Background: Primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD) is a serious and uncommon complication which can be developed months or years after a Kidney transplant. Immunosuppressive agents administered before and after transplantation to minimize the chances of allograft rejection has proved to be a double-edged sword that puts the host at risk of infectious, neoplastic and vascular diseases, including PCNS-PTLD. The immunosuppressive therapy leads to decreased innate malignant and viral immune surveillance and this has been shown to play a role in lymphoproliferative diseases after transplantation. In most cases, PCNS-PTLD is Epstein–Barr virus related. Case Description: A 60-year-old female with history of kidney transplant presented to the emergency room with history of low fever, dizziness nausea and vomiting for 1 month. MRI and CT scans showed a mass cerebellar lesion and a biopsy revealed Primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD). Conclusion: This case highlights the need for a careful long-term follow up of patients with kidney transplant. PCNS-PTLD represents a continuing long-term risk after transplantation, although less common. This case report supports observational data that suggests that peripheral blood screening for EBV DNA does not seem helpful for identification of PCNS-PTLD. Suspicion of PCNS PTLD should be considered when patients with long-term history of kidney transplant present neurological complaints.
Published in | Journal of Surgery (Volume 9, Issue 4) |
DOI | 10.11648/j.js.20210904.19 |
Page(s) | 193-198 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2021. Published by Science Publishing Group |
Central Nervous System, Primary B Cell Lymphoma, Transplantation, Kidney
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APA Style
Isabella Opoku, Lin Qin Tang, Lidan Jiang, Dan Dan Wang, Xu Yueqiao, et al. (2021). Late Primary B Cell Cerebral Lymphoma After Kidney Transplant: A Case Report and Literature Review. Journal of Surgery, 9(4), 193-198. https://doi.org/10.11648/j.js.20210904.19
ACS Style
Isabella Opoku; Lin Qin Tang; Lidan Jiang; Dan Dan Wang; Xu Yueqiao, et al. Late Primary B Cell Cerebral Lymphoma After Kidney Transplant: A Case Report and Literature Review. J. Surg. 2021, 9(4), 193-198. doi: 10.11648/j.js.20210904.19
@article{10.11648/j.js.20210904.19, author = {Isabella Opoku and Lin Qin Tang and Lidan Jiang and Dan Dan Wang and Xu Yueqiao and Ling Feng and Wang Ning}, title = {Late Primary B Cell Cerebral Lymphoma After Kidney Transplant: A Case Report and Literature Review}, journal = {Journal of Surgery}, volume = {9}, number = {4}, pages = {193-198}, doi = {10.11648/j.js.20210904.19}, url = {https://doi.org/10.11648/j.js.20210904.19}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.js.20210904.19}, abstract = {Background: Primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD) is a serious and uncommon complication which can be developed months or years after a Kidney transplant. Immunosuppressive agents administered before and after transplantation to minimize the chances of allograft rejection has proved to be a double-edged sword that puts the host at risk of infectious, neoplastic and vascular diseases, including PCNS-PTLD. The immunosuppressive therapy leads to decreased innate malignant and viral immune surveillance and this has been shown to play a role in lymphoproliferative diseases after transplantation. In most cases, PCNS-PTLD is Epstein–Barr virus related. Case Description: A 60-year-old female with history of kidney transplant presented to the emergency room with history of low fever, dizziness nausea and vomiting for 1 month. MRI and CT scans showed a mass cerebellar lesion and a biopsy revealed Primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD). Conclusion: This case highlights the need for a careful long-term follow up of patients with kidney transplant. PCNS-PTLD represents a continuing long-term risk after transplantation, although less common. This case report supports observational data that suggests that peripheral blood screening for EBV DNA does not seem helpful for identification of PCNS-PTLD. Suspicion of PCNS PTLD should be considered when patients with long-term history of kidney transplant present neurological complaints.}, year = {2021} }
TY - JOUR T1 - Late Primary B Cell Cerebral Lymphoma After Kidney Transplant: A Case Report and Literature Review AU - Isabella Opoku AU - Lin Qin Tang AU - Lidan Jiang AU - Dan Dan Wang AU - Xu Yueqiao AU - Ling Feng AU - Wang Ning Y1 - 2021/08/02 PY - 2021 N1 - https://doi.org/10.11648/j.js.20210904.19 DO - 10.11648/j.js.20210904.19 T2 - Journal of Surgery JF - Journal of Surgery JO - Journal of Surgery SP - 193 EP - 198 PB - Science Publishing Group SN - 2330-0930 UR - https://doi.org/10.11648/j.js.20210904.19 AB - Background: Primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD) is a serious and uncommon complication which can be developed months or years after a Kidney transplant. Immunosuppressive agents administered before and after transplantation to minimize the chances of allograft rejection has proved to be a double-edged sword that puts the host at risk of infectious, neoplastic and vascular diseases, including PCNS-PTLD. The immunosuppressive therapy leads to decreased innate malignant and viral immune surveillance and this has been shown to play a role in lymphoproliferative diseases after transplantation. In most cases, PCNS-PTLD is Epstein–Barr virus related. Case Description: A 60-year-old female with history of kidney transplant presented to the emergency room with history of low fever, dizziness nausea and vomiting for 1 month. MRI and CT scans showed a mass cerebellar lesion and a biopsy revealed Primary central nervous system post-transplant lymphoproliferative disorder (PCNS-PTLD). Conclusion: This case highlights the need for a careful long-term follow up of patients with kidney transplant. PCNS-PTLD represents a continuing long-term risk after transplantation, although less common. This case report supports observational data that suggests that peripheral blood screening for EBV DNA does not seem helpful for identification of PCNS-PTLD. Suspicion of PCNS PTLD should be considered when patients with long-term history of kidney transplant present neurological complaints. VL - 9 IS - 4 ER -