Abstract | BACKGROUND: OBSERVATIONS: Following EC-MPS/ prednisone therapy, disease progression was inhibited between days 30 and 45 in 9/10 patients (8 PV; 1 PF). At 18 months, 8/9 PV patients had clinically quiescent disease; EC-MPS therapy was no longer required in two patients as a result of disease remission. The remaining PV patient showed no response to treatment. The PF patient also had clinically quiescent disease but with high levels of anti-desmoglein-1. ECMPS dose was reduced to 720 mg daily in 4/9 patients by month 6. Average daily prednisone requirement decreased to 25 mg at 6 months and to 15 mg at 18 months. Three adverse events were reported: headache (two cases; one mild and one moderate) and significant increase in blood glucose (one case; moderate). CONCLUSIONS:
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Authors | Maria Rita Bongiorno, Giuseppe Pistone, Spyridoula Doukaki, Mario Aricò |
Journal | International journal of dermatology
(Int J Dermatol)
Vol. 49
Issue 6
Pg. 693-9
(Jun 2010)
ISSN: 1365-4632 [Electronic] England |
PMID | 20618478
(Publication Type: Journal Article)
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Chemical References |
- Glucocorticoids
- Immunosuppressive Agents
- Tablets, Enteric-Coated
- Mycophenolic Acid
- Prednisone
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Topics |
- Administration, Oral
- Adult
- Drug Therapy, Combination
- Female
- Follow-Up Studies
- Glucocorticoids
(administration & dosage, adverse effects)
- Humans
- Immunosuppressive Agents
(administration & dosage, adverse effects)
- Male
- Middle Aged
- Mycophenolic Acid
(administration & dosage, adverse effects, analogs & derivatives)
- Pemphigus
(drug therapy)
- Prednisone
(administration & dosage, adverse effects)
- Tablets, Enteric-Coated
- Treatment Outcome
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