Cargando…
Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel human pathogen known for its predilection on the respiratory system. Herein, we present a unique case in which a patient developed hyperhemolysis in the setting of mixed autoimmune hemolytic anemia (AIHA) secondary to SARS-CoV-2...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751182/ https://www.ncbi.nlm.nih.gov/pubmed/35028233 http://dx.doi.org/10.7759/cureus.20356 |
_version_ | 1784631630661419008 |
---|---|
author | Narula, Sonya Winkle, Sean Brand, Kenneth Shah, Farhan Fujikawa, Priscilla Truitt, Tyler Currie, Mark |
author_facet | Narula, Sonya Winkle, Sean Brand, Kenneth Shah, Farhan Fujikawa, Priscilla Truitt, Tyler Currie, Mark |
author_sort | Narula, Sonya |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel human pathogen known for its predilection on the respiratory system. Herein, we present a unique case in which a patient developed hyperhemolysis in the setting of mixed autoimmune hemolytic anemia (AIHA) secondary to SARS-CoV-2. A 33-years-old male with a past medical history of resolved immune thrombocytopenic purpura (ITP) presented to the hospital with symptoms of jaundice after being infected with SARS-CoV-2. On admission, his Hgb was 12.5 g/dL. Lab results showed indirect bilirubin of 13 mg/dL, LDH at 759 U/L, haptoglobin <10, and the percent reticulocyte count was 2.33%. A direct antiglobulin test (DAT) was also positive for C3, IgG, anti-E, in addition to both warm and cold autoantibodies. PCR was positive for COVID-19. Within two days of admission, his Hgb dropped to 5.9 g/dL. A total of seven units of packed red blood cell (pRBC) was required to achieve a Hgb of 6 g/dL in 48 hours. Patients with preexisting hematological abnormalities have a propensity to develop AIHA in the setting of the virus. The majority of the cases described in the literature were associated with warm AIHA. Our patient tested positive for both warm and cold antibodies, which may partially explain the mechanism behind hyperhemolysis in our patient. |
format | Online Article Text |
id | pubmed-8751182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-87511822022-01-12 Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 Narula, Sonya Winkle, Sean Brand, Kenneth Shah, Farhan Fujikawa, Priscilla Truitt, Tyler Currie, Mark Cureus Allergy/Immunology Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel human pathogen known for its predilection on the respiratory system. Herein, we present a unique case in which a patient developed hyperhemolysis in the setting of mixed autoimmune hemolytic anemia (AIHA) secondary to SARS-CoV-2. A 33-years-old male with a past medical history of resolved immune thrombocytopenic purpura (ITP) presented to the hospital with symptoms of jaundice after being infected with SARS-CoV-2. On admission, his Hgb was 12.5 g/dL. Lab results showed indirect bilirubin of 13 mg/dL, LDH at 759 U/L, haptoglobin <10, and the percent reticulocyte count was 2.33%. A direct antiglobulin test (DAT) was also positive for C3, IgG, anti-E, in addition to both warm and cold autoantibodies. PCR was positive for COVID-19. Within two days of admission, his Hgb dropped to 5.9 g/dL. A total of seven units of packed red blood cell (pRBC) was required to achieve a Hgb of 6 g/dL in 48 hours. Patients with preexisting hematological abnormalities have a propensity to develop AIHA in the setting of the virus. The majority of the cases described in the literature were associated with warm AIHA. Our patient tested positive for both warm and cold antibodies, which may partially explain the mechanism behind hyperhemolysis in our patient. Cureus 2021-12-12 /pmc/articles/PMC8751182/ /pubmed/35028233 http://dx.doi.org/10.7759/cureus.20356 Text en Copyright © 2021, Narula et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Allergy/Immunology Narula, Sonya Winkle, Sean Brand, Kenneth Shah, Farhan Fujikawa, Priscilla Truitt, Tyler Currie, Mark Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 |
title | Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 |
title_full | Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 |
title_fullStr | Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 |
title_full_unstemmed | Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 |
title_short | Hyperhemolysis in the Setting of Mixed-Autoimmune Hemolytic Anemia: A Rare Complication of COVID-19 |
title_sort | hyperhemolysis in the setting of mixed-autoimmune hemolytic anemia: a rare complication of covid-19 |
topic | Allergy/Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8751182/ https://www.ncbi.nlm.nih.gov/pubmed/35028233 http://dx.doi.org/10.7759/cureus.20356 |
work_keys_str_mv | AT narulasonya hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 AT winklesean hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 AT brandkenneth hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 AT shahfarhan hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 AT fujikawapriscilla hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 AT truitttyler hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 AT curriemark hyperhemolysisinthesettingofmixedautoimmunehemolyticanemiaararecomplicationofcovid19 |