OBJECTIVE: To describe a patient who developed adverse reactions to two dif
ferent lipid formulations of amphotericin B: liposomal amphotericin B (AmBi
some) and amphotericin B colloidal dispersion (ABCD, Amphocil), yet tolerat
ed amphotericin B deoxycholate (Fungizone) despite renal toxicity.
CASE SUMMARY: A 72-year-old woman with acute myelomonocytic leukemia was tr
eated with amphotericin B deoxycholate for suspected pulmonary aspergillosi
s; the drug was well tolerated but resulted; in renal failure;:Antifungal t
herapy was then changed to liposomal amphotericin B. Within 10 minutes of l
iposomal amphotericin B infusion, the patient developed severe dyspnea, che
st pain, and a feeling of imminent death. On the following day, liposomal a
mphotericin B:was switched to amphotericin B colloidal dispersion. Again, w
ithin 10 minutes of this infusion, the patient developed fever,chills hypot
ension, severe chest pain, dsypnea, and a feeling of imminent death, The pa
tient refused any further treatment with these drugs and insisted on switch
ing back to amphotericin B deoxycholate, which was then administered for 10
days and was well tolerated.
DISCUSSION: Severe adverse reactions, such as anaphylaxis, cardiac toxicity
, and respiratory failure, following administration of ail three lipid form
ulations of amphotericin B have been reported. In most reported cases, swit
ching to a different lipid formulation of amphotericin B was well tolerated
. This is in contrast to our case, where a severe reaction was repeated whe
n another lipid preparation was given, necessitating switching back to amph
otericin B deoxycholate despite its nephrotoxicity.
CONCLUSIONS: In some patients, paradoxically, lipid formulations of amphote
ricin B may be less tolerable than conventional amphotericin B.