肾病综合征
附属二院内科
诊断标准
①尿蛋白 >3.5g/d
② 血浆白蛋白低于 30g/L
③ 水肿
④血脂升高
其中①②为必备条件
病因
? 原发性
●微小病变型（儿童）
●系膜增生性
●系膜毛细血管性
●局灶节段性硬化
●膜性肾病（中老年）
? 继发性
●过敏性紫癜肾炎
●乙肝相关性肾炎
●狼疮性肾炎
●糖尿病肾病
●骨髓瘤性肾病
●肾淀粉样变性
●其它
病理生理
? 大量蛋白尿, 肾小球滤过膜分子屏障及
电荷屏障受损，通透性增加
? 血浆蛋白减低,尿丢失，蛋白摄入不足
? 水肿,血浆胶体渗透压 ↓
? 高脂血症,肝合成增加，外周利用减少
（一）微小病变型肾病：
LM,肾小球基本正常
IF,阴性
EM,广泛肾小球脏层上皮细胞足突融合
原发性肾病综合征的病理类
型及临床特征
This is a normal glomerulus by light microscopy,The glomerular capillary
loops are thin and delicate,Endothelial and mesangial cells are normal in
number,The surrounding tubules are normal,Life is good.
（一）微小病变型肾病：
LM,肾小球基本正常
IF,阴性
EM,广泛肾小球脏层上
皮细胞足突融合
原发性肾病综合征的病理类型及
临床特征
（一）微小病变型肾病
? 临床表现：
儿童，老年
典型肾综表现
15%血尿
一般无持续性高血压、肾衰
50%自发缓解,90%激素敏感，易复
发
（二）系膜增生性肾小球肾炎
■ LM,肾小球系膜细胞、系膜基质弥漫
增生
■ IF,IgA或 IgM,IgG,C3于系膜区、系
膜区及毛细血管壁颗粒样沉积
■ EM,系膜区，有时内皮下见到电子致
密物
This is Berger's disease,or IgA nephropathy,The IgA is deposited mainly in mesangium,
which then increases mesangial cellularity as shown at the arrow,Patients with IgA
nephropathy usually present with hematuria.
（二）系膜增生性肾小球肾炎
■ LM,肾小球系膜细胞、系膜基质弥漫增生
■ IF,IgA或 IgM,IgG,C3于系膜区、系
膜区及毛细血管壁颗粒样沉积
■ EM,系膜区，有时内皮下见到电子致
密物
This immunofluorescence micrograph demonstrates positivity with antibody to IgA,Note
that the pattern is that of mesangial staining,This is IgA nephropathy.
(二）系膜增生性肾小球肾炎
? 临床表现：
青少年，男性,50%前驱感染
IgA:15%肾综，几乎均有血尿
非 IgA,30%肾综,70%血尿
逐渐发生高血压、肾衰
激素、细胞毒药物反应不一
（三）系膜毛细血管性肾小球肾
炎
? 病理：
LM,系膜细胞及基质弥漫增生，毛细
血管袢呈, 双轨征,
IF,IgG,C3呈颗粒状系膜区及毛细血
管壁沉积
EM,系膜区、内皮下电子致密物沉积
This is membranoproliferative glomerulonephritis (MPGN),Those that are idiopathic are
divided into types I and II by pathologic findings,As seen here,the glomerulus has
increased overall cellularity,mainly mesangial.
This electron micrograph demonstrates a mesangial cell at the lower left that is interposing its cytoplasm at the
arrow into the basement membrane,leading to splitting and reduplication of basement membrane that is piled
up above the mesangial cytoplasm in this micrograph,This is MPGN type I,These characteristic EM changes
occur when the mesangial cell (which has a macrophage-like function) goes after subendothelial immune
deposits,but makes a mess of the basement membrane in the process.
This electron micrograph demonstrates the dense deposits in the basement membrane of
MPGN type II,There are dark electron dense deposits within the basement membrane that
often coalesce to form a ribbon-like mass of deposits.
