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Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges

BACKGROUND: Primary central nervous system lymphoma (PCNSL) is an uncommon lesion and represent 4% of all central nervous system (CNS) cancers. There have been few reports of localized isolated lymphoma developing in the fourth ventricle, with only 8 previous cases described. We present a case of an...

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Autores principales: Holanda, Tiago S. F., Pimentel, Isnara Mara Freitas, Gosch, Gabriela Oliveira, Tavora, Daniel Gurgel Fernandes, Bandeira, Luiz Anderson Bevilaqua, Filho, Flavio Leitao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610116/
https://www.ncbi.nlm.nih.gov/pubmed/36324945
http://dx.doi.org/10.25259/SNI_584_2022
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author Holanda, Tiago S. F.
Pimentel, Isnara Mara Freitas
Gosch, Gabriela Oliveira
Tavora, Daniel Gurgel Fernandes
Bandeira, Luiz Anderson Bevilaqua
Filho, Flavio Leitao
author_facet Holanda, Tiago S. F.
Pimentel, Isnara Mara Freitas
Gosch, Gabriela Oliveira
Tavora, Daniel Gurgel Fernandes
Bandeira, Luiz Anderson Bevilaqua
Filho, Flavio Leitao
author_sort Holanda, Tiago S. F.
collection PubMed
description BACKGROUND: Primary central nervous system lymphoma (PCNSL) is an uncommon lesion and represent 4% of all central nervous system (CNS) cancers. There have been few reports of localized isolated lymphoma developing in the fourth ventricle, with only 8 previous cases described. We present a case of an immunocompetent patient with isolated fourth ventricle lymphoma who did not have diffusion-weighted imaging (DWI) restriction. CASE DESCRIPTION: A 45-year-old man presented a history of headache, vomiting and weigh loss. Upon clinical examination, he presented bilateral papilledema, multidirectional nystagmus, and gait imbalance. Magnetic resonance imaging showed a solid tumor in fourth ventricle with 1.8 × 1.6 × 1.1 cm. The patient was submitted to a suboccipital telovelar approach. The pathological study showed a neoplasm composed of loose round cells. Immunohistochemistry showed positivity for CD-45 and CD-23. The diagnosis of primary CNS lymphoma of the fourth ventricle was certified. Patient was sent to complementary treatment with hematologist and radiotherapy and chemotherapy were started. CONCLUSION: PCNSL is a rare and aggressive pathology with high rates of mortality and recurrence. It requires a multidisciplinary team and multiple therapies to control the disease and deliver better quality of life and prognosis to the patient.
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spelling pubmed-96101162022-11-01 Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges Holanda, Tiago S. F. Pimentel, Isnara Mara Freitas Gosch, Gabriela Oliveira Tavora, Daniel Gurgel Fernandes Bandeira, Luiz Anderson Bevilaqua Filho, Flavio Leitao Surg Neurol Int Case Report BACKGROUND: Primary central nervous system lymphoma (PCNSL) is an uncommon lesion and represent 4% of all central nervous system (CNS) cancers. There have been few reports of localized isolated lymphoma developing in the fourth ventricle, with only 8 previous cases described. We present a case of an immunocompetent patient with isolated fourth ventricle lymphoma who did not have diffusion-weighted imaging (DWI) restriction. CASE DESCRIPTION: A 45-year-old man presented a history of headache, vomiting and weigh loss. Upon clinical examination, he presented bilateral papilledema, multidirectional nystagmus, and gait imbalance. Magnetic resonance imaging showed a solid tumor in fourth ventricle with 1.8 × 1.6 × 1.1 cm. The patient was submitted to a suboccipital telovelar approach. The pathological study showed a neoplasm composed of loose round cells. Immunohistochemistry showed positivity for CD-45 and CD-23. The diagnosis of primary CNS lymphoma of the fourth ventricle was certified. Patient was sent to complementary treatment with hematologist and radiotherapy and chemotherapy were started. CONCLUSION: PCNSL is a rare and aggressive pathology with high rates of mortality and recurrence. It requires a multidisciplinary team and multiple therapies to control the disease and deliver better quality of life and prognosis to the patient. Scientific Scholar 2022-10-14 /pmc/articles/PMC9610116/ /pubmed/36324945 http://dx.doi.org/10.25259/SNI_584_2022 Text en Copyright: © 2022 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Holanda, Tiago S. F.
Pimentel, Isnara Mara Freitas
Gosch, Gabriela Oliveira
Tavora, Daniel Gurgel Fernandes
Bandeira, Luiz Anderson Bevilaqua
Filho, Flavio Leitao
Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges
title Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges
title_full Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges
title_fullStr Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges
title_full_unstemmed Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges
title_short Immunocompetent patient with isolated primary fourth ventricle lymphoma. Unusual diagnosis, their pitfalls, and challenges
title_sort immunocompetent patient with isolated primary fourth ventricle lymphoma. unusual diagnosis, their pitfalls, and challenges
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9610116/
https://www.ncbi.nlm.nih.gov/pubmed/36324945
http://dx.doi.org/10.25259/SNI_584_2022
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