Title of article :
Kaposis Sarcoma following Allogeneic Hematopoietic Stem Cell Transplantation for Chronic Myelogenous Leukemia
Author/Authors :
Jr.، نويسنده , , Medeiros، B.C. de نويسنده , , Rezuke، W.N. نويسنده , , Ricci، A. نويسنده , , Tsongalis، G. نويسنده , , Shen، P.U.F. نويسنده , , Bona، R.D. نويسنده , , Feingold، J.M. نويسنده , , Edwards، R.L. نويسنده , , Tutschka، P.J. نويسنده , , Bilgrami، S. نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
-114
From page :
115
To page :
0
Abstract :
Unlike solid organ transplantation, Kaposiʹs sarcoma (KS) occurs rarely following hematopoietic stem cell transplantation (HSCT). In fact, only 5 cases of KS have been reported after allogeneic or autologous HSCT. The usual treatment combines a substantial decrease in, or elimination of, immunosuppressive therapy along with local measures such as surgical excision, cryotherapy or radiation therapy. A 46-year-old woman with chronic myelogenous leukemia who had received an allogeneic HSCT previously from an HLA-identical sibling, presented on day +814 with human herpes virus-8-associated KS involving her left lower extremity. She had been on continuous immunosuppressive therapy since her transplant because of chronic graft-versus-host disease. The intensity of immunosuppressive therapy was decreased once a diagnosis of KS had been established. However, the nodular lesions continued to progress in size and number. Therefore, a course of irradiation was administered to sites of bulk disease on her legs. Furthermore, thalidomide was initiated along with a topical retinoid, alitretinoin 0.1% gel applied twice daily to the nonirradiated lesions. This approach yielded a partial response in both irradiated and nonirradiated lesions over the course of the following 7 months. Both thalidomide and alitretinoin 0.1% gel appear to be beneficial in HSCT-associated KS and exhibit tolerable side effects.
Journal title :
Acta Haematologica
Serial Year :
2000
Journal title :
Acta Haematologica
Record number :
25456
Link To Document :
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