Yao Ada Lyn M, Camacho Pauline M
Osteoporosis and Metabolic Bone Disease Center, Loyola University Medical Center.
Endocr Pract. 2014 Jun;20(6):e106-11. doi: 10.4158/EP13352.CR.
We present a case of osteomesopyknosis, a nonmalignant sclerosing bone dysplasia of the axial skeleton, with unknown etiology and unknown prevalence.
We studied a 49-year-old female who suffered from back and pelvic pain. Her history was obtained, a physical examination performed, and the laboratory results and imaging diagnostics were studied to describe her disease.
A 49-year-old, perimenopausal female suffered excruciating, intermittent, dull back and pelvic pain for 1.5 years. Nonmalignant blastic bone lesions along her spine and pelvis were discovered on computed tomography (CT) and confirmed by magnetic resonance imaging (MRI) and bone scans. Other metabolic/endocrine conditions were ruled out. Her son also has similar symptoms, and corresponding changes were observed on his vertebrae MRI. Both were diagnosed with osteomesopyknosis.
Osteomesopyknosis is a rare, autosomal dominant condition characterized by nonmalignant osteosclerosis restricted to the axial skeleton. The disease may produce chronic low-grade back pain in the thoracic and lumbar regions.
我们报告一例骨致密性骨病,这是一种累及中轴骨骼的非恶性硬化性骨发育异常,病因不明,发病率未知。
我们研究了一名49岁患有背部和骨盆疼痛的女性。获取了她的病史,进行了体格检查,并研究了实验室检查结果和影像学诊断以描述她的病情。
一名49岁的围绝经期女性遭受了1.5年的剧烈、间歇性钝痛,累及背部和骨盆。计算机断层扫描(CT)发现其脊柱和骨盆有非恶性成骨性骨病变,磁共振成像(MRI)和骨扫描证实了这一结果。排除了其他代谢/内分泌疾病。她的儿子也有类似症状,其脊椎MRI检查也观察到了相应变化。两人均被诊断为骨致密性骨病。
骨致密性骨病是一种罕见的常染色体显性疾病,其特征为仅限于中轴骨骼的非恶性骨硬化。该疾病可能会导致胸腰椎区域慢性轻度背痛。