Department of Pathology, Emory University School of Medicine, Atlanta, Georgia, USA.
Renal Division, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Kidney Int. 2018 Aug;94(2):390-395. doi: 10.1016/j.kint.2018.03.016. Epub 2018 Jun 7.
A variety of criteria exist for histopathologic diagnosis of calciphylaxis, also known as calcific uremic arteriolopathy but data on their specificity are limited. To assess this, histologic findings of 38 skin biopsies performed for a suspicion of calcific uremic arteriolopathy were compared with histologic findings in skin obtained from healthy margins of 43 amputations in patients with end-stage renal disease (ESRD) without evidence of calcific uremic arteriolopathy. Abnormalities in small arteries or arterioles were present in 35% of amputation specimens and 55% of skin biopsies, and among these only thrombosis but not calcification was significantly more prevalent in skin biopsies. The prevalence of extravascular calcification did not differ. Vascular lesions were more common in skin biopsies from patients with high clinical suspicion of calcific uremic arteriolopathy (81%), significantly driven by increases in both calcification and thrombosis, compared to amputations (35%). The combination of medial calcification and thrombosis was six-fold more prevalent in high-suspicion skin biopsies than in amputation specimens. The location of affected vessels did not differ. In two autopsy cases, some but not all findings of involved skin were also present in uninvolved skin. Thus, histopathologic findings historically associated with calcific uremic arteriolopathy can also occur in viable tissue from unaffected patients with ESRD, calling into question the specificity of individual histologic findings for calcific uremic arteriolopathy. However, the combination of medial calcification and thrombosis was rare in unaffected patients and may provide a higher degree of specificity.
存在多种用于钙化性尿毒症性小动脉病(calciphylaxis)的组织病理学诊断标准,也称为钙化性尿毒症性小动脉病,但关于其特异性的数据有限。为了评估这一点,将怀疑患有钙化性尿毒症性小动脉病的 38 例皮肤活检的组织学发现与来自 43 例终末期肾病(ESRD)患者截肢健康边缘的皮肤的组织学发现进行了比较,这些患者没有钙化性尿毒症性小动脉病的证据。在截肢标本中,35%存在小动脉或小动脉异常,在皮肤活检中为 55%,而在这些标本中,只有血栓形成而不是钙化在皮肤活检中更为普遍。血管外钙化的患病率没有差异。血管病变在钙化性尿毒症性小动脉病临床高度怀疑的患者的皮肤活检中更为常见(81%),与截肢相比(35%),主要是由于钙化和血栓形成的增加。与截肢标本相比,在高度怀疑的皮肤活检中,中层钙化和血栓形成的组合更为常见(六倍)。受影响的血管的位置没有差异。在两例尸检病例中,受影响皮肤的一些但不是所有发现也存在于未受影响的皮肤中。因此,与钙化性尿毒症性小动脉病相关的组织病理学发现也可能发生在无 ESRD 患者的存活组织中,这使得个别组织病理学发现对钙化性尿毒症性小动脉病的特异性受到质疑。然而,中层钙化和血栓形成的组合在未受影响的患者中很少见,可能具有更高的特异性。