1.Diagnostic Experience in the 3 Human Brucellosis Cases by the Microbiologic, Serologic and Gene Tests.
Gyoung Yim HA ; Young Sil CHOI ; Moon Yeon KIM ; Young Hyun LEE ; Kyoung Seop LEE ; Kyu Jam HWANG ; Mi Yeon PAK
Korean Journal of Clinical Microbiology 2007;10(2):154-159
Brucellosis is a zoonosis caused by Brucella species. B. melitensis, B. suis, B. abortus and B. canis can infect humans. Recently, as the cases of bovine brucellosis have increased every year in Korea, the cases of human brucellosis have also increased among livestock workers and veterinarians in rural areas, since the first human case was reported in 2003. Because clinical manifestations of the disease are nonspecific and may be very atypical, clinicians and laboratory persons need to be active in using diagnostic tools including polymerase chain reaction in addition to the ordinary culture and serologic tests, and taking an appropriate measure to prevent intralaboratory infection. We report herein our experience in three human brucellosis cases diagnosed by cultures, serologic tests and gene detection.
Animals
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Brucella
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Brucellosis*
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Brucellosis, Bovine
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Cattle
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Humans*
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Korea
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Livestock
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Polymerase Chain Reaction
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Serologic Tests
;
Veterinarians
2.Clinicopathologic significance of tumor microenvironment CD11c, and FOXP3 expression in diffuse large B-cell lymphoma patients receiving rituximab, cyclophosphamide, anthracycline, vincristine, and prednisone (R-CHOP) combination chemotherapy.
Seul LEE ; Dong Hyun KIM ; Sung Yong OH ; So Yeon KIM ; Myeong Seok KOH ; Ji Hyun LEE ; Suee LEE ; Sung Hyun KIM ; Jong Young KWAK ; Min Gyoung PAK ; Mi Ha JU ; Hyo Jin KIM ; Jin Sook JEONG
The Korean Journal of Internal Medicine 2017;32(2):335-344
BACKGROUND/AIMS: CD11c is a dendritic cell marker in humans, which potentially induces a cytotoxic effect on lymphoma cells. Forkhead boxP3 (FOXP3) is a regulator of T lymphocyte in the microenvironment of the lymphoma. The principal objective of this study was to determine whether the tumors' microenvironment expressions of CD11c and FOXP3 are predictive of clinical outcomes in diffuse large B-cell lymphoma (DLBCL) patients receiving treatment with rituximab, cyclophosphamide, anthracycline, vincristine, and prednisone (R-CHOP) combination chemotherapy. METHODS: The study population consisted of 100 patients with DLBCL. The CD11c and FOXP3 expression in primary tumors' microenvironment were evaluated using an immunohistochemistry (IHC). RESULTS: CD11c and FOXP3 expression positivity in microenvironment were 25% and 35%, respectively. Each one counted for 1 point. In CD11c and FOXP3 stain, positive was counted as 0 and negative was 1. The points were separated into low risk (0 to 1) and high risk (2) groups. Only the extranodal DLBCL patient group analysis conveyed significant differences of progression-free survival (p = 0.019) and overall survival (p = 0.039) between the two groups. CONCLUSIONS: We can achieve possible clinical significance of lymphoma tumor microenvironments through CD11c and FOXP3 IHC stains in extranodal DLBCL patients receiving R-CHOP therapy.
B-Lymphocytes*
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Coloring Agents
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Cyclophosphamide*
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Dendritic Cells
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Disease-Free Survival
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Drug Therapy, Combination*
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Humans
;
Immunohistochemistry
;
Lymphocytes
;
Lymphoma
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Lymphoma, B-Cell*
;
Lymphoma, Large B-Cell, Diffuse
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Prednisone*
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Rituximab*
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Tumor Microenvironment*
;
Vincristine*