uncommon cone-beam computerized tomography findings in mccune-albright syndrome in an implant candidate patient: a case report
نویسندگان
چکیده
discussion in this patient we preferred following up. afterwards, total surgical lesion resection can be performed. after a long-term follow-up, the area may receive an implant. case presentation a 40-year-old female patient presented an opaque lesion at the left mandibular side of face, in a cone-beam computerized tomography (cbct) view, during the implant placement evaluations. the patient had experienced precocious puberty and had undergone hysterectomy. unilateral cafe-au-lait spots were present on patient’s left side of the face. there was no expansion in intraoral examination. the oral mucosa was also normal. no asymmetry was detected. the analysis of sample histopathology confirmed fibrous dysplasia. introduction mccune-albright syndrome is a rare disease, characterized by triad of cafe-au-lait spots, endocrinopathies and fibrous dysplasia. these bone lesions are usually revealed during the first decade of life, together with pain, pathological fractures and secondary deformities.
منابع مشابه
McCune-Albright syndrome: Report of a case
A 29- year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. On physical examination café au lait macular spots were noted on her neck, buttocks and left leg. Bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. Considering the presence of polyostotic fibrous...
متن کاملMcCune-Albright syndrome: a case report.
Fibrous dysplasia is a benign bone lesion of unknown etiology. Bone involvement usually is solitary (monostotic). Multiple forms (polyostotic) associated with extra skeletal symptoms, particularly cutaneous pigmentation, endocrine dysfunction and precocious puberty is called McCune-Albright syndrome (MAS). We report the case of a 40-year-old man who presented with left mandibular body expansion...
متن کاملMcCune-Albright syndrome. Report of a case.
The McCune Albright syndrome is seldom encountered and rarely reported in dental literature. It represents a special category of polyostic fibrous displasia associated with skin pigmentation and endocrine disturbances. We describe the case of a 9-year-old boy with the McCune Albright syndrome, who was treated for a mandibular osteolytic lesion.
متن کاملMcCune-Albright Syndrome: A Case Report and Literature Review
McCune-Albright syndrome (MAS) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. The disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities. We describe a girl patient with MAS having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. Clinical presentat...
متن کاملA Case of Mccune- Albright Syndrome
Four year old girl was evaluated for precocious puberty. Breast development and pubic hair growth had started at age 2½ year, and had been followed by vaginal bleeding resembling periods. Gaf-au-lait spots were present in most of her skin surface. Bone x-rays showed multiple cysts in pelvis and the metaphysis of femur. Diagnosis of McCune-Albright syndrome was made. Concentrations of all hormon...
متن کاملmccune-albright syndrome: report of a case
a 29- year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. on physical examination café au lait macular spots were noted on her neck, buttocks and left leg. bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. considering the presence of polyostotic fibrous dysplasia, precocious pubert...
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عنوان ژورنال:
avicenna journal of dental researchجلد ۵، شماره ۱، صفحات ۰-۰
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