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Cerebellar primary central nervous system lymphoma: Case series report
INTRODUCTION AND IMPORTANCE: Primary central nervous system lymphoma (PCNSL) is a rare cranial malignant haematological tumour. PCNSL in the cerebellar region is less common than PCNSL in other encephalic regions. A diagnosis of cerebellar PCNSL is relatively difficult to make due to its diverse ima...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403198/ https://www.ncbi.nlm.nih.gov/pubmed/35901552 http://dx.doi.org/10.1016/j.ijscr.2022.107440 |
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author | He, Minglian Zhong, Jun Li, Xuegang Chen, Yujie Li, Fei |
author_facet | He, Minglian Zhong, Jun Li, Xuegang Chen, Yujie Li, Fei |
author_sort | He, Minglian |
collection | PubMed |
description | INTRODUCTION AND IMPORTANCE: Primary central nervous system lymphoma (PCNSL) is a rare cranial malignant haematological tumour. PCNSL in the cerebellar region is less common than PCNSL in other encephalic regions. A diagnosis of cerebellar PCNSL is relatively difficult to make due to its diverse imaging manifestations. The aim of this case series report is to determine whether surgery could be used to confirm the diagnosis of cerebellar PCNSL and the effect of surgical treatment. METHODS: We report 3 cases of cerebellar PCNSL that underwent neuronavigation microsurgery under general anaesthesia. The operation was performed by author 3 and author 5. One patient underwent left lateral ventricular drainage on the fourth and tenth days after the operation due to postoperative obstructive hydrocephalus. All patients received chemotherapy or radiotherapy after histological confirmation. OUTCOMES: All patients' tumours were completely removed. One patient developed obstructive hydrocephalus twice during the perioperative period after the operation, was given drainage, and then recovered from the hospital. The other two patients recovered and were discharged smoothly without complications. One patient died 9 months after the operation, and the other two patients survived. The prognosis of 3 patients was related to tumour size and timely follow-up chemo-radiation therapy. CONCLUSION: The histology of all patients showed diffuse large B-cell lymphoma (GCB phenotype). Suspicious cerebellar PCNSL patients should undergo surgery to confirm the diagnosis, followed by radiotherapy and chemotherapy. |
format | Online Article Text |
id | pubmed-9403198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-94031982022-08-26 Cerebellar primary central nervous system lymphoma: Case series report He, Minglian Zhong, Jun Li, Xuegang Chen, Yujie Li, Fei Int J Surg Case Rep Case Series INTRODUCTION AND IMPORTANCE: Primary central nervous system lymphoma (PCNSL) is a rare cranial malignant haematological tumour. PCNSL in the cerebellar region is less common than PCNSL in other encephalic regions. A diagnosis of cerebellar PCNSL is relatively difficult to make due to its diverse imaging manifestations. The aim of this case series report is to determine whether surgery could be used to confirm the diagnosis of cerebellar PCNSL and the effect of surgical treatment. METHODS: We report 3 cases of cerebellar PCNSL that underwent neuronavigation microsurgery under general anaesthesia. The operation was performed by author 3 and author 5. One patient underwent left lateral ventricular drainage on the fourth and tenth days after the operation due to postoperative obstructive hydrocephalus. All patients received chemotherapy or radiotherapy after histological confirmation. OUTCOMES: All patients' tumours were completely removed. One patient developed obstructive hydrocephalus twice during the perioperative period after the operation, was given drainage, and then recovered from the hospital. The other two patients recovered and were discharged smoothly without complications. One patient died 9 months after the operation, and the other two patients survived. The prognosis of 3 patients was related to tumour size and timely follow-up chemo-radiation therapy. CONCLUSION: The histology of all patients showed diffuse large B-cell lymphoma (GCB phenotype). Suspicious cerebellar PCNSL patients should undergo surgery to confirm the diagnosis, followed by radiotherapy and chemotherapy. Elsevier 2022-07-21 /pmc/articles/PMC9403198/ /pubmed/35901552 http://dx.doi.org/10.1016/j.ijscr.2022.107440 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Case Series He, Minglian Zhong, Jun Li, Xuegang Chen, Yujie Li, Fei Cerebellar primary central nervous system lymphoma: Case series report |
title | Cerebellar primary central nervous system lymphoma: Case series report |
title_full | Cerebellar primary central nervous system lymphoma: Case series report |
title_fullStr | Cerebellar primary central nervous system lymphoma: Case series report |
title_full_unstemmed | Cerebellar primary central nervous system lymphoma: Case series report |
title_short | Cerebellar primary central nervous system lymphoma: Case series report |
title_sort | cerebellar primary central nervous system lymphoma: case series report |
topic | Case Series |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403198/ https://www.ncbi.nlm.nih.gov/pubmed/35901552 http://dx.doi.org/10.1016/j.ijscr.2022.107440 |
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