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Author Spotlight: Balancing Speed, Cost, and Accuracy in Neutrophil Function Assessment with NeutroFun Screen Protocol
Published on: February 9, 2024
Neutrophilic dermatoses
J Delaleu1, C Lepelletier2, A Calugareanu3
1Service de dermatologie, hôpital Saint-Louis, AP-HP, Paris, France; Inserm u976 "Human Immunology, Pathophysiology and Immunotherapy", université Paris Cité, Paris, France; Inserm u933, "Childhood genetic disorders", service de génétique, Sorbonne université, hôpital Armand-Trousseau, AP-HP, Paris, France.
Neutrophilic dermatoses (ND) involve skin inflammation with neutrophil buildup, excluding infection. They stem from immune system overactivation or myeloid cell issues, often linked to underlying conditions.
Area of Science:
- Dermatology
- Immunology
- Internal Medicine
Background:
- Neutrophilic dermatoses (ND) are inflammatory skin conditions defined by neutrophil infiltration without infection.
- Classification is based on neutrophil location and clinical presentation.
- ND pathogenesis involves innate immune system activation or myeloid cell clonal expansion.
Approach:
- Review of pathophysiology and classification of major ND types.
- Detailed examination of clinical and histopathological features.
- Highlighting diagnostic investigations for associated diseases and differential diagnoses.
Key Points:
- ND classification relies on neutrophil localization and clinical signs.
- Pathways include hereditary immune activation and somatic myeloid cell activation (e.g., VEXAS syndrome).
- Many ND patients have underlying conditions like hematologic malignancies or inflammatory diseases.
Conclusions:
- ND diagnosis requires excluding infections and considering underlying systemic diseases.
- Histopathology and clinical features guide classification and diagnosis.
- Appropriate investigations are crucial for identifying associated conditions and ruling out differentials.
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