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A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy

Acquired factor VII deficiency secondary to circulating inhibitors is rare in children but is a potentially life-threatening condition. Such a disease is challenging to diagnose and often difficult to manage. Here, we report on a newborn that presented with a catastrophic intracranial hemorrhage who...

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Autores principales: Alqarni, Nof Saadi, Algiraigri, Ali H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319681/
https://www.ncbi.nlm.nih.gov/pubmed/34350335
http://dx.doi.org/10.1016/j.ijpam.2020.12.002
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author Alqarni, Nof Saadi
Algiraigri, Ali H.
author_facet Alqarni, Nof Saadi
Algiraigri, Ali H.
author_sort Alqarni, Nof Saadi
collection PubMed
description Acquired factor VII deficiency secondary to circulating inhibitors is rare in children but is a potentially life-threatening condition. Such a disease is challenging to diagnose and often difficult to manage. Here, we report on a newborn that presented with a catastrophic intracranial hemorrhage who failed to respond to conventional supportive measures including multiple doses of fresh frozen plasma and factor VII replacement; however, he had a complete correction of prothrombin time 8 h after immunomodulatory therapies in the form of steroid and intravenous immunoglobulin. Such measures helped stabilize his bleeding and allowed urgent neurosurgical intervention.
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spelling pubmed-83196812021-08-03 A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy Alqarni, Nof Saadi Algiraigri, Ali H. Int J Pediatr Adolesc Med Case Report Acquired factor VII deficiency secondary to circulating inhibitors is rare in children but is a potentially life-threatening condition. Such a disease is challenging to diagnose and often difficult to manage. Here, we report on a newborn that presented with a catastrophic intracranial hemorrhage who failed to respond to conventional supportive measures including multiple doses of fresh frozen plasma and factor VII replacement; however, he had a complete correction of prothrombin time 8 h after immunomodulatory therapies in the form of steroid and intravenous immunoglobulin. Such measures helped stabilize his bleeding and allowed urgent neurosurgical intervention. King Faisal Specialist Hospital and Research Centre 2021-09 2020-12-09 /pmc/articles/PMC8319681/ /pubmed/34350335 http://dx.doi.org/10.1016/j.ijpam.2020.12.002 Text en © 2020 Publishing services provided by Elsevier B.V. on behalf of King Faisal Specialist Hospital & Research Centre (General Organization), Saudi Arabia. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Alqarni, Nof Saadi
Algiraigri, Ali H.
A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
title A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
title_full A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
title_fullStr A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
title_full_unstemmed A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
title_short A Neonate with Acquired Factor VII Deficiency Successfully Managed with Immunomodulatory Therapy
title_sort neonate with acquired factor vii deficiency successfully managed with immunomodulatory therapy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8319681/
https://www.ncbi.nlm.nih.gov/pubmed/34350335
http://dx.doi.org/10.1016/j.ijpam.2020.12.002
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