A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone

Central nervous system (CNS) involvement in multiple myeloma (MM) (MM-CNS) in the form of leptomeningeal myelomatosis or brain parenchyma plasmacytoma is rare, causing challenges in clinical diagnosis and treatment. We would like to report a case of leptomeningeal myelomatosis and illustrated the c...

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Main Authors: Jew Win, Kuan, Ling Chai, Sing, Pathmanathan, Rajadurai, Gong Lau, Lee, Joseph, Uchang, Sharifah Noor Akmal, Syed Husain
Format: Article
Language:English
Published: Hindawi Publishing 2022
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Online Access:http://ir.unimas.my/id/eprint/39539/1/A%20Case%20Report%20-%20Copy.pdf
http://ir.unimas.my/id/eprint/39539/
https://www.hindawi.com/journals/crihem/2022/4081971/
https://doi.org/10.1155/2022/4081971
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spelling my.unimas.ir.395392022-09-06T08:31:04Z http://ir.unimas.my/id/eprint/39539/ A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone Jew Win, Kuan Ling Chai, Sing Pathmanathan, Rajadurai Gong Lau, Lee Joseph, Uchang Sharifah Noor Akmal, Syed Husain R Medicine (General) RD Surgery Central nervous system (CNS) involvement in multiple myeloma (MM) (MM-CNS) in the form of leptomeningeal myelomatosis or brain parenchyma plasmacytoma is rare, causing challenges in clinical diagnosis and treatment. We would like to report a case of leptomeningeal myelomatosis and illustrated the challeges. A 61-year-old man was diagnosed with MM with left paravertebral plasmacytoma, R-ISS II with high suspicion of double-hit MM, either biallelic aberrancy of TP53 or del(17p) and IGH aberrancy depending on the denition chosen, treated with lenalidomide-bortezomib-dexamethasone and local radiotherapy, later developed systemic relapse and progression to MM-CNS in the form of leptomeningeal myelomatosis. A modied CNS-based treatment not reported before, consisting of daratumumab, pomalidomide, vincristine, procarbazine, and dexamethasone, brought a rapid clinical improvement and warrants a further study. Incorporation of intrathecal thiotepa into the regimen would likely increase the e�cacy. Hindawi Publishing 2022 Article PeerReviewed text en http://ir.unimas.my/id/eprint/39539/1/A%20Case%20Report%20-%20Copy.pdf Jew Win, Kuan and Ling Chai, Sing and Pathmanathan, Rajadurai and Gong Lau, Lee and Joseph, Uchang and Sharifah Noor Akmal, Syed Husain (2022) A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone. Case Reports in Hematology, 2022. pp. 1-7. ISSN 2090-6579 https://www.hindawi.com/journals/crihem/2022/4081971/ https://doi.org/10.1155/2022/4081971
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic R Medicine (General)
RD Surgery
spellingShingle R Medicine (General)
RD Surgery
Jew Win, Kuan
Ling Chai, Sing
Pathmanathan, Rajadurai
Gong Lau, Lee
Joseph, Uchang
Sharifah Noor Akmal, Syed Husain
A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone
description Central nervous system (CNS) involvement in multiple myeloma (MM) (MM-CNS) in the form of leptomeningeal myelomatosis or brain parenchyma plasmacytoma is rare, causing challenges in clinical diagnosis and treatment. We would like to report a case of leptomeningeal myelomatosis and illustrated the challeges. A 61-year-old man was diagnosed with MM with left paravertebral plasmacytoma, R-ISS II with high suspicion of double-hit MM, either biallelic aberrancy of TP53 or del(17p) and IGH aberrancy depending on the denition chosen, treated with lenalidomide-bortezomib-dexamethasone and local radiotherapy, later developed systemic relapse and progression to MM-CNS in the form of leptomeningeal myelomatosis. A modied CNS-based treatment not reported before, consisting of daratumumab, pomalidomide, vincristine, procarbazine, and dexamethasone, brought a rapid clinical improvement and warrants a further study. Incorporation of intrathecal thiotepa into the regimen would likely increase the e�cacy.
format Article
author Jew Win, Kuan
Ling Chai, Sing
Pathmanathan, Rajadurai
Gong Lau, Lee
Joseph, Uchang
Sharifah Noor Akmal, Syed Husain
author_facet Jew Win, Kuan
Ling Chai, Sing
Pathmanathan, Rajadurai
Gong Lau, Lee
Joseph, Uchang
Sharifah Noor Akmal, Syed Husain
author_sort Jew Win, Kuan
title A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone
title_short A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone
title_full A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone
title_fullStr A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone
title_full_unstemmed A Case Report of Leptomeningeal Myelomatosis and Rapid Improvement with Regimen Consisting of Daratumumab, Pomalidomide, Vincristine, Procarbazine, and Dexamethasone
title_sort case report of leptomeningeal myelomatosis and rapid improvement with regimen consisting of daratumumab, pomalidomide, vincristine, procarbazine, and dexamethasone
publisher Hindawi Publishing
publishDate 2022
url http://ir.unimas.my/id/eprint/39539/1/A%20Case%20Report%20-%20Copy.pdf
http://ir.unimas.my/id/eprint/39539/
https://www.hindawi.com/journals/crihem/2022/4081971/
https://doi.org/10.1155/2022/4081971
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