Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

82 results
Display

Prognostic utility of ADAMTS13 activity for the atypical hemolytic uremic syndrome (aHUS) and comparison of complement serology between aHUS and thrombotic thrombocytopenic purpura

Oh J, Oh D, Lee SJ, Kim JO, Kim NK, Chong SY, Huh JY, Baker RI, on behalf of the Korean TTP Registry Investigators

BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) involves dysregulation of the complement system, but whether this also occurs in thrombotic thrombocytopenic purpura (TTP) remains unclear. Although these conditions are difficult to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Differential Diagnosis and Treatment of Thrombotic Microangiopathy Syndrome

Hong J

Diagnosis of thrombotic microangiopathy (TMA) is challenging due to its close association with other forms of microangiopathic hemolytic anemia, such as malignant hypertension and disseminated intravascular coagulation, and because other...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Therapeutic Plasma Exchange in a Patient with Hemophagocytic Lymphohistiocytosis

Roh J, Kim S, Nah H, Lee K, Kim HO

A 22-year old female patient with systemic lupus erythematosus presenting microangiopathic hemolytic anemia was treated with therapeutic plasma exchange 23 times. The patient's condition and laboratory findings (aspartate aminotransferase, alanine...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical characteristics and outcomes of thrombotic microangiopathy in Malaysia

Yap YY, Sathar J, Law KB, Zulkurnain PAB, Edmund SC, Chang KM, Baker R

BACKGROUND: Thrombotic microangiopathy (TMA) with non-deficient ADAMTS-13 (a disintegrin-like and metalloprotease with thrombospondin type 1 motif 13) outcome is unknown hence the survival analysis correlating with ADAMTS-13 activity is conducted...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acute Thrombotic Thrombocytopenic Purpura with Right Heart Failure Following Total Knee Replacement Surgery

Shim S, Lim CM, Koh Y, Hong SB

Thrombotic thrombocytopenic purpura (TTP) is a life-threatening condition characterized by microangiopathic hemolytic anemia, thrombocytopenia, renal insufficiency, neurological abnormalities, and fever. Cardiac involvement is not uncommon and can be fatal; however,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Thrombotic Thrombocytopenic Purpura with Exacerbation after Incomplete Remission of Therapeutic Plasma Exchange

Sohn YH, Ihm C, Choi EH, Lee SK

Thrombotic thrombocytopenic purpura (TTP) is a rare blood disorder with a mortality rate of over 90% without prompt treatment. It is caused by congenital, idiopathic, or secondary diseases; idiopathic TTP...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of thrombotic thrombocytopenic purpura in late pregnancy

Soe AM, Tun NM, Guevara E, Shulimovich M

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Thrombotic Thrombocytopenic Purpura Associated with Bone Marrow Necrosis Complicating Metastatic Extra-Mammary Paget's Disease

Sohn JM, Lee JL, Kim BJ, Song KM, Cho YU, Kim EN, Hong JH

As extra-mammary Paget's disease is rare and usually diagnosed at early stage when it is highly curable with surgical resection, it is much rarer to see patients with recurrent metastatic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Microangiopathic Hemolytic Anemia after Myxoma Excision and Mitral Valve Repair Presenting as Hemolytic Uremic Syndrome

Park YJ, Kim SP, Shin HJ, Choi JH

Microangiopathic hemolytic anemia occurs in a diverse group of disorders, including thrombotic thrombocytopenic purpura, hemolytic uremic syndrome, and prosthetic cardiac valves. Hemolytic anemia also occurs as a rare complication after...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Rheumatoid Arthritis Accompanied by Thrombotic Thrombocytopenic Purpura

Kang SM, Lee JH, Ku IH, Kim HK, Nam KS, Park SK

Thrombotic thrombocytopenic purpura (TTP) is a blood coagulation disorder that damages numerous organs, including the kidney, heart and brain. Features indicative of TTP include thrombocytopenia, microangiopathic hemolytic anemia, neurologic symptoms,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A 22-month-old Boy with Acute Glomerulonephritis Coexistent with Hemolytic Anemia and Idiopathic Thrombocytopenia

