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Воспалительные заболевания кожи: васкулиты и васкулопатии
DOI: 10.26442/2414-3537_2018.1.28-31
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V.V.Kazlouskaya, Böer-Auer A. Inflammatory skin diseases: vasculitis and vasculopaties. Dermatology (Suppl. Consilium Medicum). 2018; 1: 28–31. DOI: 10.26442/2414-3537_2018.1.28-31
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Cutaneous vasculitis is a group of conditions that affect blood vessels of different caliber. It may be primary disease or secondary one, associated with a variety of systemic conditions. Vasculitis is classified based on the caliber of the vessel involved. The largest group of cutaneous vasculitis is leukocytoclastic vasculitis (LCV), which affects small vessels and is characterized by fibrin deposits in a vessel wall and leukocytoklasia. Herein, we will discuss the most common forms of LCV, including Henoch–Schönlein purpura, infantile acute hemorrhagic edema of infancy (Finkelstein’s disease) and urticarial vasculitis. Chronic forms of LCV (granuloma faciale and erythema elevatum diutinum) also will be discussed. In this article, we also describe histopathology of occlusive vasculopaties.
2. Yong AM, Lee SX, Tay YK. The profile of adult onset Henoch-Schonlein purpura in an Asian population. Int J Dermatology 2015; 54; 1236–41.
3. Parker L, Shahar-Nissan K, Ashkenazi-Hoffnung L et al. Acute hemorrhagic edema of infancy: the experience of a large tertiary pediatric center in Israel. WJP 2017; 13; 341–5.
4. Salim SA, Yousuf T, Patel A et al. Hypocomplementemic Urticarial Vasculitis Syndrome With Crescentic Glomerulonephritis. Am J Med Sci 2018; 355; 195–200.
5. Oliveira CC, Ianhez PE, Marques SA, Marques ME. Granuloma faciale: clinical, morphological and immunohistochemical aspects in a series of 10 patients. An Bras Dermatol 2016; 91; 803–7.
6. Llamas-Velasco M, Stengel B, Perez-Gonzalez YC, Mentzel T. Late-Stage Erythema Elevatum Diutinum Mimicking a Fibroblastic Tumor: A Potential Pitfall. Am J Dermatopathol 2017. DOI: 10.1097/DAD.0000000000001088
7. De Virgilio A, Greco A, Magliulo G et al. Polyarteritis nodosa: A contemporary overview. Autoimmunity rev 2016; 15; 564–70.
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1. Kazlouskaya V., Boer-Auer A. Inflammatory skin diseases: panniculitis. Dermatology (Suppl. Consilium Medicum). 2017; 4: 56–9.
2. Yong AM, Lee SX, Tay YK. The profile of adult onset Henoch-Schonlein purpura in an Asian population. Int J Dermatology 2015; 54; 1236–41.
3. Parker L, Shahar-Nissan K, Ashkenazi-Hoffnung L et al. Acute hemorrhagic edema of infancy: the experience of a large tertiary pediatric center in Israel. WJP 2017; 13; 341–5.
4. Salim SA, Yousuf T, Patel A et al. Hypocomplementemic Urticarial Vasculitis Syndrome With Crescentic Glomerulonephritis. Am J Med Sci 2018; 355; 195–200.
5. Oliveira CC, Ianhez PE, Marques SA, Marques ME. Granuloma faciale: clinical, morphological and immunohistochemical aspects in a series of 10 patients. An Bras Dermatol 2016; 91; 803–7.
6. Llamas-Velasco M, Stengel B, Perez-Gonzalez YC, Mentzel T. Late-Stage Erythema Elevatum Diutinum Mimicking a Fibroblastic Tumor: A Potential Pitfall. Am J Dermatopathol 2017. DOI: 10.1097/DAD.0000000000001088
7. De Virgilio A, Greco A, Magliulo G et al. Polyarteritis nodosa: A contemporary overview. Autoimmunity rev 2016; 15; 564–70.
1. Университет штата Нью-Йорк, Медицинский центр Даунстейт, США, Нью-Йорк, Бруклин;
2. Dermatologikum Clinic. 120354, Germany, Hamburg, Stephansplatz, 5
*viktoriakozlovskaya@yahoo.com
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V.V.Kazlouskaya*1, A.Böer-Auer2
1. SUNY Downstate Medical Center. USA, New-York, 450 Clarkson Street, 11203;
2. Dermatologikum Clinic. Germany, Hamburg, 120354, Stephansplatz, 5
*viktoriakozlovskaya@yahoo.com