1.Guidelines for Cancer Care during the COVID-19 Pandemic in South Korea
Jii Bum LEE ; Minkyu JUNG ; June Hyuk KIM ; Bo Hyun KIM ; Yeol KIM ; Young Seok KIM ; Byung Chang KIM ; Jin KIM ; Sung Ho MOON ; Keon-Uk PARK ; Meerim PARK ; Hyeon Jin PARK ; Sung Hoon SIM ; Hong Man YOON ; Soo Jung LEE ; Eunyoung LEE ; June Young CHUN ; Youn Kyung CHUNG ; So-Youn JUNG ; Jinsoo CHUNG ; Eun Sook LEE ; Hyun Cheol CHUNG ; Tak YUN ; Sun Young RHA
Cancer Research and Treatment 2021;53(2):323-329
At the end of 2019, the cause of pneumonia outbreaks in Wuhan, China, was identified as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In February 2020, the World Health Organization named the disease cause by SARS-CoV-2 as coronavirus disease 2019 (COVID-19). In response to the pandemic, the Korean Cancer Association formed the COVID-19 task force to develop practice guidelines. This special article introduces the clinical practice guidelines for cancer patients which will help oncologists best manage cancer patients during the COVID-19 pandemic.
2.Guidelines for Cancer Care during the COVID-19 Pandemic in South Korea
Jii Bum LEE ; Minkyu JUNG ; June Hyuk KIM ; Bo Hyun KIM ; Yeol KIM ; Young Seok KIM ; Byung Chang KIM ; Jin KIM ; Sung Ho MOON ; Keon-Uk PARK ; Meerim PARK ; Hyeon Jin PARK ; Sung Hoon SIM ; Hong Man YOON ; Soo Jung LEE ; Eunyoung LEE ; June Young CHUN ; Youn Kyung CHUNG ; So-Youn JUNG ; Jinsoo CHUNG ; Eun Sook LEE ; Hyun Cheol CHUNG ; Tak YUN ; Sun Young RHA
Cancer Research and Treatment 2021;53(2):323-329
At the end of 2019, the cause of pneumonia outbreaks in Wuhan, China, was identified as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. In February 2020, the World Health Organization named the disease cause by SARS-CoV-2 as coronavirus disease 2019 (COVID-19). In response to the pandemic, the Korean Cancer Association formed the COVID-19 task force to develop practice guidelines. This special article introduces the clinical practice guidelines for cancer patients which will help oncologists best manage cancer patients during the COVID-19 pandemic.
3.Rab25 augments cancer cell invasiveness through a β1 integrin/EGFR/VEGF-A/Snail signaling axis and expression of fascin
Bo Young JEONG ; Kyung Hwa CHO ; Kang Jin JEONG ; Yun Yong PARK ; Jin Man KIM ; Sun Young RHA ; Chang Gyo PARK ; Gordon B MILLS ; Jae Ho CHEONG ; Hoi Young LEE
Experimental & Molecular Medicine 2018;50(1):e435-
The small GTP-binding protein Rab25 is associated with tumor formation and progression. However, recent studies have shown discordant effects of Rab25 on cancer cell progression depending on cell lineage. In the present study, we elucidate the underlying mechanisms by which Rab25 induces cellular invasion. We demonstrate that Rab25 increases β1 integrin levels and subsequent activation of EGFR and upregulation of VEGF-A expression, leading to increased Snail expression, epithelial-to-mesenchymal transition and cancer cell invasiveness. Strikingly, we identify that Snail mediates Rab25-induced cancer cell invasiveness through fascin expression and that ectopic expression of Rab25 aggravates metastasis of ovarian cancer cells to the lung. We thus demonstrate a novel role of a β1 integrin/EGFR/VEGF-A/Snail signaling cascade in Rab25-induced cancer cell aggressiveness through induction of fascin expression, thus providing novel biomarkers and potential therapeutic targets for Rab25-expressing cancer cells.
Biomarkers
;
Cell Lineage
;
Ectopic Gene Expression
;
GTP-Binding Proteins
;
Lung
;
Neoplasm Metastasis
;
Ovarian Neoplasms
;
Snails
;
Up-Regulation
;
Vascular Endothelial Growth Factor A
4.Acalculous Gallbladder Perforation and Coronary Artery Aneurysm after Kidney Transplantation.
Bo Rha PARK ; Jung Hyun KANG ; Sung Joon SHIN ; Kyung Soo KIM
The Journal of the Korean Society for Transplantation 2013;27(2):57-61
Although gallbladder (GB) perforation due to acalculous cholecystitis after kidney transplantation is rarely observed, it can be life threatening and result in cholecystectomy. Coronary artery aneurysm (CAA) is also rare and may require invasive therapy depending on its diameter. We report herein the case of a 69-year-old female who developed GB perforation due to acalculous cholecystitis after kidney transplantation and underwent cholecystectomy. The patient was later invasively treated when CCA was detected by coronary angiography.
