1.Neuromyositis: A Rare Extramuscular Manifestation of Dermatomyositis
Chan Keol PARK ; Su Jin YOO ; In Seol YOO ; Jinhyun KIM ; Seung Cheol SHIM ; Seong Wook KANG
Journal of Rheumatic Diseases 2019;26(3):211-218
		                        		
		                        			
		                        			Dermatomyositis (DM) and polymyositis (PM) are representative idiopathic inflammatory myopathies characterized by symmetric and progressive proximal muscle weakness. Especially, DM is identified by characteristic skin lesions and has many extramuscular manifestations including various cardiac abnormalities, interstitial lung disease, and malignancy. However, involvement of peripheral nervous system in DM/PM is very rare and less known. The term “Neuromyositis” was introduced by Senator in 1893 to describe the concomitant involvement of the peripheral nervous system in DM/PM. Since then, a very few cases of neuromyositis have been reported mainly in the United States and Europe. Therefore, the pathogenetic mechanism and disease progression are unclear. In recent years, a few more cases were reported in Asia, specifically, China and Japan; however, none in Korea. Here, we describe a case of DM-associated neuromyositis in a 42-year-old man in Korea and review previous publications through literature research.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Asia
		                        			;
		                        		
		                        			China
		                        			;
		                        		
		                        			Dermatomyositis
		                        			;
		                        		
		                        			Disease Progression
		                        			;
		                        		
		                        			Electromyography
		                        			;
		                        		
		                        			Europe
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Japan
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Lung Diseases, Interstitial
		                        			;
		                        		
		                        			Muscle Weakness
		                        			;
		                        		
		                        			Myositis
		                        			;
		                        		
		                        			Neural Conduction
		                        			;
		                        		
		                        			Peripheral Nervous System
		                        			;
		                        		
		                        			Peripheral Nervous System Diseases
		                        			;
		                        		
		                        			Polymyositis
		                        			;
		                        		
		                        			Skin
		                        			;
		                        		
		                        			United States
		                        			
		                        		
		                        	
2.Cancer of Unknown Primary Site Mimicking Retroperitoneal Fibrosis.
Chan Keol PARK ; Su Jin YOO ; In Seol YOO ; Jinhyun KIM ; Seung Cheol SHIM ; Min Kyung YEO ; Seong Wook KANG
Korean Journal of Medicine 2018;93(6):575-581
		                        		
		                        			
		                        			Retroperitoneal fibrosis (RPF) is a rare disease characterized by marked fibro-inflammatory tissue in the retroperitoneum. Approximately 70% of cases of RPF are idiopathic, while the rest can be secondary to several other causes. The diagnosis is mainly obtained by imaging modalities such as computed tomography (CT). However, histological examination should be considered when the clinical manifestations and imaging studies suggest malignancy. In particular, in malignant diseases with retroperitoneal metastases, abnormal collagen plaques are formed from an exuberant desmoplastic response, which may not be distinguishable from RPF on CT scans. Therefore, even if CT suggests RPF, biopsy is essential to identify malignant disease because it typically results in a fatal prognosis. Here, we report a case of metastatic adenocarcinoma of unknown primary site that developed only in the retroperitoneum and was initially diagnosed as RPF based on CT findings.
		                        		
		                        		
		                        		
		                        			Adenocarcinoma
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Collagen
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Neoplasm Metastasis
		                        			;
		                        		
		                        			Neoplasms, Unknown Primary
		                        			;
		                        		
		                        			Prognosis
		                        			;
		                        		
		                        			Rare Diseases
		                        			;
		                        		
		                        			Retroperitoneal Fibrosis*
		                        			;
		                        		
		                        			Tomography, X-Ray Computed
		                        			
		                        		
		                        	
3.A Case of Sorafenib-induced DRESS Syndrome in Hepatocelluar Carcinoma.
Dong Kyun KIM ; Sung Woo LEE ; Hwa Seong NAM ; Dong Sub JEON ; Na Rae PARK ; Young Hee NAM ; Soo Keol LEE ; Yang Hyun BAEK ; Sang Young HAN ; Sung Wook LEE
The Korean Journal of Gastroenterology 2016;67(6):337-340
		                        		
		                        			
		                        			Sorafenib is currently the only targeted therapy available for advanced stage hepatocellular carcinoma (HCC). Cutaneous adverse events associated with sorafenib treatment include hand-foot skin reaction, but there has been no report of drug reaction (or rash) with eosinophilia and systemic symptoms (DRESS) syndrome. Here, we report a case of 72-year-old man with HCC and alcoholic liver cirrhosis who developed skin eruptions, fever, eosinophilia, and deteriorated hepatic and renal function under sorafenib treatment. He has since successfully recovered with conservative care.
		                        		
