Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia

Abstract Donor cell leukemia is a very rare cause of relapse after allogeneic hematopoietic cell transplantation (alloHCT). Herein, we describe an unprecedented case of donor cell‐derived chronic myelomonocytic leukemia (CMML) presenting seven years after a 51‐year‐old man received a matched‐related...

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Main Authors: Kevin C. Miller, Zaid H. Abdel Rahman, Ryan S. Robetorye, James M. Foran
Format: Article
Language:English
Published: Wiley 2020-12-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.3383
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spelling doaj-a80489a741f444e9af628d2da9a838252021-08-02T06:23:39ZengWileyClinical Case Reports2050-09042020-12-018123224322710.1002/ccr3.3383Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemiaKevin C. Miller0Zaid H. Abdel Rahman1Ryan S. Robetorye2James M. Foran3Department of Medicine Massachusetts General Hospital Boston MA USADivision of Hematology/Oncology Mayo Clinic Jacksonville FL USADepartment of Laboratory Medicine and Pathology Mayo Clinic Phoenix AZ USADivision of Hematology/Oncology Mayo Clinic Jacksonville FL USAAbstract Donor cell leukemia is a very rare cause of relapse after allogeneic hematopoietic cell transplantation (alloHCT). Herein, we describe an unprecedented case of donor cell‐derived chronic myelomonocytic leukemia (CMML) presenting seven years after a 51‐year‐old man received a matched‐related alloHCT from his 59‐year‐old brother for T‐cell acute lymphoblastic leukemia.https://doi.org/10.1002/ccr3.3383allogeneic hematopoietic cell transplantchronic myelomonocytic leukemiaCMMLdonor cell leukemiastem cell transplant
collection DOAJ
language English
format Article
sources DOAJ
author Kevin C. Miller
Zaid H. Abdel Rahman
Ryan S. Robetorye
James M. Foran
spellingShingle Kevin C. Miller
Zaid H. Abdel Rahman
Ryan S. Robetorye
James M. Foran
Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia
Clinical Case Reports
allogeneic hematopoietic cell transplant
chronic myelomonocytic leukemia
CMML
donor cell leukemia
stem cell transplant
author_facet Kevin C. Miller
Zaid H. Abdel Rahman
Ryan S. Robetorye
James M. Foran
author_sort Kevin C. Miller
title Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia
title_short Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia
title_full Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia
title_fullStr Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia
title_full_unstemmed Donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for T‐cell acute lymphoblastic leukemia
title_sort donor cell‐derived chronic myelomonocytic leukemia presenting after allogeneic hematopoietic cell transplantation for t‐cell acute lymphoblastic leukemia
publisher Wiley
series Clinical Case Reports
issn 2050-0904
publishDate 2020-12-01
description Abstract Donor cell leukemia is a very rare cause of relapse after allogeneic hematopoietic cell transplantation (alloHCT). Herein, we describe an unprecedented case of donor cell‐derived chronic myelomonocytic leukemia (CMML) presenting seven years after a 51‐year‐old man received a matched‐related alloHCT from his 59‐year‐old brother for T‐cell acute lymphoblastic leukemia.
topic allogeneic hematopoietic cell transplant
chronic myelomonocytic leukemia
CMML
donor cell leukemia
stem cell transplant
url https://doi.org/10.1002/ccr3.3383
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