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Gingival hyperplasia being the first sign of Wegener’s granulomatosis
(E-Century Publishing Corporation, 2014)
Manifestaciones neurológicas de la granulomatosis de Wegener: Caso clínico
(Sociedad Médica de Santiago, 2007)
Arteritis de takayasu con evento cerebrovascular isquémico recurrente en mujer procedente de Trujillo, Perú
(Universidad Privada Antenor Orrego, 2020)
La arteritis de Takayasu es una vasculitis crónica granulomatosa idiopática de células
gigantes, habitualmente afecta a mujeres jóvenes en edad reproductiva, se identifica por
la presencia de signos inflamatorios e ...
Takayasu Arteritis: Recent Developments
(Springer, 2019)
Purpose of Review: Takayasu arteritis (TA) is a granulomatous inflammatory disorder that affects large vessels, especially aorta and its proximal branches. Its diagnosis can be extremely challenging due to the non-specificity ...
Ceratólise auto-imune em paciente com vasculite leucocitoclástica: apresentação atípica de erythema elevatum diutinum com padrão granulomatoso
(Conselho Brasileiro de Oftalmologia, 2000-06-01)
Purpose: Leucocytoclastic vasculitis is an immune complex-mediated, small vessel disease, that is characterized clinically by the presence of palpable purpuric lesions, most often in association with rheumatic diseases. ...
Anti-neutrophil cytoplasmic antibodies in leprosy
(2007)
Introduction: Anti-Neutrophil Cytoplasmic Antibodies (ANCA) are auto-antibodies directed to intracellular components of neutrophils and used to be considered as present almost exclusively in granulomatous vasculitis. ...
CHOREA IN A CHILD WITH CHURG-STRAUSS SYNDROME
(MEDFARMA-EDICOES MEDICAS, LDA, 2010)
Introduction: Churg-Strauss syndrome (CSS) is a systemic granulomatous vasculitis rarely described in children, particularly associated with neurological involvement, exceptionally chorea. To our knowledge there are only ...
Síndrome antifosfolípido primario con hemorragia alveolar refractaria e insuficiencia mitral severa reporte de un caso y revisión de la literatura
(Asociación Colombiana de Nefrología e Hipertensión ArterialColombia, 2015-04-11)
El síndrome antifosfolípido (SAF)es un trastorno hematológico que cursa con un estado de hipercoagulabilidad de origen autoinmune, caracterizado por fenómenos trombóticos venosos o arteriales, ...
Anti-neutrophil cytoplasmic antibodies in leprosy.
(Springer Verlag, 2014)