O. Mourellou et al., THE TREATMENT OF PEMPHIGUS-VULGARIS - EXPERIENCE WITH 48 PATIENTS SEEN OVER AN 11-YEAR PERIOD, British journal of dermatology, 133(1), 1995, pp. 83-87
We present a retrospective analysis of 48 patients with pemphigus vulg
aris (PV) who were seen between 1978 and 1988. They were divided into
three treatment groups: 25 (group A) received 40-100 mg of oral predni
sone daily; eight (group B) received > 100 mg of prednisone daily; 15
(group C) received 40 mg of oral prednisone every other day and azathi
oprine 100 mg daily. A second immunosuppressive agent was subsequently
added to the treatment regimen of three patients in group A and eight
patients in group B. By 1989, 10% of the patients had been able to di
scontinue all therapy, and were in complete remission. Sixty-five per
cent of patients were on maintenance therapy, but in clinical remissio
n, Twenty-live per cent of the patients had died [eight in group A (31
%) and four in group B (50%)] either as a consequence of the disease o
r its treatment. None of the patients in group C had died. Most of the
deaths occurred during the first 2-3 months of therapy. Morbidity and
mortality were related to the severity of the disease, to the maximum
dose of prednisone required to induce remission, and to the presence
of other diseases. Patients needing a total of 5 g or more of predniso
ne to induce a remission during the acute stage had a high mortality r
ate.