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[钙化性尿毒症性小动脉病(钙化防御):发病率、临床特征及长期预后]

[Calcific uraemic arteriolopathy (calciphylaxis): incidence, clinical features and long term outcomes].

作者信息

Esteve V, Almirall J, Luelmo J, Sáez A, Andreu X, García M

机构信息

Servei de Nefrología, Corporació Sanitaria Parc Taulí, Institut Universitari Parc Taulí (UAB), Sabadell.

出版信息

Nefrologia. 2007;27(5):599-604.

Abstract

UNLABELLED

Calcific uraemic arteriolopathy, also named calciphylaxis, is a rare but serious disorder characterized by medial mural calcification of small vessel leading to tissue ischaemia. It most commonly occurs in end stage renal disease patients on dialysis or recently received renal transplant with chronic nephropathy allograft. The pathogenesis of calciphylaxis is poorly understood. Abnormalities in mineral metabolism are clearly involved, but the specific factors that induces this disorder are not completely known.

OBJECTIVES

Describe the main clinical features, outcomes and follow up of all calciphylaxis cases recorded in our dialysis unit in order to analyse the incidence, the main biologic parameters and the therapeutic background in which calciphylaxis appeared.

MATERIAL AND METHODS

We performed a descriptive study about all the calciphylaxis cases diagnosed at our dialysis unit between the years 1991 and 2005.

RESULTS

8 cases, 6 women. Mean age: 65.3 years. All the patients were on haemodialysis treatment (one previous renal transplant). Mean time on dialysis was 76.6 months. Cumulative incidence was 1.17%. The principal end stage renal disease aethiology was neprhoangioeslerosis in four patients. Secondary hiperparatyrhoidism was present in 4 patients and 2 of them had been paratyrhoidectomized previously. A second cutaneous biopsy was needed for correct diagnosis in 3 patients. Calciphylaxis distal lesions were present in 7 patients. Two cases required urgent paratyrhoidectomy in order to control calciphylaxis. Only in 2 cases a Ca x P product > 60 mg/dL was present and 3 cases had PTHi values higher than 300 pg/mL. Calcium phosphate binders and vitamin D were present in 2 and 4 cases, respectively. One patient with proximal calciphylaxis died due to skin injury infection.

CONCLUSIONS

Calciphylaxis is a rare disorder but not exceptional, related to end stage renal disease patients. The diagnosis requires a high clinical suspicion, being sometimes difficult to distinguish from other entities in spite of pathological study. Proximal distribution of calciphylaxis had worst prognostic. Metabolic disorders and therapeutics background were not different from other patients included in dialysis treatment.

摘要

未标注

钙化性尿毒症小动脉病,也称为钙化防御,是一种罕见但严重的疾病,其特征是小血管中层壁钙化导致组织缺血。它最常发生在接受透析的终末期肾病患者或近期接受肾移植并患有慢性肾病同种异体移植的患者中。钙化防御的发病机制尚不清楚。矿物质代谢异常显然与之相关,但诱发这种疾病的具体因素尚不完全清楚。

目的

描述我们透析单元记录的所有钙化防御病例的主要临床特征、结局和随访情况,以便分析钙化防御出现时的发病率、主要生物学参数和治疗背景。

材料与方法

我们对1991年至2005年间在我们透析单元诊断出的所有钙化防御病例进行了描述性研究。

结果

8例,6名女性。平均年龄:65.3岁。所有患者均接受血液透析治疗(1例曾接受肾移植)。平均透析时间为76.6个月。累积发病率为1.17%。主要的终末期肾病病因是4例患者的肾血管硬化症。4例患者存在继发性甲状旁腺功能亢进,其中2例此前已接受甲状旁腺切除术。3例患者需要进行第二次皮肤活检以明确诊断。7例患者存在钙化防御远端病变。2例患者需要紧急进行甲状旁腺切除术以控制钙化防御。仅2例患者的钙磷乘积>60mg/dL,3例患者的全段甲状旁腺激素(PTHi)值高于300pg/mL。分别有2例和4例患者使用了磷酸钙结合剂和维生素D。1例近端钙化防御患者因皮肤损伤感染死亡。

结论

钙化防御是一种罕见但并非罕见的疾病,与终末期肾病患者有关。诊断需要高度的临床怀疑,尽管进行了病理研究,但有时仍难以与其他疾病区分开来。钙化防御的近端分布预后最差。代谢紊乱和治疗背景与接受透析治疗的其他患者无异。

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