کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5716694 | 1411164 | 2017 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Disorders characterized by predominant or exclusive dermal inflammation
ترجمه فارسی عنوان
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کلمات کلیدی
Pyoderma gangrenosumHidradenitis suppurativachronic urticaria - داروی مزمن مزمنHypereosinophilic syndrome - سندرم HypereosinophilicSweet syndrome - سندرم شیرینPolymorphous light eruption - فوران نور پلیمورفDrug eruptions - فوران های مواد مخدرCutaneous lymphoid hyperplasia - هیپرپلازی لنفوئیدی پوستیUrticarial vasculitis - واسکولیت وریدیbullous pemphigoid - پمفیگوئه گوسفند
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
آسیبشناسی و فناوری پزشکی
چکیده انگلیسی
Some cutaneous inflammatory disorders are typified by a predominant or exclusive localization in the dermis. They can be further subdivided by the principal cell types into lymphocytic, neutrophilic, and eosinophilic infiltrates, and mixtures of them are also seen in a proportion of cases. This review considers such conditions. Included among the lymphoid lesions are viral exanthems, pigmented purpuras, gyrate erythemas, polymorphous light eruption, lupus tumidus, and cutaneous lymphoid hyperplasia. Neutrophilic infiltrates are represented by infections, Sweet syndrome, pyoderma gangrenosum, and hidradenitis suppurativa, as well as a group of so-called “autoinflammatory” dermatitides comprising polymorphonuclear leukocytes. Eosinophil-dominated lesions include arthropod bite reactions, cutaneous parasitic infestations, the urticarial phase of bullous pemphigoid, Wells syndrome (eosinophilic cellulitis), hypereosinophilic syndrome, and Churg-Strauss disease. In other conditions, eosinophils are admixed with neutrophils in the corium, with or without small-vessel vasculitis. Exemplary disorders with those patterns include drug eruptions, chronic idiopathic urticaria, urticarial vasculitis, granuloma faciale, and Schnitzler syndrome (chronic urticarial with a monoclonal gammopathy).
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Seminars in Diagnostic Pathology - Volume 34, Issue 3, May 2017, Pages 273-284
Journal: Seminars in Diagnostic Pathology - Volume 34, Issue 3, May 2017, Pages 273-284
نویسندگان
Mark R. Wick,