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Perioperative Management of Patients with Hemophilia during Spinal Surgery

Kobayashi , Imagama S, Ando K, Ito K, Tsushima M, Morozumi M, Tanaka S, Machino M, Ota K, Nishida Y, Ishiguro N

STUDY DESIGN: Single-center retrospective study. PURPOSE: To optimize the perioperative management of patients with hemophilia who are undergoing spinal surgery. OVERVIEW OF LITERATURE: Hemophilia is a rare disease in which there is...
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Acquired Hemophilia A Combined with Systemic Lupus Erythematosus: A Case Report and Literature Review

You J, Kim H, Park JS, Chang MH, Lee CH

Acquired hemophilia A (AHA) is a rare hemorrhagic disorder caused by autoantibodies against factor VIII (FVIII). An 80-year-old woman presented multiple bruises on her upper and lower extremities, along with...
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Differential diagnosis of childhood hemorrhagic disorders

Yoon HS

Bruising and bleeding are common events in children. The pediatrician must be able to determine whether a child's symptoms are normal or perhaps indicative of hemorrhagic disorders. A thorough medical...
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A Case of Successful Endoscopic Submucosal Dissection of Gastric Adenoma in a Patient with Congenital Factor VII Deficiency

Kim SH, Choi SH, Lee JW, Shin WJ, Bang CS, Baik GH

Congenital factor VII deficiency is a rare hemorrhagic disorder, and invasive procedures are likely to cause excessive bleeding in these patients. Endoscopic submucosal dissection (ESD) has been accepted as a...
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Analysis of factors affecting hemorrhagic diathesis and overall survival in patients with acute promyelocytic leukemia

Lee HJ, Kim DH, Lee S, Koh MS, Kim SY, Lee JH, Lee S, Oh SY, Han JY, Kim HJ, Kim SH

BACKGROUND/AIMS: This study investigated whether patients with acute promyelocytic leukemia (APL) truly fulfill the diagnostic criteria of overt disseminated intravascular coagulation (DIC), as proposed by the International Society on Thrombosis...
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Hemorrhagic Diathesis as the Presenting Symptom of Neonatal Cholestasis

Faverey LC, Vandenplas Y

A 4-week-old infant presented with a coagulation disorder resulting from a vitamin K deficiency. The vitamin K deficiency was caused by neonatal cholestasis due to biliary atresia. Jaundice, hepatomegaly and...
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Surgery in patients with congenital factor VII deficiency: A single center experience

Kim SH, Park YS, Kwon KH, Lee JH, Kim KC, Yoo MC

BACKGROUND: Congenital factor VII (FVII) deficiency is a rare hemorrhagic disorder that can cause excessive bleeding during and after surgery in affected patients. The recombinant form of activated factor VII...
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Crown removal and endodontic drainage as a last method in active gingival bleeding with liver cirrhosis and periodontitis: a case report

Choi YS, Kang SH, Kim MK, Lee CU, Yoo JH

The most common local cause of active gingival bleeding is the vessel engorgement and erosion by severe inflammation. Abnormal gingival bleeding is also associated with the systemic disturbances. Hemorrhagic disorders...
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Post-operative Bleeding due to Acquired Hemophilia Successfully Treated with Recombinant Factor VIIa: Case Report

Lee N, Yoon SH, Lim W, Kim MH, Kim HJ, Kim SK, Park JS, Seol YM, Song MK, Choi YJ, Chung JS, Cho GJ

Acquired hemophilia is a rare but potentially life-threatening hemorrhagic disorder caused by the development of autoantibodies against coagulation factor VIII. Concentrates of human factor VIII, desmopressin, activated prothrombin complex concentrates,...
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Acquired von Willebrand Syndrome Associated with Amyloidosis

Pakk H, Kim IH, Park SH, Lee DS, Park SY, Cho HI, Kim HK

Acquired von Willebrand syndrome (AvWS) is a relatively rare acquired bleeding disorder similar to inherited von Willebrand disease in terms of laboratory findings, and occurs without a personal or family...
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Ruptured Intracranial Aneurysm Successfully Treated by Clipping in a Patient with Idiopathic Thrombocytopenic Purpura: A Case Report

