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"Eun Jin Shim"

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"Eun Jin Shim"

Case Reports
[English]
A Case of Fungemia due to Rhodotorula Glutinis with Liver Cirrhosis
Jin Kyeong Park, Jae Jung Park, Jung Yoon Yoon, Jung Youn Jo, Eun Kyung Baek, Eun Jin Shim, Kwon Yu, Hee Jung Choi
Ihwa Ŭidae chi 2008;31(1):37-39.   Published online June 30, 2008
DOI: https://doi.org/10.12771/emj.2008.31.1.37

Rhodotorula species are emergent opportunistic pathogens, Particularly m mmunocompromised patients. Rhodotorula mucilaginosa was the species most frequently recovered, followed by Rhodotorula glutinis. They have been associated with endocarditis, peritonitis, meningitis and catheter-associated fungemia. We experienced a case of catheter-related blood stream infection by rhodotorula glutinis. He was 46-year old man with decompensated liver cirrhosis. He was admitted for esophageal variceal bleeding. Rhodotorula glutinis was identified on blood culture, and amphotericin B was administered for fungemia treatment.

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[English]
A Case of C-ANCA Positive Rapidly Progressive Glomerulonephritis Associated with Polyclonal Gammopathy
Eun Kyung Beak, Sun Hee Roh, Jin Kyeong Park, Jung Youn Jo, Sung Shin Kwon, Eun Jin Shim, Kyung Joo Kwon, Young Wook Noh, Kyung Jong Lee, Jung Yoon Yoon, In Seon Kim, So I Kim, Dong Ryeol Ryu, Soon Hee Sung, Ki Sook Hong
Ihwa Ŭidae chi 2008;31(1):31-35.   Published online June 30, 2008
DOI: https://doi.org/10.12771/emj.2008.31.1.31

Rapidly progressive glomerulonephritis(RPGN) is one of the most calamitous renal disease which is clinically characterized by sudden and relentless deterioration in renal function within weeks to months and associated with the pathologic finding of extensive extracapillary proliferation. Pauci-immune RPGN is mostly associated with anti neutrophil cytoplasmic antibody (ANCA) positive systemic vasculitis, but renal-limited RPGN may be found in part. We experienced a case of ANCA positive RPGN associated with polyclonal gammopathy without systemic symptoms. A 64-year-old woman was admitted with gross hematuria and azotemia. Laboratory findings revealed polyclonal gammopathy and severe anemia without definite cause, and she was diagnosed as C-ANCA positive crescentic glomerulonephritis without systemic vasculitis. She was treated with steroid pulse therapy and her renal function and anemia were progressively improved. We report herein a rare case of C-ANCA positive crescentic glomerulonephritis associated with polyclonal gammopathy and severe anemia with the review of literature.

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