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1.
Case Rep Rheumatol ; 2018: 8398453, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30327741

RESUMEN

INTRODUCTION: Inflammatory myopathies are a rare group of diseases characterized by proximal weakness. Incidence ranges from 7.98/million/year and prevalence at 14/100,000. The utility of [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) scan is increasing for the complementary diagnosis of myopathies. CASE REPORT: An 84-year-old male was admitted with a history of difficulty rising from a chair and a fall. Laboratory results showed increased creatine kinase levels of more than 50 times the normal reference values. Electromyography (EMG) showed myopathic changes, and FDG-PET/CT scan showed increased FDG uptake in bilateral quadriceps. A biopsy was performed revealing lymphocytic predominant infiltrates and myonecrosis. Prednisone and intravenous immunoglobulin (IVIG) were administered with strength improvement. The patient was discharged for further follow-up. DISCUSSION: FDG-PET/CT in inflammatory diseases has proven useful as muscle fibers have increased FDG uptake. In some cases, FDG-PET/CT is also useful in determining associated neoplastic diseases.

2.
Reumatol. clín. (Barc.) ; 7(supl.3): s37-s40, dic. 2011. tab
Artículo en Español | IBECS | ID: ibc-147316

RESUMEN

Las vasculitis asociadas a ANCA son enfermedades raras y complejas con compromiso sistémico. El desarrollo de grupos colaborativos en Europa y los Estados Unidos de América ha facilitado la realización de estudios clínicos aleatorizados para garantizar la seguridad en el tratamiento de mantenimiento de estas enfermedades. Aunque la ciclofosfamida continúa vigente para la fase de inducción, sus efectos adversos a largo plazo han propiciado el estudio de otras drogas inmunosupresoras en la fase demantenimiento. Aquí revisamos estos estudios con especial atención a los que se refieren a la combinación de medicamentos inmunosupresores y a la duración del tratamiento (AU)


ANCA-associated vasculitides are rare and complex systemic diseases. Collaborative studies in both Europe and the United States of America have been particularly important in the development of randomized clinical trials that have studied the safety of maintenance therapy for these diseases. Although cyclophosphamide continues to be the main drug utilized during induction therapy, its long-term side effects have given rise to the study of other immunosuppressive drugs for the maintenance phase. We herein review these studies with particular attention to combination therapy and the duration of treatment (AU)


Asunto(s)
Humanos , Vasculitis Asociada a Anticuerpos Citoplasmáticos Antineutrófilos/diagnóstico , Vasculitis Asociada a Anticuerpos Citoplasmáticos Antineutrófilos/tratamiento farmacológico , Quimioterapia de Mantención , Anticuerpos Monoclonales de Origen Murino/uso terapéutico , Azatioprina/uso terapéutico , Inmunoglobulinas Intravenosas/uso terapéutico , Inmunosupresores/administración & dosificación , Inmunosupresores/efectos adversos , Inmunosupresores/uso terapéutico , Quimioterapia de Inducción , Metotrexato/uso terapéutico , Ciclofosfamida/efectos adversos , Ciclofosfamida/uso terapéutico , Quimioterapia Combinada , Diagnóstico Precoz , Glucocorticoides/uso terapéutico , Isoxazoles/uso terapéutico , Ensayos Clínicos Controlados Aleatorios como Asunto , Índice de Severidad de la Enfermedad
3.
Reumatol Clin ; 7 Suppl 3: S37-40, 2011 Dec.
Artículo en Español | MEDLINE | ID: mdl-22119277

RESUMEN

ANCA-associated vasculitides are rare and complex systemic diseases. Collaborative studies in both Europe and the United States of America have been particularly important in the development of randomized clinical trials that have studied the safety of maintenance therapy for these diseases. Although cyclophosphamide continues to be the main drug utilized during induction therapy, its long-term side effects have given rise to the study of other immunosuppressive drugs for the maintenance phase. We herein review these studies with particular attention to combination therapy and the duration of treatment.


Asunto(s)
Vasculitis Asociada a Anticuerpos Citoplasmáticos Antineutrófilos/tratamiento farmacológico , Quimioterapia de Mantención , Vasculitis Asociada a Anticuerpos Citoplasmáticos Antineutrófilos/diagnóstico , Anticuerpos Monoclonales de Origen Murino/uso terapéutico , Azatioprina/uso terapéutico , Ciclofosfamida/efectos adversos , Ciclofosfamida/uso terapéutico , Quimioterapia Combinada , Diagnóstico Precoz , Glucocorticoides/uso terapéutico , Humanos , Inmunoglobulinas Intravenosas/uso terapéutico , Inmunosupresores/administración & dosificación , Inmunosupresores/efectos adversos , Inmunosupresores/uso terapéutico , Quimioterapia de Inducción , Isoxazoles/uso terapéutico , Leflunamida , Metotrexato/uso terapéutico , Ensayos Clínicos Controlados Aleatorios como Asunto , Rituximab , Índice de Severidad de la Enfermedad , Combinación Trimetoprim y Sulfametoxazol/uso terapéutico
4.
Rev Invest Clin ; 60(5): 365-74, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-19227433

RESUMEN

BACKGROUND: Preemptive therapy reduces the risk of cytomegalovirus disease in high-risk kidney transplant patients. The advantage of this strategy is that only a fraction of patients receive antiviral drugs for a limited time, which decreases costs and toxicity but requires frequent monitoring and may not prevent complications of asymptomatic cytomegalovirus replication. MATERIAL AND METHODS: Long-term graft-function and patient survival of high-risk kidney transplant patients who received preemptive therapy guided by pp65 antigenemia was compared to those whose assay remained negative throughout the first post-transplant year. RESULTS: Between August 1997 and March 2005, 24 of 272 patients were CMV D+/R-. Thirteen of the 24 (54.2%) developed a positive CMV assay during follow-up; the time between transplant and first positive antigenemia was 66.7 +/- 58.3 days (range 29-251 days). Four patients developed symptoms associated with CMV, one of whom succumbed from complications of CMV neumonitis. Overall, no significant differences were observed in SCr, eGFR, delta SCr, and delta eGFR during a 60-month followup between patients who developed CMV infection or disease and those who remained pp65 antigenemia-negative throughout the first 12 post-transplant months. Additionally, no deaths or graft loss occurred during the long-term follow up of this cohort. CONCLUSIONS: Our results suggest that in this high risk group of kidney transplant recipients, treating CMV replication using a preemptive strategy during the first posttransplant year is associated with a low rate of CMV complications and probably interferes with the alleged long-term negative indirect effects of CMV on kidney function and survival.


Asunto(s)
Antivirales/uso terapéutico , Infecciones por Citomegalovirus/prevención & control , Supervivencia de Injerto , Trasplante de Riñón , Complicaciones Posoperatorias/prevención & control , Premedicación , Adulto , Antivirales/administración & dosificación , Estudios de Cohortes , Creatinina/sangre , Citomegalovirus/inmunología , Citomegalovirus/fisiología , Infecciones por Citomegalovirus/diagnóstico , Infecciones por Citomegalovirus/epidemiología , Femenino , Estudios de Seguimiento , Supervivencia de Injerto/efectos de los fármacos , Humanos , Inmunosupresores/efectos adversos , Inmunosupresores/uso terapéutico , Trasplante de Riñón/estadística & datos numéricos , Masculino , Fosfoproteínas/sangre , Complicaciones Posoperatorias/epidemiología , Estudios Prospectivos , Riesgo , Factores de Tiempo , Proteínas de la Matriz Viral/sangre , Viremia/diagnóstico , Viremia/tratamiento farmacológico , Replicación Viral , Adulto Joven
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