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Esclerosis Sistémica en el Hospital Carlos Andrade Marín / Systemical sclerosis in Carlos Andrade Marin Hospital
González Castillo, Daniel David; Martínez Torres, Paúl Santiago; Villacís Vaca, Verónica del Pilar; Villacís Tamayo, Rómulo Abad.
  • González Castillo, Daniel David; Universidad Central del Ecuador. Medicina Interna. Quito. EC
  • Martínez Torres, Paúl Santiago; Universidad Central del Ecuador. Medicina Interna. Quito. EC
  • Villacís Vaca, Verónica del Pilar; Hospital de Especialidades Carlos Andrade Marín. Reumatología. Quito. EC
  • Villacís Tamayo, Rómulo Abad; Hospital de Especialidades Carlos Andrade Marín. Unidad de Reumatología. EC
Cambios rev. méd ; 16(1): 40-42, ene. - 2017. tab, graf
Article in Spanish | LILACS | ID: biblio-1000016
RESUMEN

Introducción:

La esclerosis sistémica es una enfermedad crónica multisistémica, caracterizada por alteraciones vasculares, activación inmune y fibrosis de tejidos y órganos. Materiales y

métodos:

Estudio descriptivo. Pacientes con diagnóstico de Esclerosis Sistémica que cumplieron los criterios de clasificación ACR-EULAR 2013, atendidos en la Unidad de Reumatología del Hospital Carlos Andrade Marín durante el año 2015.

Resultados:

De 80 pacientes, 18 presentaron esclerosis sistémica en su forma CREST; 32 como CREST incompleto; 14 en la forma difusa; uno con esclerosis sistémica sin esclerosis cutánea; 13 con síndrome de superposición; y, 2 con EMTC.

Discusión:

Las características clínicas y epidemiológicas de nuestros pacientes coincidieron con las descritas a nivel internacional.
ABSTRACT

Introduction:

Systemic sclerosis is a chronic multisystemic disease characterized by vascular disorders, immune activation, organ and tissue fibrosis.

Methods:

Descriptive study. Patients diagnosed with systemic sclerosis who met the criteria ACR- EULAR classification 2013, that receive medical care at Carlos Andrade Marín hospital.

Results:

Prevalence From 80 patients,18 had systemic sclerosis, full CREST form; 32 had incomplete CREST form; 14 had a diffuse form; one had systemic sclerosis without cutaneous impairment; 13 had overlaping syndrome and two EMTC.

Discusion:

Clinical and epidemiological characteristics of our patients were consistent with those described in the medical literature.
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: Scleroderma, Systemic / Incidence / Prevalence / Multiple Chronic Conditions Type of study: Incidence study / Observational study / Prevalence study / Prognostic study / Risk factors Limits: Female / Humans Language: Spanish Journal: Cambios rev. méd Journal subject: Medicine / Public Health Year: 2017 Type: Article Affiliation country: Ecuador Institution/Affiliation country: Hospital de Especialidades Carlos Andrade Marín/EC / Universidad Central del Ecuador/EC

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LIS

Full text: Available Index: LILACS (Americas) Main subject: Scleroderma, Systemic / Incidence / Prevalence / Multiple Chronic Conditions Type of study: Incidence study / Observational study / Prevalence study / Prognostic study / Risk factors Limits: Female / Humans Language: Spanish Journal: Cambios rev. méd Journal subject: Medicine / Public Health Year: 2017 Type: Article Affiliation country: Ecuador Institution/Affiliation country: Hospital de Especialidades Carlos Andrade Marín/EC / Universidad Central del Ecuador/EC