		                        		
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Carcinoma, Hepatocellular
		                        			;
		                        		
		                        			Drug Hypersensitivity Syndrome*
		                        			;
		                        		
		                        			Eosinophilia
		                        			;
		                        		
		                        			Fever
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Liver Cirrhosis, Alcoholic
		                        			;
		                        		
		                        			Skin
		                        			
		                        		
		                        	
4.Iliopsoas Bursitis after Transfemoral Coronary Angiography.
Jeong Chan LEE ; Chan Keol PARK ; Young KIM ; Su Jin YOO ; Seung Cheol SHIM ; Seong Wook KANG ; In Seol YOO
Keimyung Medical Journal 2016;35(1):34-38
		                        		
		                        			
		                        			A 53-year-old male was admitted to our hospital for evaluation of the second kidney transplant. A Iliopsoas Bursitis was detected on diagnostic abdominopelvic computed tomography. He had undergone a coronary angiography (CAG) due to chest pain 1 month prior to his visit. At that time, he had experienced pain on his right back and flank for some time. We found no other causes or predisposing factors associated with that problem. Thus, we report on a case of iliopsoas bursitis after CAG.
		                        		
		                        		
		                        		
		                        			Bursitis*
		                        			;
		                        		
		                        			Causality
		                        			;
		                        		
		                        			Chest Pain
		                        			;
		                        		
		                        			Coronary Angiography*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Kidney
		                        			;
		                        		
		                        			Kidney Transplantation
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Middle Aged
		                        			
		                        		
		                        	
5.Vertebral Osteomyelitis due to Mycobacterium intracellulare in an Immunocompetent Elderly Patient After Vertebroplasty.
Min Seong KIM ; Chan Keol PARK ; Kyung Mok SOHN ; Chang Hun SONG ; Shinhye CHEON ; Yeon Sook KIM
Journal of the Korean Geriatrics Society 2016;20(1):56-60
		                        		
		                        			
		                        			Mycobacterium avium complex (MAC) comprises M. intracellulare and M. avium. MAC usually causes pulmonary diseases in individuals with intact immunity, disseminated disease in patients with acquired immunodeficiency syndrome, and cervical lymphadenitis. It can also cause cutaneous disease, but musculoskeletal infection is rare. Herein, we present a case of vertebral osteomyelitis due to M. intracellulare in an elderly immunocompetent patient who underwent vertebroplasty. The patient was successfully treated with antimycobacterial drugs without surgical intervention. MAC should be considered as a causative pathogen of vertebral osteomyelitis when the patient has a history of vertebroplasty.
		                        		
		                        		
		                        		
		                        			Acquired Immunodeficiency Syndrome
		                        			;
		                        		
		                        			Aged*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lung Diseases
		                        			;
		                        		
		                        			Lymphadenitis
		                        			;
		                        		
		                        			Mycobacterium avium Complex*
		                        			;
		                        		
		                        			Mycobacterium avium-intracellulare Infection
		                        			;
		                        		
		                        			Mycobacterium*
		                        			;
		                        		
		                        			Nontuberculous Mycobacteria
		                        			;
		                        		
		                        			Osteomyelitis*
		                        			;
		                        		
		                        			Vertebroplasty*
		                        			
		                        		
		                        	
6.Predictors of the Severity and Serious Outcomes of Anaphylaxis in Korean Adults: A Multicenter Retrospective Case Study.
Young Min YE ; Mi Kyeong KIM ; Hye Ryun KANG ; Tae Bum KIM ; Seong Wook SOHN ; Young Il KOH ; Hye Kyung PARK ; Gwang Cheon JANG ; Cheol Woo KIM ; Young Koo JEE ; Gyu Young HUR ; Joo Hee KIM ; Sang Heon KIM ; Gil Soon CHOI ; Soo Keol LEE ; Hae Sim PARK
Allergy, Asthma & Immunology Research 2015;7(1):22-29
		                        		
