Literature DB >> 6376746

Bone marrow transplantation in chronic granulomatous disease.

N Kamani, C S August, S D Douglas, E Burkey, A Etzioni, H W Lischner.   

Abstract

A 5-month-old Amish infant boy with chronic granulomatous disease underwent bone marrow transplantation from his 5-year-old, histocompatible brother after a preconditioning regimen of busulfan 2 mg/kg/day for 4 days, followed by cyclophosphamide 50 mg/kg/day for 4 days. At the time of bone marrow transplantation, he was free of infection, and remained so throughout the course of the transplant. He was engrafted promptly, with complete reversal of the neutrophil function defect and no sign of graft-versus-host disease. This was followed by loss of the erythroid graft and deterioration in neutrophil function over a period of 9 months. Sixteen months after transplantation, he is free of infection and growing normally, with essentially no evidence for neutrophil engraftment.

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Year:  1984        PMID: 6376746     DOI: 10.1016/s0022-3476(84)80354-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  5 in total

1.  Bone marrow transplantation in chronic granulomatous disease.

Authors:  M C Calviño; M S Maldonado; E Otheo; A Muñoz; J M Couselo; C Burgaleta
Journal:  Eur J Pediatr       Date:  1996-10       Impact factor: 3.183

2.  Treosulfan-based conditioning regimen in a second matched unrelated peripheral blood stem cell transplantation for a pediatric patient with CGD and invasive aspergillosis, who experienced initial graft failure after RIC.

Authors:  Maja Agnieszka Klaudel-Dreszler; Krzysztof Kalwak; Magdalena Kurenko-Deptuch; Beata Wolska-Kusnierz; Edyta Heropolitanska-Pliszka; Barbara Pietrucha; Bożena Mikoluc; Ewa Gorczyńska; Marek Ussowicz; Alicja Chybicka; Ewa Bernatowska
Journal:  Int J Hematol       Date:  2009-10-29       Impact factor: 2.490

3.  Clinical features and prognoses of 23 patients with chronic granulomatous disease followed for 21 years by a single hospital in Japan.

Authors:  Shinichi Kobayashi; Shizuko Murayama; Sayaka Takanashi; Kumiko Takahashi; Sachiko Miyatsuka; Tomoko Fujita; Sadato Ichinohe; Yuichi Koike; Toshitaka Kohagizawa; Hirosumi Mori; Yasushi Deguchi; Kaoru Higuchi; Hiroaki Wakasugi; Tatsuya Sato; Yasuyuki Wada; Masato Nagata; Nobuhiko Okabe; Osamu Tatsuzawa
Journal:  Eur J Pediatr       Date:  2008-03-12       Impact factor: 3.183

4.  Bone marrow aplasia following donor lymphocyte infusion in 4-year-old patient with chronic granulomatous disease after allogeneic stem cell transplantation: case report.

Authors:  Magdalena Cienkusz; Monika Lejman; Nel DĄbrowska-Leonik; Marta Choma; Katarzyna Drabko
Journal:  Cent Eur J Immunol       Date:  2020-09-24       Impact factor: 2.085

5.  An Experience of Donor Lymphocyte Infusion after Reduced-Intensity Conditioning Allogeneic Hematopoietic Stem Cell Transplantation for Chronic Granulomatous Disease.

Authors:  Tahereh Rostami; Azadeh Kiumarsi
Journal:  Pediatr Rep       Date:  2020-12-11
  5 in total

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