Grundmann-Kollmann M, Behrens S, Gruss C, Gottlöber P, Peter R U, Kerscher M
Department of Dermatology, University of Ulm, Germany.
J Am Acad Dermatol. 2000 Jan;42(1 Pt 1):134-6. doi: 10.1016/s0190-9622(00)90023-9.
Graft-versus-host disease is a frequent complication of allogenic bone marrow transplantation. Approximately 10% of patients suffering from chronic graft-versus-host disease develop sclerodermic graft-versus-host disease of the skin, which often does not respond to conventional immunosuppressive therapy. An alternative to immunosuppressive treatment is photochemotherapy. We describe a patient with chronic sclerodermic graft-versus-host disease who did not respond to a combination therapy of cyclosporine and prednisone and later mycophenolate mofetil plus prednisone. A combination therapy of mycophenolate mofetil (2 g/day) and low-dose UVA(1) therapy (single dose, 20 J/cm(2), 4 times per week over 6 weeks) resulted in striking clinical improvement of sclerodermic graft-versus-host disease.
移植物抗宿主病是同种异体骨髓移植常见的并发症。约10%患有慢性移植物抗宿主病的患者会发展为皮肤硬皮病样移植物抗宿主病,这种病通常对传统免疫抑制治疗无反应。光化学疗法是免疫抑制治疗的一种替代方法。我们描述了一名患有慢性硬皮病样移植物抗宿主病的患者,其对环孢素和泼尼松联合治疗以及后来的霉酚酸酯加泼尼松治疗均无反应。霉酚酸酯(2克/天)与低剂量UVA(1)疗法(单次剂量,20焦耳/平方厘米,每周4次,共6周)联合治疗使硬皮病样移植物抗宿主病的临床症状得到显著改善。