1.Value of Ultrasound in Rheumatologic Diseases.
Taeyoung KANG ; Laura HORTON ; Paul EMERY ; Richard J WAKEFIELD
Journal of Korean Medical Science 2013;28(4):497-507
The use of musculoskeletal ultrasound in rheumatology clinical practice has rapidly increased over the past decade. Ultrasound has enabled rheumatologists to diagnose, prognosticate and monitor disease outcome. Although international standardization remains a concern still, the use of ultrasound in rheumatology is expected to grow further as costs fall and the opportunity to train in the technique improves. We present a review of value of ultrasound, focusing on major applications of ultrasound in rheumatologic diseases.
Humans
;
Magnetic Resonance Imaging
;
Musculoskeletal System/ultrasonography
;
Osteoarthritis/ultrasonography
;
Rheumatic Diseases/*ultrasonography
;
Sjogren's Syndrome/ultrasonography
;
Spondylarthropathies/ultrasonography
;
Synovitis/ultrasonography
;
Tendinopathy/ultrasonography
;
Vasculitis/ultrasonography
2.Wegener`s Granulomatosis of the Ureter Mimicking Ureteral Tumor.
Hong Jin SUH ; Dong Hwan LEE ; Bong Hyeon NAM ; Joong Ho KIM ; Jang Min OH ; Hong Woo RHEE
Korean Journal of Urology 1997;38(5):561-564
Wegener`s granulomatosis (WG) is a multisystem disorder of unknown origin characterized by necrotizing granulomatous vasculitis. WG usually affects the upper respiratory tract, lungs, and kidneys with focal glomerulonephritis, but almost any organ can be affected. The ureter is primarily an unusual location for lesions of WG. A 30-year-old woman presented with intermittent right flank pain and hematuria. A renal ultrasound demonstrated unilateral hydronephrosis and a retrograde pyelography revealed a filling defect at right mid ureter and a computed tomography displayed marked concentric thickening of the right ureteral wall which was mimicking ureteral tumor. At nephroureterectomy, the right ureter was found to be obstructed by dense, intramural fibroinflammatory reaction. There was a necrotizing granulomatous vasculitis in the muscle layer of the ureter. Our case represents the rare occurrence of WG presenting ureteral bstruction.
Adult
;
Female
;
Flank Pain
;
Glomerulonephritis
;
Hematuria
;
Humans
;
Hydronephrosis
;
Kidney
;
Lung
;
Respiratory System
;
Ultrasonography
;
Ureter*
;
Urography
;
Vasculitis
3.Posterior Tibial Artery Aneurysm: A Case Report.
Ji Hoon KIM ; Yong Pil CHO ; Je Hong AHN ; Soo Jung CHOI ; Gil Hyun KANG ; Myoung Sik HAN ; Hyuk Jai JANG ; Yong Ho KIM ; Jin Ho KWAK ; Youn Baik CHOI
Journal of the Korean Society for Vascular Surgery 2005;21(2):171-174
Aneurysms of the infrapopliteal arteries are rare and they are commonly associated with trauma. We report here on a rare case of a true aneurysm of the posterior tibial artery in a sixty-year-old female. There was no history of trauma, and the serologic tests for the possibility of vasculitis were all negative. The color Doppler ultrasound examination and the multi-detector computed tomographic scan confirmed the diagnosis of a posterior tibial artery aneurysm and these tests revealed no evidence of aneurysms or occlusive lesions in the other arteries. Aneurysmectomy and end-to-end microvascular anastomosis were performed successfully. Preoperative multi- detector computed tomographic scanning is a valuable, noninvasive diagnostic tool to delineate not only the state of the aneurysm, but also that of the distal arterial tree.
Aneurysm*
;
Arteries
;
Diagnosis
;
Female
;
Humans
;
Serologic Tests
;
Tibial Arteries*
;
Ultrasonography
;
Vasculitis
4.Vessel Wall Imaging of the Intracranial and Cervical Carotid Arteries.
Young Jun CHOI ; Seung Chai JUNG ; Deok Hee LEE
Journal of Stroke 2015;17(3):238-255
Vessel wall imaging can depict the morphologies of atherosclerotic plaques, arterial walls, and surrounding structures in the intracranial and cervical carotid arteries beyond the simple luminal changes that can be observed with traditional luminal evaluation. Differentiating vulnerable from stable plaques and characterizing atherosclerotic plaques are vital parts of the early diagnosis, prevention, and treatment of stroke and the neurological adverse effects of atherosclerosis. Various techniques for vessel wall imaging have been developed and introduced to differentiate and analyze atherosclerotic plaques in the cervical carotid artery. High-resolution magnetic resonance imaging (HR-MRI) is the most important and popular vessel wall imaging technique for directly evaluating the vascular wall and intracranial artery disease. Intracranial artery atherosclerosis, dissection, moyamoya disease, vasculitis, and reversible cerebral vasoconstriction syndrome can also be diagnosed and differentiated by using HR-MRI. Here, we review the radiologic features of intracranial artery disease and cervical carotid artery atherosclerosis on HR-MRI and various other vessel wall imaging techniques (e.g., ultrasound, computed tomography, magnetic resonance, and positron emission tomography-computed tomography).
Arteries
;
Atherosclerosis
;
Carotid Arteries*
;
Early Diagnosis
;
Electrons
;
Magnetic Resonance Imaging
;
Moyamoya Disease
;
Phenobarbital
;
Plaque, Atherosclerotic
;
Stroke
;
Ultrasonography
;
Vasculitis
;
Vasoconstriction
5.Carotid artery intima-media thickness in Behcet's disease patients without significant cardiovascular involvement.
