- Comparison of Clinical, Angiographic Features and Outcome in Takayasu's Arteritis and Behçet's Disease With Arterial Involvement
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Choi SJ, Koo HJ, Yang DH, Kang JW, Oh JS, Hong S, Kim YG, Yoo B, Lee CK
- KMID: 2471951
- J Rheum Dis.
- 2020 Apr;27(2):100-109.
- doi: 10.4078/jrd.2020.27.2.100
OBJECTIVE: Takayasu's arteritis (TAK) is a vasculitis that primarily involves the aorta and its branches. In Behçet's disease (BD), systemic vasculitis is one of major manifestations. We aimed to compare... -
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- A Case of Cutaneous Leukocytoclastic Vasculitis Associated with Granulocyte Colony-Stimulating Factor: An Unusual Presentation
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Yoon D, Byun HJ, Oh SJ, Park JH, Lee DY
- KMID: 2471345
- Ann Dermatol.
- 2020 Apr;32(2):164-167.
- doi: 10.5021/ad.2020.32.2.164
Drug-induced vasculitis is an inflammation of small-sized blood vessel caused by the use of drugs. It accounts for approximately 10% of acute cutaneous vasculitis. Propylthiouracil, hydralazine, and allopurinol have been... -
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- History and Future of Treatment for Acute Stage Kawasaki Disease
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Ishii M, Ebato T, Kato H
- KMID: 2468036
- Korean Circ J.
- 2020 Feb;50(2):112-119.
- doi: 10.4070/kcj.2019.0290
Kawasaki disease is a form of vasculitis, mainly in small and medium arteries of unknown origin, occurring frequently in childhood. It is the leading form of childhood-onset acquired heart disease... -
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- An Atypical Extraintestinal Manifestation in a Child with Ulcerative Colitis: Cutaneous Leukocytoclastic Vasculitis
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Oh SJ, Choi Y, Kim CR, Park JH, Lee JH, Lee DY
- KMID: 2467210
- Ann Dermatol.
- 2020 Feb;32(1):90-91.
- doi: 10.5021/ad.2020.32.1.90
No abstract available. -
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- Surviving Takayasu's Arteritis—A Young Girl with Long Segment Stenosis of the Descending Thoracic Aorta and Myocarditis
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Abas SI, Ramli KA, Tiong KG, Mohammed Y
- KMID: 2469177
- Cardiovasc Imaging Asia.
- 2020 Jan;4(1):34-36.
- doi: 10.22468/cvia.2019.00157
We report the case of a 12-year-old girl who presented with heart failure symptoms that were treated as dilated cardiomyopathy. The echocardiogram showed a dilated left ventricle, poor ejection fraction,... -
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- Clinical Usefulness of Neutrophil-Lymphocyte Ratio as a Predictor of Henoch–Schönlein Nephritis
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Kim M, Suh WS
- KMID: 2470410
- Soonchunhyang Med Sci.
- 2019 Dec;25(2):110-116.
- doi: 10.0000/sms.2019.25.2.110
OBJECTIVE: Henoch–Schönlein purpura is the most widespread systemic vasculitis during childhood. This study evaluated the relationship between neutrophil-lymphocyte ratio (NLR) and Henoch–Schönlein nephritis, which is important for the long-term prognosis... -
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- A case of gastroduodenal ulcer complicating Kawasaki disease
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Sohn H, Kim K, Koh H, Kim S
- KMID: 2469723
- Pediatr Emerg Med J.
- 2019 Dec;6(2):81-85.
- doi: 10.22470/pemj.2019.00087
Kawasaki disease (KD) is a systemic vasculitis associated with various clinical manifestations and complications, such as gastrointestinal abnormalities. We report a 3-year-old boy who presented with hematemesis and diffuse gastroduodenal... -
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- Primary Ocular Toxoplasmosis Presenting to Uveitis Services in a Non-endemic Setting
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Bhikoo R, Damato EM, Guest S, Sims J
- KMID: 2465131
- Korean J Ophthalmol.
- 2019 Dec;33(6):514-519.
- doi: 10.3341/kjo.2019.0092
PURPOSE: This study sought to describe the different clinical features and presentations of primary ocular toxoplasmosis in a setting not demonstrating an outbreak of disease. METHODS: This was a retrospective review... -
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- Controlling Nutritional Status Score is Associated with All-Cause Mortality in Patients with Antineutrophil Cytoplasmic Antibody-Associated Vasculitis
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Ahn SS, Jung SM, Song JJ, Park YB, Lee SW
- KMID: 2463795
- Yonsei Med J.
- 2019 Dec;60(12):1164-1173.
- doi: 10.3349/ymj.2019.60.12.1164
PURPOSE: The controlling nutritional status (CONUT) score was developed to detect undernutrition in patients. Here, we investigated whether the CONUT score estimated at diagnosis could help predict poor outcomes [all-cause... -
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- Two Cases of Localized Myeloperoxidase-Antineutrophil Cytoplasmic Antibody-Associated Vasculitis Manifested with Intractable Otitis Media
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Lee E, Chung WH
- KMID: 2466716
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2019 Nov;62(11):657-662.
