Summary of GN secondary causes
1.Type of GN#
| Type of GN | Secondary causes |
|---|---|
| MCD | (Atypical infection/virus/AIR/allergy/lymphoma/drugs) I(rare): HCV(MPGN, cryoglobuline type II多, 可MCD, collapsing FSGS, MGN, IgAN, TMA, TIN), syphilis(MGN>MCD), HIV(多collapsing FSGS, 可MCD, MPGN/cryoglobulin/lupus like GN/IgAN, fibrillary GN, immunotactoid GN(?)), mycoplasma(可MCD, MPGN), TB(多amyloidosis, 可MCD, collapsing FSGS, IgAN), Ehrlichiosis(tickborne), Lyme disease, Echinococcus(絛蟲) I:allergy related?(30% MCD Pts有allergy(含food allergy); 有些report有記載oligoantigenic diet induced remission!)(所以和食物, 花粉, 某些植物(常春藤, 橡木...), 塵蟎, 蜜蜂叮咬...有關); many AIR(association); HSCT/GVHD(比MN早發生) M(degree of proteinuria大多和malignancy的嚴重度成正比):HL(0.4% Pts have MCD), leukemia, NHL, solid cancers很少見(solid cancers多MGN) M:NSAID(most common cause of secondary MCD)(MCD>MGN; AIN, pre-renal), gold(MGN>MCD), penicillamine(MGN>MCD), Lithium(MCD, FSGS, CTIN, NDI), Interferon(MCD/FSGS, 也可以ATN, TMA), Penicillin/beta-lactam/rifampin(多AIN; beta-lactam可ATN, MCD; rifampin類似NSAID), Sulfasalazine and 5-ASA, Aredia(MCD/FSGS) and other bisphosphonate(Zometa也可ATN), tamoxifen(MCD), anthracyclines(doxorubicin, daunorubicin...可MCD, FSGS(因為會傷害podocytes)) C:PCKD(association) |
| MCD/FSGS variant-Idiopathic mesangial proliferative GN | 感染後腎炎恢復期(resolving PIGN)、輕微狼瘡腎炎(LN class II)、早期或輕微 IgAN、自體免疫風濕疾病之次發表現 |
| MCD/FSGS variant-IgMN | 多為 idiopathic; 亦見於自體免疫疾病(SLE, RA)、血液腫瘤、或非特異性免疫球蛋白於硬化區之物理性截留 |
| MCD/FSGS variant-C1q nephropathy | 診斷前必須排除 SLE(無 SLE 臨床與血清學證據); 亦可次發於病毒感染、DM、HIV 等非特異性沉積 |
| FSGS | 1.FSGS(collapsing type) - 大多因為HIV/B19(可collapsing FSGS, cryoglobulin) - I:CMV, TB(also amyloidosis, MCD, collapsing FSGS, IgAN) - I:lupus/MCTD, AOSD(可mesangial GN, collapsing FSGS, secondary amyloidosis(AA), IN), cerebral arteritis, IgAN, post-renal transplant - M:MM/MGUS, acute monoblastic leukemia/hemophagocytic syndrome(主要是TMA) - M:DM(可以collapsing FSGS??), drugs(Heroin?, interferon(可MCD/FSGS, ATN, TMA)/anabolic steroid(MCD, FSGS)/pamidronate(MCD, FSGS), sirolimus(可以TMA, collapsing FSGS, MPGN(due to TMA?), MN, IgAN(後三者少見)) - C:APOL1 gene, mitochondrial cytopathy(Dr.蔡宜蓉:mitochondrial disease大多是用Fanconi syndrome來表現)/other genetics/也可以idiopathic - H:Sickle cell anemia(會hematuria(papillary necrosis), MPGN, collapsing FSGS, secondary FSGS(due to cTIN?)) 2.FSGS(all) - I:HIV(collapsing), B19(collapsing), also EBV(MN, FSGS, cryoglobulinemia, TIN)/CMV(collapsing FSGS, cryoglobulin, TIN)/HCV - I:any GN causing glomerular injury, TMA, post-renal transplantation(collapsing), AIR diseases... - M:lymphoma(其他癌症少見, 有也是case reports; RCC and thymoma多一點點); 不過MM/acute monoblastic leukemia/hemophagocytic syndrome和collapsing FSGS有關 - M:drugs(Heroin)(collapsing), interferon(collapsing), Lithium(MCD, FSGS, cTIN, NDI), Pamidronate/alendronate(Zometa也 cause tubular injury)(collapsing), anabolic steroid(collapsing), anthracycline(FSGS related), 可MCD, FSGS), CNI(secondary FSGS); Sirolimus(可以TMA, collapsing FSGS, MPGN(due to TMA?), MGN, IgAN(後三者少見)), DM可以collapsing FSGS(?)