Results: 19

Climatério e lúpus eritematoso sistêmico

Femina; 51 (6), 2023
O lúpus eritematoso sistêmico é uma doença crônica, complexa e multifatorial que apresenta manifestações em vários órgãos. O seu acometimento ocorre 10 vezes mais no sexo feminino do que no masculino. É uma doença com uma clínica variada e com graus variados de gravidade, causando fadiga, ma...

Síndrome antifosfolipídico en pediatría: a propósito de un caso

Arch. argent. pediatr; 119 (6), 2021
El síndrome antifosfolipídico (SAF) es infrecuente en la edad pediátrica (3 %) y se presenta como eventos trombóticos de lechos vasculares y/o abortos espontáneos, asociado a la presencia de anticuerpos antifosfolipídicos (aFL). Este síndrome puede ser primario o asociado a alguna enfermedad sist�...

Resultados obstétricos en gestantes diagnosticadas de síndrome antifosfolípido

Rev. Méd. Clín. Condes; 32 (1), 2021
INTRODUCCIÓN: El síndrome antifosfolípido (SAF) es una enfermedad autoinmune caracterizada por la aparición de trombosis, complicaciones obstétricas y la presencia de anticuerpos antifosfolípidos. El objetivo de este estudio fue evaluar los resultados obstétricos en gestantes ...

Retinal ischemia as the first manifestation of antiphospholipid antibody syndrome

Rev. bras. oftalmol; 80 (1), 2021
ABSTRACT Antiphospholipid antibody syndrome (APS) is characterized by the development of venous and/or arterial thrombosis and by gestational morbidity (recurrent fetal losses) in the presence of antiphospholipid antibodies. We report the case of a 38-year-old woman who was diagnosed with primary APS fro...

Síndrome antifosfolipídico, lupus eritematoso sistémico y tromboembolismo pulmonar
Antiphospholipid syndrome, systemic lupus erythematosus and pulmonary thromboembolism. Case presentation

Rev. cuba. reumatol; 22 (3), 2020
El síndrome antifosfolipídico o de Hughes, como también se le conoce, puede aparecer de manera aislada o asociado a otras enfermedades autoinmunes como el lupus eritematoso sistémico. La asociación de ambas entidades puede causar varias complicaciones, como el tromboembolismo pulmonar. Se presenta e...

Endocarditis de Libman-Sacks de válvulas nativas derechas en contexto de síndrome antifosfolípido y lupus eritematoso sistémico: ¡cuando el tratamiento marca la diferencia!

Rev. chil. anest; 49 (4), 2020
We report the case of a 54 years old woman with antiphospholipid syndrome in irregular therapy, admitted due to exertional dyspnea and orthopnea. The transthoracic echocardiogram showed dilated cardiomyopathy with biventricular systolic dysfunction, pulmonary hypertension and masses related to the pulmon...

Antiphospholipid antibody syndrome and infertility

Abstract Antiphospholipid antibody syndrome (APS) is a systemic, autoimmune, prothrombotic disease characterized by persistent antiphospholipid antibodies (aPLs), thrombosis, recurrent abortion, complications during pregnancy, and occasionally thrombocytopenia. The objective of the present study was to r...

Antiphospholipid syndrome and neurofibromatosis type I: a coincidence or new association?

Arq. bras. oftalmol; 82 (2), 2019
ABSTRACT - Numerous studies have reported on structural vascular anomalies and ischemia associated with neurofibromatosis type 1 that are thought to stem from dysfunction of neurofibromin, the neurofibromatosis type 1 protein. Documented cases of associated antiphospholipid syndrome fulfilling the accept...

Pigmented purpura and cutaneous vascular occlusion syndromes

An. bras. dermatol; 93 (3), 2018
Abstract: Purpura is defined as a visible hemorrhage in the skin or mucosa, which is not evanescent upon pressure. Proper classification allows a better patient approach due to its multiple diagnoses. Purpuras can be categorized by size, morphology, and other characteristics. The course varies according ...