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1.
Arch Virol ; 165(1): 33-42, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31630275

RESUMEN

Hepatocellular carcinoma (HCC) is a major public health issue in Africa. In Tunisia, hepatitis B virus (HBV) is known to be an important risk factor for HCC in the south of the country, but the role played by hepatitis C virus (HCV) still remains unclear. The aim of the current case-control study was to identify risk factors for HCC development in the northern part of the country. Clinical and biological data including viral hepatitis status (serological and molecular) and non-infectious risk factors from 73 patients with HCC and 70 control subjects without hepatic diseases were collected. The mean age of the patients was 63 ± 10 years, and the ratio of males to females was 1.1. HCC occurred in cirrhotic liver in 72.0% of the cases. HCV infection was the dominant risk factor (64.3% of cases); the presence of HBV was observed in 53.4% of the cases. Occult hepatitis B and C were implicated, respectively, in 30.1% and 9.6% of the cases. HCV genotype 1b was predominant. Patients originating from western Tunisia formed a homogeneous group, characterized by significantly higher rates of tattoos or scarifications (83%) and HCV infection (80%) than those from other parts of the country. Chronic HCV infection is currently the primary risk factor for HCC in Tunisia; HBV infection remains frequent in its overt or occult infection forms. Traditional esthetic practices apparently contribute to increasing the burden of terminal liver diseases in western Tunisia.


Asunto(s)
Carcinoma Hepatocelular/epidemiología , Hepatitis B/epidemiología , Hepatitis C/epidemiología , Cirrosis Hepática/virología , Neoplasias Hepáticas/epidemiología , Adulto , Anciano , Anciano de 80 o más Años , Carcinoma Hepatocelular/virología , Estudios de Casos y Controles , Femenino , Genotipo , Hepatitis B/complicaciones , Hepatitis C/complicaciones , Humanos , Cirrosis Hepática/complicaciones , Neoplasias Hepáticas/virología , Masculino , Persona de Mediana Edad , Medición de Riesgo , Túnez/epidemiología
2.
Joint Bone Spine ; 75(1): 73-5, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17900962

RESUMEN

Primary intestinal lymphangiectasis (PIL), also known as Waldmann's disease, is a rare protein-losing enteropathy characterized by abnormal enlargement of the lymphatic ducts in the bowel wall. The symptoms usually start in early infancy. We report a case of osteomalacia in a 63-year-old patient with delayed-onset of PIL, for which she was on dietary treatment. She presented with a 3-year history of mechanical pain in the back and pelvis. Mild ascites and edema with functional impairment of the lower limbs were noted. The neurological evaluation was normal. Blood tests showed hypocalcemia, hypophosphatemia, alkaline phosphatase elevation, and evidence of intestinal malabsorption. Radiographs of the pelvis disclosed a fracture, Looser's zones in the iliopubic rami and left femoral neck, and a washed-out appearance of the vertebras. Dual-energy X-ray absorptiometry showed bone loss with T-score values of -1.2SD at the lumbar spine and -2.5SD at the femoral necks. A diagnosis of osteomalacia related to vitamin D deficiency was given. Serum 25-OH-vitamin D was 18.2ng/ml (normal, 20-40ng/ml) and serum parathyroid hormone was 620pg/ml (normal, 15-65pg/ml), suggesting secondary hyperparathyroidism. Intramuscular vitamin D was given, together with oral calcium and an adequate diet. At follow-up 8 months later, small improvements were noted in the symptoms and absorptiometry findings.


Asunto(s)
Linfangiectasia Intestinal/complicaciones , Osteomalacia/etiología , Edad de Inicio , Femenino , Humanos , Hiperparatiroidismo Secundario/etiología , Linfangiectasia Intestinal/epidemiología , Persona de Mediana Edad , Osteomalacia/diagnóstico
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