RÉSUMÉ
OBJECTIVE: This study aimed to evaluate the injury patterns in pediatric patients with an orbital wall fracture (OWF) and to identify the differences in injury patterns between preschool and school-aged patients with OWF who presented to the emergency department. METHODS: We performed a retrospective observational study in the emergency department of a tertiary hospital between January 2004 and March 2014. A total of 177 pediatric patients (7 years) pediatric groups. RESULTS: The inferior wall was the most common fracture site in both the preschool and school-aged pediatric groups (50.0% vs. 64.4%, P=0.15). The male-to-female ratio and the mechanism of injury showed significant differences between the two age groups. Violence was the most common mechanism of injury in the school-aged pediatric group (49.3%), whereas falls from a height caused OWF in approximately half of the patients in the preschool pediatric group (42.9%). Concomitant injuries and facial fractures had a tendency to occur more frequently in the school-aged pediatric group. CONCLUSION: Significant differences according to the sex and mechanisms of injury were identified in preschool and school-aged pediatric patients with OWF.
Sujet(s)
Enfant , Humains , Chutes accidentelles , Services des urgences médicales , Service hospitalier d'urgences , Os de la face , Lésions traumatiques de la face , Étude d'observation , Orbite , Fractures orbitaires , Études rétrospectives , Centres de soins tertiaires , ViolenceRÉSUMÉ
Pneumatosis cystoides intestinalis is a rare condition characterized by gas-filled cysts within the bowel wall. It may be idiopathic or secondary to a variety of disorders. Associated conditions include chronic obstructive pulmonary disease, the use of non-steroidal anti-inflammatory drugs, collagen vascular disease, organ transplantation, and necrotizing enterocolitis. Approximately 15% of cases are idiopathic. We present a case of pneumatosis cystoides intestinalis complicated by pneumoperitoneum in chronic respiratory failure due to a post-tuberculosis destroyed lung. Successful palliation involved paracentesis of the peritoneal air and oxygen therapy.
Sujet(s)
Collagène , Entérocolite nécrosante , Poumon , Transplantation d'organe , Oxygène , Paracentèse , Pneumatose kystique de l'intestin , Pneumopéritoine , Broncho-pneumopathie chronique obstructive , Insuffisance respiratoire , Transplants , Maladies vasculairesRÉSUMÉ
Lipomas are common soft tissue tumors that are located in the body tissues containing adipose tissues. However, lipomas arising from the walls of a vein are very rare. Intravascular lipomas have been described most commonly in association with the inferior vena cava. Intravascualar lipomas involving the subclavian vein are rare. We are reporting a case of an asymptomatic lipoma of the right subclavian vein, growing into the right brachiocephalic vein.
Sujet(s)
Veines brachiocéphaliques , Lipome , Veine subclavière , Veines , Veine cave inférieureRÉSUMÉ
Venous thrombosis and thromboembolism appear to occur more often in patient with inflammatory bowel disease (IBD). The cause of thrombotic complications in IBD is generally considered to be associated with hypercoagulable conditions. Its prevalence rate ranges from 1% to 8% in clinical studies and rises to 39% in autopsy, but the renal vein thrombosis is very rare complication in ulcerative colitis patient. A 24-year-old man presented with intermittent abdominal pain and hematochezia for 6 months and recently developed pitting edema for few weeks. He was diagnosed as severe ulcerative colitis involving whole colon combined with thrombosis in both renal veins by colonoscopy and computed tomography scan of abdomen. We used steroid for the treatment of ulcerative colitis and both intravenous lower molecular weight heparin and warfarin for renal vein thrombosis. His symptoms were improved after treatment and maintained with mesalazine and warfarin. Follow-up abdominal CT scan showed complete resolution of both renal vein thrombosis. Currently he has been followed up for 2 years with oral mesalazine.
Sujet(s)
Humains , Mâle , Jeune adulte , Anticoagulants/usage thérapeutique , Rectocolite hémorragique/complications , Coloscopie , Héparine/usage thérapeutique , Protéine S/métabolisme , Veines rénales , Tomodensitométrie , Thrombose veineuse/complications , Warfarine/usage thérapeutiqueRÉSUMÉ
Streptococcus constellatus (S. constellatus) is a commensal microorganism belonging to the "Streptococcus milleri" group, but may cause infections in different locations in immunocompromised patients. The infection of S. constellatus has high mortality and morbidity due to its tendency to cause abscesses in infected patients, which require immediate surgical drainage for effective treatment. We report on a 72-year-old woman with end stage renal disease, who suffered from dyspnea and general weakness that had developed over 7 days. Chest CT showed loculated pleural effusion. S. constellatus was cultured from exudative pleural effusions and confirmed by an analysis of 16S rRNA sequence. The patient was treated with drainage of pleural effusion and piperacillin/tazobactam for 5 weeks.