Subject(s)
Male , Female , Humans , Middle Aged , Aged , Low Back Pain/diagnosis , Low Back Pain/etiology , Low Back Pain/therapyABSTRACT
Background: Polymorphisms of Fc receptors for IgG (FcgR) have been proposed as a genetic factor that influences susceptibility for systemic lupus erythematosus (SLE). Human FcgRIIa has 2 codominantly expressed alleles, H131 and R131, which differ at amino acid position 131 in the second extracelular domain (histidine or arginine respectively) and differ substantially in their ability to bind human IgG2. The H131 allele binds IgG2 efficiently, whereas R131 binds it poorly. Because IgG2 is a poor activator of the classical complement pathway, the H131 is essential for the disposal of IgG2 immune complexes. Aim: To determine the distribution of FcgRIIA genes in a cohort of Chilean SLE patients, with or without a history of lupus nephritis. Patients and methods: We studied 52 Chilean SLE patients fulfilling the 1982 American College of Rheumatology (ACR) criteria, 20 of whom had a history of nephritis, and 44 ethnically matched disease-free controls. FcgRIIa allotypes were genotyped by PCR. Results: No significant association was observed between the low affinity FcgRII receptor (FcgRIIa-R131) and the presence of SLE or lupus nephritis. However, genotype frequencies in SLE patients but not in controls, departed from the proportions predicted by the Hardy-Weinberg equilibrium, suggesting this locus might be related to the disease. Conclusions: Our results suggest that in Chilean patients with SLE, as well as in many other populations, the R131 allotype is not a major factor predisposing to the development of SLE or lupus nephritis
Subject(s)
Humans , Lupus Erythematosus, Systemic/genetics , Polymorphism, Genetic/genetics , Immunoglobulin G , Receptors, IgE , Alleles , Genotype , Kidney DiseasesSubject(s)
Humans , Signs and Symptoms , Vasculitis/diagnosis , Antibodies, Antineutrophil Cytoplasmic , Arthralgia/etiology , Clinical Diagnosis , Giant Cell Arteritis/diagnosis , Lymphomatoid Granulomatosis/diagnosis , Polyarteritis Nodosa/diagnosis , Takayasu Arteritis/diagnosis , Vasculitis/classification , Vasculitis/etiologySubject(s)
Humans , Consciousness/physiology , Diagnostic Techniques, Cardiovascular , Diagnostic Techniques, Otological , Physical Examination/methods , Nutritional Status/physiology , Gait Disorders, Neurologic/diagnosis , Vision Tests , Breast Diseases/diagnosis , Cardiovascular Diseases/diagnosis , Diagnostic Techniques, Obstetrical and Gynecological , Ear Diseases/diagnosis , Peripheral Vascular Diseases/diagnosis , Skin Pigmentation/physiology , Respiratory Sounds/diagnosis , Spinal Diseases/diagnosis , Thyroid Diseases/diagnosis , Articulation Disorders/diagnosisSubject(s)
Humans , Blood Chemical Analysis/methods , Clinical Laboratory Techniques/classification , Leukocyte Count , Blood Sedimentation , Heart , Electrocardiography/methods , Rheumatic Diseases/diagnosis , Eosinophilia/diagnosis , Lipids , Biomarkers , Radiography, Thoracic/methods , Radiography, Abdominal , Sensitivity and Specificity , Urine/chemistryABSTRACT
The prevalence of Lyme disease in Chile is unknown. To study the existence and epidemiology of Lyme Disease in Chile. One hundred eighteen patients with signs or symptoms suggestive of Lyme disease were studied. Antibodies against Borrelia burgdorferi were measured using ELISA and indirect immunofluorescence screening tests. Positive cases were confirmed with ELISA using a purified antigen and Western Blot analysis. Human biological samples and ticks were cultured in BSK-H medium. Five patients, 3 with dermatological manifestations and two with facial palsy and other neurological symptoms, had antibodies against Borrelia, measured by ELISA and indirect immunofluorescence. However, the presence of IgM antibodies by ELISA using purified antigen, was confirmed in only one case. All sera and cerebrospinal fluids were negative on Western Blot analysis. No plasma, skin, CFS or thick culture yielded Borrelia. We could not confirm the existence of Lyme disease in Chile. Positive screening with negative confirmatory test suggests false positive non-specific reactivity or that local Borrelia are antigenically different compared to North American strains