、HTN、severe obesity - C:congenital/familial(genetic/familial autonomic insufficiency, cyanotic heart disease, alport syndrome - NPHS1 gene mutation(AR, 和nephrin有關) -->glucocorticoid-resistant nephrotic syndrome - NPHS2 gene mutation(AR, 和podocin有關) -->glucocorticoid-resistant nephrotic syndrome - Alpha-actinin-4 gene mutation(AD, 和actin有關) - TRPC6(AD, gain of function of podocyte的Ca channel, Ca進入後激活calmodulin/calcineurin/NFAT, NFAT會破壞 synaptopodin(所以CNI可治療FSGS)), INF2, MYO1E gene...... - AR較多, 多出生後就發病 - AD較少, 多adolescent or young adult發病 - 若是黑人則和APO L1 gene(chromosome 22)有關 - APOL1 G1/G2雙變異與非洲裔HIVAN、高血壓腎硬化及collapsing FSGS高度相關〔PMID 20647424〕 - H:sickle cell anemia, hemophagocytic syndrome(TMA, collapsing FSGS) - O:advanced renal disease, reflux nephropathy |
| Secondary MGN | I:HBV(較常見於小孩, 和HBeAg and anti-HBeAg Ab的immunocomplex(所以C1q(+))沉積在subepithelial/subendothelial/mesangial area有關(所以HBeAg seroconversion有可能MGN就spontaneous resolve, 但成人常不resolve); 有microscopic hematuria, 可hypocomplements, negative PLA2R Ab(但一小部分HBV, HCV, malignancy related MGN也可以anti-PLA2R Ab(+)...); 可cryoglobulin, MPGN, IgAN(due to chronic liver disease?)), HCV, syphilis(因為Treponemal antigen deposits in glomerulus, MGN>MCD), EBV, malaria(MPGN, cryoglobulinemia, MGN) - 沒有HIV(HIV多collapsing FSGS, 可MCD, MPGN/cryoglobulin/lupus like GN/IgAN, AIN(AIN可能是因為virus, drugs...)), 有的話可能是因為HBV or syphilis - 標靶抗原與次發病因關聯:NELL-1與惡性腫瘤及含硫藥物/硫辛酸相關;EXT1/EXT2與SLE/自體免疫強相關(LN class V)〔PMID 31061139〕;THSD7A約20%合併惡性腫瘤;SEMA3B見於小兒;FAT1見於造血幹細胞移植GVHD |
| SLE type V | I:SLE type V(10-20% lupus nephritis為type V; 可hypocomplements但不常見, 所以MCTD也會MGN但奇特的是MCTD都IgG3(-)) - Sjogren's syndrome(可MGN(rare), MPGN, 其他GN(rare), amyloidosis(AA), cryoglobulinemia, IN(多chronic IN with NDI, type I RTA(also II), hypokalemia...), RTA type I(25% sjogren可有一點type I RTA, 大多mild) and II [RTA主要是因為IN導致的tubular injury]; 也可以Bartter's syndrome, Gitelman's syndrome(=2M GN+...)), RA(可MGN, MPGN, mesangial GN, 可IgAN, secondary amyloidosis(AA), drugs related(NSAID, MTX, CsA, Golds(1-3%MGN; 也可MCD)), vasculitis(=3M GN+IgA類+...)), autoimmune thyroiditis(因為Ab+thyroglobulin沉積在subepithelial site; 可MGN, 可MPGN), GVHD(MGN>MCD; 可能是donor lymphocytes打glomerular Ag, 治療和iMN一樣; MGN多發生在post-HSCT後8-14M且within 2M after GVHD(+)); post renal transplantation(可recurrence(typical 1yr after renal transplantation); 也可以de novo MGN(多比recurrent MGN晚開始); 不過uptodate建議Rituximab>Endoxan in renal transplantation的MGN(和chronic