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Early diagnosis and successful treatment of a patient with transfusion‐associated GVHD with autologous peripheral blood progenitor cell transplantation
Author(s) -
Hutchinson Kendra,
Kopko Patricia M.,
Muto Kathryn N.,
Tuscano Joseph,
O'Donnell Robert T.,
Holland Paul V.,
Richman Carol,
Paglieroni Teresa G.,
Wun Theodore
Publication year - 2002
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1046/j.1537-2995.2002.00253.x
Subject(s) - medicine , pancytopenia , rash , transplantation , immunosuppression , fludarabine , chronic lymphocytic leukemia , hematopoietic stem cell transplantation , gastroenterology , surgery , cyclophosphamide , immunology , leukemia , chemotherapy , bone marrow
BACKGROUND : Transfusion‐associated GVHD (TA‐GVHD) is an uncommon complication of blood transfusion. Diagnosis of TA‐GVHD is difficult, and it is usually rapidly fatal. There are few documented sur‐ vivors of TA‐GVHD. CASE REPORT : A 61‐year‐old woman with chronic lymphocytic leukemia (CLL) was treated with fludarabine followed by combination chemotherapy and high‐dose radioimmunotherapy and peripheral blood progenitor cell (PBPC) rescue. She was transfused with nonirradiated blood components at an outside hospital and presented 10 days later with rash, elevated liver enzymes, and progressive pancytopenia. Skin biopsy was consistent with GVHD, and HLA typing of lymphocytes from the patient demonstrated mixed chimerism. The patient was treated with solumedrol and cyclosporin A, followed by high‐dose cyclophosphamide and antithymocyte globulin and autologous PBPC infusion. She had rapid engraftment, resolution of skin rash, and normalization of liver function abnormalities. She is in good health with normal blood counts and no evidence of CLL 34 months after transplantation. CONCLUSION : TA‐GVHD occurs in the setting of an immunocompromised recipient receiving nonirradiated blood components. A typical presentation includes skin rash, liver function abnormalities, and pancytopenia. Demonstration of mixed chimerism by HLA typing facilitated diagnosis in this patient. High‐dose immunosuppression, facilitated by the availability of autologous PBPCs, resulted in a successful outcome.