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Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report

BACKGROUND: Various therapeutic options are available for the management of Langerhans cell histiocytosis. However, treatment administered to control this disease may be complicated by acute leukemia. CASE PRESENTATION: A 34 years old male was diagnosed to have Langerhans cell histiocytosis in March...

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Autores principales: Al-Anazi, Khalid A, Alshehri, Abdulrahman, Al-Zahrani, Hazza A, Al-Mohareb, Fahad I, Maghfoor, Irfan, Ajarim, Dahish
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527498/
https://www.ncbi.nlm.nih.gov/pubmed/18710527
http://dx.doi.org/10.1186/1757-1626-1-101
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author Al-Anazi, Khalid A
Alshehri, Abdulrahman
Al-Zahrani, Hazza A
Al-Mohareb, Fahad I
Maghfoor, Irfan
Ajarim, Dahish
author_facet Al-Anazi, Khalid A
Alshehri, Abdulrahman
Al-Zahrani, Hazza A
Al-Mohareb, Fahad I
Maghfoor, Irfan
Ajarim, Dahish
author_sort Al-Anazi, Khalid A
collection PubMed
description BACKGROUND: Various therapeutic options are available for the management of Langerhans cell histiocytosis. However, treatment administered to control this disease may be complicated by acute leukemia. CASE PRESENTATION: A 34 years old male was diagnosed to have Langerhans cell histiocytosis in March 1999. Unfortunately, the cytotoxic chemotherapy and radiotherapy given to control the repeated relapses and exacerbations of the primary disease predisposed him to therapy-induced myelodysplastic syndrome which transformed into acute myeloid leukemia. After achieving complete remission of his leukemia, the patient received an allogeneic hematopoietic stem cell transplant. The allograft was complicated by chronic graft versus host disease that was controlled by various immunosuppressive agents and extracorporal photophoresis. CONCLUSION: Management of complicated cases of histiocytosis requires various therapeutic modalities and a multidisciplinary approach. Having complications of therapy eg myelodysplasia or acute leukemia make the outcome more dismal and the management options limited to aggressive forms of treatment. High dose chemotherapy followed by an allograft may be a curative option not only for therapy-related myelodysplasia/acute leukemia, but also for frequently relapsing and poorly controlled Langerhans cell histiocytosis.
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spelling pubmed-25274982008-09-01 Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report Al-Anazi, Khalid A Alshehri, Abdulrahman Al-Zahrani, Hazza A Al-Mohareb, Fahad I Maghfoor, Irfan Ajarim, Dahish Cases J Case Report BACKGROUND: Various therapeutic options are available for the management of Langerhans cell histiocytosis. However, treatment administered to control this disease may be complicated by acute leukemia. CASE PRESENTATION: A 34 years old male was diagnosed to have Langerhans cell histiocytosis in March 1999. Unfortunately, the cytotoxic chemotherapy and radiotherapy given to control the repeated relapses and exacerbations of the primary disease predisposed him to therapy-induced myelodysplastic syndrome which transformed into acute myeloid leukemia. After achieving complete remission of his leukemia, the patient received an allogeneic hematopoietic stem cell transplant. The allograft was complicated by chronic graft versus host disease that was controlled by various immunosuppressive agents and extracorporal photophoresis. CONCLUSION: Management of complicated cases of histiocytosis requires various therapeutic modalities and a multidisciplinary approach. Having complications of therapy eg myelodysplasia or acute leukemia make the outcome more dismal and the management options limited to aggressive forms of treatment. High dose chemotherapy followed by an allograft may be a curative option not only for therapy-related myelodysplasia/acute leukemia, but also for frequently relapsing and poorly controlled Langerhans cell histiocytosis. BioMed Central 2008-08-18 /pmc/articles/PMC2527498/ /pubmed/18710527 http://dx.doi.org/10.1186/1757-1626-1-101 Text en Copyright © 2008 Al-Anazi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Al-Anazi, Khalid A
Alshehri, Abdulrahman
Al-Zahrani, Hazza A
Al-Mohareb, Fahad I
Maghfoor, Irfan
Ajarim, Dahish
Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
title Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
title_full Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
title_fullStr Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
title_full_unstemmed Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
title_short Successful outcome of Langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
title_sort successful outcome of langerhans cell histiocytosis complicated by therapy-related myelodysplasia and acute myeloid leukemia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2527498/
https://www.ncbi.nlm.nih.gov/pubmed/18710527
http://dx.doi.org/10.1186/1757-1626-1-101
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