		                        			
		                        			PURPOSE: Differences in definitions of the condition, relevant triggers, and the geographical locations of study centers, cause estimates of the prevalence of anaphylaxis to vary. Recent epidemiological data indicate that the incidence of anaphylaxis is rising. METHODS: To investigate the causes and clinical features of anaphylaxis in Korean adults, factors associated with the severity of the condition, and serious outcomes, a retrospective medical record review was performed on adult patients diagnosed with anaphylaxis between 2007 and 2011 in 15 University Hospitals of South Korea. RESULTS: A total of 1,806 cases (52% male, age 16-86 years) were reported. Cutaneous symptoms (84.0%), combined with respiratory (53.9%) and/or cardiovascular (55.4%) symptoms, were the most frequent presentations. Using a recognized grading system, 1,776 cases could be classified as either mild, 340; moderate, 690; or severe, 746. Although eliciting factors varied significantly by age, gender, and regional and seasonal factors, drugs (46.5%; including nonsteroidal anti-inflammatory drugs, antibiotics, and radiocontrast media) were the most common cause of anaphylaxis, followed by foods (24.2%), insect stings (16.4%), exercise (5.9%), and unknown etiology (7.0%). All of age, multi-organ involvement, a history of allergic disease, and drug-induced anaphylaxis, were significant predictors of serious outcomes requiring hospital admission or prolongation of hospital stay. Epinephrine auto-injectors were prescribed for 7.4% of reported cases. CONCLUSIONS: The principal causes of anaphylaxis in Korean adults were drugs, food, and insect stings. Drug-associated anaphylaxis, a history of allergic disease, multi-organ involvement, and older age, were identified as predictors of serious outcomes.
		                        		
		                        		
		                        		
		                        			Adult*
		                        			;
		                        		
		                        			Anaphylaxis*
		                        			;
		                        		
		                        			Anti-Bacterial Agents
		                        			;
		                        		
		                        			Epidemiology
		                        			;
		                        		
		                        			Epinephrine
		                        			;
		                        		
		                        			Hospitals, University
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Incidence
		                        			;
		                        		
		                        			Insect Bites and Stings
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Length of Stay
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Medical Records
		                        			;
		                        		
		                        			Prevalence
		                        			;
		                        		
		                        			Retrospective Studies*
		                        			;
		                        		
		                        			Seasons
		                        			
		                        		
		                        	
7.A Case of Intravascular Large B-cell Lymphoma Mimicking Systemic Lupus Erythematosus.
Chan Keol PARK ; Jeong Chan LEE ; Seong Wook KANG ; Seung Cheol SHIM ; Hwan Jung YUN ; Jin Man KIM ; In Seol YOO
Korean Journal of Medicine 2015;89(6):746-751
		                        		
		                        			
		                        			Intravascular large B-cell lymphoma (IVLBCL) is a rare subtype of non-Hodgkin's lymphoma (NHL) and that progresses rapidly and is usually fatal. Because it usually presents with nonspecific symptoms, such as fever, the early diagnosis of IVLBCL is very difficult and it is often misdiagnosed as another disease. Systemic lupus erythematosus (SLE) is an autoimmune disease that affects various organs. The clinical manifestation of SLE ranges from rash and arthritis through anemia and thrombocytopenia to serositis, nephritis, seizures, and psychosis. Thus, it can be easily confused with many other disorders. We report a case of IVLBCL mimicking SLE in the initial diagnosis.
		                        		
		                        		
		                        		
		                        			Anemia
		                        			;
		                        		
		                        			Arthritis
		                        			;
		                        		
		                        			Autoimmune Diseases
		                        			;
		                        		
		                        			B-Lymphocytes*
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Early Diagnosis
		                        			;
		                        		
		                        			Exanthema
		                        			;
		                        		
		                        			Fever
		                        			;
		                        		
		                        			Lupus Erythematosus, Systemic*
		                        			;
		                        		
		                        			Lymphoma
		                        			;
		                        		
		                        			Lymphoma, B-Cell*
		                        			;
		                        		
		                        			Lymphoma, Non-Hodgkin
		                        			;
		                        		
		                        			Nephritis
		                        			;
		                        		
		                        			Psychotic Disorders
		                        			;
		                        		
		                        			Seizures
		                        			;
		                        		
		                        			Serositis
		                        			;
		                        		
		                        			Thrombocytopenia
		                        			
		                        		
		                        	
8.Seasonal and regional variations in the causes of anaphylaxis in Korean adults.
Yeon Kyung LEE ; Mi Kyeong KIM ; Hye Ryun KANG ; Tae Bum KIM ; Seong Wook SOHN ; Hye Kyung PARK ; Young Il KOH ; Gwang Cheon JANG ; Cheol Woo KIM ; Young Koo JEE ; Gyu Young HUR ; Joo Hee KIM ; Sang Heon KIM ; Gil Soon CHOI ; Soo Keol LEE ; Hae Sim PARK ; Young Min YE
Allergy, Asthma & Respiratory Disease 2015;3(3):187-193
		                        		
