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IgG4-Related Disease: Dataset of 235 Consecutive Patients

机译:IgG4相关疾病:235名连续患者的数据集

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摘要

Immunoglobulin G4-related disease (IgG4-RD) is a recently discovered systemic condition, in which various organ manifestations are linked by a similar histological appearance. Our knowledge of this condition is still fragmented, as most studies have examined only a few dozen patients or focused on a particular organ manifestation. This study was conducted to learn the demography and patient characteristics of IgG4-RD using a large cohort. A total of 235 consecutive patients with IgG4-RD, diagnosed in 8 general hospitals in the same medical district, were identified by searching the institutions’ radiology database. Inclusion criteria were histology-proven IgG4-RD according to the Pathology Consensus Statement and/or definitive type 1 autoimmune pancreatitis meeting the International Consensus Diagnostic Criteria. Clinical notes and images of selected patients were retrospectively reviewed. All patients were adults (M/F = 4/1). The median age was 67 years (range 35–86). Nine tenths were diagnosed in their 50s to 70s. Among 486 manifestations identified in total, the most common was pancreatitis diagnosed in 142 patients (60%), followed by sialadenitis (34%), tubulointerstitial nephritis (23%), dacryoadenitis (23%), and periaortitis (20%). The majority of patients (95%) had at least 1 of the 5 most common manifestations. Male and female patients differed in their organ manifestations (periaortitis more common in males and sialodacryoadenitis more common in females). Serum IgG4 (normal ≤135 mg/dL) was elevated to >135 mg/dL in 208 patients (88%) and >270 mg/dL in 167 (71%). The IgG4 value was significantly higher in patients with multiorgan involvement than in those with a single manifestation (median 629 mg/dL vs 299 mg/dL, P 10% in 194 (89%). Corticosteroids were effective, but the relapse rate was estimated to be 24% in the study period (median 37 months). During the follow-up, 15 malignant diseases were diagnosed in 13 patients (6%). This figure is similar to the incidence (12.9 cancers) expected from the Japanese nationwide study for cancer epidemiology (standardized incidence ratio 1.16). In conclusion, this reliable dataset could improve the characterization of IgG4-RD, particularly its unique demography and the frequency of each organ manifestation.
机译:免疫球蛋白G4相关疾病(IgG4-RD)是最近发现的一种全身性疾病,其中各种器官表现都通过相似的组织学表现联系在一起。我们对这种疾病的了解仍然是零散的,因为大多数研究仅检查了几十名患者或关注特定器官的表现。进行这项研究的目的是使用大型队列研究IgG4-RD的人口统计学和患者特征。通过搜索该机构的放射学数据库,共鉴定了在同一医学区的8家综合医院中确诊的235例IgG4-RD连续患者。入选标准是根据病理学共识声明进行组织学验证的IgG4-RD和/或符合国际共识诊断标准的确定的1型自身免疫性胰腺炎。回顾性分析所选患者的临床笔记和图像。所有患者均为成人(男/女= 4/1)。中位年龄为67岁(范围35-86)。在50到70年代,有十分之九的人被诊断出来。在总共鉴定出的486种表现中,最常见的是在142例患者中诊断出的胰腺炎(60%),其次是骨腺炎(34%),肾小管间质性肾炎(23%),泪腺炎(23%)和腹膜炎(20%)。大多数患者(95%)至少有5种最常见的表现之一。男性和女性患者的器官表现有所不同(男性腹膜炎多见,女性唾液酸腺腺炎多见)。 208名患者(88%)的血清IgG4(正常值≤135mg / dL)升高至> 135 mg / dL,而167名患者(71%)升高至> 270 mg / dL。多器官受累患者的IgG4值明显高于单一表现的患者(中位值629 mg / dL与299 mg / dL,194%P 10%(89%)。皮质类固醇有效,但估计复发率在研究期间(平均37个月)为24%。在随访期间,有13位患者被诊断出15种恶性疾病(6%),这一数字与日本全国性研究预期的发病率(12.9种癌症)相似总之,这个可靠的数据集可以改善IgG4-RD的特性,特别是其独特的人口统计学和每个器官表现的频率。

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