Mackensen Friederike, Smith Justine R, Rosenbaum James T
Casey Eye Institute, Oregon Health & Science University, Portland, Oregon, USA.
Ophthalmology. 2007 May;114(5):995-9. doi: 10.1016/j.ophtha.2007.01.002. Epub 2007 Mar 26.
Tubulointerstitial nephritis and uveitis syndrome (TINU) is a specific form of uveitis that is unfamiliar to most ophthalmologists. Thus, it is frequently overlooked in differential diagnosis. We hypothesized that recognition of subsets of uveitis can facilitate the diagnosis of rare entities such as TINU.
Retrospective case series.
One thousand nine hundred eighty-five patients with uveitis.
We performed a computerized database analysis of patients evaluated for uveitis at the Casey Eye Institute from September 1985 until May 2005. The database includes details about ocular inflammation, including specific diagnosis, anatomic location, laterality, continuity, onset, complications, HLA-B27 status, and relative diagnostic certainty. Additionally, we reviewed all charts of patients diagnosed with TINU or with a presentation of uveitis that was typical of TINU (i.e., bilateral sudden-onset anterior uveitis).
Prevalence of TINU in identifiable subsets of patients with uveitis, visual acuity (VA), and renal function.
Individuals with TINU (n = 33) represented 1.7% of all patients with uveitis. However, TINU was diagnosed in 32 of the 316 patients (10%) presenting with bilateral sudden-onset anterior uveitis and in 20 of 62 of these patients (32%) who were younger than 20 years. Creatinine levels were more likely to be elevated in patients older than 40. Most patients maintained excellent VA and did not develop clinically significant renal impairment.
Tubulointerstitial nephritis and uveitis syndrome is a common cause of uveitis among patients who present with bilateral sudden-onset anterior uveitis. The size of this series clarifies the understanding of the relationship between renal and ocular disease; facilitates recognition of the syndrome; and adds to the knowledge on prognosis, complications, and role of antecedent medications.
肾小管间质性肾炎并葡萄膜炎综合征(TINU)是一种大多数眼科医生并不熟悉的葡萄膜炎特殊类型。因此,在鉴别诊断中它常被忽视。我们推测,认识葡萄膜炎的不同亚组有助于诊断像TINU这样的罕见疾病。
回顾性病例系列研究。
1985例葡萄膜炎患者。
我们对1985年9月至2005年5月在凯西眼科研究所接受葡萄膜炎评估的患者进行了计算机数据库分析。该数据库包含有关眼部炎症的详细信息,包括具体诊断、解剖位置、单侧或双侧、炎症连续性、发病情况、并发症、HLA - B27状态以及相对诊断确定性。此外,我们查阅了所有被诊断为TINU或具有典型TINU表现(即双侧急性前葡萄膜炎)的患者病历。
葡萄膜炎患者可识别亚组中TINU的患病率、视力(VA)和肾功能。
TINU患者(n = 33)占所有葡萄膜炎患者的1.7%。然而,在316例表现为双侧急性前葡萄膜炎的患者中,有32例(10%)被诊断为TINU,在这些患者中,62例年龄小于20岁的患者中有20例(32%)被诊断为TINU。40岁以上患者的肌酐水平更有可能升高。大多数患者保持了良好的视力,且未出现具有临床意义的肾功能损害。
肾小管间质性肾炎并葡萄膜炎综合征是双侧急性前葡萄膜炎患者中葡萄膜炎的常见病因。本系列研究的规模明确了对肾脏和眼部疾病之间关系的理解;有助于识别该综合征;并增加了关于预后、并发症以及先前用药作用的知识。