骨斑病

The patient was diagnosed with osteopoikilosis, characterized by multiple spotted bone densities throughout the skeleton.
患者被诊断为骨斑点症，其特征是全身骨骼中存在多个斑点状骨密度。
Osteopoikilosis is an uncommon genetic skeletal disorder that often presents as asymptomatic.
骨斑点症是一种罕见的遗传性骨骼疾病，通常表现为无症状。
In the X-ray report, osteopoikilosis manifested as numerous small, round, and well-defined spots in the bones.
在X光报告中，骨斑点症表现为骨内存在许多小而圆、边界清晰的斑点。
Although osteopoikilosis is benign, it can sometimes be mistaken for metastatic bone disease.
尽管骨斑点症是良性的，但有时可能会被误诊为转移性骨病。
People with osteopoikilosis typically have no associated symptoms unless it's complicated by other conditions like melorheostosis.
骨斑点症患者通常没有相关症状，除非它与其它如梅洛赫斯特综合症等病症并发。
A family history of osteopoikilosis suggests its autosomal dominant inheritance pattern.
家族中有骨斑点症病例表明了该病可能具有常染色体显性遗传模式。
Treatment for osteopoikilosis primarily focuses on managing any related pain or complications rather than targeting the condition itself.
对骨斑点症的治疗主要集中在管理任何相关的疼痛或并发症上，而不是针对病症本身。
Despite being a congenital condition, osteopoikilosis may not be detected until adulthood during routine radiographic examination.
尽管骨斑点症是一种先天性疾病，但在常规放射学检查中可能直到成年后才会被发现。
There is currently no cure for osteopoikilosis; however, periodic monitoring to ensure no malignancy development is recommended.
目前尚无法治愈骨斑点症；然而，建议定期监测以确保未发生恶性病变。
Cases of osteopoikilosis are often incidentally discovered during imaging studies performed for unrelated reasons.
骨斑点症病例往往在因其他原因进行影像学检查时偶然发现。