1.Epidemiological and clinical features of Behcet's disease in Korea.
Dongsik BANG ; Kyeong Han YOON ; Han Gil CHUNG ; Eung Ho CHOI ; Eun So LEE ; Sungnack LEE
Yonsei Medical Journal 1997;38(6):428-436
Behcet's disease occurs with a high prevalence in the Far East including Korea. In this report we inspected 1,155 patients with Behcet's disease and collected information concerning the clinical and epidemiologic features of Behcet's disease in Korea. In summary, patients in their 30s were the most common, with the most common age of onset in the 20s; the sex ratio was 0.63:1 with female predominance; according to revised Shimizu's classification, the order of frequency of the different types was incomplete (38.2%), suspected (25.4%), possible (20.3%) and complete (16.1%); oral ulcers were the most frequent major symptom (97.5%) and the most common initial symptom (78.5%); erythema nodosum-like lesion (55.3%) was the most common type of skin lesion; a seasonal aggravation of the disease was observed in 21.3% of patients; and the most common type of childhood onset Behcet's disease was suspected type.
Adolescence
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Adult
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Age Distribution
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Aged
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Behcet's Syndrome/epidemiology*
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Behcet's Syndrome/complications
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Behcet's Syndrome/classification
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Child
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Female
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Human
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Korea/epidemiology
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Male
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Middle Age
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Sex Distribution
2.Epidemiological features of Adamantiades-Behcet's disease in Germany and in Europe.
Christos C ZOUBOULIS ; Ina KOTTER ; Djalil DJAWARI ; Wilhelm KIRCH ; Peter K KOHL ; Falk R OCHSENDORF ; Wolfgang KEITEL ; Rudolf STADLER ; Uwe WOLLINA ; Ehrhardt PROKSCH ; Rolf SOHNCHEN ; Helmut WEBER ; Harald P GOLLNICK ; Erhard HOLZLE ; Klaus FRITZ ; Thomas LICHT ; Constantin E ORFANOS
Yonsei Medical Journal 1997;38(6):411-422
The German Registry of Adamantiades-Behcet's disease was founded in 1990 in Berlin and it provides current data on the epidemiology, the clinical manifestations and the course of the disease in Germany on a continuous basis. A total of 218 patients, including 89 German and 100 Turkish patients, had been reported to the German Registry until October 1997. One hundred and ninety-six patients fulfilled the criteria of the Behcet's disease classification tree. The prevalence of the disease evaluated in Berlin-West was 1.68/100,000 in 1989 and had risen to 2.26/100,000 by 1994. The median age of onset was 25 years (range 5 to 66 years; German-Turks, ns). Juvenile disease was recorded in 6.9% of patients. The complete clinical picture according to the criteria of the International Study Group of Behcet's Disease developed in 15.5 months. The interval between onset of the disease and diagnosis was 35 months, which was significantly longer than the duration of the development of the complete clinical picture (p < 0.0001). The disease was diagnosed later in German (48.5 months) than in Turkish patients (25.5 months, p = 0.003). While German patients presented an equal male-to-female ratio, a male predominance was shown in Turkish patients (M:F 2.1:1, p = 0.022). Familial occurrence was detected in 2.0% of German and 15.9% of Turkish patients (p = 0.013). The frequencies of major clinical manifestations were: oral ulcers 99%, skin lesions 76%, genital ulcers 75%, ocular manifestations 59%, arthritis 59%, and positive pathergy test 52%. Clinical differences between German and Turkish patients were only found in the frequency of ocular lesions (48% vs. 66%, p = 0.025). Oral ulcers were with 72% the most common onset symptom of the disease followed by erythema nodosum (9%), uveitis (7%), arthritis (7%), genital ulcers (3%), superficial thrombophlebitis (2%) and papules/sterile pustules (2%). Uveitis and erythema nodosum as onset symptoms shortened the median interval to diagnosis to 1.5 and 15 months, respectively, while arthritis delayed diagnosis (43.5 months; p = 0.029). A severe course developed in 25% of the patients; irreversible retinal vasculitis to blindness in 15%, sterile meningoencephalitis in 8%, severe arthritis in 5%, hemoptysis in 2%, lethal outcome in 2% and bowel perforation in 1%. The relative risk of HLA-B5 positive German natives developing the disease. HLA-B5 was confirmed as a marker of severe prognosis. Cardiolipin autoantibodies were associated with cutaneous vasculitis and superficial thrombophlebitis was correlated with systemic vessel involvement.
