Am. J. Respir. Crit. Care Med., Vol 151, No. 4, 04 1995, 1006-1010.
Diffuse alveolar hemorrhage in allogeneic bone marrow transplantation. A postmortem study
C Agusti, J Ramirez, C Picado, A Xaubet, E Carreras, E Ballester, A Torres, C Battochia and R Rodriguez-Roisin
Department of Pathologic Anatomy, University of Barcelona, Spain.
To define better the syndrome of diffuse alveolar hemorrhage (DAH), we
conducted a postmortem study in 77 patients who died of pulmonary
complications, distributed into three groups. Group A included 47 patients
with hematologic diseases treated with allogeneic bone marrow transplant
(BMT); Group B, 20 patients with hematologic diseases treated with
conventional chemotherapy; and Group C, 10 patients without hematologic
diseases. The diagnosis of DAH was established when there was blood in at
least 30% of the lung tissue evaluated without evidence of infection or any
other pathologic change that could account for its presence. The presence
of an associated pulmonary complication was considered only when there was
normal lung parenchyma between both blood and the specific lesions. Diffuse
alveolar hemorrhage was shown in 11 patients 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 pulmonary 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 patients with confirmed DAH in Group A, who had been
submitted to a bronchoscopic examination within 1 wk of death, 4 had normal
BAL fluid; by contrast, 7 of 13 patients without DAH had hemorrhagic BAL
fluid.(ABSTRACT TRUNCATED AT 250 WORDS)
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Copyright © 1995 American Thoracic Society
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