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首页> 外文期刊>Asia Oceania Journal of Nuclear Medicine & Biology >Sagliker Syndrome in a Patient with Secondary Hyperparathyroidism and Chronic Renal Insufficiency: A Case Report
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Sagliker Syndrome in a Patient with Secondary Hyperparathyroidism and Chronic Renal Insufficiency: A Case Report

机译:继发性甲状旁腺功能亢进和慢性肾功能不全患者的Sagliker综合征:一例报告

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Sagliker syndrome is a rare form of renal osteodystrophy resulted from untreated secondary hyperparathyroidism. It is described by severe skeletal deformities, high level of PTH in patients with chronic renal failure, and deformed face. This paper reports a 44-year-old male patient with the mentioned characteristics. In addition to the unique clinical features, high levels of ALP and PTH hormones encouraged us to search for syndrome-like a disease, which clinically and paraclinically matched the Sagliker syndrome.This case highlights the importance of clinicians’ attention for earlymonitoring and appropriate treatment as it is shown to be effective in preventing irreversible complications such as soft tissue and bone abnormalities and cardiovascular impairment in patients with Sagliker syndrome. Therefore, considering the syndrome isrecommended as one of the diagnostic hypothesis in young patients with renal insufficiency, secondary hyperparathyroidism, and skeletal deformities.
机译:Sagliker综合征是罕见的继发性甲状旁腺功能亢进导致的肾性骨营养不良。严重的骨骼畸形,慢性肾功能不全患者的PTH水平高以及面部畸形可以描述该疾病。本文报道了一名具有上述特征的44岁男性患者。除了独特的临床特征外,高水平的ALP和PTH激素还鼓励我们寻找与Sagliker综合征在临床上和旁临床上相匹配的类似综合征的疾病。该病例强调了临床医生重视早期监测和适当治疗的重要性。它被证明可有效预防Sagliker综合征患者不可逆的并发症,例如软组织和骨骼异常以及心血管损害。因此,建议将该综合征作为肾功能不全,继发性甲状旁腺功能亢进和骨骼畸形的年轻患者的诊断假说之一。

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