Adolescence
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Adult
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Aged
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Behcet's Syndrome/epidemiology*
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Behcet's Syndrome/complications
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Child
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Child, Preschool
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Europe/epidemiology
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Female
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Germany/epidemiology
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Human
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Male
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Middle Age
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Prognosis
3.Cutaneous Manifestations of Behcet's Syndrome.
Moon Soo YOON ; Seung Hun LEE ; Dong Sik BANG ; Sungnack LEE
Yonsei Medical Journal 1987;28(4):291-296
The clinical features of cutaneous manifestations in 411 patients with Behcet's syndrome were studied. 302 patients (73.5%) had skin lesions. The frequency with which the following skin lesions were noted was, in decreasing order; erythema nodosum-like lesion, papulopustular eruption, erythema multiforme-like lesion, thrombophlebitis, ulcer and Sweet's syndrome-like lesion. More than two types of skin lesions were seen in 86 patients (28.5%), the combination of the skin lesions being in decreasing order, erythema nodosum-like lesion and papulopustular eruption; erythema multiforme-like lesion and papulopustular lesion; erythema nodosum-like lesion and thrombophlebitis. A skin pathergy test was performed on 245 patients, and a positive reaction was seen in 97 patients (39.6%). This study showed the high incidence, wide spectrum and importance of skin lesions as a major symptom in Behcet's syndrome.
Adolescent
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Adult
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Aged
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Behcet Syndrome/complications*
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Behcet Syndrome/epidemiology
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Child
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Female
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Human
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Male
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Middle Age
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Skin Diseases/classification
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Skin Diseases/epidemiology*
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Skin Diseases/etiology
4.Esophageal Involvement in Behcet's Disease.
Mohamed Habib HOUMAN ; Imed Ben GHORBEL ; Mounir LAMLOUM ; Monia KHANFIR ; Amel BRAHAM ; Slim HAOUET ; Nourreddine SAYEM ; Hajer LASSOUED ; Mohamed MILED
Yonsei Medical Journal 2002;43(4):457-460
Esophageal involvement in Behcet's disease is very rare, and normally is observed as aphtosis and esophagitis, but serious complications such as erosions, perforations, and stenosis may occur. We carried out this prospective study to evaluate the prevalence of esophageal involvement in Behcet's disease and to establish if routine endoscopy and/or manometry are necessary. Twenty-three patients who fulfilled the diagnostic criteria of the international study group for Behcet's disease were enrolled. None were taking drugs or had disease that might produce esophageal abnormalities or alter any existing changes due to the Behcet's disease itself. Twenty- three patients underwent esophagogastroduodenoscopy by a single observer. Esophageal biopsies were performed in thirteen patients and esophageal manometry in twenty. At the beginning of the study, the disease activity was defined by the presence of more than one symptom related to Behcet's disease, and upon the classification of Behcet's disease. Of the twenty three patients enrolled two were excluded from final analysis because of the presence of hiatus hernia. Thus, 13 men and 8 women, ranging in age from 20 to 63 years with a mean age of 36.2 years were included. Ten patients (47.6%) had active disease and four (19%) complained of upper gastrointestinal symptoms at the time of the study. Fourteen patients had endoscopic, manometric and/or microscopic abnormalities. Esophageal manometry was performed in twenty patients and was abnormal in 7 cases (35%). Esophageal biopsies were done in 13 patients and revealed histopathological abnormalities in 5 cases. Microscopic findings showed vasculities in one case, and non-specific inflammatory infiltration mainly consisting of neutrophils in 4 cases. Our results suggest that the prevalence of esophageal involvement in Behcet's disease is rather high and occur even in asymptomatic patients, but that this usually does not result in specific abnormalities.
