recent history of intensive ch
emotherapy are predisposing factors for the development of fulminant h
emorrhagic S. maltophilia pneumonia. Since some of the infections and
colonizations developed despite prophylactic administration of antibac
terial agents with documented in vitro activity against the pathogen a
nd none was controlled by such agents, it is clear an efficient treatm
ent strategy needs to be developed.