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Clinical Manifestations and Significance of Mononeuritis Multiplex in Systemic Necrotizing Vasculitis

Kim J, Cha HS, Seo GH, Ahn HJ, Lee CK, Koh JH, Kim HS, Choi DC, Koh EM

  • KMID: 1544920
  • J Korean Rheum Assoc.
  • 1999 Mar;6(1):23-30.
No abstract available.
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A Case of Rheumatoid Vasculitis Involving Hepatic Artery in Early Rheumatoid Arthritis

Lee JE, Kim IJ, Cho MS, Lee J

Rheumatoid vasculitis is a rare, but most serious extra-articular complications of long-standing, seropositive rheumatoid arthritis (RA). Vasculitis of hepatic artery is an extremely rare but severe manifestation of rheumatoid vasculitis....
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A Case of Churg-Strauss Syndrome

Heo K, Sunwoo IN, Chi JG

  • KMID: 2065910
  • J Korean Neurol Assoc.
  • 1989 Dec;7(2):377-382.
Churg-Strauss syndrome is one of idiopathic, systemic necrotizing vasulitides and characterized by a history of asthma or allergic rhinitis, eosinophilia of peripheral blood and variable symptoms of the systemic vasculitis....
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A Case of Polyarteritis Nodosa Mimicking Systemic Lupus Erythematosus

Lee KH, Nam DH, Lee HW, Ryu TH, Lee CH, Lee SK

  • KMID: 2334857
  • J Korean Rheum Assoc.
  • 2007 Dec;14(4):427-430.
Polyarteritis nodosa (PAN) is a rare systemic necrotizing vasculitis involving multiple organ system. Systemic lupus erythematousus (SLE) also presented as a vasculitic symptoms. So, systemic vasculitis and SLE share some...
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3 Cases of Mononeuropathy Multiplex Associated with Systematic Vasculitis

Kim BJ, Park KW, Song GG, Lee YH, Koh SB, Han JH, Lee DH

  • KMID: 1659738
  • J Korean Neurol Assoc.
  • 1996 Dec;14(4):1007-1017.
Peripheral nervous system involvement is common in systemic vasculitis, occurring most frequently in the polyarteritis nodosa (PAN) group of disorders and in rheumatoid vasculitis. Within the polyarteritis nodosa group of...
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Necrotizing Vasculitis of the Gallbladder: A case report

Lee AW, Lee YS, Kang SJ, Kim BK, Shim SI

  • KMID: 1725538
  • Korean J Pathol.
  • 1999 Apr;33(4):292-294.
We report a case of necrotizing arteritis involving the gallbladder. This case was clinically diagnosed as cholelithiasis with cholecystitis, and necrotizing arteritis was found in the surgically resected specimen. Vascular...
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Mononeuritis Multiplex in Association with Anti-neutrophil Cytoplasmic Autoantibody(?) Vasculitis: A case report

Kim MS, Kim HS, Hwang CM, Ahn KH

  • KMID: 2136843
  • J Korean Acad Rehabil Med.
  • 1997 Oct;21(5):1039-1044.
Mononeuritis multiplex may be a manifestation of systemic vasculitis or of other illnesses such as sarcoidosis, diabetes, lymphoma, and AIDS. Anti-neutrophil cytoplasmic autoantibody(ANCA) is a serologic marker for pauci-immune crescentic...
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Treatment of Chronic Wound in a Patient with Systemic Vasculitis

Lim JS, Kim HJ, Joo HS, Choi YS

  • KMID: 2120068
  • J Korean Soc Plast Reconstr Surg.
  • 2006 Jan;33(1):116-119.
Management of chronic wound has been a great problem to many surgeons because the wound is usually associated with an underlying disease of the patient. Without accurate diagnosis and treatment...
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Isolated Angiitis of Cntral Nervous System: A case Report

Kim JS, Seo DC

  • KMID: 2065909
  • J Korean Neurol Assoc.
  • 1989 Dec;7(2):373-376.
Isolated angiitis of central nervous system is a rare clinicopathologic entity characterized by vasculitis restricted to the vessels of the central nervous system without other apparent systemic vasculitis. We report...
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ANCA-Associated Vasculitic Neuropathy with Concurrent Pulmonary Tuberculosis

Seok JI, Park SH, Kim KC

  • KMID: 2343432
  • J Korean Neurol Assoc.
  • 2012 Feb;30(1):42-44.
Antineutrophil cytoplasmic antibodies (ANCA) are closely linked to primary systemic vasculitis, and ANCA detection has became an important diagnostic hallmark of ANCA-associated vasculitis (AAV). However, it has been reported that...
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A case of Wegener's granulomatosis complicated by non-small cell lung cancer