ABMR有關)); sarcoidosis(35-50% renal involvement; 多non-caseating granulomatous AIN+vitamin D related nephrocalcinosis and nephrolithiasis; 可GN(rare, 可MGN, MPGN, IgAN, crescent (口訣:MMAC)...); 可obstructive uropathy(lymph nodes, retroperitoneal fibrosis, stones, direct ureter involvement)); IgG-4 disease(TIN>>>MGN/mesangial GN/MPGN/MCD/IgAN/HSP/amyloidosis(AA); 也會hypocomplements雖然機制不太清楚, 因為IgG4不太激活complements)(=4M GN+IgA類) - M:(5-20% Pts of MN, 尤其>65y/o; 原因是tumor Ag deposits in glomerulus->Ab接上去->激活complements; 也有可能是malignancy表現出的Ag和podocyte Ag一樣, 如有report說tumor表現THSD7A):多為solid cancer尤其lung(26%), prostate(15%), GI...; hematologic malignancy(14%, CLL, lymphoma...)也可但較少見; 診斷MN時大多是clinically apparent cancer - M:NSAID(MCD>MGN), anti-TNF alpha(可new lupus nephritis, MGN, pauci-immune GN, crescent GN, MGN), bucillamine, Penicillamine(7%; MGN>MCD; 可crescent GN), Tiopronin(結構像Penicillamine), Gold(1-3%; MGN>MCD)[大多是治療RA的藥], captopril, probenecid, Mercury(MGN>>MCD; also tubular dysfunction)... - 多使用drugs後6-12M出現, 不過也可以3-4年才出現; 停藥後多9-12M resolution, 也可以upto 2-3 years(因為slow clearance of subepithelial immune deposits and slow remodeling of the disorganized GBM; podocytes類的回復比較慢...) |
| IgAN/HSP | (感覺呼吸道/腸胃道疾病, HIV/lymphoma, liver疾病等會產生IgA或是IgA無法代謝的疾病就可能IgA deposit-->其中某些人會IgA nephropathy) I:HCV, HIV, disseminated TB, dermatitis herpetiformis I:RA, celiac disease(1/3 Pts腎臟會堆積IgA但大多無IgA nephropathy; 如果IgA nephropathy有腸胃道症狀要小心Celiac disease, HSP), IBD, seronegative arthritis(特別是AS), GPA(可能是因為常upper airway infection), IgG-4 disease, sarcoidosis M:SCLC, HL and T cell lymphoma(本身產生IgA?) M:smoking(呼吸到刺激?), sirolimus(可以TMA, collapsing FSGS, MPGN(due to TMA?), MN, IgAN(後三者少見; 和sarcoidosis口訣都是MMAC, 雖然C不同)) O:Chronic liver disease(含HBV/HCV...), liver cirrhosis(因為IgA removal by the Kupffer cells下降; 很多Pts腎臟會堆積IgA但大多無IgA nephropathy) C:在Africa and central America有familial IgAN(大多為AD with incomplete penetrance) |
| PSGN/IRGN | 1.PSGN from GAS, 不過group C, group G streptococcus也有case例 |
| MPGN | (簡單來說就是許多慢性感染, 許多AIR, MGUS/MIDD, TMA) I:chronic infection, 尤其HCV(HBV也可), 其他的virus(HIV...) /bacteria(mycoplasma(MCD, MPGN), abscess, IE, osteomyelitis, shunt nephritis...) /fungus/parasites(P. malariae(可MN), schistosoma, toxoplasma(可AIN)...) chronic infection也可 - URI也可以誘發MPGN(應該是本來體質就有問題??) - 回思IE可MPGN(其實應該算是IRGN)... - PSGN廣義來說也算MPGN的一種(不過應該沒有double contour?) |
2.FSGS(all)#
- (FSGS 之次發原因、感染、藥物、血液疾患及詳細遺傳基因清單,完整彙整於本檔 §1 表格,以及專章 FSGS §2 之「FSGS/SRNS 重要基因速查表」)
- APOL1-mediated kidney disease (AMKD):非洲裔帶有 G1/G2 雙風險等位基因者,顯著增加高血壓腎硬化、HIVAN 及 collapsing FSGS 之發病風險〔PMID 20647424〕
3.Secondary MGN(次發 membranous pattern)#
- 標靶抗原與次發病因關聯(2020-2025新考點):
- NELL-1(~5-10%):與惡性腫瘤(多固態腫瘤)及外源性含硫製劑(lipoic acid 硫辛酸、傳統草藥、NSAID)強相關;IgG1 主