Choi JE, Joo SP, Seo BR, Kim TS

  • KMID: 2029756
  • Korean J Cerebrovasc Surg.
  • 2008 Jun;10(2):383-386.
We report here on a case of a ruptured left posterior communicating artery (P-com) aneurysm that was treated by clipping in a patient with idiopathic thrombocytopenic purpura (ITP) and steroids...
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A Case of Childhood Acute Idiopathic Thrombocytopenic Purpura Aggravated Following Treatment at a Herbal Clinic

Kim JW, Kim YL

  • KMID: 2302366
  • Korean J Dermatol.
  • 2006 Jan;44(1):100-102.
Idiopathic thrombocytopenic purpura (ITP) is a hemorrhagic disorder due to accelerated sequestration of antibody-sensitized platelets. Acute ITP occurs most frequently in children and rarely persists for more than 6 months....
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Acute Ammonium Dichromate Poisoning: A Case Report

Choi DH, Joo MD, Jun DH, Choi WI, Lee DP

  • KMID: 2331406
  • J Korean Soc Emerg Med.
  • 2004 Jun;15(3):201-204.
Soluble compounds of chromium are widely used in industrial processes, including printing, photography, pyrotechnics, dyeing, electroplating, aircraft, shipbuilding, and leather tanning. Exposure in industry is generally via the inhalation of...
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Hemorrhagic Cystitis Following Allogeneic Hematopoietic Cell Transplantation

Lee GW, Lee JH, Choi SJ, Kim S, Seol M, Kim WK, Lee JS, Lee KH

We conducted a retrospective study to investigate the incidence, risk factors, and clinical features of hemorrhagic cystitis (HC) following allogeneic hematopoietic cell transplantation (allo-HCT). Adult patients who developed HC after...
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A Case of Kasabach-Merritt syndrome with generalized hemorrhagic diathesis

Park J, Yang WY, Yang YM, Lee DH, Choi WS

  • KMID: 2119643
  • J Korean Soc Plast Reconstr Surg.
  • 1999 Nov;26(6):1177-1181.
Kasabach-Merritt syndrome is the association of thrombocytopenia, disorder of coagulation, spontaneous bleeding and enlargement of a hemangima or extensive hemangiomatosis, which can be often life threatening. We experienced a three...
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A Case of TypeI Glanzmann's Thrombasthenia Diagnosed by Flow Cytometry

Lee MS, Shin CH, Kim KY, Son DW, Chung HR, Kim DH

  • KMID: 1946332
  • J Korean Pediatr Soc.
  • 1999 Jan;42(1):133-137.
Glanzmann's thrombasthenia is a rare autosomal recessive hemorrhagic disorder of platelet function with missing or abnormal platelet plasma membrane glycoprotein IIb-IIIa, which functions as a receptor for fibrinogen. We have...
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Clinical Feature of von Willebrand Disease

Lee KS, Choi EJ

  • KMID: 1535332
  • Korean J Pediatr Hematol Oncol.
  • 1998 Oct;5(2):278-284.
PURPOSE: Although von Willebrand disease is the most frequent hereditary hemorrhagic disorder. Its biological characteristics make some difficulties in diagnosing this common disease, so careful individual history taking and laboratory...
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Postoperative Severe Hemorrhage Due to Disseminated Intravascular Coagulation: A case report

Chung EB, Park SH, Lee JH, Lee KN, Moon JI

Disseminated intravascular coagulation (DIC) is a pathological syndrome in which activation of coagulation cascade leads to fibrin clot formation, consumption of platelets and coagulation factors, and secondary fibrinolysis. We report...
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A Case of Unusual Clinical Course in Patient with Hemorrhagic Fever with Renal Syndrome Associated with Secondary Amyloidosis

Lee JE, Do YR, Kim SI, Lee WS, Song HS

  • KMID: 2038500
  • Korean J Hematol.
  • 1997 Nov;32(3):440-445.
Hemorrhagic fever with renal syndrome (HFRS) is a symptom complex of fever, chill, myalgia, hemorrhagic diathesis and acute renal failure. We experienced a case of non-oliguric HFRS associated severe thrombocytopenia....
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Diagnosis and Treatment of Childhood Hemorrhagic Disorders

Kim HK

  • KMID: 1747713
  • J Korean Pediatr Soc.
  • 1996 Jul;39(7):901-907.
No abstract available.
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