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1.
J Rheum Dis ; 30(1): 53-57, 2023 Jan 01.
Article in English | MEDLINE | ID: mdl-37476529

ABSTRACT

Central nervous system (CNS) manifestations of systemic lupus erythematosus (SLE) are diverse and often difficult to distinguish from SLE-unrelated events. CNS vasculitis is a rare manifestation, which is seen in less than 10% of post-mortem studies, and lesions with multifocal cerebral cortical microinfarcts associated with small-vessel vasculitis are the predominant feature. However, CNS vasculitis presenting as a tumor-like mass lesion in SLE has rarely been reported. Herein, we report a case of cerebral vasculitis mimicking a brain tumor in a 39-year-old female with SLE. A biopsy of the brain mass revealed fibrinoid necrosis and leukocytoclastic vasculitis. The neurological deficits and systemic symptoms improved after treatment with corticosteroids and immunosuppressive agents. To the best of our knowledge, there are no reports of biopsy-proven cerebral vasculitis presenting as a brain mass in patients with SLE in Korea.

2.
Arthritis Res Ther ; 23(1): 258, 2021 10 13.
Article in English | MEDLINE | ID: mdl-34641970

ABSTRACT

OBJECTIVE: Patients with rheumatoid arthritis (RA) are almost twice as likely to develop cardiovascular disease (CVD) as those without. However, traditional CVD risks have been shown to underperform in RA patients; thus, we aimed to identify new surrogate risk factors to better reflect their atherosclerotic burden. METHODS: A total of 380 RA patients with carotid atherosclerosis data were analyzed in this prospective cohort study. The primary outcome was carotid plaque progression over the 3-year follow-up period. Risk parameters assessed for the progression of carotid plaque were categorized as demographics, traditional CVD risks, RA-related risks, and bone parameters. RESULTS: The progression of carotid plaque was associated with the level of rheumatoid factor (p = 0.025), serum C-terminal telopeptide of type-I collagen (CTX-I) (p = 0.014), and femur and distal radius bone mass density (BMD) (p = 0.007 and 0.004, respectively), as well as traditional CVD risk factors. In multivariable analyses, the bone parameters of serum CTX-I and distal radius BMD proved to be independent predictors of the progression of carotid plaque along with hyperlipidemia, smoking, and baseline carotid plaque (all, p < 0.05). Adding both serum CTX-I and distal radius BMD increased the carotid plaque progression prediction model's percentage of explained variance from 24 to 30%. CONCLUSION: High serum CTX-I and lower radius BMD, reflecting high bone turnover, were independent risk factors for the progression of carotid plaque in RA patients, implicating the direct or indirect role of bone metabolism on the atherosclerotic burden.


Subject(s)
Arthritis, Rheumatoid , Carotid Artery Diseases , Plaque, Atherosclerotic , Biomarkers , Bone Density , Carotid Arteries , Carotid Artery Diseases/diagnostic imaging , Humans , Plaque, Atherosclerotic/diagnostic imaging , Prospective Studies , Radius
3.
Rheumatology (Oxford) ; 54(5): 808-15, 2015 May.
Article in English | MEDLINE | ID: mdl-25305139

ABSTRACT

OBJECTIVE: Patients with RA have an increased risk of atherosclerosis and cardiovascular (CV) diseases compared with the general population. The aim of this study was to evaluate the role of inflammatory burden in the formation of carotid plaques in patients with RA. METHODS: We performed carotid artery US to measure the carotid intima-media thickness (IMT) and plaques in 406 patients with RA and 209 age- and sex-matched healthy controls. To assess the inflammatory burden, the area under the curve (AUC) of ESR over time was calculated. RESULTS: The carotid plaque frequency and mean IMT were significantly increased in patients with RA relative to controls. After adjustment for age and gender, the presence of carotid plaques in patients with RA was associated with HAQ score, tender joint count (TJC), swollen joint count (SJC), 28-joint DAS, ESR, CRP, LEF use, current corticosteroid dose and the number of conventional CV risk factors. After multivariate regression analysis, the factors significantly associated with plaque formation were TJC (P = 0.002), ESR (P = 0.002) and the number of conventional CV risk factors (P = 0.041). Among 194 RA patients with ESR AUC data, the presence of carotid plaque was independently associated with both the ESR AUC and number of conventional CV risk factors, which showed a synergistic interaction. CONCLUSION: Cumulative inflammatory burden contributes to the development of carotid atherosclerosis through a synergistic interaction with conventional CV risk factors in patients with RA.


