Results 21 to 30 of about 930 (179)
Recommendations for the Clinical Approach to Immune Thrombocytopenia: Spanish ITP Working Group (GEPTI) [PDF]
, 2023 Glucocorticoids; Intravenous immunoglobulins; Primary immune thrombocytopeniaGlucocorticoides; Immunoglobulines intravenoses; Trombocitopènia immune primàriaGlucocorticoides; Inmunoglobulinas intravenosas; Trombocitopenia inmune primariaPrimary immune ...
Bernardo, Angel +6 more
core +1 more source
Necrolisis epidérmica tóxica. Terapia en UCI con inmunoglobulinas intravenosas en un caso
Revista médica de Chile, 2000 We report a 27 years old homosexual male with AIDS that was admitted to the ICU dehydrated, with fever and severe malaise. He had irregular bullae, an extensive purpuric exanthema and a zone of epidermic detachment in the right arm. A toxic epidermal necrolysis was diagnosed and therapy with i.v. immunoglobulins was started.
Andresen H, Max +4 more
openaire +3 more sources
Vitiligo y terapia con inmunoglobulina intravenosa: a propósito de un paciente con síndrome de Sjögren [PDF]
Revista médica de Chile, 2011 Vitiligo is associated with other autoimmune diseases. We report a 52-year-old male with a Sjögren syndrome that was treated with monthly pulses of intravenous immunoglobulin for a chronicinflammatory demyelinating polyradiculoneuropathy. The neurological disorder responded adequately to the treatment and the patient also noted a marked remission of ...
Alejandro Badilla P, Carolina Díaz G
openaire +3 more sources
Síndrome de Stevens-Johnson/necrolisis epidérmica tóxica tratado con inmunoglobulinas intravenosas
Actas Dermo-Sifiliográficas, 2005 Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are part of the same disease spectrum, but are differentiated by the degree of skin detachment. In TEN, more than 30 % of the body's surface area is affected; thus, it is a serious process, whose frequency is estimated at 1.2-6 cases per million population/year. We describe the case of
Manuela Yuste +6 more
openaire +1 more source
Using Intravenous Inmunoglobulin in an Atypical Case of Lambert Eaton Síndrome.
Medisur, 2007 A 48 year-old hypertensive, smoker patient who started presenting a generalized weakness, pait instability,visual disorders and uncontrolled blood pressure is presented. At physical examination quadriparesis and weakness extraocular muscles were found. A
Erélido Hernández Valero +1 more
doaj +2 more sources
Neurología (English Edition), 2015 Background: There is increasing evidence supporting that neuromyelitis optica (NMO) is an inflammatory humoral mediated disorder associated with NMO-IgG/AQP-4 antibodies.
C. de Andrés +4 more
doaj +1 more source
Trombocitopenia inmune primaria en pacientes de edad avanzada : experiencia en un centro [PDF]
, 2011 Estudi descriptiu dels pacients majors de 60 anys amb diagnòstic de trombocitopènia immune primària en un centre. S'han revisat característiques bàsiques en el moment de l'inici de la malaltia, així com les diferents línies de tractament, resposta ...
López Pavía, María de la Encarnación +2 more
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Neurología, 2015 Resumen: Antecedentes: La neuromielitis óptica (NMO) es una enfermedad predominantemente humoral mediada por anticuerpos IgG-NMO/AQP-4. Sin embargo, no se conoce bien la contribución de las diferentes subpoblaciones de células B y T en su patogenia o en
C. de Andrés +4 more
doaj +1 more source
Síndrome de Susac Revisión bibliográfica [PDF]
, 2019 El síndrome de Susac constituye una entidad clínica caracterizada por una triada que se compone de encefalopatía, oclusiones de la arteria retiniana y pérdida de audición.
Pablo-Torres López-Brea, Rodrigo
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Inflammatory miopathy associated with anti-SRP auto-antibodies and its response to endovenous therapy: systematic review [PDF]
, 2022 Trabajo de fin de grado. Grado en Medicina. Curso académico 2021-2022Introducción: La miopatía inflamatoria por anticuerpos anti-SRP es un subtipo de miopatía necrosante inmunomediada caracterizada por la presencia de dichos anticuerpos.
Escribano Iglesias, María
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