Twenty-four patients with cancer met predetermined criteria for a diagnosis
of zygomycosis over a 10-year period at our institution. All had hematolog
ic malignancy, and most had either neutropenia or steroid use as a risk fac
tor. Pulmonary involvement mimicking invasive aspergillosis was the most co
mmon presentation, and dissemination was seen in 58% of patients on whom au
topsies were performed. Three-fourths of the patients with pulmonary zygomy
cosis had pathogenic microorganisms other than zygomycetes isolated from re
spiratory specimens. The sensitivity of cultures in detecting zygomycetes f
rom respiratory specimens was low. A culture positive for zygomycetes was t
ypically a preterminal finding in the fatal, acute cases. Two-thirds of the
patients died. Favorable outcome seemed to correlate with lack of pulmonar
y involvement, surgical debridement, neutrophil recovery, and a cumulative
total amphotericin B dose of 2000 mg. Therapy with high-dose amphotericin B
, combined with aggressive surgery and immune reconstitution, offers the be
st chance for survival of cancer patients with zygomycosis.