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Total: 19 |
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| PMID (PMCID) | ||
|---|---|---|
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31031392 |
OTHER | |
| Primary membranous nephropathy with concomitant IgA nephropathy. | ||
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Khorsan R, Hanna RM, Ameen K, Arman F, Nobakht N, Hasnain H, Hyunh A, Rastogi A. Saudi J Kidney Dis Transpl. 2019;30(2):531-536. |
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| IgA nephropathy is one of the most common autoimmune glomerular diseases in the world and presents with a spectrum of disease ranging from asymptomatic mild hematuria and proteinuria to rapidly progressive crescentic glomerulonephritis. | ||
|
30227733 |
FEMALE | Middle Aged |
| [Rapidly progressive proliferative glomerulonephritis with monoclonal immunoglobulin G deposits despite the mild histological changes. Case report]. | ||
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Bajcsi D, Constantinou K, Krenacs L, Barabas Z, Molnar S, Nyiraty S, Abraham G, Ivanyi B. Orv Hetil. 2018;159(38):1567-1572. |
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| The proteinuria and dysmorphic microhematuria suggested rapidly progressive glomerulonephritis. | ||
|
27077635 |
FEMALE | Child |
| Severe acute kidney injury in children owing to infective endocarditis-associated immune complex glomerulonephritis: a report of two cases. | ||
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Krishnamurthy S, Chandrasekaran V, Mahadevan S, Priyamvada PS, Rajesh NG. Paediatr Int Child Health. 2017;37(2):144-147. |
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| The cases illustrate that crescentic glomerulonephritis or severe diffuse proliferative glomerulonephritis should be considered as possible complications in children presenting with haematuria, proteinuria and severe AKI. | ||
|
27077635 |
FEMALE | Child |
| Severe acute kidney injury in children owing to infective endocarditis-associated immune complex glomerulonephritis: a report of two cases. | ||
|
Krishnamurthy S, Chandrasekaran V, Mahadevan S, Priyamvada PS, Rajesh NG. Paediatr Int Child Health. 2017;37(2):144-147. |
||
| Renal involvement in infective endocarditis (IE) may manifest with different clinical patterns, including diffuse proliferative glomerulonephritis and crescentic glomerulonephritis, which may lead to haematuria and/or proteinuria. | ||
|
28679995 |
MALE | Middle Aged |
| Thrombotic microangiopathy due to malignant hypertension complicated with late-onset bleeding after renal biopsy. | ||
|
Ameda S, Kuroda H, Yamada M, Sato K, Miura S, Sakano H, Shibata T, Uemura N, Abe T, Fujii S, Maeda M, Fujita M, Kobune M, Kato J. Rinsho Ketsueki. 2017;58(6):637-642. |
||
| A renal biopsy was done to evaluate pathology of high proteinuria, hematuria, and rapidly progressive glomerulonephritis. | ||
|
26841801 |
FEMALE | Adult |
| The transition of renal histopathology after immunosuppressive therapy in a woman with renal limited ANCA-associated vasculitis: a case report and literature review. | ||
|
Li XY, Liang YS, Pai P. Clin Exp Rheumatol. 2016;34(3 Suppl 97):S115-20. |
||
| AAGN is commonly described as a pauci-immune necrotising crescentic glomerulonephritis, but immune complex depositions have been frequently identified under electronic microscopy and is associated with greater levels of proteinuria. | ||
|
26950980 |
FEMALE | Middle Aged |
| [Rituximab therapy in the treatment of anti-neutrophil cytoplasmic antibody (ANCA) -positive interstitial pneumonia: case report]. | ||
|
Miyaoka T, Itabashi M, Kumon S, Akiyama K, Iwabuchi Y, Kataoka H, Moriyama T, Takei T, Nitta K. Nihon Jinzo Gakkai Shi. 2016;58(1):38-44. |
||
| On the first admission, severe renal dysfunction, proteinuria, hematuria, and an elevated titer of MPO-ANCA were observed, and the woman was diagnosed with rapidly progressive glomerulonephritis because of MPA. | ||
|
26458570 |
MALE | |
| [A case of MPO-ANCA positive hypertrophic pachymeningitis associated with vascular inflammation in the kidney biopsy]. | ||
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Takewaki D, Tsuji Y, Kasai T, Yoshida T, Nakagawa M, Mizuno T. Rinsho Shinkeigaku. 2015;55(11):844-7. |
||
| Because proteinuria and hematuria were detected on urinalysis, we performed a kidney biopsy, leading to the diagnosis of crescentic glomerulonephritis. | ||
|
25121358 (4602443) |
MALE | Adult |
| Membranous nephropathy with crescents in a patient with Hashimoto's thyroiditis: a case report. | ||
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Thajudeen B, John SG, Ossai NO, Riaz IB, Bracamonte E, Sussman AN. Medicine (Baltimore). 2014;93(8):e63. |
||
| A renal biopsy revealed coexistent necrotizing and crescentic glomerulonephritis and membranous nephropathy.The final diagnosis was necrotizing, crescentic glomerulonephritis with superimposed membranous nephropathy likely secondary to Hashimoto's thyrodiitis.Induction treatment with oral cyclophosphamide and prednisone was started.At the end of 6 months of treatment, there was improvement in renal function and proteinuria and maintenance treatment with azathioprine and low-dose prednisone was initiated. | ||
