A Fatal Case of Neuroblastoma Complicated by Posterior Reversible Encephalopathy with Rapidly Evolving Transplantation-Associated Thrombotic Microangiopathy

Author:

Matsui Motohiro12ORCID,Makimoto Atsushi13ORCID,Saito Yuya4,Enokizono Mikako5ORCID,Matsuoka Kentaro36,Yuza Yuki1

Affiliation:

1. Department of Hematology/Oncology, Tokyo Metropolitan Children’s Medical Center, Tokyo 183-8561, Japan

2. Division of Molecular Epidemiology, Jikei University School of Medicine, Tokyo 105-8461, Japan

3. Department of Laboratory Medicine, Tokyo Metropolitan Children’s Medical Center, Tokyo 183-8561, Japan

4. Department of Pediatrics, Tama-Hokubu Medical Center, Tokyo 189-8511, Japan

5. Department of Radiology, Tokyo Metropolitan Children’s Medical Center, Tokyo 183-8561, Japan

6. Department of Pathology, Tokyo Metropolitan Children’s Medical Center, Tokyo 183-8561, Japan

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.

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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