Uzun C.Adali M.K.Koten M.Karasalihoglu A.R.2024-06-122024-06-1219990300-0729https://hdl.handle.net/20.500.14551/17053We report a 19-year old female patient with the McCune-Albright syndrome, which is a rare disease consisting of polyostotic fibrous dysplasia (FD) of bone associated with brown pigmented areas of the skin and several endocrine dysfunctions. The patient had FD involving the paranasal sinuses, the middle turbinate and the skull. The endocrine dysfunction of the patient concerns both growth hormone and prolactin hypersecretion. Because the patient had no major symptoms, neither surgical nor medical treatment was applied. Five-year follow-up revealed no complication and enlargement of the lesion.eninfo:eu-repo/semantics/closedAccessFibrous Dysplasia; Growth Hormone; Mccune-Albright Syndrome; Paranasal Sinuses; SkullGrowth Hormone; Prolactin; Adolescent; Albright Syndrome; Article; Cafe Au Lait Spot; Case Report; Edema; Epistaxis; Face Asymmetry; Facial Bone; Female; Fibrous Dysplasia; Growth Hormone Release; Headache; Human; Hyperprolactinemia; Hypertelorism; Hypertrophy; Nose Malformation; Nose Obstruction; Nose Septum; Paranasal Sinus; Telecanthus; Adolescent; Disease Progression; Female; Fibrous Dysplasia, Polyostotic; Follow-Up Studies; Humans; Paranasal Sinuses; Tomography, X-Ray ComputedArticle3731221242-s2.0-003275663810567991Q1