中华肾脏病杂志
中華腎髒病雜誌
중화신장병잡지
2014年
7期
481-485
,共5页
李融融%李航%文煜冰%黄庆元%段琳%李艳
李融融%李航%文煜冰%黃慶元%段琳%李豔
리융융%리항%문욱빙%황경원%단림%리염
显微镜检查,电子%病理学,临床%血尿%肾小球轻微病变%薄基底膜肾病%系膜增生性肾小球肾炎
顯微鏡檢查,電子%病理學,臨床%血尿%腎小毬輕微病變%薄基底膜腎病%繫膜增生性腎小毬腎炎
현미경검사,전자%병이학,림상%혈뇨%신소구경미병변%박기저막신병%계막증생성신소구신염
Microscopy,electron%Pathology,clinical%Hematuria%Glomerular minor lesion%Thin basement membrane nephropathy%Mesangial proliferative glomerulonephritis
目的 对肾小球轻微病变(glomerular minor lesion,GML)进行临床及电镜病理的分类总结,进一步明确该病理表现的性质及意义,探讨其与临床表现的相关性.方法 纳入北京协和医院2003年1月7日至2008年12月2日经光镜及免疫荧光病理诊断为GML、同时电镜病理资料完整的患者148例,回顾性分析其临床及病理资料.结果 孤立性血尿是患者最常见的临床表现,其次为血尿合并少量蛋白尿及单纯蛋白尿,部分患者可并存高血压、特殊自身免疫表现、肝炎标志物阳性等.经电镜检查明确,GML可最终呈现各种不同的病理表现:薄基底膜肾病(66.2%)、系膜增生性肾小球肾炎(20.3%)、Alport综合征(2.7%)、膜性肾病(3.4%)以及正常组织(4.7%)等.结合临床与病理,表现为孤立性血尿的GML患者,经电镜病理检查诊断为薄基底膜肾病的可能性最大(76.9%).部分患者存在蛋白尿、高血压等提示不良预后的情况.结论 GML只是一种对肾脏病理表现的粗泛描述,对应的电镜病理具有较大异质性,临床意义各异,需积极完善电镜病理,结合临床特点,明确最终诊断,指导治疗.
目的 對腎小毬輕微病變(glomerular minor lesion,GML)進行臨床及電鏡病理的分類總結,進一步明確該病理錶現的性質及意義,探討其與臨床錶現的相關性.方法 納入北京協和醫院2003年1月7日至2008年12月2日經光鏡及免疫熒光病理診斷為GML、同時電鏡病理資料完整的患者148例,迴顧性分析其臨床及病理資料.結果 孤立性血尿是患者最常見的臨床錶現,其次為血尿閤併少量蛋白尿及單純蛋白尿,部分患者可併存高血壓、特殊自身免疫錶現、肝炎標誌物暘性等.經電鏡檢查明確,GML可最終呈現各種不同的病理錶現:薄基底膜腎病(66.2%)、繫膜增生性腎小毬腎炎(20.3%)、Alport綜閤徵(2.7%)、膜性腎病(3.4%)以及正常組織(4.7%)等.結閤臨床與病理,錶現為孤立性血尿的GML患者,經電鏡病理檢查診斷為薄基底膜腎病的可能性最大(76.9%).部分患者存在蛋白尿、高血壓等提示不良預後的情況.結論 GML隻是一種對腎髒病理錶現的粗汎描述,對應的電鏡病理具有較大異質性,臨床意義各異,需積極完善電鏡病理,結閤臨床特點,明確最終診斷,指導治療.
목적 대신소구경미병변(glomerular minor lesion,GML)진행림상급전경병리적분류총결,진일보명학해병리표현적성질급의의,탐토기여림상표현적상관성.방법 납입북경협화의원2003년1월7일지2008년12월2일경광경급면역형광병리진단위GML、동시전경병리자료완정적환자148례,회고성분석기림상급병리자료.결과 고립성혈뇨시환자최상견적림상표현,기차위혈뇨합병소량단백뇨급단순단백뇨,부분환자가병존고혈압、특수자신면역표현、간염표지물양성등.경전경검사명학,GML가최종정현각충불동적병리표현:박기저막신병(66.2%)、계막증생성신소구신염(20.3%)、Alport종합정(2.7%)、막성신병(3.4%)이급정상조직(4.7%)등.결합림상여병리,표현위고립성혈뇨적GML환자,경전경병리검사진단위박기저막신병적가능성최대(76.9%).부분환자존재단백뇨、고혈압등제시불량예후적정황.결론 GML지시일충대신장병리표현적조범묘술,대응적전경병리구유교대이질성,림상의의각이,수적겁완선전경병리,결합림상특점,명학최종진단,지도치료.
Objective To analyze cases diagnosed with glomerular minor lesion (GML) by light microscopy and immunofluorescence,uncover their final pathology diagnosis by electron microscopy,and thereby clarify the pathological and clinical meaning of GML.Methods One hundred and forty-eight patients receiving renal biopsy between 2003 and 2008 in Peking Union Medical College Hospital,with diagnosis of GML described by light microscopy and immunofluorescence examination were retrospectively studied.All the clinical data and pathological observation were collected and analyzed,including intact results of electron microscopic examination which were considered as golden standards of pathological diagnosis.Results The 148 patients with GML had heterogenous clinical features,with isolated hematuria as the most common presentation.Electron microscopy revealed various pathological presentations:thin basement membrane nephropathy (TBMN,66.2%),mesangial proliferative glomerulonephritis (MsPGN,20.3%),Alport syndrome (2.7%),membranous nephropathy (MN,3.4%),normal tissue (4.7%).Among GML patients with isolated hematuria,TBMN ranked as the most common pathology (76.9%).Conclusions GML is only an equivocal description of pathological manifestation by light microscopy and immunofluorescence examination.And electron microscopy is necessary to obtain accurate pathology diagnosis for patients undergoing renal biopsies.