- EXT1/EXT2:與自體免疫/SLE 強相關(尤 LN class V),多為年輕女性,預後佳〔PMID 31061139〕
- THSD7A(~1-5%):約 20% 合併惡性腫瘤
- SEMA3B:見於小兒膜性腎病最常見抗原
- FAT1:造血幹細胞移植後(GVHD 相關)
- CNTN1:合併慢性脫髓鞘多發性神經病變 (CIDP)
- I:HBV(較常見於小孩, 和HBeAg and anti-HBeAg Ab的immunocomplex(所以C1q(+))沉積在subepithelial/subendothelial/mesangial area有關(所以HBeAg seroconversion有可能MGN就spontaneous resolve, 但成人常不resolve); 有microscopic hematuria, 可hypocomplements, negative PLA2R Ab(但一小部分HBV, HCV, malignancy related MGN也可以anti-PLA2R Ab(+)...); 可cryoglobulin, MPGN, IgAN(due to chronic liver disease?)), HCV, syphilis(因為Treponemal antigen deposits in glomerulus, MGN>MCD), EBV, malaria(MPGN, cryoglobulinemia, MGN)
- 沒有HIV(HIV多collapsing FSGS, 可MCD, MPGN/cryoglobulin/lupus like GN/IgAN, AIN(AIN可能是因為virus, drugs...)), 有的話可能是因為HBV or syphilis
4.SLE type V(10-20% lupus nephritis)(type V: 可hypocomplement但不常見)#
- I:SLE type V(10-20% lupus nephritis為type V; 可hypocomplements但不常見, 所以MCTD也會MGN但奇特的是MCTD都IgG3(-))
- Sjogren's syndrome(可MGN(rare), MPGN, 其他GN(rare), amyloidosis(AA), cryoglobulinemia, IN(多chronic IN with NDI, type I RTA(also II), hypokalemia...), RTA type I(25% sjogren可有一點type I RTA, 大多mild) and II [RTA主要是因為IN導致的tubular injury]; 也可以Bartter's syndrome, Gitelman's syndrome(=2M GN+...)), RA(可MGN, MPGN, mesangial GN, 可IgAN, secondary amyloidosis(AA), drugs related(NSAID, MTX, CsA, Golds(1-3%MGN; 也可MCD)), vasculitis(=3M GN+IgA類+...)), autoimmune thyroiditis(因為Ab+thyroglobulin沉積在subepithelial site; 可MGN, 可MPGN), GVHD(MGN>MCD; 可能是donor lymphocytes打glomerular Ag, 治療和iMN一樣; MGN多發生在post-HSCT後8-14M且within 2M after GVHD(+)); post renal transplantation(可recurrence(typical 1yr after renal transplantation); 也可以de novo MGN(多比recurrent MGN晚開始); 不過uptodate建議Rituximab>Endoxan in renal transplantation的MGN(和chronic ABMR有關)); sarcoidosis(35-50% renal involvement; 多non-caseating granulomatous AIN+vitamin D related nephrocalcinosis and nephrolithiasis; 可GN(rare, 可MGN, MPGN, IgAN, crescent (口訣:MMAC)...); 可obstructive uropathy(lymph nodes, retroperitoneal fibrosis, stones, direct ureter involvement)); IgG-4 disease(TIN>>>MGN/mesangial GN/MPGN/MCD/IgAN/HSP/amyloidosis(AA); 也會hypocomplements雖然機制不太清楚, 因為IgG4不太激活complements)(=4M GN+IgA類)
- M:(5-20% Pts of MN, 尤其>65y/o; 原因是tumor Ag deposits in glomerulus->Ab接上去->激活complements; 也有可能是malignancy表現出的Ag和podocyte Ag一樣, 如有report說tumor表現THSD7A):多為solid cancer尤其lung(26%), prostate(15%), GI...; hematologic malignancy(14%, CLL, lymphoma...)也可但較少見; 診斷MN時大多是clinically apparent cancer
- M:NSAID(MCD>MGN), anti-TNF alpha(可new lupus nephritis, MGN, pauci-immune GN, crescent GN, MGN), bucillamine, Penicillamine(7%; MGN>MCD; 可crescent GN), Tiopronin(結構像Penicillamine), Gold(1-3%; MGN>MCD)[大多是治療RA的藥], captopril, probenecid, Mercury(MGN>>MCD; also tubular dysfunction)...
