Delayed <scp>post‐COVID‐19</scp> hemophagocytic lymphohistiocytosis in patient with <scp>XIAP</scp> deficiency-Reference-Cited by-同舟云学术

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Delayed post‐COVID‐19 hemophagocytic lymphohistiocytosis in patient with XIAP deficiency

Published:2023-09 Issue:9 Volume:34 Page:
ISSN:0905-6157
Container-title:Pediatric Allergy and Immunology
language:en
Short-container-title:Pediatric Allergy Immunology

Author:

Chen Jonathan H.¹,Arceri Talia²,Datta Rahul²,Sullivan Kathleen E.²^ORCID

Affiliation:

1. Department of Internal Medicine, Lankenau Medical Center Main Line Health Wynnewood Pennsylvania USA

2. Division of Allergy and Immunology, Department of Pediatrics, Perelman School of Medicine, The Children's Hospital of Philadelphia University of Pennsylvania Philadelphia Pennsylvania USA

Publisher

Wiley

Subject

Immunology,Immunology and Allergy,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.14028

Reference11 articles.

1. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

2. XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease

3. Secondary hemophagocytic lymphohistiocytosis in a post‐COVID‐19 patient;Bandaru SS;Cureus,2022

4. Secondary hemophagocytic lymphohistiocytosis in post‐COVID‐19 patients: a report of two cases;Kalita P;Cureus,2021

5. Hemophagocytic lymphohistiocytosis, a new cause of death during ‘post-acute COVID-19 syndrome?’ A case report

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