首页> 外文期刊>Peritoneal dialysis international: Journal of the International Society for Peritoneal Dialysis >Uremic tumoral calcinosis in patients on peritoneal dialysis: clinical, radiologic, and laboratory features.
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Uremic tumoral calcinosis in patients on peritoneal dialysis: clinical, radiologic, and laboratory features.

机译:腹膜透析患者的尿毒症肿瘤煅烧:临床,放射学和实验室特征。

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BACKGROUND: Uremic tumoral calcinosis (UTC) has been analyzed in uremic patients on hemodialysis, but little is known about UTC in peritoneal dialysis (PD). In this study, we aimed to characterize UTC in uremic patients on PD. METHODS: We retrospectively reviewed uremic patients on PD who developed UTC over a 9-year period. Clinical, radiologic, and laboratory features; treatments; and outcomes in those patients were assessed. One of the patients (case 7) is described as a case example. RESULTS: The study enrolled 7 patients with a mean age of 41 years. Mean time from PD to UTC was 45.3 months. All patients were anuric but adequately dialyzed. Cardinal symptoms were local tenderness and limited range of joint motion. Lesions were mostly multifocal (n=6) and predominantly involved shoulders, hands, feet, hips, and wrists. Metatarsophalangeal joint UTC was misdiagnosed as tophaceous gout in 2 patients. Main laboratory findings were hyperphosphatemia (7.9 +/- 0.8 mg/dL), high CaxP product [>65 mg(2)/dL(2) (range: 81.1 +/- 11.5 mg(2)/dL(2))], secondary hyperparathyroidism (SHPT) with various levels of intact parathyroid hormone (iPTH: 592.2 +/- 315.2 pg/mL; <250 pg/mL in 2 patients). Medical treatments for UTC included P restriction, non-Ca-based phosphate binders, and adequate dialysis with low-Ca dialysate, but all treatments were ineffective. Parathyroidectomy (n=3) can partially ameliorate UTC, but only 1 patient (case 7), who had extremely high iPTH (1085 pg/mL), manifested hungry bone syndrome (HBS) and had remarkable resolution of UTC. By contrast, in patients who underwent renal transplantation (n=3), UTC completely resolved by about 1 year after surgery. CONCLUSIONS: Uremic tumoral calcinosis develops in anuric PD patients with uncontrolled hyperphosphatemia; it is usually multifocal, occurring around the weight-bearing joints or overused smaller joints. Aggressive medical therapy alone is ineffective, and parathyroidectomy appears to be unsatisfactory except in the presence of severe SHPT with postoperative HBS.
机译:背景:在血液透析的尿毒症患者中对尿毒症肿瘤煅烧(UTC)进行了分析,但对腹膜透析(PD)中的UTC知之甚少。在这项研究中,我们旨在表征PD尿毒症患者的UTC。方法:我们回顾性研究了在9年内出现UTC的PD尿毒症患者。临床,放射学和实验室特征;治疗;并评估了这些患者的结局。将其中一名患者(案例7)作为案例进行说明。结果:该研究招募了7名平均年龄为41岁的患者。从PD到UTC的平均时间为45.3个月。所有患者均为无尿,但已充分透析。主要症状是局部压痛和关节活动受限。病变多为多灶性(n = 6),主要累及肩膀,手,脚,臀部和手腕。 2趾关节UTC被误诊为2例吞咽痛风。实验室的主要发现是高磷酸盐血症(7.9 +/- 0.8 mg / dL),高CaxP产物[> 65 mg(2)/ dL(2)(范围:81.1 +/- 11.5 mg(2)/ dL(2))] ,继发性甲状旁腺功能亢进症(SHPT)和各种水平的完整甲状旁腺激素(iPTH:592.2 +/- 315.2 pg / mL; 2名患者<250 pg / mL)。 UTC的药物治疗包括磷限制剂,非钙基磷酸盐结合剂以及用低钙透析液进行充分透析,但所有治疗均无效。甲状旁腺切除术(n = 3)可以部分改善UTC,但只有1名患者(病例7),其iPTH极高(1085 pg / mL),表现出饥饿骨综合征(HBS),并且具有显着的UTC分辨率。相比之下,在接受肾移植的患者(n = 3)中,UTC在手术后约一年后完全消退。结论:无控制性高磷血症的无尿PD患者发展为尿毒症肿瘤钙化。它通常是多灶性的,发生在负重关节周围或过度使用的较小关节周围。仅仅积极的药物治疗是无效的,并且甲状旁腺切除术似乎不能令人满意,除非存在严重的SHPT伴术后HBS。

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