- A Case of a 14-Year-Old Girl Who Developed Dermatomyositis Associated with Mycoplasma pneumoniae Infection
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Moon HJ, Yang JK, In DH, Kwun DH, Jo HH, Chang SH
- KMID: 2317773
- Soonchunhyang Med Sci.
- 2015 Dec;21(2):130-133.
- doi: 10.0000/sms.2015.21.2.130
Extrapulmonary manifestations of Mycoplasma pneumoniae infection are not uncommon and involvement of every organ system has been reported. However, association of inflammatory myositis with M. pneumoniae infection is rare. Here,... -
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- Thrombotic Thrombocytopenic Purpura after Stent Insertion in Patient with Colon Cancer
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Kwun DH, Yun J, Kim SH, Kim HJ, Kim CK, Park SK, Hong DS
- KMID: 2317751
- Soonchunhyang Med Sci.
- 2014 Dec;20(2):176-179.
- doi: 10.0000/sms.2014.20.2.176
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,... -
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- A Case of Synchronous Gastrointestinal Multiple Lymphomatous Polyposis and Gastric Adenocarcinoma
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Jeong JI, Shin JW, Shin DW, Chun JH, Kim JH, Jeong SY, Kwun DH, Shin MK, Koo YS
- KMID: 1772574
- Korean J Gastroenterol.
- 1999 Dec;34(6):827-831.
Multiple lymphomatous polyposis (MLP) is a rare type of malignant gastrointestinal lymphoma characterized by multiple polyps involving long segments of the gastrointestinal tract. The malignant cells of MLP share morphological,... -
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- A Case of Systemic Lupus Erythematosus with Mediastinal Lymphadenopathy
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Chung SY, Shin DW, Shin JW, Chan JH, Kim JH, Jeong JI, Kwun DH, Shin MK, Song TE
- KMID: 2202529
- J Korean Rheum Assoc.
- 1999 Jun;6(2):192-196.
Approximately half of the patients with systemic lupus erythematosus(SLE) develop localized or diffuse lymphadenopathy during the evolution of the disease. But hilar and mediastinal lymph node enlargement due to SLE... -
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- A case of rotor syndrome
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Kim JH, Koo YS, Jeong JI, Jeong SY, Kwun DH, Shin DW, Hahn BC, Suh DJ
- KMID: 2306223
- Korean J Med.
- 2000 Jul;59(1):109-113.
Rotor syndrome is a rare benign familial disorder characterized by chronic, fluctuating, nonhemolytic and predominantly conjugated hyperbilirubinemia with normal liver tissue. In contrast to Dubin-Johnson syndrome, there is no liver hyperpigmentation in... -
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- Features of atherosclerosis in hemodialysis patients
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Park KA, Jo HM, Han JS, Kim MJ, Kwun DH, Park MY, Choi SJ, Kim JK, Hwang SD
- KMID: 2224296
- Kidney Res Clin Pract.
- 2013 Dec;32(4):177-182.
BACKGROUND: Cardiovascular disease is the main cause of mortality in dialysis patients. Carotid intima-media thickness (CIMT) is used as a surrogate marker of early atherosclerosis. Atherosclerosis can cause vascular access... -
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