Abstract:

Herediter multiple exostosis (HME) is an autosomal dominant transitional syndrome, characterized by exostosis that originate from the jukstaepifizer area of long bones. The main defect is the excess growth of a large number of benign bones (exostosis or osteochondrom) in the jukstaepifizer areas where the endocondral bone formation is deteriorated and the endocondral bone formation is deteriorated. The population is 1/50,000. Clinically, the main approach is the presence of one or more severe, painless masses near the joint. These osteochondroms can also cause growth tension, painful local symptoms, veins, tendons, nerve pressures, limitations in joint movements and neurological findings. Here, the patient, who was diagnosed with HME with a breast pain complaint with the clinic of breast diseases and identified solitary pulmonary nodes in the lung graph, was presented as a rare cause in the distinctive diagnosis of solitary pulmonary nodes.

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