A5063550172- Tumors and Oncological Cases
- Sexual Differentiation and Disorders
- Oral and Maxillofacial Pathology
- Genital Health and Disease
- Bone Tumor Diagnosis and Treatments
- Cleft Lip and Palate Research
- Craniofacial Disorders and Treatments
- Hemostasis and retained surgical items
- Teratomas and Epidermoid Cysts
- Female Genital Mutilation/Cutting Issues
- Vascular Malformations and Hemangiomas
- Congenital Ear and Nasal Anomalies
- Bone health and treatments
University of Lausanne
2021-2024
Hôpital Riviera-Chablais
2024
Lymphatic malformations (LMs) are classified as macrocystic, microcystic or mixed. Treatment depends on their characteristics: surgery, sclerotherapy, both combined, systemic treatment observation. This study aims to analyze the surgical and interventional management of LMs in children over last two decades our university hospital.Management born with between 2000 2019 was reviewed. Parameters collected were: malformation characteristics, type treatment, symptoms, imaging, timing diagnosis...
Background: This study reviews the surgical and functional outcomes of children diagnosed with a bilateral cleft lip palate treated by same team following specific protocols 18 years after surgery during follow-up. Methods: Based on single-center retrospective design, demographic data were gathered authors from international institutions. Most quantitative in nature, descriptive statistical non-parametric tests employed for analysis. All born 1982 to 2002 considered. Children affected...
Abstract Background Managing wounds and scars in children presents a significant challenge for surgical rehabilitation teams. Studies have already explored the potential of fish skin grafts with Omega-3 hard-to-heal lower extremity chronic ulcers deep-burn management. Aims The purpose this study is to assess safety outcome intact when used as replacement therapy pediatric population. Methods This article was conducted adherence our hospital's ethical guidelines. Patients enrolled were...
Clitoral enlargement in the pediatric population is a rare condition, usually related to problems of sexual differentiation, but malignant and benign clitoral lesions have also been described. We report case newborn infant, investigated at birth for an intersex disorder because clitoromegaly. Hormonal screening was normal ultrasound (US) did not show pelvic or abdominal mass. Three weeks later, lesion larger, tense erythematous. An abscess suspected. A drainage then performed,...
Hereditary multiple exostosis (HME) is a rare skeletal genetic disorder with and disseminated osteochondromas. Costal localization found in 40% of cases. Surgery for asymptomatic lesions remains controversial, but some can be life-threatening. We report the case 10-year-old girl HME, who developed sharp costal compressing hepatic parenchyma, which prophylactic resection was decided. The complete excision lesion performed through extraperitoneal approach under video-assisted laparoscopy...