Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant

Background: Post-transplant lymphoproliferative disorders (PTLD) are rare immunosuppression complications affecting 5% of transplant patients. Isolated central nervous system (CNS)-PTLD without nodal or extra-nodal organ involvement is rarely reported and is difficult to diagnose due to the non-spec...

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Main Authors: Austin Feindt, Montserrat Lara-Velazquez, Ahmad Alkhasawneh, Dinesh Rao, Raafat Makary, Keith Dombrowski, Daryoush Tavanaiepour, Gazanfar Rahmathulla
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/11/23/7058
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author Austin Feindt
Montserrat Lara-Velazquez
Ahmad Alkhasawneh
Dinesh Rao
Raafat Makary
Keith Dombrowski
Daryoush Tavanaiepour
Gazanfar Rahmathulla
author_facet Austin Feindt
Montserrat Lara-Velazquez
Ahmad Alkhasawneh
Dinesh Rao
Raafat Makary
Keith Dombrowski
Daryoush Tavanaiepour
Gazanfar Rahmathulla
author_sort Austin Feindt
collection DOAJ
description Background: Post-transplant lymphoproliferative disorders (PTLD) are rare immunosuppression complications affecting 5% of transplant patients. Isolated central nervous system (CNS)-PTLD without nodal or extra-nodal organ involvement is rarely reported and is difficult to diagnose due to the non-specific clinical manifestations and imaging features overlapping with other common CNS lesions. Case presentation: We present a case of a 72-year-old female subjected to a renal transplant 11 years ago with progressively worsening headaches and confusion. Imaging revealed vasogenic edema in the left frontal and bilateral temporal lobes. She was subjected to a craniotomy and excisional biopsy to obtain tissue for diagnostic and therapeutic interventions. Pathology examination showed atypical EBV-positive lymphoplasmacytic infiltrate, consistent with Polymorphic type PTLD. Conclusions: Patients diagnosed with PTLD need to have close monitoring of immunosuppressive medications while in the hospital. Early diagnosis is essential for patient survival with PTLD, as their health can deteriorate fast.
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spelling doaj.art-cda288ae27194c278fa61148a873c3c72023-11-24T11:22:13ZengMDPI AGJournal of Clinical Medicine2077-03832022-11-011123705810.3390/jcm11237058Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal TransplantAustin Feindt0Montserrat Lara-Velazquez1Ahmad Alkhasawneh2Dinesh Rao3Raafat Makary4Keith Dombrowski5Daryoush Tavanaiepour6Gazanfar Rahmathulla7School of Medicine, University of South Florida School of Medicine, 12901 Bruce B Downs Blvd., Tampa, FL 33612, USADepartment of Neurological Surgery, University of Florida College of Medicine, 653-1 8th St. W, Jacksonville, FL 32209, USADepartment of Pathology, University of Florida College of Medicine, 8th St. W, Jacksonville, FL 32209, USADepartment of Radiology, University of Florida College of Medicine, 8th St. W, Jacksonville, FL 32209, USADepartment of Pathology, University of Florida College of Medicine, 8th St. W, Jacksonville, FL 32209, USADepartment of Neurosurgery and Brain Repair, USF Health, 2 Tampa General Cir, Tampa, FL 33606, USADepartment of Neurological Surgery, University of Florida College of Medicine, 653-1 8th St. W, Jacksonville, FL 32209, USADepartment of Neurological Surgery, University of Florida College of Medicine, 653-1 8th St. W, Jacksonville, FL 32209, USABackground: Post-transplant lymphoproliferative disorders (PTLD) are rare immunosuppression complications affecting 5% of transplant patients. Isolated central nervous system (CNS)-PTLD without nodal or extra-nodal organ involvement is rarely reported and is difficult to diagnose due to the non-specific clinical manifestations and imaging features overlapping with other common CNS lesions. Case presentation: We present a case of a 72-year-old female subjected to a renal transplant 11 years ago with progressively worsening headaches and confusion. Imaging revealed vasogenic edema in the left frontal and bilateral temporal lobes. She was subjected to a craniotomy and excisional biopsy to obtain tissue for diagnostic and therapeutic interventions. Pathology examination showed atypical EBV-positive lymphoplasmacytic infiltrate, consistent with Polymorphic type PTLD. Conclusions: Patients diagnosed with PTLD need to have close monitoring of immunosuppressive medications while in the hospital. Early diagnosis is essential for patient survival with PTLD, as their health can deteriorate fast.https://www.mdpi.com/2077-0383/11/23/7058lymphoproliferative disorderorgan transplantationEpstein–Barr virus infections
spellingShingle Austin Feindt
Montserrat Lara-Velazquez
Ahmad Alkhasawneh
Dinesh Rao
Raafat Makary
Keith Dombrowski
Daryoush Tavanaiepour
Gazanfar Rahmathulla
Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant
Journal of Clinical Medicine
lymphoproliferative disorder
organ transplantation
Epstein–Barr virus infections
title Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant
title_full Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant
title_fullStr Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant
title_full_unstemmed Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant
title_short Post-Transplant Lymphoproliferative Disorder: A Rare Case of CNS Involvement following Renal Transplant
title_sort post transplant lymphoproliferative disorder a rare case of cns involvement following renal transplant
topic lymphoproliferative disorder
organ transplantation
Epstein–Barr virus infections
url https://www.mdpi.com/2077-0383/11/23/7058
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