Successful management of a pregnancy complicated by ollier disease and coagulation factors deficiency – A rare case report

Introduction: Ollier disease (OD) is a rare, non-hereditary bone disease characterized by multiple enchondromas with a predilection for the appendicular skeleton or pelvis. Its prevalence is estimated at 1:100,000 people. Patients with OD have a 20-53% increased risk of malignant transformation into chondrosarcoma, visceral, hematologic or gonadal-related malignancies.This is the first case described in Poland and the third in the world of a pregnant patient with Ollier disease.
Source: European Journal of Obstetrics, Gynecology, and Reproductive Biology - Category: OBGYN Authors: Source Type: research