Résumé
Pulmonary capillary haemangiomatosis (PCH) is a rare disorder of unknown aetiology, characterised by proliferating capillaries that invade the pulmonary interstitium, alveolar septae and the pulmonary vasculature. It is often mis-diagnosed as primary pulmonary hypertension and pulmonary veno-occlusive disease. Pulmonary capillary haemangiomatosis is a locally aggressive benign vascular neoplasm of the lung. We report the case of a 19-year-old female who was referred to us in the early post-partum period with severe pulmonary artery hypertension, which was diagnosed as PCH by open lung biopsy.
Sujets)
Biopsie , Diagnostic différentiel , Femelle , Hémangiome capillaire/diagnostic , Hémangiome capillaire/physiopathologie , Hémangiome capillaire/thérapie , Humains , Hypertension pulmonaire/diagnostic , Hypertension pulmonaire/étiologie , Hypertension pulmonaire/physiopathologie , Hypertension pulmonaire/thérapie , Poumon/anatomopathologie , Poumon/imagerie diagnostique , Tumeurs du poumon/diagnostic , Tumeurs du poumon/physiopathologie , Tumeurs du poumon/thérapie , Oxygénothérapie/méthodes , Chirurgie thoracique vidéoassistée/méthodes , Jeune adulteRésumé
The ideal goal of prosthetic dentistry is to restore the form and function of the missing structures as close to natural as possible. The introduction of implants have revolutionized the field of restorative dentistry and this article evaluates the merits and demerits of the immediate loading implants