Acalculous Cholecystitis
;
Aneurysm
;
Cholecystectomy
;
Coronary Angiography
;
Coronary Vessels
;
Female
;
Gallbladder
;
Humans
;
Kidney
;
Kidney Transplantation
5.Beta-Thalassemia Minor Is Associated with IgA Nephropathy.
Jung Hyun KANG ; Bo Rha PARK ; Kyung Soo KIM ; Do Yeun KIM ; Hee Jin HUH ; Seok Lae CHAE ; Sung Joon SHIN
Annals of Laboratory Medicine 2013;33(2):153-155
No abstract available.
Aged
;
Anemia/diagnosis
;
Bone Marrow Cells/pathology
;
Chromosomes, Human, Pair 11
;
Electrophoresis
;
Glomerulonephritis, IGA/complications/*diagnosis
;
Hematuria/pathology
;
Hemoglobin A/analysis
;
Heterozygote
;
Humans
;
Male
;
Renal Insufficiency/diagnosis
;
beta-Globins/genetics
;
beta-Thalassemia/*diagnosis/etiology
6.A Case of Acute Kidney Injury due to Retroperitoneal Sarcoma.
Bo Rha PARK ; Won Gun KWACK ; Jong Ho LEE ; Jong Sun CHOI ; Sung Joon SHIN ; Kyung Soo KIM
Korean Journal of Nephrology 2010;29(5):611-616
Retroperitoneal sarcoma is a rare tumor accounting for 1-2% of all solid malignancies. These tumors are usually large when diagnosed because of their typically silent nature and should be distinguished from other retroperitoneal masses for adequate management. In spite of an apparent complete resection which is the only potential curative treatment, the high rate of local recurrence is the major problem of retroperitoneal sarcoma; therefore, patients with high-grade tumors should undergo regular and continuous follow-ups. Postrenal acute kidney injury (AKI) results from a urinary outflow tract compression due to the mass effect of retroperitoneal sarcoma, which is one of less common causes of postrenal AKI and has not been reported in Korea. We report a case that an 81-year-old-woman with undifferentiated retroperitoneal sarcoma presented with postrenal AKI and improved after complete resection.
Accounting
;
Acute Kidney Injury
;
Follow-Up Studies
;
Humans
;
Korea
;
Recurrence
;
Retroperitoneal Neoplasms
;
Sarcoma
7.A Case of Hepatocellular Carcinoma of Unknown Origin, Presenting as Huge Abdominal Mass in an 82-year-old Female Patient.
Bo Rha PARK ; Yun Jeong LIM ; Jeong Ill SUH ; Eo Jin KIM ; Jong Sun CHOI ; Yong Seok LEE ; Jin Ho LEE
Journal of the Korean Geriatrics Society 2008;12(3):171-175
Hepatocellular carcinoma(HCC) of unknown origin presents unusually in the elderly as a huge abdominal mass. Though most commonly associated with viral infections, about 10% of HCC in Korea arise from an unknown cause. HCC of unknown origin has a varying clinical picture and prognosis. It is known to have relatively good reserve liver function and rarely complications with previous cirrhosis or active hepatitis. Its pathogenesis may be not associated with an inflammation-dysplasia-carcinoma sequence. We recently managed an unusual case of moderately differentiated hepatocellular carinoma of unknown origin presenting with a huge abdominal mass. The 82-year-old female patient had no history of viral hepatitis and no other metabolic diseases were diagnosed. She received palliative care.
Aged
;
Aged, 80 and over
;
Carcinoma, Hepatocellular
;
Female
;
Fibrosis
;
Hepatitis
;
Humans
;
Korea
;
Liver
;
Metabolic Diseases
;
Neoplasms, Unknown Primary
;
Prognosis
8.Diagnosis of Antibiotic-Associated Diarrhea and Pseudomembranous Colitis by Direct Detection of Clostridium difficile Toxin B Gene.