		                        			
		                        			PURPOSE: To investigate whether causes of anaphylaxis vary according to regions and seasons in Korean adults. METHODS: Based on previous retrospective studies of anaphylaxis between 2007 and 2011 at the 15 university hospitals. Regions were classified into 4 groups: region I, Seoul; region II, Gyeonggi; region III, Chungcheong; and region IV, Chonnam and Busan. The cases induced by 5 major allergens including drugs, food, bee sting, radiocontrast media, and exercise, were analyzed in the present study. RESULTS: Among a total of 1,661 cases reported (53% male, 45.9+/-16.0 years), 367 (22.2%), 706 (42.5%), 319 (19.2%), and 269 cases (16.2%) were enrolled in regions I, II, III, and IV, respectively. Of the 5 major allergens, drugs (37.3%) were the most frequently reported, followed by food (25.7%), bee sting (17.9%), radiocontrast media (12.9%), and exercise (6.2%). There was no significant difference in the total occurrence of anaphylaxis in 4 seasons (374 in spring, 460 in summer, 460 in autumn, and 367 in winter). Multiple logistic regression analysis revealed that drug-induced anaphylaxis was significantly associated with the winter season (odds ratio [OR] 1.0 vs. OR 0.597, P<0.05 for spring; OR 1.0 vs. OR 0.481, P<0.01 for summer; OR 1.0 vs. OR 0.653, P<0.05 for autumn). Food-associated anaphylaxis was mainly reported in region I, whereas the frequency of insect sting was relatively higher in regions II, III, and IV than in region I. Older age and female gender were significantly associated with drug-induced anaphylaxis. CONCLUSION: Specific causative allergens of anaphylaxis in adults may vary according to age, gender, region, and season in Korea.
		                        		
		                        		
		                        		
		                        			Adult*
		                        			;
		                        		
		                        			Allergens
		                        			;
		                        		
		                        			Anaphylaxis*
		                        			;
		                        		
		                        			Bees
		                        			;
		                        		
		                        			Bites and Stings
		                        			;
		                        		
		                        			Busan
		                        			;
		                        		
		                        			Contrast Media
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Geographic Locations
		                        			;
		                        		
		                        			Gyeonggi-do
		                        			;
		                        		
		                        			Hospitals, University
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Insect Bites and Stings
		                        			;
		                        		
		                        			Jeollanam-do
		                        			;
		                        		
		                        			Korea
		                        			;
		                        		
		                        			Logistic Models
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Seasons*
		                        			;
		                        		
		                        			Seoul
		                        			
		                        		
		                        	
9.Dermatomyositis in an Allogeneic Stem Cell Transplant Recipient with Graft-Versus-Host Disease.
Young KIM ; Seong Wook KANG ; Deog Yeon JO ; Chan Keol PARK ; Kyu Sang SONG ; Jin Man KIM ; Jinhyun KIM
Korean Journal of Medicine 2014;86(4):523-527
		                        		
		                        			
		                        			Dermatomyositis (DM) is an autoimmune disease characterized by subacute-onset proximal symmetric muscle weakness, skin abnormalities, and muscle inflammation. Descriptions of DM as a complication of chronic graft-versus-host disease (cGVHD) are very rare. We report a 50-year-old woman who developed DM associated with cGVHD after allogeneic stem cell transplantation.
		                        		
		                        		
		                        		
		                        			Autoimmune Diseases
		                        			;
		                        		
		                        			Dermatomyositis*
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Graft vs Host Disease*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Inflammation
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Muscle Weakness
		                        			;
		                        		
		                        			Skin Abnormalities
		                        			;
		                        		
		                        			Stem Cell Transplantation
		                        			;
		                        		
		                        			Stem Cells*
		                        			;
		                        		
		                        			Transplantation*
		                        			
		                        		
		                        	
10.Localized Mesenteric Vasculitis in a Patient with Polymyalgia Rheumatica.
Seung Taek SONG ; Young KIM ; Chan Keol PARK ; Su Jin YOO ; Jin Hyun KIM ; Seong Wook KANG ; In Seol YOO
Journal of Rheumatic Diseases 2014;21(5):253-256
		                        		
		                        			
		                        			Polymyalgia rheumatica (PMR) is an uncommon disorder characterized by bilateral pain and stiffness in the shoulder and pelvic girdles. Polymyalgia rheumatica and giant cell arteritis (GCA) occur in the same patient population and share a common pathogenesis. Giant cell arteritis predominantly affects the cranial arteries and rarely involves the gastrointestinal tract. Moreover, giant cell arteritis has rarely been reported in Asians. Here, we present a case with 62-year-old Asian woman who developed polymyalgia rheumatica with localized vasculitis in the mesenteric arteries.
		                        		
		                        		
		                        		
		                        			Arteries
		                        			;
		                        		
		                        			Asian Continental Ancestry Group
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Gastrointestinal Tract
		                        			;
		                        		
		                        			Giant Cell Arteritis
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Mesenteric Arteries
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Polymyalgia Rheumatica*
		                        			;
		                        		
		                        			Shoulder
		                        			;
		                        		
		                        			Vasculitis*
		                        			
		                        		
		                        	
            
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