SAT0345 Histopathological Differences between Single-Organ Cutaneous Small Vessel Vasculitis and Other Cutaneous Vasculitis Associated with Systemic Involvement
| Autor: | Roman Blanco, M. Marcellán, Javier Loricera, Susana Armesto, M.Ά. González-Gay, W. Salcedo, M.A. González-Lόpez, Francisco Ortiz-Sanjuán, C. Fernández-Díaz, M. Lacalle-Calderόn, Carmen González-Vela, S. Hermana-Ramírez, M. Lόpez-Escobar, Vanesa Calvo-Río, J.L. Hernández |
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| Rok vydání: | 2016 |
| Předmět: |
Pathology
medicine.medical_specialty Lymphocytosis business.industry Immunology medicine.disease Cryoglobulinemia General Biochemistry Genetics and Molecular Biology Group B Neutrophilia Rheumatology Immunology and Allergy Medicine Eosinophilia medicine.symptom business Vasculitis Microscopic polyangiitis Cutaneous small-vessel vasculitis |
| Zdroj: | Annals of the Rheumatic Diseases. 75:792.1-792 |
| ISSN: | 1468-2060 0003-4967 |
| DOI: | 10.1136/annrheumdis-2016-eular.4846 |
| Popis: | Background Cutaneous vasculitis (CV) encompasses a wide and heterogeneous group of disorders characterized by the presence of necrotizing inflammatory lesions in the cutaneous blood vessels. Single-organ cutaneous small vessel vasculitis (SoCSVV) is, according to 2012 Chapel-Hill criteria, a vasculitis confined to the skin. Objectives Our aim was to compare the histopathological findings of skin biopsies from patients with SoCSVV and those with systemic involvement. Methods From a series of patients with CV, we selected 3 groups: group a) SoCSVV; group b) CV with systemic involvement; group c) subgroup of patients of group b with involvement of 3 organs other than the skin. A comparative study between the group a) with the other two groups (b and c) was performed. Results Group a) was integrated by 9 patients (7 W/2 M; mean age, 64±16 years). In the group b) 43 patients were included (18 W/25M; mean age, 54±21 years). The underlying conditions were: severe bacterial infections (n=12), hypersensitivity vasculitis with involvement of other organs besides the skin (n=10), HSP (n=9), panarteritis nodosa (n=4), microscopic polyangiitis (n=2), cryoglobulinemia (n=2), malignancy (n=2), SLE (n=1) and Sjogren9s syndrome (n=1). Finally, 7 patients (3 W/4 M; mean age, 50 ± 20 years) were included in group c) . The underlying conditions were: severe bacterial infections (n=3), HSP (n=3) and cryoglobulinemia (n=1). The results of histopathological comparison of group a) with the groups b) and c) are shown in the table. Although no parameter reached statistical significance, in our series we observed that the greater systemic involvement was more frequently associated with tissue neutrophilia, pustular dermatosis and deep involvement of arterioles. By contrast, SoCSVV tend to develop greater tissue eosinophilia and tissue lymphocytosis, whilst the intensity of the inflammatory infiltrate was lower. On the other hand, none of the samples of patients with SoCSVV showed involvement of deep arterioles. Conclusions In this series we observed that qualitative and quantitative histological differences were correlated with the degree of systemic involvement. However, these results need to be tested in prospective studies with a larger number of patients. Acknowledgement “Fondo de Investigaciones Sanitarias” PI12/00193 (Spain) and RETICS Programs, RD08/0075 (RIER) and RD12/0009/0013 from “Instituto de Salud Carlos III” (ISCIII) (Spain). Disclosure of Interest None declared |
| Databáze: | OpenAIRE |
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