Cianciolo Rachel E, Rhodes James L, Haskins Mark E, Clubb Fred J, Lees George E
Department of Public Health and Pathobiology, North Caroline State University, Raleigh, North Carolina, USA.
Comp Med. 2011 Oct;61(5):441-4.
Renal failure was diagnosed in an 11-mo-old male domestic shorthair cat from a colony with mucopolysaccharidosis type I lysosomal storage disease. Grossly, the kidneys were enlarged and bulged on cut section. Histology revealed tubular necrosis and regeneration with severe interstitial macrophage accumulation. Tubular epithelial cells and interstitial macrophages were distended by abundant, large cytoplasmic vacuoles. Electron microscopy demonstrated severe tubular epithelial vacuolar degeneration with lysosomes distended by granular debris and mineral precipitates. Interstitial macrophages contained similarly distended lysosomes. Although the initial cause of the tubular injury was not identified, the presence of macrophages laden with storage product most likely exacerbated the disease. The macrophage infiltrate may have caused tubular ischemia by compressing peritubular capillaries and separating tubules from their blood supply. Because the kidney is not normally affected in MPS I, this case is an unusual presentation of a well-characterized disease. Furthermore, this report documents the diagnostic workflow used to investigate a single case of feline acute renal failure in the setting of numerous at-risk laboratory animals.
在一个患有I型黏多糖贮积症溶酶体贮积病的群体中,一只11月龄的雄性家养短毛猫被诊断出肾衰竭。大体上,肾脏肿大,切面膨出。组织学检查显示肾小管坏死和再生,伴有严重的间质巨噬细胞积聚。肾小管上皮细胞和间质巨噬细胞被大量大的细胞质空泡扩张。电子显微镜显示严重的肾小管上皮空泡变性,溶酶体被颗粒碎片和矿物质沉淀扩张。间质巨噬细胞含有类似扩张的溶酶体。虽然肾小管损伤的最初原因尚未确定,但充满贮积产物的巨噬细胞的存在很可能加剧了疾病。巨噬细胞浸润可能通过压迫肾小管周围毛细血管并使肾小管与其血液供应分离而导致肾小管缺血。由于肾脏在MPS I中通常不受影响,该病例是一种特征明确疾病的不寻常表现。此外,本报告记录了在众多有风险的实验动物背景下用于调查一例猫急性肾衰竭的诊断流程。