- 多使用drugs後6-12M出現, 不過也可以3-4年才出現; 停藥後多9-12M resolution, 也可以upto 2-3 years(因為slow clearance of subepithelial immune deposits and slow remodeling of the disorganized GBM; podocytes類的回復比較慢...)
5.IgAN/HSP#
- (感覺呼吸道/腸胃道疾病, HIV/lymphoma, liver疾病等會產生IgA或是IgA無法代謝的疾病就可能IgA deposit-->其中某些人會IgA nephropathy)
- I:HCV, HIV, disseminated TB, dermatitis herpetiformis
- I:RA, celiac disease(1/3 Pts腎臟會堆積IgA但大多無IgA nephropathy; 如果IgA nephropathy有腸胃道症狀要小心Celiac disease, HSP), IBD, seronegative arthritis(特別是AS), GPA(可能是因為常upper airway infection), IgG-4 disease, sarcoidosis
- M:SCLC, HL and T cell lymphoma(本身產生IgA?)
- M:smoking(呼吸到刺激?), sirolimus(可以TMA, collapsing FSGS, MPGN(due to TMA?), MN, IgAN(後三者少見; 和sarcoidosis口訣都是MMAC, 雖然C不同))
- O:Chronic liver disease(含HBV/HCV...), liver cirrhosis(因為IgA removal by the Kupffer cells下降; 很多Pts腎臟會堆積IgA但大多無IgA nephropathy)
- C:在Africa and central America有familial IgAN(大多為AD with incomplete penetrance)
6.PSGN/IRGN#
- 1.PSGN from GAS, 不過group C, group G streptococcus也有案例
7.MPGN#
- (簡單來說就是許多慢性感染, 許多AIR, MGUS/MIDD, TMA)
- I:chronic infection, 尤其HCV(HBV也可); 其他的virus(HIV...)/bacteria(mycoplasma(MCD, MPGN), abscess, IE, osteomyelitis, shunt nephritis...)/fungus/parasites(P. malariae(可MN), schistosoma, toxoplasma(可AIN)...) chronic infection也可
- URI也可以誘發MPGN(應該是本來體質就有問題??)
- 回思IE可MPGN(其實應該算是IRGN)...
- PSGN廣義來說也算MPGN的一種(不過應該沒有double contour?)
- HCV:typically shows granular deposition of IgM, C3, and both κ and λ light chains +/- IgG; C1q is typically negative(may also be seen with other viral infections)
- I:尤其LN(less often=>Sjögren's syndrome or systemic sclerosis(因為malignant HTN而TMA?) or RA or IgG-4 disease or sarcoidosis or APS(因為TMA?)) or autoimmune thyroiditis(可MGN, MPGN)
- D/D
- SLE會"full house" pattern, including IgG, IgM, IgA, C1q, C3, κ and λ light chains
- TMA immunofluorescence是(-)的
- M:monoclonal gammopathy(尤其LCDD, monoclonal IgG disease; 小心MM, CLL, B cell lymphoma)(所以MIDD可以有MPGN pattern, 但大多是nodular pattern); Rares: NHL, RCC, melanoma
- monoclonal gammopathy:characterized by deposition of monotypic κ or λ light chains but not both. MPGN associated with heavy-chain deposition may show immunoglobulin deposition(heavy-chain isotypes) in the absence of either light chain(=HCDD?)
