Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid

Familial hemophagocytic lymphohistiocytosis (FHL) is a rare fatal autosomal recessive disorder of immune dysregulation. The disease presents most commonly in the first year of life; however, symptomatic presentation throughout childhood and adulthood has also been identified. Biallelic mutation in t...

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Detalles Bibliográficos
Autores principales: Mian, Agrima, Kumari, Kalpana, Kaushal, Seema, Fazal, Farhan, Kodan, Parul, Batra, Atul, Kumar, Prabhat, Baitha, Upendra, Jorwal, Pankaj, Soneja, Manish, Sharma, Mehar Chand, Biswas, Ashutosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: São Paulo, SP: Universidade de São Paulo, Hospital Universitário 2019
Materias:
Article- Autopsy Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6655852/
https://www.ncbi.nlm.nih.gov/pubmed/31440481
http://dx.doi.org/10.4322/acr.2019.101

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6655852/
https://www.ncbi.nlm.nih.gov/pubmed/31440481
http://dx.doi.org/10.4322/acr.2019.101

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