|
25121358 (4602443) |
MALE | Adult |
| Membranous nephropathy with crescents in a patient with Hashimoto's thyroiditis: a case report. | ||
|
Thajudeen B, John SG, Ossai NO, Riaz IB, Bracamonte E, Sussman AN. Medicine (Baltimore). 2014;93(8):e63. |
||
| A renal biopsy revealed coexistent necrotizing and crescentic glomerulonephritis and membranous nephropathy.The final diagnosis was necrotizing, crescentic glomerulonephritis with superimposed membranous nephropathy likely secondary to Hashimoto's thyrodiitis.Induction treatment with oral cyclophosphamide and prednisone was started.At the end of 6 months of treatment, there was improvement in renal function and proteinuria and maintenance treatment with azathioprine and low-dose prednisone was initiated. | ||
|
24969202 |
MIXED_SAMPLE | Child |
| Treatment of severe henoch-schonlein purpura nephritis with mycophenolate mofetil. | ||
|
Nikibakhsh AA, Mahmoodzadeh H, Karamyyar M, Hejazi S, Noroozi M, Macooie AA. Saudi J Kidney Dis Transpl. 2014;25(4):858-63. |
||
| In two cases with rapidly progressive glomerulonephritis without response to steroid, after treatment with MMF, significant improvement in kidney function and proteinuria were observed. | ||
|
22975555 |
FEMALE | |
| Myeloperoxidase anti-cytoplasmic antibody related crescentic glomerulonephritis in a patient with IgG3lamda monoclonal immunoglobulin deposition disease with membranous features. | ||
|
Ito A, Miura N, Kimura Y, Maeda S, Suzuki K, Kitagawa W, Morita H, Banno S, Imai H. Intern Med. 2012;51(17):2393-7. |
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| A 68-year-old woman showed rapidly progressive glomerulonephritis based on the fact that she had 1+ proteinuria (1.1 g/day), a 3+ occult blood reaction, blood urea nitrogen of 32.4 mg/dL, serum creatinine of 2.96 mg/dL, and myeloperoxidase (MPO)-anti-neutrophil cytoplasmic antibodies (ANCA) at 52 ELISA Unit (normal range: below 10). | ||
|
17496401 |
MIXED_SAMPLE | Adult |
| Goodpasture's syndrome - four case reports. | ||
|
Salam N, Rezki H, Fadili W, Hachim K, Ramdani B. Saudi J Kidney Dis Transpl. 2007;18(2):235-8. |
||
| All patients had rapidly progressive glomerulonephritis (RPGN) with proteinuria and microscopic hematuria. | ||
|
16471470 |
FEMALE | Middle Aged |
| Bullous Systemic Lupus Erythematosus as an Initial Manifestation of SLE. | ||
|
Fujimoto W, Hamada T, Yamada J, Matsuura H, Iwatsuki K. J Dermatol. 2005;32(12):1021-7. |
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| Because of the appearance of marked proteinuria, a subsequent renal biopsy, and serological tests, the patient was diagnosed with rapidly progressive glomerulonephritis and systemic lupus erythematosus. | ||
|
15909597 |
FEMALE | Middle Aged |
| Crescentic post-streptococcal glomerulonephritis with nephrotic syndrome in the adult: is aggressive therapy warranted? | ||
|
Raff A, Hebert T, Pullman J, Coco M. Clin Nephrol. 2005;63(5):375-80. |
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| The prognosis for adults with acute post-streptococcal glomerulonephritis (PSGN) who present with crescentic glomerulonephritis and nephrotic proteinuria is not known. | ||
|
15840673 |
MIXED_SAMPLE | Adult |
| Development of glomerulonephritis during anti-TNF-alpha therapy for rheumatoid arthritis. | ||
|
Stokes MB, Foster K, Markowitz GS, Ebrahimi F, Hines W, Kaufman D, Moore B, Wolde D, D'Agati VD. Nephrol Dial Transplant. 2005;20(7):1400-6. |
||
| Two individuals presented with new onset renal insufficiency, haematuria and proteinuria, and renal biopsies showed pauci-immune necrotizing and crescentic glomerulonephritis. | ||
|
15830277 |
FEMALE | Middle Aged |
| The increase of antiglomerular basement membrane antibody following pauci-immune-type crescentic glomerulonephritis. | ||
|
Kitagawa W, Miura N, Yamada H, Nishikawa K, Futenma A, Imai H. Clin Exp Nephrol. 2005;9(1):69-73. |
||
| Proteinuria, hematuria, and elevated BUN (47.8 mg/dl) and creatinine (3.4 mg/dl) suggested rapidly progressive glomerulonephritis. | ||
|
11579530 |
FEMALE | |
| [Elderly-onset anticentromere antibody-positive pulmonary-renal syndrome: report of an autopsy case]. | ||
|
Oide T, Iwamura A, Yamamoto H, Aizawa K, Inoue K, Itoh N, Ikeda S. Nihon Kokyuki Gakkai Zasshi. 2001;39(7):498-503. |
||
| Because of hematuria, proteinuria with various casts, renal dysfunction and anemia, a clinically diagnosis of rapidly progressive glomerulonephritis was made. | ||
|
9428460 |
FEMALE | |
| Rifampicin-associated acute renal failure: pathophysiologic, immunologic, and clinical features. | ||
|
De Vriese AS, Robbrecht DL, Vanholder RC, Vogelaers DP, Lameire NH. Am J Kidney Dis. 1998;31(1):108-15. |
||
| The other cases of rifampicin-associated ARF were unrelated to this subgroup: two cases of rapidly progressive glomerulonephritis, five cases of acute interstitial nephritis, and four cases of light chain proteinuria were recorded. | ||