Yoo Rha HONG ; Seok Hoon JEONG ; Kyung Bo KIM ; Sang Ho LEE ; Kyung Hyun CHOI ; Seun Ja PARK ; Mooin PARK ; Byung Chan JEON
Infection and Chemotherapy 2003;35(5):241-248
BACKGROUND: Clostridium difficile is the major cause of antibiotic-associated diarrhea (AAD) and pseudomembranous colitis (PMC). This study was designed to investigate predisposing factors of AAD or PMC and to evaluate the efficiency of nested PCR assay for direct detection of toxin B gene in the treatment and prognosis of these diseases. METHODS: From January to December, 2002, stool specimens from 142 patients in Kosin Medical Center, Busan, were tested for the detection of toxigenic C. difficile strains. Toxin B gene in C. difficile was detected by nested PCR. And chart review was performed to investigate the antibiotics or anticancer drug history, clinical symptoms, treatment regimens, and prognosis. RESULTS: Among 142 stool specimens, 56 specimens showed positive for the toxin B gene in C. difficile strains by PCR. Forty two percents (47/113) of stool specimens from patients with AAD and all of specimens from eight patiens with PMC were C. difficile toxin B gene positive. Administration of antibiotics or anticancer drugs was stopped in 92.7% of toxin B gene-positive cases, but those were stopped in only 48.5% of toxin B gene-negative cases. The cure rate was higher in positive cases (82%) than negative ones (71%). CONCLUSION: It is concluded that nested PCR assay for the direct detection of C. difficile toxin B gene was helpful in rapid diagnosis and treatment of AAD or PMC.
Anti-Bacterial Agents
;
Busan
;
Causality
;
Clostridium difficile*
;
Clostridium*
;
Diagnosis*
;
Diarrhea*
;
Enterocolitis, Pseudomembranous*
;
Humans
;
Polymerase Chain Reaction
;
Prognosis
9.Diagnosis of Antibiotic-Associated Diarrhea and Pseudomembranous Colitis by Direct Detection of Clostridium difficile Toxin B Gene.
Yoo Rha HONG ; Seok Hoon JEONG ; Kyung Bo KIM ; Sang Ho LEE ; Kyung Hyun CHOI ; Seun Ja PARK ; Mooin PARK ; Byung Chan JEON
Infection and Chemotherapy 2003;35(5):241-248
BACKGROUND: Clostridium difficile is the major cause of antibiotic-associated diarrhea (AAD) and pseudomembranous colitis (PMC). This study was designed to investigate predisposing factors of AAD or PMC and to evaluate the efficiency of nested PCR assay for direct detection of toxin B gene in the treatment and prognosis of these diseases. METHODS: From January to December, 2002, stool specimens from 142 patients in Kosin Medical Center, Busan, were tested for the detection of toxigenic C. difficile strains. Toxin B gene in C. difficile was detected by nested PCR. And chart review was performed to investigate the antibiotics or anticancer drug history, clinical symptoms, treatment regimens, and prognosis. RESULTS: Among 142 stool specimens, 56 specimens showed positive for the toxin B gene in C. difficile strains by PCR. Forty two percents (47/113) of stool specimens from patients with AAD and all of specimens from eight patiens with PMC were C. difficile toxin B gene positive. Administration of antibiotics or anticancer drugs was stopped in 92.7% of toxin B gene-positive cases, but those were stopped in only 48.5% of toxin B gene-negative cases. The cure rate was higher in positive cases (82%) than negative ones (71%). CONCLUSION: It is concluded that nested PCR assay for the direct detection of C. difficile toxin B gene was helpful in rapid diagnosis and treatment of AAD or PMC.
Anti-Bacterial Agents
;
Busan
;
Causality
;
Clostridium difficile*
;
Clostridium*
;
Diagnosis*
;
Diarrhea*
;
Enterocolitis, Pseudomembranous*
;
Humans
;
Polymerase Chain Reaction
;
Prognosis
10.A case of thrombotic thrombocytopenic purpura in systemic lupus erythematosus.
Bo Suk KIM ; Jun Hyeop AN ; Woo Hyung BAE ; Sam Suk PARK ; Ho Jin SHIN ; Sung Il KIM ; Im Su KWAK ; Ha Yeon RHA
Korean Journal of Medicine 2001;60(6):593-596
Thrombotic thrombocytopenic purpura (TTP) rarely may be seen in association with autoimmune processes such as scleroderma, rheumatoid arthritis, polyarteritis nodosa, Sj gren's syndrome, and systemic lupus erythematosusus (SLE). The diagnosis of TTP as a syndrome distinct from SLE may be challenging, because both processes may present with some or all elements of the classic pentad considered pathognomonic of the former: microangiopathic hemolytic anemia, fever, thrombocytopenia, neurological deficits, and renal abnormalities. We describe a patient with synchronous TTP and SLE, and review the literature.
Anemia, Hemolytic
;
Arthritis, Rheumatoid
;
Diagnosis
;
Fever
;
Humans
;
Lupus Erythematosus, Systemic*
;
Polyarteritis Nodosa
;
Purpura, Thrombotic Thrombocytopenic*
;
Thrombocytopenia

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