Subject(s)
Arthritis, Rheumatoid/blood , Arthritis, Rheumatoid/complications , Carotid Intima-Media Thickness , Carotid Stenosis/epidemiology , Inflammation/blood , Inflammation/complications , Adult , Aged , Area Under Curve , Biomarkers/blood , Blood Sedimentation , C-Reactive Protein/metabolism , Carotid Arteries/diagnostic imaging , Case-Control Studies , Female , Humans , Male , Middle Aged , Regression Analysis , Risk Factors
4.
Korean J Intern Med ; 29(6): 814-21, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25378981

ABSTRACT

BACKGROUND/AIMS: We investigated the electromyography (EMG) findings and demographic, clinical, and laboratory features that may predict the development of malignancy in patients with idiopathic inflammatory myopathy (IIM). METHODS: In total, 61 patients, 36 with dermatomyositis and 25 with polymyositis, were included. Patients were divided into those with and without malignancies, and comparisons were made between the groups in terms of their demographic, clinical, laboratory, and EMG findings. RESULTS: The frequencies of malignancies associated with dermatomyositis and polymyositis were 22% and 8%, respectively. Patients with malignancies showed a significantly higher incidence of dysphagia (odds ratio [OR], 21.50; 95% confidence interval [CI], 3.84 to 120.49), absence of interstitial lung disease (ILD; OR, 0.12; 95% CI, 0.01 to 0.98), and complex repetitive discharge (CRD) on the EMG (OR, 26.25; 95% CI, 2.67 to 258.52), versus those without. After adjustment for age, dysphagia and CRD remained significant, while ILD showed a trend for a difference but was not statistically significant. Multivariate analysis revealed that the CRD conferred an OR of 25.99 (95% CI, 1.27 to 531.86) for malignancy. When the frequency of malignancy was analyzed according to the number of risk factors, patients with three risk factors showed a significantly higher incidence of malignancy, versus those with fewer than two (p = 0.014). CONCLUSIONS: We demonstrated for the first time that CRD on the EMG was an additional independent risk factor for malignancy in IIM. Further studies on a larger scale are needed to confirm the importance of CRD as a risk factor for malignancy in IIM.


Subject(s)
Dermatomyositis/diagnosis , Electromyography , Muscle, Skeletal/innervation , Neoplasms/etiology , Polymyositis/diagnosis , Action Potentials , Adult , Aged , Dermatomyositis/complications , Dermatomyositis/physiopathology , Female , Humans , Logistic Models , Male , Middle Aged , Multivariate Analysis , Muscle, Skeletal/pathology , Odds Ratio , Polymyositis/complications , Polymyositis/physiopathology , Predictive Value of Tests , Retrospective Studies , Risk Factors
5.
Endoscopy ; 46(11): 981-6, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25321618

ABSTRACT

We investigated the clinical and endoscopic features of gastrointestinal lesions in adults with Henoch-Schönlein purpura (HSP) causing gastrointestinal bleeding. The study included 24 adult HSP patients with gastrointestinal hemorrhage who underwent both upper gastrointestinal endoscopy and colonoscopy. The controls were 27 adult HSP patients without gastrointestinal hemorrhage. Patients with gastrointestinal bleeding showed higher frequencies of purpura on the upper extremities and trunk, and of elevated serum C-reactive protein (CRP). The rate of concurrent lesions in both the upper and lower gastrointestinal tracts was 91.7 %. The second portion of duodenum and terminal ileum were most frequently and severely involved. Leukocytoclastic vasculitis was detected in severe lesions and was significantly associated with mucosal ischemic changes. Most lesions (95.7 %) dramatically improved after corticosteroid therapy. This study suggests that both upper and lower gastrointestinal examinations are necessary for proper evaluation of gastrointestinal bleeding in patients with HSP.


Subject(s)
Colonic Diseases/etiology , Duodenal Diseases/etiology , Endoscopy, Gastrointestinal , Gastrointestinal Hemorrhage/etiology , IgA Vasculitis/complications , Ileal Diseases/etiology , Adolescent , Adult , Anti-Inflammatory Agents/therapeutic use , C-Reactive Protein/metabolism , Colonic Diseases/blood , Colonic Diseases/pathology , Colonoscopy , Duodenal Diseases/blood , Duodenal Diseases/pathology , Female , Gastrointestinal Hemorrhage/blood , Gastrointestinal Hemorrhage/pathology , Humans , IgA Vasculitis/drug therapy , IgA Vasculitis/pathology , Ileal Diseases/blood , Ileal Diseases/pathology , Intestinal Mucosa/blood supply , Ischemia/etiology , Male , Middle Aged , Prednisone/therapeutic use , Retrospective Studies , Torso , Upper Extremity , Young Adult
6.
Korean Circ J ; 42(12): 857-60, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23323126

ABSTRACT

A 73-year-old man with a history of hypertension and ascending aortic dissection was hospitalized for aggravated abdominal pain and general ache for 3 months. Follow-up CT showed aggravated abdominal aortic hematoma with aneurysm, atherosclerotic periaortitis and bilateral hydronephrosis. An initial laboratory finding showed elevated levels of inflammatory markers and renal dysfunction. Positron emission tomography-CT showed an increased standardized uptake values level in the aortic arch, descending thoracic aorta, major branch, abdominal aorta, and common iliac artery. For bilateral hydronephrosis, a double J catheter insertion was performed. Tissue specimens obtained from previous surgery on the aorta indicated the infiltration of lympho-plasma cells without granuloma formation in the aortic wall. After a combined therapy of high dose steroid therapy with azathioprine, the patient's initial complaints of abdominal pain, weakness and azotemia improved. This case was diagnosed as chronic periaortitis based on aortic inflammation at biopsy, which was complicated with retroperitoneal fibrosis and ureteric obstruction.

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