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Successful eradication of leptomeningeal plasma cell disease

Plasma cell leukaemia (PCL) is a rare and aggressive form of malignant monoclonal gammopathy characterized by the presence of high levels of plasma cells in peripheral blood. Central nervous system involvement of PCL has no established treatment and an extremely poor prognosis. We here present a 59-...

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Autores principales: Bruserud, Øyvind, Hansen, Bent-Are, Vetti, Nils, Johansen, Silje, Reikvam, Håkon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031028/
https://www.ncbi.nlm.nih.gov/pubmed/29992033
http://dx.doi.org/10.1093/omcr/omy038
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author Bruserud, Øyvind
Hansen, Bent-Are
Vetti, Nils
Johansen, Silje
Reikvam, Håkon
author_facet Bruserud, Øyvind
Hansen, Bent-Are
Vetti, Nils
Johansen, Silje
Reikvam, Håkon
author_sort Bruserud, Øyvind
collection PubMed
description Plasma cell leukaemia (PCL) is a rare and aggressive form of malignant monoclonal gammopathy characterized by the presence of high levels of plasma cells in peripheral blood. Central nervous system involvement of PCL has no established treatment and an extremely poor prognosis. We here present a 59-year-old male patient diagnosed with PCL, initially treated with induction chemotherapy followed by autologous peripheral blood hematopoietic stem cell transplantation. After achieving a partial response, he relapsed and presented with leptomeningeal disease. He was then successfully treated with dexamethasone, pomalidomide, and an intrathecal combination of methotrexate, methylprednisolone and cytarabine. This cleared his cerebrospinal fluid from plasma cells achieving a durable partial response.
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spelling pubmed-60310282018-07-10 Successful eradication of leptomeningeal plasma cell disease Bruserud, Øyvind Hansen, Bent-Are Vetti, Nils Johansen, Silje Reikvam, Håkon Oxf Med Case Reports Case Report Plasma cell leukaemia (PCL) is a rare and aggressive form of malignant monoclonal gammopathy characterized by the presence of high levels of plasma cells in peripheral blood. Central nervous system involvement of PCL has no established treatment and an extremely poor prognosis. We here present a 59-year-old male patient diagnosed with PCL, initially treated with induction chemotherapy followed by autologous peripheral blood hematopoietic stem cell transplantation. After achieving a partial response, he relapsed and presented with leptomeningeal disease. He was then successfully treated with dexamethasone, pomalidomide, and an intrathecal combination of methotrexate, methylprednisolone and cytarabine. This cleared his cerebrospinal fluid from plasma cells achieving a durable partial response. Oxford University Press 2018-07-03 /pmc/articles/PMC6031028/ /pubmed/29992033 http://dx.doi.org/10.1093/omcr/omy038 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Bruserud, Øyvind
Hansen, Bent-Are
Vetti, Nils
Johansen, Silje
Reikvam, Håkon
Successful eradication of leptomeningeal plasma cell disease
title Successful eradication of leptomeningeal plasma cell disease
title_full Successful eradication of leptomeningeal plasma cell disease
title_fullStr Successful eradication of leptomeningeal plasma cell disease
title_full_unstemmed Successful eradication of leptomeningeal plasma cell disease
title_short Successful eradication of leptomeningeal plasma cell disease
title_sort successful eradication of leptomeningeal plasma cell disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031028/
https://www.ncbi.nlm.nih.gov/pubmed/29992033
http://dx.doi.org/10.1093/omcr/omy038
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