- M:chronic and healed TMA/TTP/HUS
- C:complement dysregulation(尤其complement factor H deficiency)(也是一種TMA), complement deficiency(C2 or C3) +/- partial lipodystrophy, α1-Antitrypsin deficiency(也和AAV相關)
8.Cryoglobulinemia#
- Type I(10-15%)
- Monoclonal Ab:多為IgG or IgM; 但也可以是IgA or light chain
- 非IC deposit-->no decreased complement but可hyperviscosity syndrome
- From
- M(B cells系列):(MM, WM, CLL...) >>> MGUS
- Monoclonal Ab:多為IgG or IgM; 但也可以是IgA or light chain
- Type II(mixed cryoglobulinemia)(50-60%)
- Polyclonal IgG and monoclonal IgM(against the IgG; =rheumatoid factor)
- IC deposit in BV-->vasculitis(small vessel leukocytoclastic vasculitis)-->C4↓↓, C3↓
- From
- I(主):HAV, HBV, HCV, EBV, CMV(collapsing FSGS, cryoglobulinemia, TIN), HIV, B19, IE, streptococcus, fungus, malaria, Ameba
- I:SLE, Sjogren, RA, PAN
- M:B cell lymphoma, solid cancers
- HCV>>>AIR>idiopathic>LPD>other infections
- Polyclonal IgG and monoclonal IgM(against the IgG; =rheumatoid factor)
- Type III(也是mixed cryoglobulinemia)(25-30%)
- Polyclonal IgG and polyclonal IgM
- IC deposit in BV-->vasculitis(small vessel leukocytoclastic vasculitis) -->C4↓↓, C3↓
- From(不就和type II一樣???)
- I:as above, 尤其HCV(仍多)
- Polyclonal IgG and polyclonal IgM
9.TMA#
- 詳見專章TMA(TTP-aHUS and secondary)
- 小心有一些是drugs related:
- 劑量依賴毒性:CNI(CsA/FK506), mTORi(sirolimus), gemcitabine, mitomycin C, cisplatin, bleomycin, anti-VEGF/TKI(bevacizumab, sunitinib, sorafenib)
- 免疫媒介/idiosyncratic:quinine, ticlopidine, clopidogrel
- (註:minocycline, hydralazine, procainamide, isoniazid是drug-induced lupus和AAV的藥, 不是TMA的藥, 勿混淆)
10.LN / AAV#
- (註:LN 本身次發於 SLE;drug-induced lupus 如 minocycline, hydralazine, procainamide, isoniazid…;以下為 AAV 的 ANCA 分型/次發成因)
- 1.比較少c-ANCA和p-ANCA都(+), 除了cocaine(with levamisole(cutting agent in cocaine) contamination) user導致的vasculitis
- 2.c-ANCA(more ENT and respiratory tract involved)
- GPA(90%(+); c:75-80%, p:10-15%)
- α1-Antitrypsin deficiency(?, α1-Antitrypsin是in vivo PR3 inhibitor)
- 3.P-ANCA(more 肺腎skin involved; 註:P-ANCA較易resistance but較少relapse)
- EGPA(50%(+); c:15%, p:35%), MPA(70-90%(+); 多p-ANCA)
- Renal limited vasculitis(=idiopathic crescent GN; 90%(+), c:10%, p:80%)
- Anti-GBM disease(10-40%(+); 多p-ANCA)
- 4.Atypical P-ANCA(IFA(+), ELISA(-))
- 註:有發現AAV Pts似乎和cancer association, 但是是based on case reports/series, 所以證據不強
- SLE(p:20-30%) and other AIR diseases...
- LN若為crescent GN有30% P-ANCA(+), 其他的immunocomplex GN若是crescent GN也有25% P-ANCA(+)
- UC/PSC(p:40-70%), CD(p:10-27%), AIH
- Cystic fibrosis
- IE/bacteremia/TB/aspergillus...(感染相關)
- Drugs induced vasculitis(PTU, -mazole, Apresoline(SLE相關), procainamide(SLE相關), isoniazid(SLE相關), minocycline(SLE相關), allopurinol, phenytoin, penicillamine, rifampicin, Cefotaxime, indomethacin, clozapine...)
- PTU:30% Pts, 多months~yrs出現p-ANCA(+)(因為PTU累積在neutrophil並bind and alter MPO antigen), 但有vasculitis的僅占一小部分, DC drugs後大多會recovery
- Apresoline:會有DLE and ANCA-associated vasculitis; 後者常有anti-DsDNA, high titer P-ANCA, renal involvement, 常需要immunosuppressive Tx and DC drugs
- 小心GPA/MPA有report of concurrent other GN(anti-GBM disease, MGN(crescents maybe due to concurrent anti-GBM or ANCA disease), IgAN, PSGN, LN)
- 有IgAN, PSGN因為AAV其實部分和infection有關?