Adult
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Behcet Syndrome/*complications
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Esophageal Diseases/*epidemiology
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Esophagoscopy
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Esophagus/pathology
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Female
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Human
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Male
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Manometry
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Middle Age
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Prevalence
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Prospective Studies
5.Carpal Tunnel Syndrome in Behcet's Disease.
Jungsoo LEE ; Suhyun CHO ; Do Young KIM ; Zhenlong ZHENG ; Hoon PARK ; Dongsik BANG
Yonsei Medical Journal 2015;56(4):1015-1020
PURPOSE: Behcet's disease (BD) is a chronic inflammatory disease characterized by orogenital ulcers, skin and ocular lesions, in addition to articular, vascular, and neurologic symptoms. Carpal tunnel syndrome (CTS), can also occur in BD patients secondary to inflammation in the connective tissues, vessels, and tendons, as well as nerve involvement in BD itself. However, reports of patients who have CTS in BD are rare. The aim of this study was to evaluate the clinical characteristics of CTS in BD patients. MATERIALS AND METHODS: Retrospective analysis of the medical records of 1750 BD patients, and 14 (0.8%) BD patients who were diagnosed with CTS was performed at the BD Specialty Clinic of Severance Hospital. Patient demographics, disease activity/severity for both diseases, and the clinical characteristics of CTS in BD were recorded and analyzed. RESULTS: All 14 BD patients with CTS were women. Twelve patients (85.7%) were diagnosed with active BD. The CTS was mild in 8 patients (57.2%), moderate in 3 patients (21.4%), and severe in 3 patients (21.4%). Ten patients (71.4%) had BD prior to the diagnosis of CTS, and these 10 patients all had active BD. CONCLUSION: CTS can occur as a result of the inflammation associated with BD and can also be the presenting symptom of nerve involvement in BD. CTS can also develop as the initial symptom of BD. Therefore, a higher degree of suspicion should be maintained for CTS in patients with BD and vice versa; however, the exact relationship is uncertain.
Adult
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Age Distribution
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Aged
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Behcet Syndrome/complications/diagnosis/*epidemiology
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Carpal Tunnel Syndrome/diagnosis/*epidemiology
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Female
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Humans
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Inflammation
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Male
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Middle Aged
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Retrospective Studies
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Sex Distribution
6.Morbidity of Solid Cancer in Behcet's Disease: Analysis of 11 Cases in a Series of 506 Patients.
So Young NA ; Jaeyoung SHIN ; Eun So LEE
Yonsei Medical Journal 2013;54(4):895-901
PURPOSE: Behcet's disease (BD) is rarely reported to be associated with malignancies in the literature. However, the frequency of cancer in BD patients remains unknown. This study evaluated cancer morbidity in BD patients compared with that in the general population of Korea. MATERIALS AND METHODS: A retrospective chart review was performed on 506 patients visiting our hospital from 1994 to 2011 for BD. We analyzed the standardized morbidity rate (SMR), which is the ratio of observed to expected malignancies. Furthermore, we reviewed cases of solid cancer in BD patients in the literature. RESULTS: Of the 506 patients with BD, 11 (2.17%) developed cancer. We found a variety of solid cancers without predominance and no hematologic malignancies. The total number of cancers observed was less than expected, which was determined from the statistical data of the National Cancer Information Center of Korea, with an SMR of 0.023 (95% confidence interval, 0.012-0.039). CONCLUSION: BD may be associated with a lower cancer-related morbidity compared with the general population of Korea.
Adult
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Behcet Syndrome/*complications/drug therapy/epidemiology
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Female
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Follow-Up Studies
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Humans
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Male
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Middle Aged
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Neoplasms/*epidemiology/etiology/surgery
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Republic of Korea/epidemiology
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Retrospective Studies
7.Epidemiologic and Clinical Survey of Behcet's Disease in Korea: the First Multicenter Study.