Park HW, Seo BS, Jung SJ, Lee JH

Hemolytic anemia and thrombocytopenia are rare clinical manifestations of acute glomerulonephritis. Initially, in all such cases, a diagnosis of hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, systemic lupus erythematosus, and amyloidosis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Two Different Coagulopathy Episodes in a Single Patient with Metastatic Prostate Cancer

Rheem I, Lee G

We reported a case of two different episodes of critical coagulopathy in a single patient with metastatic prostate cancer (mPC). The patient initially visited the emergency room with a huge...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Successful Treatment with Low-dose Rituximab in a Patient with Plasma Exchange-refractory Idiopathic Thrombotic Thrombocytopenic Purpura

Song KH, Hong J, Hwang H, Kang E, Park J, Ahn JY, Lee JH

Thrombotic thrombocytopenic purpura (TTP) is a clinical syndrome characterized by micro-angiopathic hemolytic anemia, thrombocytopenia, fever, renal disorders, and neurological manifestations. Its clinical course is rapid and the mortality rate is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Adult-Onset Still's Disease with Thrombotic Thrombocytopenic Purpura

Lee TH, Lee JM, Lee SY, Cho NH, Son CN, Kim JM, Kim SH

Adult-onset Still's disease (AOSD) is a rare systemic inflammatory disorder that affects multiple organs and is fatal in some cases. Thrombotic thrombocytopenic purpura (TTP), another rare disease, is characterized by...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Hemosuccus Pancreaticus Associated with Pseudoaneurysm of Splenic Artery

Cho YH, Kwon CI, Jin SM, Song SH, Park HJ, Shin DK, Park PW

Splenic artery pseudoaneurysm (SAP) is a rare condition, occurring from many causes like pancreatitis, peptic ulcer, surgery, abdominal trauma and iatrogenic origins. SAP poses a great challenge to clinicians because...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Thrombotic Thrombocytopenic Purpura and Rhabdomyolysis Associated With Acute Renal Failure in Hypothyroidism

Lee J, Lee KW, Yun SM, Shin HC, Nam SM, Cho NY

Myopathy due to hypothyroidism can be detected in its early stage, but as the symptom is mild, complications such as rhabdomyolysis are rare. Thrombotic thrombocytopenic purpura in hypothyroidism is not...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Thrombotic Thrombocytopenic Purpura after Stent Insertion in Patient with Colon Cancer

Kwun DH, Yun J, Kim SH, Kim HJ, Kim CK, Park SK, Hong DS

Thrombotic thrombocytopenic purpura (TTP), a fatal disease, is mostly idiopathic but can occur secondary to cancer, infection, transplantation, pregnancy, surgery, or drugs. The mechanism of TTP is still unknown, however,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Thrombotic Thrombocytopenic Purpura associated with Clopidogrel in a Patient with Acute Cerebral Infarction

Park J, Lee Y, Park H, Min J, Ko Y, Kim YO

Clopidogrel is an antiplatelet agent prescribed widely to prevent stent thrombosis after coronary or peripheral vascular interventions and for stroke prophylaxis. The side effects of this drug include gastrointestinal symptoms,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Postoperative Thrombotic Thrombocytopenic Purpura in a Cardiac Surgery Patient: A Case Report

Choi EJ, Lee S

Although thrombotic thrombocytopenic purpura (TTP) is a rare disease, when it develops in a post-cardiac surgery patient, it may have a fatal outcome. Since the frequency of early-onset thrombocytopenia in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Sunitinib-Associated Thrombotic Thrombocytopenic Purpura

Kim EJ, Choi YM, Lee SW, Ha YJ, Lee JL

  • KMID: 2267896
  • Korean J Med.
  • 2013 Feb;84(2):303-307.
Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome (TTP-HUS) is an acute condition with abnormalities of multiple organ systems. It is characterized by microangiopathic hemolytic anemia and thrombocytopenia. Several chemotherapeutic agents...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr