A peptide-based erythropoietin-receptor agonist for pure red-cell aplasia.
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n engl j med 362;7 nejm.org february 18, 2010 656 neous regression is never observed, whereas such regression occurs in of 35% of patients with bowenoid papulosis.2 One may wonder whether the complete regression of lesions that was observed in some patients in this clinical trial could be related to a spontaneous regression of multifocal lesions, particularly in very young women (e.g., Patient 11, who was 23 years of age) or in patients with a recent onset (<9 months) of the disease (Patients 11, 27, 29, and 30) or with very small lesions (Patients 11, 16, 27, 29, and 30, who had lesions ranging from 2 cm2 to 8 cm2). Our clinical study involving six women who presented with bowenoid papulosis included a woman who was 23 years of age and who had multifocal lesions (measuring 10 cm2) that underwent spontaneous regression.3
[1] I. Macdougall,et al. A peptide-based erythropoietin-receptor agonist for pure red-cell aplasia. , 2009, The New England journal of medicine.
[2] I. Macdougall,et al. Treatment of erythropoietin-induced pure red cell aplasia: a retrospective study , 2004, The Lancet.
[3] F. Locatelli,et al. Revised European best practice guidelines for the management of anaemia in patients with chronic renal failure. , 2004, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.