（三）系膜毛细血管性肾炎
? 临床表现：
青壮年男性,70%前驱感染
60%肾综,30%急性肾炎综合征
肉眼血尿
肾损、高血压出现早,10年 50%肾
衰
激素效果差
附属二院内科
诊断标准
①尿蛋白 >3.5g/d
② 血浆白蛋白低于 30g/L
③ 水肿
④血脂升高
其中①②为必备条件
病因
? 原发性
●微小病变型（儿童）
●系膜增生性
●系膜毛细血管性
●局灶节段性硬化
●膜性肾病（中老年）
? 继发性
●过敏性紫癜肾炎
●乙肝相关性肾炎
●狼疮性肾炎
●糖尿病肾病
●骨髓瘤性肾病
●肾淀粉样变性
●其它
病理生理
? 大量蛋白尿, 肾小球滤过膜分子屏障及
电荷屏障受损，通透性增加
? 血浆蛋白减低,尿丢失，蛋白摄入不足
? 水肿,血浆胶体渗透压 ↓
? 高脂血症,肝合成增加，外周利用减少
（一）微小病变型肾病：
LM,肾小球基本正常
IF,阴性
EM,广泛肾小球脏层上皮细胞足突融合
原发性肾病综合征的病理类
型及临床特征
This is a normal glomerulus by light microscopy,The glomerular capillary
loops are thin and delicate,Endothelial and mesangial cells are normal in
number,The surrounding tubules are normal,Life is good.
（一）微小病变型肾病：
LM,肾小球基本正常
IF,阴性
EM,广泛肾小球脏层上
皮细胞足突融合
原发性肾病综合征的病理类型及
临床特征
（一）微小病变型肾病
? 临床表现：
儿童，老年
典型肾综表现
15%血尿
一般无持续性高血压、肾衰
50%自发缓解,90%激素敏感，易复
发
（二）系膜增生性肾小球肾炎
■ LM,肾小球系膜细胞、系膜基质弥漫
增生
■ IF,IgA或 IgM,IgG,C3于系膜区、系
膜区及毛细血管壁颗粒样沉积
■ EM,系膜区，有时内皮下见到电子致
密物
This is Berger's disease,or IgA nephropathy,The IgA is deposited mainly in mesangium,
which then increases mesangial cellularity as shown at the arrow,Patients with IgA
nephropathy usually present with hematuria.
（二）系膜增生性肾小球肾炎
■ LM,肾小球系膜细胞、系膜基质弥漫增生
■ IF,IgA或 IgM,IgG,C3于系膜区、系
膜区及毛细血管壁颗粒样沉积
■ EM,系膜区，有时内皮下见到电子致
密物
This immunofluorescence micrograph demonstrates positivity with antibody to IgA,Note
that the pattern is that of mesangial staining,This is IgA nephropathy.
(二）系膜增生性肾小球肾炎
? 临床表现：
青少年，男性,50%前驱感染
IgA:15%肾综，几乎均有血尿
非 IgA,30%肾综,70%血尿
逐渐发生高血压、肾衰
激素、细胞毒药物反应不一
（三）系膜毛细血管性肾小球肾
炎
? 病理：
LM,系膜细胞及基质弥漫增生，毛细
血管袢呈, 双轨征,
IF,IgG,C3呈颗粒状系膜区及毛细血
管壁沉积
EM,系膜区、内皮下电子致密物沉积
This is membranoproliferative glomerulonephritis (MPGN),Those that are idiopathic are
divided into types I and II by pathologic findings,As seen here,the glomerulus has
increased overall cellularity,mainly mesangial.
This electron micrograph demonstrates a mesangial cell at the lower left that is interposing its cytoplasm at the
arrow into the basement membrane,leading to splitting and reduplication of basement membrane that is piled
up above the mesangial cytoplasm in this micrograph,This is MPGN type I,These characteristic EM changes
occur when the mesangial cell (which has a macrophage-like function) goes after subendothelial immune
deposits,but makes a mess of the basement membrane in the process.
This electron micrograph demonstrates the dense deposits in the basement membrane of
MPGN type II,There are dark electron dense deposits within the basement membrane that
often coalesce to form a ribbon-like mass of deposits.
（三）系膜毛细血管性肾炎
? 临床表现：
青壮年男性,70%前驱感染
60%肾综,30%急性肾炎综合征
肉眼血尿
肾损、高血压出现早,10年 50%肾
衰
激素效果差
