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1.
Korean Journal of Medicine ; : 254-258, 2015.
Artículo en Coreano | WPRIM | ID: wpr-102972

RESUMEN

Common variable immunodeficiency (CVID) is a heterogeneous group of primary immune deficiencies in adults characterized by hypogammaglobulinemia, recurrent bacterial infections, and a higher incidence of autoimmune diseases. More than 25% of CVID patients also have autoimmune diseases such as autoimmune hemolytic anemia, immune thrombocytopenic purpura, rheumatoid arthritis, and systemic lupus erythematosus. However, the pathogenesis of autoimmunity in CVID remains obscure. We report a 56-year-old woman with CVID and Sjogren's syndrome. In addition to a long history of recurrent upper respiratory infections, acute gastroenteritis, and cellulitis, she has also suffered from persistent xerostomia and xerophthalmia for the past 10 years. Serologic studies revealed hypogammaglobulinemia (low levels of IgG, IgA, and IgM in serum) and the presence of anti-Ro antibodies, and salivary scintigraphy indicated salivary gland involvement. These findings led to a diagnosis of CVID and Sjogren's syndrome, which was treated by monthly intravenous immunoglobulin therapy.


Asunto(s)
Adulto , Femenino , Humanos , Persona de Mediana Edad , Agammaglobulinemia , Anemia Hemolítica Autoinmune , Anticuerpos , Artritis Reumatoide , Enfermedades Autoinmunes , Autoinmunidad , Infecciones Bacterianas , Celulitis (Flemón) , Inmunodeficiencia Variable Común , Diagnóstico , Gastroenteritis , Inmunización Pasiva , Inmunoglobulina A , Inmunoglobulina G , Inmunoglobulina M , Incidencia , Lupus Eritematoso Sistémico , Púrpura Trombocitopénica Idiopática , Cintigrafía , Infecciones del Sistema Respiratorio , Glándulas Salivales , Síndrome de Sjögren , Xeroftalmia , Xerostomía
2.
The Ewha Medical Journal ; : 121-125, 2014.
Artículo en Coreano | WPRIM | ID: wpr-80978

RESUMEN

Systemic lupus erythematosus (SLE) is a chronic inflammatory disease of unknown etiology and is characterized by presence of variable pathogenic auto-antibodies and multiple organ involvement. Serositis is common in SLE, but peritoneal involvement is relatively rare. This is a case report of 28-year-old female who initially presented with abdominal pain and ascites. After ruling out many other possibilities such as liver cirrhosis, neoplasm, and infectious etiologies, we confirmed SLE with clinical features, serologic tests and radiological findings. To conclude, her abdominal pain and ascites were caused by lupus peritonitis. After administration of corticosteroid therapy, her symptoms fairly improved.


Asunto(s)
Adulto , Femenino , Humanos , Dolor Abdominal , Ascitis , Cirrosis Hepática , Lupus Eritematoso Sistémico , Peritonitis , Pruebas Serológicas , Serositis
3.
Korean Journal of Medicine ; : 651-654, 2014.
Artículo en Coreano | WPRIM | ID: wpr-151946

RESUMEN

Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease. In patients with SLE, the prevalence of antiphospholipid antibodies is considerably higher, and is largely responsible for thrombosis. Splenic infarction is a rare complication of arterial thrombosis in patients with SLE. It is important to consider splenic infarction in a patient with SLE complaining of left upper quadrant (LUQ) pain because of the possibility of severe infarction-related complications, such as subcapsular hemorrhage and splenic rupture. We report a case of solitary splenic infarction in a patient with SLE. The only symptom was LUQ pain of 3-day duration. Lupus anticoagulant activity was positive and abdominal-pelvic computed tomography (CT) was consistent with splenic infarction. She did not show any other evidence of thrombotic events. The patient was diagnosed with antiphospholipid syndrome that presented as a splenic infarction in a SLE patient.


Asunto(s)
Humanos , Anticuerpos Antifosfolípidos , Síndrome Antifosfolípido , Enfermedades Autoinmunes , Hemorragia , Inhibidor de Coagulación del Lupus , Lupus Eritematoso Sistémico , Prevalencia , Infarto del Bazo , Rotura del Bazo , Trombosis
4.
Tuberculosis and Respiratory Diseases ; : 233-236, 2014.
Artículo en Inglés | WPRIM | ID: wpr-155552

RESUMEN

Catamenial hemoptysis is a rare condition, characterized by recurrent hemoptysis associated with the presence of intrapulmonary or endobronchial endometrial tissue. Therapeutic strategies proposed for intrapulmonary endometriosis with catamenial hemoptysis consist of medical treatments and surgery. Bronchial artery embolization is a well-established modality in the management of massive or recurrent hemoptysis, but has seldom been used for the treatment of catamenial hemoptysis. We report a case of catamenial hemoptysis associated with pulmonary parenchymal endometriosis, which was successfully treated by a bronchial artery embolization.


Asunto(s)
Femenino , Arterias Bronquiales , Embolización Terapéutica , Endometriosis , Hemoptisis
5.
Endocrinology and Metabolism ; : 574-578, 2014.
Artículo en Inglés | WPRIM | ID: wpr-14694

RESUMEN

Our aim was to examine whether serum testosterone concentrations are in fact low in hospitalized men with poorly controlled type 2 diabetes compared with healthy men. In this study, 79 men aged 40 years or older (41 healthy men and 38 men with type 2 diabetes) were included. Total testosterone and sex hormone-binding globulin levels were measured. The average duration of diagnosed diabetes was 10.8 years and the mean glycated hemoglobin value was 10.8%. Total testosterone concentrations were lower in men with type 2 diabetes than in healthy men, after adjusting for age and body mass index (3.83+/-0.32 ng/mL vs. 5.63+/-0.31 ng/mL, P<0.001). In conclusion, this study shows that serum testosterone concentrations are lower in hospitalized men with poorly controlled type 2 diabetes than in healthy men. Therefore, men with poorly controlled type 2 diabetes should undergo further assessment for hypogonadism.


Asunto(s)
Humanos , Masculino , Índice de Masa Corporal , Diabetes Mellitus Tipo 2 , Hemoglobina Glucada , Hipogonadismo , Globulina de Unión a Hormona Sexual , Testosterona
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