[LANTHANUM DEPOSITS AS A RARE DIFFERENTIAL DIAGNOSIS OF VILLOUS ATROPHY].

Harefuah Pub Date : 2024-11-01
Rachel Gingold-Belfer, Matan Siterman, Shira Goldman, Lucille Hayman Manzur
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Abstract

Introduction: Up to 5% of patients with newly diagnosed celiac disease have negative serology. Although seronegative celiac, is the most common cause for villous atrophy, there are other differential diagnoses that should be ruled out when we find villous blunting without positive serology for celiac disease. The aetiologies are usually divided into 5 categories: immune-mediated, infectious, iatrogenic, inflammatory and infiltrative. We hereby report a case of 39 years old male, with end-stage renal failure and pancreatic insufficiency. He was treated with peritoneal dialysis and was a candidate for combined kidney-pancreas transplantation. Hyperphosphatemia is a common complication in patients with end-stage renal disease. In order to reduce his serum phosphate levels, he was treated with a high dose of lanthanum carbonate, one of the most effective and safe non-calcium-based phosphate binders. During weight loss investigation, he underwent gastroscopy that demonstrated duodenal denudated mucosa with villous blunting. Biopsy showed complete villous atrophy and accumulation of foreign material in mucosal histiocytes. Von Kossa staining, that was performed, emphasized the depositions of the foreign material that has been identified as lanthanum. Consequently, the treatment with lanthanum was stopped and replaced by another phosphate binder. This case illustrates a rare differential diagnosis of villous atrophy typical for end-stage renal disease patients, that can be categorized as an iatrogenic and infiltrative aetiology for villous atrophy. Since the long-term consequences of lanthanum deposition in tissue are unknown, this case also emphasizes the need for a multidisciplinary approach for treating dialysis patients, in order to understand which phosphate binder was provided.

[镧沉积是绒毛萎缩的罕见鉴别诊断]。
介绍:在新确诊的乳糜泻患者中,血清学阴性者高达 5%。虽然血清学阴性的乳糜泻是导致绒毛萎缩的最常见原因,但当我们发现绒毛发育不良而乳糜泻血清学检测未呈阳性时,还应排除其他鉴别诊断。病因通常分为 5 类:免疫介导型、感染性、先天性、炎症性和浸润性。我们在此报告一例 39 岁的男性患者,他患有终末期肾衰竭和胰腺功能不全。他接受了腹膜透析治疗,是肾胰联合移植的候选者。高磷血症是终末期肾病患者常见的并发症。为了降低血清磷酸盐水平,他接受了大剂量碳酸镧治疗,碳酸镧是最有效、最安全的非钙磷酸盐结合剂之一。在减肥调查期间,他接受了胃镜检查,结果显示十二指肠粘膜变性,绒毛变细。活检显示绒毛完全萎缩,粘膜组织细胞内有异物堆积。冯-科萨染色法显示,异物沉积已被确认为镧。因此,医生停止了镧的治疗,并用另一种磷酸盐粘合剂取而代之。本病例是典型的终末期肾病患者绒毛萎缩的罕见鉴别诊断,可归类为绒毛萎缩的先天性和浸润性病因。由于镧沉积在组织中的长期后果尚不清楚,本病例还强调了采用多学科方法治疗透析患者的必要性,以便了解提供的是哪种磷酸盐结合剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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