Subject(s)
Humans , Male , Female , Child, Preschool , Adolescent , Adult , Middle Aged , Lyme Disease/epidemiology , Borrelia burgdorferi/pathogenicity , Tick Infestations/complications , Enzyme-Linked Immunosorbent Assay , Cross-Sectional Studies , Antibodies/isolation & purificationABSTRACT
We report a previously healthy 24 years old woman, that presented with an acute abdomen due to a mesenteric vasculitis. The diagnostic study demonstrated the presence of a systemic lupus erythematosus with a type IV nephropathy. Posterior to intestinal resection and immunosuppresive therapy, the patient had a satisfactory evolution
Subject(s)
Humans , Female , Adult , Vasculitis/complications , Abdomen, Acute/etiology , Lupus Erythematosus, Systemic/complications , Vasculitis/surgery , Mesentery/pathologyABSTRACT
Trienta y dos pacientes con hallazgos clínicos y patológicos de Lupus Eritematoso Sistémico (LES) fueron identificados en una revisión de necropsias en un período de veinte años en el Hospital del Salvador. Veintiséis pacientes (81,3%) tuvieron manifestaciones anatomopatológicas de compromiso cardiovascular (CV), ya que fuera directo o mediante hipertensión arterial. Solamente en 5 casos se hizo el diagnóstico clínico de compromiso CV directo (con insuficiencia valvular, insuficiencia cardiaca o pericarditis). En la necropsia se encontraron 13 casos de pericarditis (43,8%), 4 casos de miocarditis(12,5%), 4 casos de endocarditis verrucosa de Libman-Sacks (12,5%) de la válvula mitral y 1 caso de fibrosis endomiocárdica. No se hallaron pacientes con arteritis coronaria, aunque 11 tenían un grado discreto de ateroesclerosis. En 15 pacientes se hizo el diagnóstico clínico de hipertensión arterial (46,8%), mientras en 30 (93,75%) hubo hallazgos patológicos de nefritis lúpica. A pesar de la alta incidencia de hallazgos patológicos, la insuficiencia cardiaca clínica fue rara, documentándose solamente en 3 casos de esta serie (9,3%). La utilización rutinaria en la actualidad de exámenes no invasivos (especialmente ecocardiografía) debería facilitar el reconocimiento y ayudar al manejo del compromiso CV en el LES
Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Cardiovascular Diseases/etiology , Lupus Erythematosus, Systemic/complications , Lupus Erythematosus, Systemic/pathologySubject(s)
Adult , Aged , Humans , Male , Lymphatic Diseases/pathology , Granuloma, Lethal Midline/pathology , Diagnosis, DifferentialABSTRACT
Se presenta la experiencia en 7 pacientes con antecedentes de pérdida recurrente del embarazo (x=3,7 rango 2-6) con AACL(+) en las cuales se descartó otra etiología; éstas pacientes totalizaban 26 gestaciones no tratadas concluidas en 24 pérdidas fetales (constando en 9 la muerte fetal in útero) y 2 RN vivos. La duración promedio de esas gestaciones fue 17,4 semanas (rango 8-37). Fueron tratadas con prednisona 20 mg/día y ASA 100 mg/día obteniéndose 7 RN vivos y 1 mortinato. En todas las pacientes se obtuvo descenso de los AACL. La duración promedio de las gestaciones tratadas fue de 31,7 semanas (rango 26-28). Se concluye que la presencia de AACL se correlaciona con alta mortalidad y bajo peso fetal y que con el tratamiento se obtiene gestaciones significativamente más largas que en las no tratadas y mayor relación de niños vivos respecto al número de embarazos