Author:
Fassihi Hiva,Iqbal Kamran,Garibaldinos Trish,Sarkany Robert,Scarisbrick Julia,Novaković Ljubomir
Abstract
Abstract
Chronic graft-versus-host disease (GVHD) is a frequent complication after allogeneic hematopoietic stem cell transplantation (HSCT). Approximately 10% of patients with GVHD develop sclerodermatous changes, which can cause significant morbidity and are often refractory to standard systemic immunosuppression. We present two cases of sclerodermatous GVHD. The first is a 39-year-old man, who had a matched sibling, undergoing allogeneic HSCT for severe aplastic anemia. The second patient is a 7-year-old boy, who had an allogeneic HSCT from his HLA-identical mother for acute myeloid leukemia (AML). Both patients presented with widespread sclerotic changes, resulting in joint contractures and significant functional difficulties. Studies have shown UVA1 phototherapy to be a promising and well tolerated treatment modality in patients with sclerotic skin diseases. Both of our patients were treated with UVA1, which resulted in a significant skin softening, improvement in joint mobility and quality of life. UVA1 appears to be an effective treatment for refractory sclerodermatous GVHD; however, long-term clinical studies in larger groups are needed to accurately evaluate its efficacy and safety.
Reference32 articles.
1. Alteration of subcutaneous tissue in systemic scleroderma;Fleischmajer;Arch Dermatol,1972
2. High - dose therapy in the treatment of patients with atopic dermatitis;Krutmann;J Am Acad Dermatol,1992
3. Chronic graft versus host disease;Baird;Curr Opin Hematol,2006
4. phototherapy and PUVA photochemotherapy in connective tissue diseases and related disorders : a research based;Breuckmann;review Dermatology,2004
5. Decreased collagenase expression in cultured systemic sclerosis fibroblasts;Takeda;J Invest Dermatol,1994
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