1.A Case of Choriocarcinoma after Evacuation of Partial Mole.
Hyun CHO ; Jejung LEE ; Hajung CHO ; Kyunghee KO ; Hyungbae MOON ; Heunggon KIM
Korean Journal of Obstetrics and Gynecology 2004;47(12):2511-2514
Persistent gestational trophoblastic tumor develops in about 15-25% after evacuation of complete mole, and arises in about 4-5% after removal of partial mole. Especially there is reported that choriocarcinoma after evacuation of partial mole is extremely rare, and it is well responded to systemic chemotherapy. We have experienced that a case of choriocarcinoma which was developed after evacuation of partial mole. So we report this case with a brief review of literatures.
Choriocarcinoma*
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Drug Therapy
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Female
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Pregnancy
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Trophoblastic Neoplasms
2.Inherited protein S deficiency due to a novel nonsense mutation in the PROS1 gene in the patient with recurrent vascular access thrombosis: A case report.
Eun Jin CHO ; Yong Chul KIM ; Jin Ho HWANG ; Hajung LEE ; Sung Sup PARK ; So Yeon KIM ; Suhnggwon KIM ; Ho Jun CHIN
Kidney Research and Clinical Practice 2012;31(1):72-75
Vascular access thrombosis is one of the major causes of morbidity in patients maintained on chronic hemodialysis. Thrombophilia has been recognized as a risk factor of vascular access thrombosis. The authors report a case of inherited protein S deficiency associated with vascular access thrombotic events. DNA sequence analysis of the PROS1 gene identified a novel heterozygous nonsense mutation in exon 10 by transition of AAG (lysine) to TAG (stop codon) at codon 473 (c.1417A>T, p.K473X). Results from the study suggest that the inherited protein S deficiency due to a PROS1 gene mutation may cause vascular access thrombosis in hemodialysis patients.
Codon
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Codon, Nonsense
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Exons
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Humans
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Protein S
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Protein S Deficiency
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Renal Dialysis
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Risk Factors
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Sequence Analysis, DNA
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Thrombophilia
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Thrombosis
3.Proliferative Glomerulopathy with Unusual Subendothelial Deposits of Striated Structure in Multiple Myeloma.
Yun Gyoo LEE ; Dong Yeop SHIN ; Hyun Jung LEE ; Se Youn CHOI ; Jae yoon PARK ; Shin young AHN ; Hajung LEE ; Yunjung OH ; Kyung Chul MOON ; Kook Hwan OH ; Inho KIM
Korean Journal of Nephrology 2010;29(6):772-775
A 50-year-old woman was admitted for the evaluation of proteinuria and renal biopsy. On the basis of the serum monoclonal protein, marrow plasma cell dyscrasia and end organ damage (nephrotic range proteinuria), multiple myeloma was diagnosed. A renal biopsy showed a membranoproliferative glomerulonephritis pattern of injury and unusual organized deposits of striated structure in the subendothelial space, which were identified as non-amyloid non-immunoglobulin-derived deposits. These deposits contained regularly stacked straight electron-dense bands, which have not been described in the setting of paraproteinemia and/or plasma cell dyscrasia.
Biopsy
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Bone Marrow
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Female
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Glomerulonephritis, Membranoproliferative
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Humans
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Middle Aged
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Multiple Myeloma
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Paraproteinemias
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Proteinuria