Her AY, Lee HY, Kang G, Song SY

  • KMID: 2143009
  • Korean J Med.
  • 2007 Sep;73(3):336-341.
Vasculitis may be a manifestation of the paraneoplastic syndrome in association with solid and hematological cancers. There are few reports of paraneoplastic antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis in patients with...
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A Case of Systemic Vasculitis Presented as Fever of Unknown Origin

Jung ES, Kim CH, Hyun YY, Ko GJ, Hwang BY, Cheong HJ, Kim WJ, Won NH

  • KMID: 1808208
  • Infect Chemother.
  • 2004 Dec;36(6):377-380.
Fever of unknown origin (FUO) means fever that does not resolve spontaneously in the period expected for self-limited infection and whose cause cannot be ascertained despite considerable diagnostic efforts. We...
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A Case of Polyarteritis Nodosa Successfully Treated with Deflazacort

Choi JH, Kim DH, Park SH, Shin WG, Lee JH, Kang IS

  • KMID: 2102005
  • J Korean Rheum Assoc.
  • 1999 Sep;6(3):283-286.
Polyarteritis nodosa(PAN), a systemic vasculitis involving multiple organs including the nervous system, requires a long-term glucocorticoid therapy. Deflazacort is a synthetic glucocorticoid, which has been claimed to have less side...
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A Benign Biliary Stricture Complicating Isolated Polyarteritis Nodosa

Lee WJ, Jang YH, Kim YT, Yoon YB, Kim CY, Kim SW, Kim WH

  • KMID: 2240396
  • Korean J Gastroenterol.
  • 2000 Mar;35(3):400-404.
Polyarteritis nodosa, a disease of the vasculitis of small- and medium-sized arteries, has diverse symptoms and signs. Gastrointestinal involvement is common, but localized involvement of the biliary tree or pancreas is very...
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A Case of Kikuchi Disease Accompanied with Bilateral Retinal Vasculitis

Bae J, Kim J, Heo ST, Seong GM, Jeong JH, Kim JH

Kikuchi disease, also called histiocytic necrotizing lymphadenitis, is an uncommon, idiopathic and generally self-limited disease, characterized by cervical lymphadenopathy. It can present systemic symptoms and signs, but ocular involvement is...
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A Case of Left Atrial Myxomoa Presented as Pseudovasculitis

Kim JE, Koh EM, Kim DK, Chang SH, Park PW, Han JH

  • KMID: 2251474
  • Korean J Med.
  • 1997 Nov;53(5):709-713.
Left atrial myxoma is well-known mimicker of systemic vasculitis. In general, however, these patients showed some symptoms and signs of cardiovascular disease. We experienced a patient with left atrial myxoma...
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Update on the Classification Criteria for Vasculitis

Kim HW, Hur JW

The systemic vasculitides are a group of diverse diseases characterized by blood vessel inflammation. The existing classification criteria are intended to create homogeneous patient groups for research and not to...
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Small Intestinal Infarction Associated with Henoch-Schoenlein Purpura

Han MK, Park YI, Kim JH, Lee JJ, Kang HY

  • KMID: 2335571
  • J Korean Pediatr Soc.
  • 2002 Jan;45(1):125-130.
Henoch-Schoenlein purpura, also known as anaphylactoid purpura, is characterized by palpable purpura, colicky abdominal pain, gastrointestinal hemorrhage, arthralgias, and renal involvement. Histopathologically, the condition represents a vasculitis, and in fact,...
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Medical Treatment of Vasculitis; Anti-TNF-alpha Treatment

Jun JB

  • KMID: 1941114
  • J Korean Soc Vasc Surg.
  • 2003 May;19(1):1-4.
The major treatment of systemic vasculitis, such as Wegener's granulomatosis and polyarteritis nodosa, is based on the combination of corticosteroids and immunosuppressive drugs, such as cyclophosphamide. This therapy has been...
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Ileocolonoscopic Diagnosis of Ileal Vasculitis in Henoch - Schonlein Purpura Mimicking Acute Abdomen prior to the Development of Skin Lesions

Kim MS, Kim HS, Park SJ, Baik SK, Lee DK, Kwon SO, Cho MY

  • KMID: 2084985
  • Korean J Gastroenterol.
  • 2001 May;37(5):379-383.
Henoch-Schonlein purpura is an immunologically mediated systemic vasculitis of small vessel in the skin, joints, gastrointestinal (GI) tract, or kidneys. The patients typically show palpable purpura with one or more...
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