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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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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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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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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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A Case of cytophagic Histiocytic Panniculitis

Chun BN, Shin HJ, Yu HJ, Son SJ

  • KMID: 2231306
  • Korean J Dermatol.
  • 1989 Oct;27(5):589-592.
We describe a case of typical cytophagic histiocytic panniculitis occuring in 10-year-old male. He had recurrent subcutaneous nodules, fever, pancytopenia and abnormal liver function tests since 5 months of his...
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Anesthetic Management for Patient with Hemophilia A

Lee SR, Kim KH, Seung IS

Numerous advances have been applied for the management of hemophiliac patients and the life expectancy of them was markedly improved. But they have many problems yet such as transmission...
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A Case of Benign Cytophagic Histiocytic Panniculitis

Lee JH, Han EH, Kwon KS, Chung TA

  • KMID: 2230846
  • Korean J Dermatol.
  • 1994 Feb;32(1):99-104.
Cytophagic histiocytic panniculitis is a histiocytic disorder which is characterized by recurrent subcutaneous nodules, fever, pancytopenia, and abnormal hepatocyte function. Most patients had systemic involvement with hepatosplenomegaly and pancytopenia and,...
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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 Cytophagic Histiocytic Panniculitis

Lee DW, Park BC, Houh D, Kim SY, Kim HO, Kim CW

Cytophagic histiocytic panniculitis(CHP) is a histiocytic disorder that was first described by Winkelmann and Crotty in 1980. We have recently experienced a case of CHP is a 21-year-old female who...
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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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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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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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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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A Case of Acute Renal Failure due to Massive Blood Loss during Gastrectomy

Han YM

Often anesthesiologists are experienced to performe the inevitable blood transfusion during massive blood loss. Red blood cells are transfused primarily to increase transport of oxygen to tissues. An increase in...
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A Case of Spinal Epidural Hematoma due to Arteriovenous Malformation

Lee YH, Oh SW, Kim SW, Chun YK

  • KMID: 2208262
  • J Korean Pediatr Soc.
  • 1996 Mar;39(3):431-435.
Spinal epidural hematoma results from various causes such as use of anticoagulants, hemorrhagic diathesis, pregnancy, labor, arteriovenous malformation and spinal anesthesia as well as idiopathic orgin. We report a 3-year-old...
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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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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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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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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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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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