Total: 14 |
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PMID (PMCID) | ||
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28341428 |
FEMALE | Child |
Renal papillary necrosis in patients with sickle cell disease: How to recognize this 'forgotten' diagnosis. | ||
Henderickx MMEL, Brits T, De Baets K, Seghers M, Maes P, Trouet D, De Wachter S, De Win G. J Pediatr Urol. 2017;13(3):250-256. |
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It is known to be associated with sickle cell hemoglobinopathies; however a wide range of etiologies are possible, and it is therefore not the first diagnosis clinicians consider in patients with sickle cell disease who present with hematuria. | ||
28341428 |
FEMALE | Child |
Renal papillary necrosis in patients with sickle cell disease: How to recognize this 'forgotten' diagnosis. | ||
Henderickx MMEL, Brits T, De Baets K, Seghers M, Maes P, Trouet D, De Wachter S, De Win G. J Pediatr Urol. 2017;13(3):250-256. |
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This study aims to remind clinicians of this "forgotten" diagnosis and what signs to look for in pediatric patients with sickle cell disease who present with hematuria. | ||
28341428 |
FEMALE | Child |
Renal papillary necrosis in patients with sickle cell disease: How to recognize this 'forgotten' diagnosis. | ||
Henderickx MMEL, Brits T, De Baets K, Seghers M, Maes P, Trouet D, De Wachter S, De Win G. J Pediatr Urol. 2017;13(3):250-256. |
||
These findings are illustrated with a case of a 9-year old girl with sickle cell disease who was referred with painless gross hematuria. | ||
25035790 |
OTHER | |
A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation. | ||
Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22. |
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Despite the fact that immunoglobulin A nephropathy is the most commonly diagnosed glomerulonephritis worldwide, an association between this entity and sickle cell disease has not yet been reported, probably because all cases of hematuria in patients with sickle cell disease have been regarded as secondary to sickle cell disease. | ||
25035790 |
OTHER | |
A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation. | ||
Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22. |
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This case report describes a novel case of a patient with sickle cell disease who presented with proteinuria and microscopic dysmorphic (glomerular) hematuria. | ||
25035790 |
OTHER | |
A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation. | ||
Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22. |
||
Despite the fact that immunoglobulin A nephropathy is the most commonly diagnosed glomerulonephritis worldwide, an association between this entity and sickle cell disease has not yet been reported, probably because all cases of hematuria in patients with sickle cell disease have been regarded as secondary to sickle cell disease. | ||
25035790 |
OTHER | |
A novel case report of sickle cell disease-associated immunoglobulin A nephropathy: the diagnostic value of erythrocyte dysmorphism evaluation. | ||
Silva GE, Teixeira AC, Vergna JG, Salgado-Filho N, Crivellentti LZ, Costa RS, Dantas M. Int J Clin Exp Med. 2014;7(6):1619-22. |
||
Despite the fact that immunoglobulin A nephropathy is the most commonly diagnosed glomerulonephritis worldwide, an association between this entity and sickle cell disease has not yet been reported, probably because all cases of hematuria in patients with sickle cell disease have been regarded as secondary to sickle cell disease. | ||
23619113 |
FEMALE | |
Hyperhemolysis in sickle cell disease. | ||
Aragona E, Kelly MJ. J Pediatr Hematol Oncol. 2014;36(1):e54-6. |
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An 18-year-old female with sickle cell disease presented with thigh pain, dark urine, and hematuria within 72 hours of receiving a blood transfusion. | ||
19669800 |
MALE | Child |
Two cases of hematuria with hemoglobin C trait. | ||
Spencer JD, Sanders JT, Ault BH. Pediatr Nephrol. 2009;24(12):2455-7. |
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Patients with sickle cell disease commonly experience painless hematuria. | ||
19669800 |
MALE | Child |
Two cases of hematuria with hemoglobin C trait. | ||
Spencer JD, Sanders JT, Ault BH. Pediatr Nephrol. 2009;24(12):2455-7. |
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Hematuria may be found in patients with sickle cell trait, sickle cell anemia, and sickle cell hemoglobin C disease, but it is believed to be uncommon in patients with other hemoglobinopathies, such as hemoglobin C disease and hemoglobin C trait. | ||
15593260 |
MALE | Adult |
Cytologic features of renal medullary carcinoma. | ||
Assad L, Resetkova E, Oliveira VL, Sun W, Stewart JM, Katz RL, Caraway NP. Cancer. 2005;105(1):28-34. |
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Renal medullary carcinoma should be considered in the differential diagnosis of patients who present with hematuria or a renal mass, especially in young black men with sickle cell disease or trait. | ||
7871949 |
MIXED_SAMPLE | Adult |
Hematuria in sickle cell anemia--not always benign: evidence for excess frequency of sickle cell anemia in African Americans with renal cell carcinoma. | ||
Baron BW, Mick R, Baron JM. Acta Haematol. 1994;92(3):119-22. |
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Hematuria in sickle cell anemia--not always benign: evidence for excess frequency of sickle cell anemia in African Americans with renal cell carcinoma. | ||
7871949 |
MIXED_SAMPLE | Adult |
Hematuria in sickle cell anemia--not always benign: evidence for excess frequency of sickle cell anemia in African Americans with renal cell carcinoma. | ||
Baron BW, Mick R, Baron JM. Acta Haematol. 1994;92(3):119-22. |
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Hematuria in sickle cell anemia--not always benign: evidence for excess frequency of sickle cell anemia in African Americans with renal cell carcinoma. | ||
682269 |
FEMALE | Adult |
Conservative surgery for refractory sickle cell hematuria. | ||
Douglas LL, Pawaroo J. J Urol. 1978;120(3):385-6. |
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Two cases of recurrent hematuria from sickle cell disease are described. |