- doi: 10.3342/kjorl-hns.2018.00850
Localized form of myeloperoxidase-antineutrophil cytoplasmic antibody-associated vasculitis (MPO-AAV) in the ear is a rare disease. It manifests as a sudden otalgia with hearing loss accompanied by dizziness and facial nerve... -
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- A Case of Henoch-Schönlein Purpura with Fulminant Complications and Its Long-term Outcome
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Lee DH, LEE ES, Hong J, Park KH, Pai KS
- KMID: 2464940
- Child Kidney Dis.
- 2019 Oct;23(2):128-133.
- doi: 10.3339/jkspn.2019.23.2.128
Henoch-Schönlein purpura (HSP) is a systemic vasculitis characterized by purpura, arthritis, abdominal pain, and nephritis. Gastrointestinal involvement can manifest as pain, intussusception, intestinal bleeding, and intestinal perforation. We report a... -
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- A pediatric case of eosinophilic granulomatosis with polyangiitis accompanied by heart failure mimicking an asthma attack
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Kim MJ, Lee BR, Park JS, Choi YJ, Song MK, Lee S, Suh DI
- KMID: 2461399
- Allergy Asthma Respir Dis.
- 2019 Oct;7(4):212-217.
- doi: 10.4168/aard.2019.7.4.212
Eosinophilic granulomatosis with polyangiitis (EGPA, also known as the Churg-Strauss syndrome) is a disorder characterized by asthma, peripheral eosinophilia and systemic vasculitis. It rarely occurs in children, so that physicians... -
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- The association between asthma and Kawasaki disease
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Choi BS
- KMID: 2461393
- Allergy Asthma Respir Dis.
- 2019 Oct;7(4):173-178.
- doi: 10.4168/aard.2019.7.4.173
Kawasaki disease (KD) is a systemic vasculitis and the most common cause of acquired heart disease among preschool-aged children. Asthma is one of the most common chronic illness of childhood.... -
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- A Case of Primary Central Nervous System Vasculitis That Worsened Despite Early Corticosteroid Therapy
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Yoon SY, Park KS, Park SH, Park JY
- KMID: 2461193
- Brain Tumor Res Treat.
- 2019 Oct;7(2):164-167.
- doi: 10.14791/btrt.2019.7.e37
Primary central nervous system vasculitis (PCNSV) is rare, and the diagnosis is difficult to make because of its variable radiologic expressions. Early corticosteroid therapy often is effective. Herein we report... -
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- Frosted Branch Angiitis Secondary to Granulomatosis with Polyangiitis
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Kim DY, Jeong J, Kim JY
- KMID: 2459534
- Korean J Ophthalmol.
- 2019 Oct;33(5):485-486.
- doi: 10.3341/kjo.2019.0033
No abstract available. -
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- Understanding the importance of cerebrovascular involvement in Kawasaki disease
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Yeom JS, Cho JY, Woo HO
- KMID: 2464382
- Korean J Pediatr.
- 2019 Sep;62(9):334-339.
- doi: 10.3345/kjp.2019.00143
Kawasaki disease (KD) is a systemic vasculitis in infants and young children. However, its natural history has not been fully elucidated because the first case was reported in the late... -
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- Ruptured Suprarenal Abdominal Aortic Pseudoaneurysm with Superior Mesenteric and Celiac Arteries Occlusion, Revealing Behçet’s Disease: A Case Report
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Rashaideh , Janho KE, Jalokh M, Ajarmeh ES, As’ad M
- KMID: 2460013
- Vasc Spec Int.
- 2019 Sep;35(3):160-164.
- doi: 10.5758/vsi.2019.35.3.160
Behçet’s disease (BD) is a multisystemic, chronic autoimmune inflammatory vasculitic disease with an unknown etiology. Although the literature reports that vascular involvement occurs in 7% to 38% of all BD... -
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- Unilateral Cutaneous Vasculitis on Lower Limb in Patient with Unilateral Lymphedema
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Kim JS, Woo YR, Kim M, Park HJ
- KMID: 2456665
- Ann Dermatol.
- 2019 Aug;31(Suppl):S20-S21.
- doi: 10.5021/ad.2019.31.S.S20
No abstract available. -
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- Unilateral Cutaneous Vasculitis on Lower Limb in Patient with Unilateral Lymphedema
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Kim JS, Woo YR, Kim M, Park HJ
- KMID: 2456638
- Ann Dermatol.
- 2019 Aug;31(Suppl 1):S20-S21.
- doi: 10.5021/ad.2019.31.S.S20
No abstract available. -
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- Eosinophilic Granulomatosis with Polyangiitis: Experiences in Korean Patients
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Choi CB, Park YB, Lee SW
- KMID: 2452950
- Yonsei Med J.
- 2019 Aug;60(8):705-712.
- doi: 10.3349/ymj.2019.60.8.705
Eosinophilic granulomatosis with polyangiitis (EGPA) is one form of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Identical to what has been called Churg-Strauss syndrome, EGPA exhibits both allergic and vasculitis features. EGPA... -
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