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Granulomatous amebic encephalitis following hematopoietic stem cell transplantation
BACKGROUND: Granulomatous amebic encephalitis (GAE) is rare, but often fatal. The infection has been documented predominantly among the immunocompromised population or among those with chronic disease. To date, however, there have only been eight cases regarding the infection following hematopoietic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604647/ https://www.ncbi.nlm.nih.gov/pubmed/26539322 http://dx.doi.org/10.4103/2152-7806.166788 |
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author | Doan, Ninh Rozansky, Gregory Nguyen, Ha Son Gelsomino, Michael Shabani, Saman Mueller, Wade Johnson, Vijay |
author_facet | Doan, Ninh Rozansky, Gregory Nguyen, Ha Son Gelsomino, Michael Shabani, Saman Mueller, Wade Johnson, Vijay |
author_sort | Doan, Ninh |
collection | PubMed |
description | BACKGROUND: Granulomatous amebic encephalitis (GAE) is rare, but often fatal. The infection has been documented predominantly among the immunocompromised population or among those with chronic disease. To date, however, there have only been eight cases regarding the infection following hematopoietic stem cell transplantation (HSCT). CASE DESCRIPTION: A 62-year-old female with a history of relapsed diffuse large B-cell lymphoma, recently underwent peripheral blood autologous stem cell transplant after BEAM conditioning (day 0). On day +15, she began to exhibit worsening fatigue, generalized weakness, and fever. Symptoms progressed to nausea, emesis, somnolence, confusion, and frontal headaches over the next few days. Imaging demonstrated multifocal ill-defined vasogenic edema with patchy enhancement. The patient was started on broad antibiotics, antifungals, and seizure prophylaxis. Evaluation for bacterial, fungal, mycobacterial, and viral etiologies was fruitless. Her mental status progressively deteriorated. On day +22, she exhibited severe lethargy and went into pulseless electrical activity arrest, requiring chest compressions. The episode lasted <2 min and her pulse was restored. She was taken to the operating room for a brain biopsy. Postoperatively, her right pupil began to dilate compared to the left; she demonstrated extensor posturing in her upper extremities and withdrawal in her lower extremities. Repeat computed tomography demonstrated progressive edema. Given poor prognosis and poor neurological examination, the family opted for withdrawal of care. Final pathology was consistent with Acanthamoeba GAE. CONCLUSION: The authors report the third case of GAE after autologous stem cell transplant, and the ninth case overall after HSCT. This case is unusual due to its rapid clinical presentation after HSCT compared to prior literature. The case highlights the need for high suspicion of Acanthamoeba infection in this patient population. |
format | Online Article Text |
id | pubmed-4604647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46046472015-11-04 Granulomatous amebic encephalitis following hematopoietic stem cell transplantation Doan, Ninh Rozansky, Gregory Nguyen, Ha Son Gelsomino, Michael Shabani, Saman Mueller, Wade Johnson, Vijay Surg Neurol Int Surgical Neurology International: Unique Case Observations BACKGROUND: Granulomatous amebic encephalitis (GAE) is rare, but often fatal. The infection has been documented predominantly among the immunocompromised population or among those with chronic disease. To date, however, there have only been eight cases regarding the infection following hematopoietic stem cell transplantation (HSCT). CASE DESCRIPTION: A 62-year-old female with a history of relapsed diffuse large B-cell lymphoma, recently underwent peripheral blood autologous stem cell transplant after BEAM conditioning (day 0). On day +15, she began to exhibit worsening fatigue, generalized weakness, and fever. Symptoms progressed to nausea, emesis, somnolence, confusion, and frontal headaches over the next few days. Imaging demonstrated multifocal ill-defined vasogenic edema with patchy enhancement. The patient was started on broad antibiotics, antifungals, and seizure prophylaxis. Evaluation for bacterial, fungal, mycobacterial, and viral etiologies was fruitless. Her mental status progressively deteriorated. On day +22, she exhibited severe lethargy and went into pulseless electrical activity arrest, requiring chest compressions. The episode lasted <2 min and her pulse was restored. She was taken to the operating room for a brain biopsy. Postoperatively, her right pupil began to dilate compared to the left; she demonstrated extensor posturing in her upper extremities and withdrawal in her lower extremities. Repeat computed tomography demonstrated progressive edema. Given poor prognosis and poor neurological examination, the family opted for withdrawal of care. Final pathology was consistent with Acanthamoeba GAE. CONCLUSION: The authors report the third case of GAE after autologous stem cell transplant, and the ninth case overall after HSCT. This case is unusual due to its rapid clinical presentation after HSCT compared to prior literature. The case highlights the need for high suspicion of Acanthamoeba infection in this patient population. Medknow Publications & Media Pvt Ltd 2015-10-07 /pmc/articles/PMC4604647/ /pubmed/26539322 http://dx.doi.org/10.4103/2152-7806.166788 Text en Copyright: © 2015 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, 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 | Surgical Neurology International: Unique Case Observations Doan, Ninh Rozansky, Gregory Nguyen, Ha Son Gelsomino, Michael Shabani, Saman Mueller, Wade Johnson, Vijay Granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
title | Granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
title_full | Granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
title_fullStr | Granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
title_full_unstemmed | Granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
title_short | Granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
title_sort | granulomatous amebic encephalitis following hematopoietic stem cell transplantation |
topic | Surgical Neurology International: Unique Case Observations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604647/ https://www.ncbi.nlm.nih.gov/pubmed/26539322 http://dx.doi.org/10.4103/2152-7806.166788 |
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