- 也可以反過來..., 這些crescent immunocomplex GN 25%合併ANCA(+)(註:若是non-crescent immunocomplex GN其ANCA(+)<5%)
11.Anti-GBM disease#
- 誘發/次發成因:吸菸(誘發肺出血)、碳氫化合物/有機溶劑暴露、呼吸道感染、ESWL 體外震波碎石或腎外傷、Alemtuzumab 治療後
- 遺傳關聯:易感 HLA-DRB1*15:01、DR4;保護 HLA-DRB1*01 與 DRB1*07
- 詳見Anti-GBM disease
12.Congo red and thioflavine-T#
- 1.Fibrillary GN
- negative(nonamyloid) fibrillar glomerular deposition diseases
- DNAJB9 為特異性免疫染色標記(Andeen JASN 2018; PMID 29097624)〔PMID 29097624〕
- 可和HCV相關
- AIR(15%)
- most often CD, SLE, Graves' disease, ITP
- 可和anti-GBM disease相關
- Monoclonal gammopathy(17%)
- Malignancy(23%)
- 可以發生在GN前 or 後10年
- 2.Immunotactoid glomerulopathy
- 大多有monoclonal gammopathy with restricted light chains(either k or λ)
- 所以要小心survey lymphoproliferative disorders(尤其CLL or B cell lymphoma)
- 但似乎HCV or cryoglobulinemia or anti-GBM disease or SLE也可immunotactoid glomerulopathy
- negative(nonamyloid) fibrillar glomerular deposition diseases
- Fibronectin glomerulopathy
- Autosomal dominant congenital disease(亞洲人有)
- Collagenofibrotic glomerulopathy
- AR
- More frequently in adult Indian populations in a sporadic, non-familial manner
- AR
- Nail-patella syndrome
- Autosomal dominant congenital disease
- Amyloidosis
- 1.AL
- 可with MM, P(PNS, ANS)OE(pituitary, thyroid, adrenal↓)MS, WM(註:IgM-associated AL amyloidosis, 較少cardiac involvement), lymphoplasmacytic lymphoma, NHL, CLL
- 2.AA
- I
- TB(amyloidosis(AA), also MCD, collapsing FSGS, IgAN), leprosy, COPD, cystic fibrosis, subacute IE, osteomyelitis, chronic pyelonephritis, skin ulcers
- Whipple's disease
- HBV(?)
- I(60%)
- RA(常>15yrs), IBD/sero (-) spondyloarthropathy, FMF(familial Mediterranean fever), AOSD, SLE(rare, 原因未知, 不過 SAA level抽起來確實比RA低), vasculitis(Giant cell arteritis, Takayasu arteritis, Behcet's diseases, PAN), IgG-4 related diseases
- RA以前常有glomerular AA depositions and 常常ESRD
- 隨著治療進步,現在不常見, 因為大多發生在poor controlled, seropositive, long-standing and 有 extraarticular manifestation的RA
- RA可cresent GN(uncommon), 可能因為RA本身造成的GN or amyloid fibril-induced ruptures in the capillary loops
- RA以前常有glomerular AA depositions and 常常ESRD
- RA(常>15yrs), IBD/sero (-) spondyloarthropathy, FMF(familial Mediterranean fever), AOSD, SLE(rare, 原因未知, 不過 SAA level抽起來確實比RA低), vasculitis(Giant cell arteritis, Takayasu arteritis, Behcet's diseases, PAN), IgG-4 related diseases
- 其他AL, AA也可以crescent GN但是很少見
- I
- M
- 尤其HL, RCC
- 可Hairy cell leukemia, castleman disease
- 可Lung/GI/GU adenocarcinoma, hepatic adenoma, BCC
- Others
- Drugs abuser(感染相關?)
- Gout(case report)
- 1.AL
13.MIDD#
- 大多還是from MM(LCDD or LHCDD都約50%有MM, HCDD約25%有MM), 不過也可from WM, CLL, nodal marginal zone lymphoma or chronic infection or autoimmune