Dongsik BANG ; Ju Hee LEE ; Eun So LEE ; Sungnack LEE ; Jong Soo CHOI ; Young Keun KIM ; Baik Kee CHO ; Jai Kyoung KOH ; Young Ho WON ; Nack In KIM ; Seok Don PARK ; Hong Jun AHN ; Yoon Woo LEE ; Han Young WANG ; Won Woo LEE ; Hee Chul EUN ; Eun Sup SONG ; Sung Won LEE ; Chang Woo LEE ; Chong Ju LEE ; Jae Ho PARK ; Yeong Wook SONG ; Sang Tae KIM ; Chong Yeol KIM ; Jang Kyu PARK ; Kyung Sool KWON
Journal of Korean Medical Science 2001;16(5):615-618
The prevalence of Behcet's disease is the highest in the East Asian and the Medi-terranean countries. Behcet's disease is also distributed in the Asian countries, but the nationwide survey has not been performed in Korea yet. The Korean Study Group for Behcet's Disease, founded in 1999, conducted a multicenter, retrospective survey on epidemiologic and clinical features of the patients with Behcet's disease from 20 hospitals around the nation from 1997 to 1999. Of 3,497 patients, 1,527 were classified into complete or incomplete type of Behcet's disease according to the revised Shimizu's classification. The sex ratio was 1:1.75 with the female predominance. Geographical distribution showed the highest frequency in Seoul (38.5%). Clinically, 98.8% had oral ulcers, 83.2% had genital ulcers, 84.3% had skin lesions and 50.9% had ocular lesions. As for the minor clinical manifestations, articular symptoms were the most frequent. The pathergy test showed positive in 15.4% of patients and revealed a higher positive rate in males (20.2%) than in females (12.7%). In conclusion, we performed the first multicenter study on Behcet's disease in Korea and revealed the female predominance, higher frequency of ocular lesions, and lower positivity of pathergy test in the patients.
Adolescence
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Adult
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Aged
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Behcet's Syndrome/complications/*epidemiology
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Child
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Child, Preschool
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Female
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Human
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Infant
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Korea/epidemiology
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Male
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Middle Age
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Prevalence
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Retrospective Studies
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Sex Distribution
8.The Prevalence and Clinical Characteristics of Esophageal Involvement in Patients with Behcet's Disease: A Single Center Experience in Korea.
Seung Woo YI ; Jae Hee CHEON ; Jie Hyun KIM ; Sang Kil LEE ; Tae Il KIM ; Yong Chan LEE ; Won Ho KIM
Journal of Korean Medical Science 2009;24(1):52-56
While a significant amount of clinical information has been reported concerning intestinal involvement in Behcet's disease (BD), esophageal involvement in BD has not yet been studied extensively. The aim of this study was to evaluate the prevalence of esophageal involvement in BD and its clinical characteristics. We retrospectively reviewed the medical records of 842 patients diagnosed with BD at a single tertiary institution in Korea between January 1990 and June 2006. Of the 842 patients with BD, 129 patients (15.3%) experienced upper gastrointestinal symptoms that required inspection through esophagogastroduodenoscopy. Esophageal involvement was found in 6 (4.7%) of the 129 patients. The activity index of Behcet's disease did not differ among patients with or without esophageal involvement. All patients with esophageal involvement responded well to medical treatment and no one experienced serious complications. The results of our study demonstrate that the prevalence of esophageal involvement in BD is very low and that most patients with such involvement face few complications and respond well to medical treatment.
Adolescent
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Adult
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Aged
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Behcet Syndrome/*complications/diagnosis/epidemiology
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Child
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Child, Preschool
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Endoscopy, Digestive System
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Esophageal Diseases/diagnosis/epidemiology/*etiology
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Female
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Humans
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Korea
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Male
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Medical Records
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Middle Aged
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Prevalence
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Retrospective Studies
9.Renal Manifestations in 2007 Korean Patients with Behcet's Disease.
