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- calcinosis universalis 全身性钙质沉着
- Scrotal calcinosis: Is the cause still unknown? 阴囊钙质沉着症:病因是否仍不清楚?
- James Gregory gave in in his "Geometriae Pars Universalis" a method of rectifying curves. james Gregory在他的《几何的通用部分》中给出了计算曲线长度的方法。
- James Gregory gave in his "Geometriae Pars Universalis" a method of rectifying curves. James Gregory在他的《几何的通用部分》中给出了计算曲线长度的方法。
- The main chemistry formations are silica.The major cemented matters are calcinosis. 砾岩的主要成分是矽质，胶结物主要为钙质。
- No epithelial cells were found. hence. a cytological diagnosis of idiopathic calcinosis of the scrotum was suggested. 因未发现上皮细胞.;因此建议对阴囊自发性钙沈淀症进行细胞性诊断
- A case of localized linear discoid lupus erythematosus with cutaneous calcinosis is reported. 报告1例线状盘状红斑狼疮伴皮肤钙沉着症。患者女,36岁。
- Alopecia universalis is the rarest form of alopecia areata and presents itself as the loss of hair over the entire scalp and body. 脱发泛是稀有形式斑秃，并提出自己的损失头发整个头皮和身体。
- Three cases of alopecia universalis during PEG-IFN and ribavirin combination therapy have been reported in the literature. 国内外文献已报道3例在聚乙二醇干扰素与利巴韦林联合治疗过程中出现普脱的案例。
- Method:A case of scrotal calcinosis was analyzed and the literatue was reviewed. 方法:分析1例阴囊特发性钙盐沉着症的诊断与治疗并复习相关文献。
- No epithelial cells were found, hence, a cytological diagnosis of idiopathic calcinosis of the scrotum was suggested. 因未发现上皮细胞，因此建议对阴囊自发性钙沈淀症进行细胞性诊断。
- Methods Eleven intervertebral discs with Calcinosis in 9 cases were evaluated retrospectively. 方法对9例11个钙化性椎间盘病的颈椎片进行回顾性分析。
- Conclusion:Scrotal calcinosis is an extremely uncommon.Scrotal calcinosis has to be differentiated with steatocystoma multiplex. 结论:阴囊特发性钙盐沉着症临床罕见,本病需与多发性脂囊瘤相鉴别。
- One calcification faded away in 3 months.Conclusion: Intervertebral calcinosis in children is a benign self-limited disease. 结果：4例患儿中发现5处椎间盘钙化，经对症治疗后症状消失，其中一处椎间盘钙化在3个月后消失。
- If sclerodactyly is seen along with calcinosis, Raynaud's phenomenon, esophageal dysmotility, and telangietastias, then the best diagnosis is CREST syndrome. 如果指端硬皮病伴钙化;雷诺现象，食道蠕动障碍和毛细血管扩张症;称为CREST综合症.
- No cellular structures were noted. Histopathology confirmed the diagnosis of idiopathic calcinosis of the scrotum. No recurrence was observed after a six months' follow-up period. 并未发现细胞性结构。组织病理学确认这项对阴囊自发性钙沈淀症所做的诊断。经过六个月追踪治疗期后病患未再发。
- Conclusion: Intervertebral calcinosis in children is a benign self-limited disease.Familiar with its pathophysiologic course will help to avoid unnecessary surgery. 结论：儿童钙化性椎间盘病是良性自限性疾病，认识该病的病理生理过程，避免不必要的手术创伤。
- Result:A 37-year-old man,with hard and white nodule on the Scrotum for 7 years.Histological examination of white nodule showed Calcinosis of the Scrotum. 结果:患者男,37岁,阴囊起白色硬性结节7a,病理符合阴囊特发性钙盐沉着症。
- No cellular structures were noted. Histopathology confirmed the diagnosis of idiopathic calcinosis of the scrotum. No recurrence was observed after a six months＇ follow-up period. 并未发现细胞性结构.;组织病理学确认这项对阴囊自发性钙沈淀症所做的诊断
- acrodystrophia universalis hereditaria 遗传性普遍性肢营养不良
