Literature DB >> 20846242

Solid organ transplants following hematopoietic stem cell transplant in children.

Nancy Bunin1, Virginia Guzikowski, Elizabeth R Rand, Samuel Goldfarb, Jorge Baluarte, Kevin Meyers, Kim M Olthoff.   

Abstract

SOT may be indicated for a select group of pediatric patients who experience permanent organ failure following HSCT. However, there is limited information available about outcomes. We identified eight children at our center who received an SOT following an HSCT. Patients were six months to 18 yr at HSCT. Diseases for which children underwent HSCT included thalassemia, Wiskott-Aldrich syndrome, Shwachman-Diamond/bone marrow failure, sickle cell disease (SCD), erythropoietic porphyria (EP), ALL, chronic granulomatous disease, and neuroblastoma. Time from HSCT to SOT was 13 days to seven yr (median, 27 months. Lung SOT was performed for two patients with BO, kidney transplants for three patients, and liver transplants for three patients (VOD, chronic GVHD). Seven patients are alive with functioning allografts 6-180 months from SOT. Advances in organ procurement, operative technique, immunosuppressant therapy, and infection control may allow SOT for a select group of patients post-HSCT. However, scarcity of donor organs available in a timely fashion continues to be a limiting factor. Children who have undergone HSCT and develop single organ failure should be considered for an SOT if there is a high likelihood of cure of the primary disease.
© 2010 John Wiley & Sons A/S.

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Year:  2010        PMID: 20846242     DOI: 10.1111/j.1399-3046.2010.01401.x

Source DB:  PubMed          Journal:  Pediatr Transplant        ISSN: 1397-3142


  2 in total

Review 1.  Solid organ transplantation following end-organ failure in recipients of hematopoietic stem cell transplantation in children.

Authors:  Kiran Upadhyay; Richard N Fine
Journal:  Pediatr Nephrol       Date:  2013-08-16       Impact factor: 3.714

2.  [Clinical analysis of lung transplantation in eight patients with obstructive bronchiolitis syndrome after hematopoietic stem cell transplantation].

Authors:  L L Wang; H Y Wang; Y F Shen; M Z Lu; J Y Chen; B Wu
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2017-11-14
  2 in total

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