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עמוד בית
Wed, 05.08.26

REVIEWS

IMAJ | volume 28

Journal 8, August 2026
pages: 535-542

Inborn Neutrophil Disorders: A Unique Case of Chronic Granulomatous Disease and a Review of the Literature

1 Department of Pediatrics A and Immunology Service, Safra Children's Hospital, Jeffrey Modell Foundation Center, Sheba Medical Center, Tel Hashomer, Israel 2 Pediatric Immunology Services, Safra Children's Hospital, Jeffrey Modell Foundation Center, Sheba Medical Center, Tel Hashomer, Israel 3 Clinical Immunology, Angioedema and Allergy Unit Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel 4 Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel 5 Recanati School of Medicine, Reichman University, Herzliya, Israel 6 Israel Association of Allergy and Clinical Immunology, Israel Medical Association, Ramat Gan, Israel

Summary

Neutrophils serve as a cornerstone of innate immunity. Beyond their classical antimicrobial repertoire, these cells are versatile and capable of shaping the adaptive immune response through direct interactions with dendritic cells and lymphocytes in addition to cytokine-mediated effects. Additional functional phenotypes have also been described with regard to cancer and chronic inflammation. The clinical importance of neutrophils in host defense is perhaps best illustrated by the spectrum of inborn neutrophil disorders, ranging from congenital neutropenia to defects of adhesion and phagocytosis. We present a patient with clinical and laboratory features of hemophagocytic lymphohistiocytosis with a bacterial infection. The patient was subsequently found to carry a homozygous variant in the NCF2 gene, establishing a diagnosis of autosomal recessive chronic granulomatous disease (CGD). This presentation, combining cytokine storm with ongoing infection-driven inflammation, exemplifies the multifaceted role of neutrophils in health and disease. In this review, we provide clinical and immunological insights into neutrophil disorders, illustrated through a case of CGD as a paradigm of primary neutrophil dysfunction.

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