A5016064426- Neuroblastoma Research and Treatments
- Melanoma and MAPK Pathways
- Lung Cancer Research Studies
- Cutaneous Melanoma Detection and Management
- CAR-T cell therapy research
- Thyroid and Parathyroid Surgery
- Genetic factors in colorectal cancer
- Digestive system and related health
- Congenital Diaphragmatic Hernia Studies
- Metastasis and carcinoma case studies
- Thyroid Cancer Diagnosis and Treatment
Ministry of Health
2023
Ministry of Health of the Russian Federation
2020
Genetically caused medullary thyroid cancer (MTC) is associated with unfavorable survival prognosis, so it makes necessary to develop new diagnostic techniques reveal pre-clinical stage of disease as well introduce into clinical practice the effective method tumor prevention. The article represents first in Russia summary experience prophylactic thyroidectomy have been executed period 1998 – 2015 yeas among ten bearers RET gene germlinemutation families hereditary including syndrome MEN2A...
Introduction. Skin melanoma in children is a very rare disease that differs many aspects from skin adults. The conventional criteria for clinical diagnostics of observed adults are often absent and adolescents, making it difficult to make diagnosis on time. Objective. aim the study assess significance various diagnostic analysis case congenital pigment neoplasm child. Materials methods. melanocytic lesion wrist joint area girl 5 months old. During primary diagnosis, an ultrasound examination...
Background . Hereditary polyposis syndromes (HPS) are a group of rare genetic diseases characterized by multiple epithelial lesions in the gastrointestinal tract (GIT) with high risk malignancy and neoplasia development other localizations. The case follow-up tactics hereditary polyposes have significant differences, differential diagnosis can be complicated due to phenotype variability clinical manifestations similarity. Objective. aim study is determine role molecular testing endoscopic...