Results 71 to 80 of about 6,385 (228)

LESIONES CUTÁNEAS ASOCIADAS A FACTORES ESTIMULANTES DE COLONIAS EN UNA PACIENTE CON CÁNCER DE PULMÓN

open access: yesRevistas Argentina de Medicina, 2017
Se conoce como síndrome de Sweet a una dermatosis neutrofílica que se manifiesta como placas cutáneas sensibles o dolorosas de aparición brusca. El factor estimulante de colonias de granulocitos (G-CSF) es un factor de crecimiento hematopoyético cuya ...
Alexis Ostinelli   +2 more
doaj   +2 more sources

Type I interferonopathies in pediatric rheumatology. [PDF]

open access: yes, 2016
Defective regulation of type I interferon response is associated with severe inflammatory phenotypes and autoimmunity. Type I interferonopathies are a clinically heterogenic group of Mendelian diseases with a constitutive activation of this pathway that ...
Candotti, F.   +4 more
core   +2 more sources

Erosive pustular dermatosis of the lower legs (EPDL): A rarely diagnosed neutrophilic dermatosis of the elderly

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Erosive pustular dermatosis of the lower legs (EPDL) is a rarely diagnosed, chronic inflammatory skin disease that occurs predominantly in elderly people. Predisposing factors include skin atrophy, chronic venous insufficiency, and trauma. Although the pathogenesis of EPDL has not yet been conclusively clarified, there are ongoing discussions ...
Joachim Dissemond   +3 more
wiley   +1 more source

Sweet’s syndrome in a granulocytopenic patient with acute myeloid leukemia on FLT3 inhibitor

open access: yesJournal of Community Hospital Internal Medicine Perspectives, 2020
Introduction Gilteritinib is a FLT3 kinase inhibitor approved for FLT3-mutated acute myeloid leukemia (AML). We present a case of febrile neutropenia and neutrophilic dermatosis consistent with Sweet’s syndrome (SS).
Anish Paudel   +4 more
doaj   +1 more source

Caso para diagnóstico [PDF]

open access: yes, 2012
Pyodermatitis-pyostomatitis vegetans is a rare mucocutaneous dermatosis characterized by pustular and vegetating lesions of the skin and oral mucosa. It is considered a highly specific marker for inflammatory bowel diseases.
Costa, Izelda Maria Carvalho   +1 more
core   +3 more sources

Primary cicatricial alopecias: a review of histopathologic findings in 38 patients from a clinical University Hospital in Sao Paulo, Brazil [PDF]

open access: yes, 2008
BACKGROUND: Scarring alopecias are classified into primary and secondary types according to the initial site of inflammation. In primary scarring alopecias, the hair follicle is the main target of destruction; the term secondary cicatricial alopecia ...
MOURE, Emanuella Rosyane Duarte   +3 more
core   +1 more source

Cryptococcoid Sweet syndrome: a case report

open access: yesFrontiers in Medicine
Cryptococcoid Sweet syndrome (cSS) is a recently described clinical and histological variant of Sweet syndrome (SS). Its cutaneous presentation is similar to the classical form of SS but it includes atypical findings, such as capsular and yeast-like ...
Martina Volonté   +9 more
doaj   +1 more source

Diagnostic Agreement in Subepidermal Blistering Diseases: Is ELISA Test Reliable as Direct Immunofluorescence? A Systematic Review, Meta‐Analysis, and Trial Sequential Analysis

open access: yesJournal of Oral Pathology &Medicine, EarlyView.
ABSTRACT Objectives Direct immunofluorescence (DIF) is the gold standard for diagnosing subepidermal blistering diseases (SBDs). However, DIF requires specialized expertise; therefore, alternative immunological methods such as enzyme‐linked immunosorbent assays (ELISA) are worth exploring. The aim of this review was to evaluate the diagnostic agreement
Romeo Patini   +9 more
wiley   +1 more source

A Dermal Plaque on the Arm

open access: yes
JEADV Clinical Practice, EarlyView.
Claudine Howard‐James   +3 more
wiley   +1 more source

TNF Inhibitor Therapy in Corticosteroid‐Resistant or ‐Dependent Pediatric Neutrophilic Dermatosis

open access: yesPediatric Dermatology, EarlyView.
ABSTRACT Neutrophilic dermatoses are rare in children. Systemic corticosteroids are the first‐line treatment, but guidelines for second‐line therapies are lacking. We report five cases of children with systemic steroid‐resistant/dependent neutrophilic dermatoses, successfully treated with tumor necrosis factor inhibitors.
Laure Chêne   +7 more
wiley   +1 more source

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