Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge

We report a case based on simultaneous occurrence of Waldenström macroglobulinemia, myeloma and amyloidosis as a collision neoplasm. The strangeness and severity of the case presented a diagnostic and therapeutic challenge, which required individualised treatment and close follow‐up to achieved stri...

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Autores principales: Ceballos, Candela, Alburquerque, Cristina, Zabalza, Amaya, Quispe, Iván, Panizo, Ángel, Burguete, Yolanda, Redondo, Ana Margarita, Mateos, María Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019880/
https://www.ncbi.nlm.nih.gov/pubmed/35474975
http://dx.doi.org/10.1002/ccr3.5769
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author Ceballos, Candela
Alburquerque, Cristina
Zabalza, Amaya
Quispe, Iván
Panizo, Ángel
Burguete, Yolanda
Redondo, Ana Margarita
Mateos, María Carmen
author_facet Ceballos, Candela
Alburquerque, Cristina
Zabalza, Amaya
Quispe, Iván
Panizo, Ángel
Burguete, Yolanda
Redondo, Ana Margarita
Mateos, María Carmen
author_sort Ceballos, Candela
collection PubMed
description We report a case based on simultaneous occurrence of Waldenström macroglobulinemia, myeloma and amyloidosis as a collision neoplasm. The strangeness and severity of the case presented a diagnostic and therapeutic challenge, which required individualised treatment and close follow‐up to achieved stringent complete response.
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spelling pubmed-90198802022-04-25 Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge Ceballos, Candela Alburquerque, Cristina Zabalza, Amaya Quispe, Iván Panizo, Ángel Burguete, Yolanda Redondo, Ana Margarita Mateos, María Carmen Clin Case Rep Case Reports We report a case based on simultaneous occurrence of Waldenström macroglobulinemia, myeloma and amyloidosis as a collision neoplasm. The strangeness and severity of the case presented a diagnostic and therapeutic challenge, which required individualised treatment and close follow‐up to achieved stringent complete response. John Wiley and Sons Inc. 2022-04-20 /pmc/articles/PMC9019880/ /pubmed/35474975 http://dx.doi.org/10.1002/ccr3.5769 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Ceballos, Candela
Alburquerque, Cristina
Zabalza, Amaya
Quispe, Iván
Panizo, Ángel
Burguete, Yolanda
Redondo, Ana Margarita
Mateos, María Carmen
Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge
title Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge
title_full Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge
title_fullStr Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge
title_full_unstemmed Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge
title_short Concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: A diagnostic and therapeutic challenge
title_sort concomitant lymphoplasmacytic lymphoma, multiple myeloma, and amyloidosis: a diagnostic and therapeutic challenge
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019880/
https://www.ncbi.nlm.nih.gov/pubmed/35474975
http://dx.doi.org/10.1002/ccr3.5769
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