Sung Bin CHO ; Jihyun KIM ; Shin Wook KANG ; Tae Hyun YOO ; Zhenlong ZHENG ; Suhyun CHO ; Hye Sun LEE ; Dongsik BANG
Yonsei Medical Journal 2013;54(1):189-196
PURPOSE: Behcet's disease (BD) theoretically affects all sizes and types of blood vessels and results in multi-organ involvement. However, renal BD has not been fully characterized, though the kidneys are histologically rich in blood vessels. MATERIALS AND METHODS: A total of 2007 patients who fulfilled the diagnostic criteria for BD were enrolled in this study. We reviewed the medical records and test results of the BD patients and used univariate and multivariate logistic regression analyses to determine the clinical significance of renal involvement in BD. RESULTS: Among the 2007 BD patients, we noted hematuria in 412 (20.5%) and proteinuria in 29 (1.4%). Univariate analysis showed that the BD patients with hematuria were predominantly female and older, had higher erythrocyte sedimentation rates (ESRs), and more frequently presented with genital ulcerations. BD patients with proteinuria had higher ESR levels compared to BD patients without proteinuria. In the multivariate analysis, age, sex, and ESR were found to be significantly associated with hematuria in BD patients, whereas only ESR was associated with proteinuria in BD patients. We also found that IgA nephropathy was the most common pathologic diagnosis in 12 renal BD patients who underwent renal biopsies. CONCLUSION: We suggest that routine urinalysis and serum renal function tests be performed for the early detection of renal BD, especially in older female BD patients with recurrent hematuria, high ESR levels, and frequent genital ulcers, as well as in BD patients with proteinuria and high ESR levels.
Adolescent
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Adult
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Age Factors
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Aged
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Aged, 80 and over
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Behcet Syndrome/*complications/epidemiology/*metabolism
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Biopsy
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Female
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Glomerulonephritis, IGA/complications/diagnosis
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Hematuria/complications/diagnosis
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Humans
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Kidney/*pathology
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Kidney Diseases/*diagnosis
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Logistic Models
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Male
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Middle Aged
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Multivariate Analysis
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Proteinuria/complications/diagnosis
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Republic of Korea
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Young Adult
10.Overlooked Management and Risk Factors for Anemia in Patients with Intestinal Behcet's Disease in Actual Clinical Practice.
Bun KIM ; Soo Jung PARK ; Sung Pil HONG ; Jae Hee CHEON ; Tae Il KIM ; Won Ho KIM
Gut and Liver 2015;9(6):750-755
BACKGROUND/AIMS: Anemia in patients with inflammatory bowel disease significantly affects the quality of life. The aim of this study was to investigate the frequency of and risk factors for anemia and to describe the management of anemia in patients with intestinal Behcet's disease (BD) in actual clinical practice. METHODS: We included 64 patients with intestinal BD who visited the outpatient clinic of a tertiary referral center in June 2011 and had available laboratory data for the subsequent 6 months. RESULTS: Anemia was detected in 26 patients (40.6%). After 6 months, anemia was still present in 14 of these patients (53.8%). The cause of anemia was investigated in eight patients (30.8%), and oral iron supplementation was prescribed to four patients (15.4%). Of these four patients, two (50%) recovered completely within 6 months. Anemia was associated with a high Disease Activity Index for Intestinal Behcet's Disease (DAIBD, p=0.024), erythrocyte sedimentation rate (p=0.003), and C-reactive protein (p=0.049) in univariate analysis. In multivariate analysis, the factor predictive for anemia in patients with intestinal BD was a higher DAIBD (> or =40; odds ratio, 4.08; 95% confidence interval, 1.21 to 13.71; p=0.023). CONCLUSIONS: Although anemia is common in intestinal BD patients, its clinical importance is overlooked in daily practice. Moderate to severe disease activity is predictive of anemia.
Adult
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Anemia/drug therapy/epidemiology/*etiology
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Behcet Syndrome/blood/*complications/pathology
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Blood Sedimentation
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C-Reactive Protein/analysis
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Dietary Supplements
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Disease Management
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Female
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Humans
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Intestinal Diseases/blood/*complications/pathology
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Iron/therapeutic use
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Male
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Middle Aged
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Multivariate Analysis
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Odds Ratio
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Predictive Value of Tests
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Risk Factors
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Severity of Illness Index
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Trace Elements/therapeutic use