输尿管原发性局限性淀粉样变性,表现为输尿管结石

Se Min Jang, Hulin Han, Young Jin Jun, Jongmin Sim, Hye In Ahn, Tchun Yong Lee, Ki-Seok Jang, Seung Sam Paik
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引用次数: 1

摘要

原发性尿路局限性淀粉样变性是一种罕见的疾病,在临床表现和诊断影像学研究中通常与恶性肿瘤或炎症相似。我们报告一位77岁男性患者,在左侧输尿管上部出现局部淀粉样变。患者就诊主诉无痛性肉眼血尿和排尿困难1个月。实验室检查仅发现血尿。尿细胞学检查无明显异常。腹部电脑断层显示输尿管内有钙化的阻塞肿块。临床表现为输尿管结石或恶性肿瘤。行肾输尿管切除术。输尿管呈节段性纤维化增厚伴管腔梗阻。镜检显示有淡色嗜酸性无定形物质沉积,并伴有钙化和骨化。刚果红染色显示淀粉样蛋白沉积,偏光显微镜呈阳性。虽然其发病率很少见,但在输尿管肿瘤病变的鉴别诊断中应考虑局限性淀粉样变,以避免不必要的手术。
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Primary localized amyloidosis of the ureter presenting as a ureteral stone

Primary localized amyloidosis of the urinary tract is a rare disease, usually mimicking a malignancy or inflammation in its clinical presentation and in diagnostic imaging studies. We present a case of localized amyloidosis arising in the left upper ureter in a 77-year-old man. The patient visited the hospital complaining of painless gross hematuria and dysuria for 1 month. Laboratory examination revealed hematuria only. Urine cytology was unremarkable. Abdominal computed tomography revealed an obstructing mass with calcification in the ureter. The clinical impression was of a ureteral stone or malignancy. A nephroureterectomy was performed. The ureter showed segmental fibrotic thickening with luminal obstruction. Microscopic examination revealed deposition of pale-eosinophilic amorphous material with calcification and ossification. Congo-red staining showed amyloid deposits with positive polarizing microscopic findings. Although its incidence is rare, localized amyloidosis should be considered in the differential diagnosis of ureteral tumorous lesions to avoid unnecessary surgery.

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