A5049715856- Oral and Maxillofacial Pathology
- Bone Tumor Diagnosis and Treatments
- Sarcoma Diagnosis and Treatment
- Tumors and Oncological Cases
- Full-Duplex Wireless Communications
- Antenna Design and Analysis
- Polyomavirus and related diseases
- Tuberous Sclerosis Complex Research
- Vascular Tumors and Angiosarcomas
- Soft tissue tumor case studies
- Renal cell carcinoma treatment
- Genetics, Bioinformatics, and Biomedical Research
- Salivary Gland Tumors Diagnosis and Treatment
- Cancer-related molecular mechanisms research
- Skin Diseases and Diabetes
- Reconstructive Surgery and Microvascular Techniques
- Renal and related cancers
- DNA Repair Mechanisms
- Cardiac tumors and thrombi
- Genomics and Chromatin Dynamics
- Nonmelanoma Skin Cancer Studies
- Protein Structure and Dynamics
- Autoimmune Bullous Skin Diseases
- Ear and Head Tumors
- Wound Healing and Treatments
Centre hospitalier régional d'Orléans
2016-2023
Centre Hospitalier Universitaire de Tours
2013-2016
Université de Tours
2013-2016
Inserm
2016
Service de la Santé Publique
2015
Thion Medical (France)
2013-2014
Laboratoire de Biochimie
2013
Recently, YAP1 fusion genes have been demonstrated in eccrine poroma and porocarcinoma, the diagnostic use of immunohistochemistry has highlighted this setting. In other organs, loss expression can reflect rearrangement or transcriptional repression, notably through RB1 inactivation. context, our objective was to re-evaluate performance for diagnosis porocarcinoma.The C-terminal part protein evaluated by 543 cutaneous epithelial tumours, including 27 poromas, 14 porocarcinomas 502 tumours....
Interstitial granulomatous dermatitis (IGD) is a rare skin condition, which in half of the cases associated with rheumatoid arthritis, lupus erythematosus or other inflammatory diseases [1]. Drug causality has been suspected [2-5]. We report case IGD occurring during SAPHO syndrome treated for one month leflunomide (Arava®). Leflunomide was withdrawn no resolution IGD, but exacerbation rheumatism. Ustekinumab (Stelara®) started and disappearance [...]
Angiosarcomas are rare aggressive neoplasms that can occur secondary to chronic lymphedema (Stewart-Treves syndrome). Although angiosarcomas commonly described after-mastectomy and/or after-radiotherapy, few cases have been reported in association with of congenital origin. We report the clinical, pathological, and cytogenetic findings a case cutaneous epithelioid clear cells angiosarcoma occurred 21-year-old woman hemibody lymphedema. Surgical biopsies tumor mass revealed diffuse...
Rhabdomyomas are the most common benign cardiac tumors. They may often be associated with tuberous sclerosis. In many cases, rhabdomyomas undergo spontaneous regression. Here, we report unusual case of an infant a large nonobstructive right ventricular rhabdomyoma at birth and four months age, which subsequently caused severe ventricle outflow tract obstruction six prompting surgery to remove tumor. Close monitoring should done in infants rhabdomyomas.