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Your search keyword '"Rybicki Z"' showing total 4 results
Start Over Author "Rybicki Z" Topic bone marrow transplantation
4 results on '"Rybicki Z"'

1. Allogeneic bone marrow transplantation from HLA-identical siblings following conditioning with busulphan and cyclophosphamide.

Author

Wiktor-Jedrzejczak W, Szczylik C, Matej H, Pojda Z, Ratajczak MZ, Myc A, Siekierzyński M, Kansy J, Kłos M, and Rybicki Z

Subjects
Adolescent, Adult, Busulfan administration & dosage, Child, Combined Modality Therapy, Cyclophosphamide administration & dosage, Female, HLA Antigens, Hematologic Diseases drug therapy, Hematologic Diseases surgery, Humans, Infant, Leukemia drug therapy, Leukemia surgery, Male, Transplantation, Homologous, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Bone Marrow Transplantation methods
Published
1991

2. Allogeneic bone marrow transplantation from HLA-identical siblings following conditioning with busulfan and cyclophosphamide. First results.

Author

Wiktor-Jedrzejczak W, Szczylik C, Matej H, Pojda Z, Ratajczak MZ, Myc A, Siekierzyński M, Kansy J, Kłos M, and Rybicki Z

Subjects
Adolescent, Adult, Anemia, Aplastic mortality, Anemia, Aplastic surgery, Child, Child, Preschool, Female, Humans, Infant, Leukemia, Myelogenous, Chronic, BCR-ABL Positive mortality, Leukemia, Myelogenous, Chronic, BCR-ABL Positive surgery, Leukemia, Myeloid, Acute mortality, Leukemia, Myeloid, Acute surgery, Male, Precursor Cell Lymphoblastic Leukemia-Lymphoma mortality, Precursor Cell Lymphoblastic Leukemia-Lymphoma surgery, Bone Marrow Transplantation, Busulfan therapeutic use, Cyclophosphamide therapeutic use
Abstract

In the time period from November 1984 to January 1987 eight allogeneic bone marrow transplantation were performed from HLA-identical siblings. The theoretical chance of success in this group was between 21 and 50%, according to the recent data of the International Bone Marrow Transplant Registry, depending on the diagnosis and clinical condition. The average chance was 37.5%. Haemopoietic reconstitution was achieved in 6 recipients, while 2 died of early complications (cytostatic induced hepatocellular damage and fungal sepsis). Another 3 patients died of complications of the intermediate period (pulmonary bleeding, virus hepatitis, graft rejection). The remaining 3 recipients are alive, in excellent clinical condition, including one girl surviving more than 2 years after the transplantation.

Published
1989

3. [Allogeneic transplantation of HLA-compatible bone marrow. Initial results].

Author

Jedrzejczak WW, Matej H, Szczylik C, Pojda Z, Ratajczak MZ, Myc A, Siekierzyński M, Kansy J, Kłos M, and Rybicki Z

Subjects
Adult, Bone Marrow immunology, Child, Female, Hematologic Diseases immunology, Histocompatibility Testing, Humans, Male, Preoperative Care, Transplantation, Isogeneic, Bone Marrow Transplantation, HLA Antigens analysis, Hematologic Diseases therapy, Postoperative Complications etiology
Published
1988

4. [Rejection of allogeneic bone marrow transplant. Case report].

Author

Szczylik C, Ratajczak M, Dumański Z, Myc A, Siekierzyński M, Rybicki Z, Kłos M, Zaboklicki S, Zaborowski P, and Nowakowska B

Subjects
Adult, Bone Marrow Transplantation immunology, Graft vs Host Disease diagnosis, HLA Antigens immunology, Humans, Leukemia, Myeloid, Acute immunology, Male, Time Factors, Bone Marrow Transplantation adverse effects, Graft Rejection immunology, Graft vs Host Disease etiology, Leukemia, Myeloid, Acute surgery
Abstract

In a patient aged 22 years with acute myeloblastic leukaemia during complete remission an allogenic transplant of bone marrow identical in the HLA antigen range was rejected despite administration before transplantation of a full marrow-ablating dose of busulphan (16 mg/kg) and severe graft-versus-host disease. Graft rejection manifested itself as disappearance of its haemopoietic function which was confirmed during the life and on autopsy. The case deserves attention in view of the rarity of HLA-identical marrow graft rejections in patients treated for leukaemias.

Published
1988

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