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A Fatal Case of Neuroblastoma Complicated by Posterior Reversible Encephalopathy with Rapidly Evolving Transplantation-Associated Thrombotic Microangiopathy.
Matsui, Motohiro; Makimoto, Atsushi; Saito, Yuya; Enokizono, Mikako; Matsuoka, Kentaro; Yuza, Yuki.
Afiliação
  • Matsui M; Department of Hematology/Oncology, Tokyo Metropolitan Children's Medical Center, Tokyo 183-8561, Japan.
  • Makimoto A; Division of Molecular Epidemiology, Jikei University School of Medicine, Tokyo 105-8461, Japan.
  • Saito Y; Department of Hematology/Oncology, Tokyo Metropolitan Children's Medical Center, Tokyo 183-8561, Japan.
  • Enokizono M; Department of Laboratory Medicine, Tokyo Metropolitan Children's Medical Center, Tokyo 183-8561, Japan.
  • Matsuoka K; Department of Pediatrics, Tama-Hokubu Medical Center, Tokyo 189-8511, Japan.
  • Yuza Y; Department of Radiology, Tokyo Metropolitan Children's Medical Center, Tokyo 183-8561, Japan.
Children (Basel) ; 10(3)2023 Mar 03.
Article em En | MEDLINE | ID: mdl-36980064
ABSTRACT

BACKGROUND:

Transplantation-associated thrombotic microangiopathy (TA-TMA) is a severe complication of hematopoietic stem cell transplantation and is sometimes fatal. OBSERVATIONS A 4-year-old, male patient with stage M neuroblastoma (NBL) who had received an allogeneic bone marrow transplantation (BMT) from his sibling five months previously presented with rapidly progressive posterior reversible encephalopathy (PRES) complicated with TA-TMA. Although the patient was transferred to the pediatric intensive care unit, he died within one week after the onset of the latest symptoms.

CONCLUSIONS:

This is the first description of a fatal case of NBL complicated by PRES with rapidly evolving TA-TMA after an allogenic BMT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article