C. Agusti et al., DIFFUSE ALVEOLAR HEMORRHAGE IN ALLOGENEIC BONE-MARROW TRANSPLANTATION- A POSTMORTEM STUDY, American journal of respiratory and critical care medicine, 151(4), 1995, pp. 1006-1010
Citations number
24
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
To define better the syndrome of diffuse alveolar hemorrhage (DAH), we
conducted a postmortem study in 77 patients who died of pulmonary com
plications, distributed into three groups. Group A included 47 patient
s with hematologic diseases treated with allogeneic bone marrow transp
lant (BMT); Group B, 20 patients with hematologic diseases treated wit
h conventional chemotherapy; and Group C, 10 patients without hematolo
gic diseases. The diagnosis of DAH was established when there was bloo
d in at least 30% of the lung tissue evaluated without evidence of inf
ection or any other pathologic change that could account for its prese
nce. The presence of an associated pulmonary complication was consider
ed only when there was normal lung parenchyma between both blood and t
he specific lesions. Diffuse alveolar hemorrhage was shown in 11 patie
nts in Group A (23%) compared with 1 patient in Group B (5%) (p < 0.05
). Of the 11 patients with DAH in Group A, 10 had some associated pulm
onary complication: 7 presented with diffuse alveolar damage (DAD), 2
with associated bacterial pneumonia and 1 with invasive aspergillosis,
2 others had an associated cytomegalovirus (CMV) pneumonitis, and the
remaining patients had an associated herpes pneumonia. There were no
clinical differences between patients with and without DAH. Of 8 patie
nts with confirmed DAH in Group A, who had been submitted to a broncho
scopic examination within 1 wk of death, 4 had normal BAL fluid; by co
ntrast, 7 of 13 patients without DAH had hemorrhagic BAL fluid. It is
concluded that (1) DAH is a common contributing factor to death in pat
ients treated with allogeneic BMT; (2) DAH usually occurs in associati
on with other pulmonary complications; and (3) the validity of BAL in
the diagnosis of DAH appears to be poor in this study.