- A Case of Pneumocystis jirovecii Pneumonia Following CMV Duodenitis in a Kidney Transplant Patient
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Kim HW, Kim MG, Woo YS, Boo CS, Jo SK, Kim HK, Jo WY, Lee KG, Kim HO, Oh CR, Kim JH
- KMID: 1477258
- Korean J Nephrol.
- 2008 Sep;27(5):631-637.
Solid organ transplant recipients are at increased risk for various opportunistic infections because of their immunocompromised state. Pneumocystis jirovecii (carinii) infection has posed serious problems in these patients which can... -
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- A Case of Successfully Treated Pneumocystis jiroveci Pneumonia in CMV-associated IgA Nephropathy
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Lee MY, Jang SH, Park MJ, Hwang WM, Yun SR
- KMID: 1806940
- Infect Chemother.
- 2012 Dec;44(6):491-494.
- doi: 10.3947/ic.2012.44.6.491
A range of infections including cytomegalovirus (CMV) infections are associated with IgA nephropathy. Several reports have suggested that the risk of Pneumocystis infections is lower in the presence of preceding... -
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- Pneumocystis jirovecii Pneumonia with Granulomatous Reaction in the Lung and the Liver Discovered at Autopsy
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Kim MY, Bak S, Park S, Choi M, Lee SD
- KMID: 2350697
- Korean J Leg Med.
- 2016 Aug;40(3):88-92.
- doi: 10.7580/kjlm.2016.40.3.88
We report the case of a 42-year-old woman who died in hospital from severe respiratory failure, 10 days after the onset of symptoms. Autopsy and microscopic examination identified features of... -
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- Systemic New Antifungal Agents
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Cho YK
- KMID: 1517366
- Korean J Med Mycol.
- 2003 Dec;8(4):147-156.
Voriconazole is a second-generation triazole that has an enhanced antifungal spectrum, compared with older triazoles. It will likely become the drug of choice for treatment of invasive aspergillosis and many... -
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- Successful Treatment with Rituximab and Immunoadsorption for an Auto-Antibody Induced Bile Salt Export Pump Deficiency in a Liver Transplanted Patient
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Quintero J, Juamperez , Gonzales E, Julio E, Mercadal-Hally M, Collado-Hilly M, MarÃn-Sánchez A, Charco R
- KMID: 2471627
- Pediatr Gastroenterol Hepatol Nutr.
- 2020 Mar;23(2):174-179.
- doi: 10.5223/pghn.2020.23.2.174
We present an 8 years old girl who was diagnosed at 6 months of age of Progressive Familial Intrahepatic Cholestasis type 2. Although liver transplantation (LT) was classically considered curative... -
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