Transplantation-associated thrombotic microangiopathy isolated to a congenital anomaly of the lung

Pediatr Transplant. 2017 Feb;21(1). doi: 10.1111/petr.12824. Epub 2016 Nov 24.

Abstract

TA-TMA is a post-hematopoietic stem cell transplant complication with clinical features of hemolytic anemia and thrombocytopenia. A 26-month-old child who had had an allogeneic transplant for treatment of DBA developed severe TA-TMA with heavy red blood cell and platelet transfusion dependence. Incidentally, he was found to have a lung sequestration. TA-TMA resolved and transfusion dependence resolved after resection of the sequestration. The finding suggests the malformation vasculature was selectively vulnerable to the trigger of TA-TMA-raising perhaps a clue to basic pathophysiology of TA-TMA and/or vascular malformations.

Keywords: allogeneic stem cell transplantation; anemia; child; graft-vs-host disease; lung diseases; pediatric hematopoietic stem cell.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Erythrocyte Transfusion
  • Erythrocytes
  • Graft vs Host Disease / etiology*
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Humans
  • Lung / abnormalities*
  • Lung Diseases / congenital*
  • Male
  • Platelet Transfusion
  • Thrombotic Microangiopathies / etiology*
  • Transplantation, Homologous
  • Treatment Outcome