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A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum
INTRODUCTION: Human granulocytic anaplasmosis (HGA) is a potentially fatal tick-borne disease caused by the obligate intracellular bacterium Anaplasma phagocytophilum. It is most commonly found in the Northeastern and Midwestern parts of the United States especially during spring and summer months....
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/PMC8851287/ https://www.ncbi.nlm.nih.gov/pubmed/35198193 http://dx.doi.org/10.1016/j.amsu.2022.103366 |
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author | Song, David Almas, Talal Abdelghffar, Mohamed Jain, Samkit Geetha, Harinivaas Shanmugavel Shah, Vaibhav Nagarajan, Vikneswaran Raj Alshareef, Norah Gunasaegaram, Varman Ravintharan, Keesha Tan, Sze Teng John, Arun |
author_facet | Song, David Almas, Talal Abdelghffar, Mohamed Jain, Samkit Geetha, Harinivaas Shanmugavel Shah, Vaibhav Nagarajan, Vikneswaran Raj Alshareef, Norah Gunasaegaram, Varman Ravintharan, Keesha Tan, Sze Teng John, Arun |
author_sort | Song, David |
collection | PubMed |
description | INTRODUCTION: Human granulocytic anaplasmosis (HGA) is a potentially fatal tick-borne disease caused by the obligate intracellular bacterium Anaplasma phagocytophilum. It is most commonly found in the Northeastern and Midwestern parts of the United States especially during spring and summer months. The clinical picture of anaplasmosis is varied ranging from common symptoms such as fever, headache and myalgia to rarer presentations such as pancytopenia. CASE PRESENTATION: We present a case of a 62 year old male who presented with watery diarrhea, fever, and pancytopenia. Although there is a broad differential for pancytopenia, a thorough history provides clues regarding the diagnosis. In our patient, a recent history of camping in Upstate New York was suggestive of an infectious etiology from a tick borne illness. CLINICAL DISCUSSION: A tick-borne panel guided us to identify the diagnosis of HGA. Although the exact underlying pathogenesis of tick-borne illnesses leading to pancytopenia is still unknown, the pancytopenia is postulated to be due to a multi-nodal mechanism involving immune and non immune platelet destruction, global bone marrow suppression, hemophagocytic lymphohistiocytosis and myelosuppressive chemokines release. CONCLUSION: We hope that this case report elucidates the importance of obtaining a meticulous history in guiding clinicians towards prompt diagnosis, even in instances where there may be an evolving clinical picture. |
format | Online Article Text |
id | pubmed-8851287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-88512872022-02-22 A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum Song, David Almas, Talal Abdelghffar, Mohamed Jain, Samkit Geetha, Harinivaas Shanmugavel Shah, Vaibhav Nagarajan, Vikneswaran Raj Alshareef, Norah Gunasaegaram, Varman Ravintharan, Keesha Tan, Sze Teng John, Arun Ann Med Surg (Lond) Case Report INTRODUCTION: Human granulocytic anaplasmosis (HGA) is a potentially fatal tick-borne disease caused by the obligate intracellular bacterium Anaplasma phagocytophilum. It is most commonly found in the Northeastern and Midwestern parts of the United States especially during spring and summer months. The clinical picture of anaplasmosis is varied ranging from common symptoms such as fever, headache and myalgia to rarer presentations such as pancytopenia. CASE PRESENTATION: We present a case of a 62 year old male who presented with watery diarrhea, fever, and pancytopenia. Although there is a broad differential for pancytopenia, a thorough history provides clues regarding the diagnosis. In our patient, a recent history of camping in Upstate New York was suggestive of an infectious etiology from a tick borne illness. CLINICAL DISCUSSION: A tick-borne panel guided us to identify the diagnosis of HGA. Although the exact underlying pathogenesis of tick-borne illnesses leading to pancytopenia is still unknown, the pancytopenia is postulated to be due to a multi-nodal mechanism involving immune and non immune platelet destruction, global bone marrow suppression, hemophagocytic lymphohistiocytosis and myelosuppressive chemokines release. CONCLUSION: We hope that this case report elucidates the importance of obtaining a meticulous history in guiding clinicians towards prompt diagnosis, even in instances where there may be an evolving clinical picture. Elsevier 2022-02-11 /pmc/articles/PMC8851287/ /pubmed/35198193 http://dx.doi.org/10.1016/j.amsu.2022.103366 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 Report Song, David Almas, Talal Abdelghffar, Mohamed Jain, Samkit Geetha, Harinivaas Shanmugavel Shah, Vaibhav Nagarajan, Vikneswaran Raj Alshareef, Norah Gunasaegaram, Varman Ravintharan, Keesha Tan, Sze Teng John, Arun A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum |
title | A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum |
title_full | A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum |
title_fullStr | A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum |
title_full_unstemmed | A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum |
title_short | A rare case of delayed anaplasma phagocytophilum-induced pancytopenia: A diagnostic conundrum |
title_sort | rare case of delayed anaplasma phagocytophilum-induced pancytopenia: a diagnostic conundrum |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851287/ https://www.ncbi.nlm.nih.gov/pubmed/35198193 http://dx.doi.org/10.1016/j.amsu.2022.103366 |
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