Hara Shigeo, Yamaguchi Yutaka, Hara Shigeko, Tanimoto Akihide, Seki Kunihiko, Matsushita Hiroshi, Tomikawa Shinji, Kuzuhara Keihachiro
Department of Pathology, Toranomon Hospital, Tokyo, Japan.
Clin Transplant. 2005;19 Suppl 14:32-40. doi: 10.1111/j.1399-0012.2005.00402.x.
We conducted the present study to elucidate the fate of post-transplant mesangial IgA deposit under the long-term observation. Out of a total of 45 cases with post-transplant mesangial IgA deposition, nine cases with more than 4 yr of follow-up term were enrolled in this study, and clinicopathologic characteristics were described. The study included three men and six women with a mean age of 34.2 yr. The average observation time from the detection of mesangial IgA deposition was 6.1 yr. Three cases were categorized as recurrent IgA nephropathy, while six cases were classified into latent mesangial IgA deposition. One case with hypertension developed end-stage renal disease. The significant improvement in microscopic hematuria was observed in one recurrent IgA nephropathy case. Microscopic findings included mild mesangial stalk thickening in all but one case. IgA deposition demonstrated a significant decrease in three latent mesangial IgA deposition cases. No apparent reduction in dense deposit quantity was observed on electron microscopy. There was no association between clinicopathologic findings and the regimen of anti-immunosuppressive agents. This study showed the improvement of the disease activity did occur in both recurrent IgA nephropathy and latent mesangial IgA deposition. Further investigation of latent mesangial IgA deposition may present the important clue to the pathogenesis of IgA nephropathy.
我们开展本研究以在长期观察下阐明移植后系膜IgA沉积物的转归。在总共45例有移植后系膜IgA沉积的病例中,9例随访期超过4年的病例被纳入本研究,并描述其临床病理特征。该研究包括3名男性和6名女性,平均年龄为34.2岁。从检测到系膜IgA沉积起的平均观察时间为6.1年。3例被归类为复发性IgA肾病,而6例被归类为潜伏性系膜IgA沉积。1例患有高血压的患者发展为终末期肾病。在1例复发性IgA肾病病例中观察到镜下血尿有显著改善。镜下表现除1例病例外均包括轻度系膜基质增厚。在3例潜伏性系膜IgA沉积病例中,IgA沉积显著减少。电镜检查未观察到致密沉积物数量有明显减少。临床病理表现与免疫抑制剂治疗方案之间无关联。本研究表明复发性IgA肾病和潜伏性系膜IgA沉积的疾病活动度均有改善。对潜伏性系膜IgA沉积的进一步研究可能为IgA肾病的发病机制提供重要线索。