Hesse E, Brand J, Bastian L, Krettek C, Meller R
Department of Orthopaedics and Cell Biology, Yale University School of Medicine, 333 Cedar Street, SHM-IE 55, P.O. Box 208044, New Haven, CT 06520-8044, USA.
Unfallchirurg. 2008 Jul;111(7):553-8. doi: 10.1007/s00113-007-1368-6.
Melorheostosis is a rare, benign, and sporadically occurring osteosclerosis of unknown cause. The onset of the disease is usually in early adulthood. Melorheostosis affects both genders, develops progressively, and is usually limited to one side of the human body. The sclerosis originates predominantly from the cortices of the long bones of the lower limbs and rarely the upper limbs. Frequently, the sclerosis involves the soft tissue surrounding the affected bones which may cause limitations in the range of motion, contractures, deformities, and pain. Melorheostosis is usually diagnosed by radiograms. Pain relief and restoration of the full range of motion are the primary goals of the therapeutic approach. A good outcome cannot always be achieved and a recurrence of the disease happens very often.
肢骨纹状肥大是一种罕见的、良性的、偶发的病因不明的骨硬化症。该病通常在成年早期发病。肢骨纹状肥大男女均可发病,呈进行性发展,且通常局限于人体一侧。硬化主要起源于下肢长骨的皮质,上肢很少受累。通常,硬化累及患骨周围的软组织,这可能导致活动范围受限、挛缩、畸形和疼痛。肢骨纹状肥大通常通过X线片诊断。缓解疼痛和恢复全范围活动是治疗方法的主要目标。不一定总能取得良好的效果,而且该病经常复发。