Unusual association of a positive pANCA pauci-immune extracapillary glomerulonephritis in a lupus patient [0.03%]
一名系统性红斑狼疮患者的pANCA阳性寡免疫局灶节段性坏死性肾小球肾炎病例报告
W Fadili,N H Bassit,Z E Ghali et al.
W Fadili et al.
Succesfully treated Curvularia lunata peritonitis in a peritoneal dialysis patient [0.03%]
腹膜透析患者曲霉属肺阵发性紧张素成功治疗体会
U Kalawat,G S Reddy,Y Sandeep et al.
U Kalawat et al.
Reversible dialysis-dependent renal failure due to undiagnosed renovascular disease [0.03%]
误诊血管病变所致可逆性血液透析依赖性肾功能衰竭病例报告
R Jha,D Gude,G Narayan et al.
R Jha et al.
Renovascular disease (RVD) can present with resistant hypertension, acute or rapidly progressive renal failure and occasionally nephrotic proteinuria. Revascularization plays an important role in controlling blood pressure and preserving re...
Catastrophic antiphospholipid antibody syndrome in a child with thrombotic microangiopathy [0.03%]
抗磷脂抗体综合征合并血栓性微血管病的儿童个案報告
N Prasad,D Bhadauria,N Agarwal et al.
N Prasad et al.
Thrombotic microangiopathic hemolytic anemia (TMHA) is not uncommon in clinical nephrology practice while antiphospholipid syndrome (APS) is uncommon. Although less than 1% of patients with APS develop catastrophic APS (CAPS), its potential...
Contrasting approaches to end of life and palliative care in end stage kidney disease [0.03%]
终末期肾病患者的姑息治疗和安乐死的不同方法及观点
A N Koshy,R Mace,L Youl et al.
A N Koshy et al.
With increased numbers of the elderly, including nursing home patients, being accepted for end-stage kidney disease (ESKD) management, there is heightened interest and focus on end of life decisions, advanced care planning and directives, w...
Chronic tubulointerstitial nephritis in a solitary kidney of a child with Noonan syndrome [0.03%]
诺顿综合征儿童独肾慢性间质性肾炎
V Golay,R Pandey,A Roychowdhary
V Golay
Noonan syndrome is a genetic disorder with involvement of many organ systems; facial dysmorphism and cardiovascular defects being the common abnormalities. Renal involvement is uncommon and abnormalities of the genitourinary system are usua...
Postrenal transplant laryngeal and visceral leishmaniasis - A case report and review of the literature [0.03%]
肾移植后喉部和内脏利什曼病一例报告及文献回顾
P K Jha,M Vankalakunti,V Siddini et al.
P K Jha et al.
Visceral leishmaniasis (kala-azar) is a disease caused by protozoa of genus Leishmania. It is currently regarded as the second most dreaded parasitic disease, next to malaria. There have been very few case reports of visceral leishmaniasis ...
Hereditary ADAMTS 13 deficiency presenting as recurrent acute kidney injury [0.03%]
ADAMTS13缺陷遗传导致反复急性肾损伤
T E Jamale,N K Hase,M Kulkarni et al.
T E Jamale et al.
We report here a case of 26-year-old male who presented with history of recurrent acute renal failure associated with microangiopathic hemolytic anemia and thrombocytopenia. ADAMTS 13 deficiency due to mutation in the gene encoding for ADAM...
P Mukhopadhyay,M Rathi,H S Kohli et al.
P Mukhopadhyay et al.
Spontaneous perirenal hematoma following ruptured microaneurysm is an unusual but serious complication of polyarteritis nodosa. We describe a young male who presented with spontaneous perirenal hematoma and was subsequently diagnosed to hav...