Immune reconstitution inflammatory syndrome after hematopoietic stem cell transplantation in a FOXN1-deficient patient
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Erişim
info:eu-repo/semantics/embargoedAccessTarih
2023Yazar
Çorbalı, OsmanGemici Karaaslan, Hatice Betül
Aydemir, Sezin
Önal, Pınar
Kendir Demirkol, Yasemin
Nepesov, Serdar
Kıykım, Ayça
Çokuğraş, Haluk
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Çorbalı, O., Gemici Karaaslan, H. B., Aydemir, S., Önal, P., Kendir Demirkol, Y., Nepesov, S. ... Çokuğraş, H. (2023). Immune reconstitution inflammatory syndrome after hematopoietic stem cell transplantation in a FOXN1-deficient patient. Journal of Pediatric Hematology/Oncology, 45(5), 275-277. https://dx.doi.org/10.1097/MPH.0000000000002677Özet
The FOXN1 gene mutation is a unique disorder that causes the nude severe combined immunodeficiency phenotype. In patients with severe combined immunodeficiency, hematopoietic stem cell transplantation (HSCT) is life-saving if performed earlier. Thymic transplantation is the curative treatment for FOXN1 deficiency because the main pathology is thymic stromal changes. In this report, we describe the clinical features of a Turkish patient with a homozygous FOXN1 mutation treated with HSCT from his human leukocyte antigen-matched sibling. On follow-up, he showed Bacille Calmette Guerin adenitis and was evaluated as having immune reconstitution inflammatory syndrome. By presenting our patient, we aimed to draw attention to the development of HSCT and subsequent immune reconstitution inflammatory syndrome as a treatment option in patients with FOXN1 deficiency.
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Journal of Pediatric Hematology/OncologyCilt
45Sayı
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