Seo Na HONG ; Jong Chun PARK ; Nam Sik YOON ; Sang Rok LEE ; Kye Hun KIM ; Young Joon HONG ; Hyung Wook PARK ; Ju Han KIM ; Youngkeun AHN ; Myung Ho JEONG ; Jeong Gwan CHO ; Jung Chaee KANG
The Korean Journal of Internal Medicine 2008;23(2):87-93
BACKGROUND/AIMS: Behcet's disease (BD) is a systemic disorder associated with a characteristic vasculitis that can involve both veins and arteries of all sizes. Endothelial activation or injury is a characteristic feature of BD. Endothelial dysfunction is widely regarded as being the initial lesion in the development of atherosclerosis. The carotid artery intima-media thickness (IMT) is a widely accepted marker of subclinical atherosclerosis. We aimed to determine the carotid IMT in BD patients with using high-resolution B-mode Doppler ultrasonography. METHODS: We studied 40 patients (24 males, mean age: 39.1+/-8.5 years) who were diagnosed by the international diagnostic criteria of Behcet's disease and 20 healthy controls (13 males, mean age: 40.2+/-5.1 years), and the two groups were matched by age and gender. No subject in either group had a history of atherosclerosis or its complications. The clinical data, including the age of onset, the duration of disease, a history of medication, the activity score and the laboratory data were analyzed. RESULTS: The carotid IMT in the BD group was significantly higher than that in the control group (0.71+/-0.22 mm vs. 0.59+/-0.09 mm, respectively, p<0.01). Cardiac and major vessel involvements were not identified in the BD group. However, minor vascular involvements were documented in 2 patients with deep vein thrombosis, in 4 patients with superficial thrombophlebitis and in 2 patients with pseudoaneurysm. The carotid IMT in the patients with posterior uveitis or retinal vasculitis was higher than that of the patients without these findings (0.85+/-0.21 mm vs. 0.64+/-0.10 mm, respectively, p=0.007), but there was no difference of the IMT according to minor vascular involvement. CONCLUSIONS: Despite that there was no significant cardiovascular involvement in the BD patients, the carotid IMT was significantly higher in the BD patients as compared with the healthy controls.
Adult
;
Behcet Syndrome/complications/diagnosis/*pathology
;
Carotid Arteries/*pathology/ultrasonography
;
Case-Control Studies
;
Endothelium, Vascular/pathology
;
Female
;
Humans
;
Male
;
Prognosis
;
Prospective Studies
;
Risk Factors
;
Tunica Intima/*pathology/ultrasonography
;
Tunica Media/*pathology/ultrasonography
;
Ultrasonography, Doppler
;
Vasculitis/pathology
6.Acute Scrotum in an Infant with Kawasaki Disease.
Ha Young KANG ; Eun Young JOO ; Dong Hyun KIM ; Young Jin HONG
Pediatric Infection & Vaccine 2017;24(1):60-64
Kawasaki disease (KD) is a systemic vasculitis that occurs predominantly in infants and young children. The etiology of KD is unknown and coronary heart disease is a major complication of KD. Acute scrotum is a rare complication of acute KD, and not as well recognized as other manifestations of the disease. We report a 2-month-old boy with acute scrotum in the acute phase of KD. He was treated with intravenous immunoglobulin (total 2 g/kg) and aspirin (50 mg/kg/day). The treatment was effective in resolving his fever and other clinical symptoms, but 2 days after starting treatment he experienced scrotal swelling. Scrotal ultrasound and transillumination were used in the diagnosis of acute scrotum. After 2 months, a follow-up testicular ultrasound revealed a remission of the acute scrotum. Subsequently, he has been followed up for KD.
Aspirin
;
Child
;
Coronary Disease
;
Diagnosis
;
Fever
;
Follow-Up Studies
;
Humans
;
Immunoglobulins
;
Infant*
;
Male
;
Mucocutaneous Lymph Node Syndrome*
;
Scrotum*
;
Systemic Vasculitis
;
Testicular Hydrocele
;
Transillumination
;
Ultrasonography
;
Urological Manifestations
7.Spontaneous Rupture of Renal Artery Aneurysm in a Patient with Untreated Hypertension.
Ji Il KIM ; Hak Jun SEO ; Ok Ran SHIN ; Sun Wha SONG ; Eun Mi WHANG ; Kang JU ; Young Soo KIM ; Sun Ae YOUN ; Young Ok KIM
Korean Journal of Nephrology 2003;22(6):763-766
Spontaneous rupture of renal artery aneurysm is a rare, but life threatening complication with high mortality. The etiology of non-traumatic renal artery aneurysm is fibromuscular dysplasia, atherosclerosis, vasculitis, and pregnancy. We here report a case of spontaneous rupture of renal artery aneurysm in a patient with untreated hypertension. A 39-year-old non-pregnant woman complained of sudden onset of right flank and lower quadrant abdominal pain. Ultrasonography showed large fluid collection in right lower abdomen. Emergency laparotomy demonstrated huge retroperitoneal hematoma due to spontaneous rupture of right renal artery aneurysm. Microscopic examination of the aneurysmal wall revealed intimal hyperplasia without atherosclerotic change.
Abdomen
;
Abdominal Pain
;
Adult
;
Aneurysm*
;
Atherosclerosis
;
Emergencies
;
Female
;
Fibromuscular Dysplasia
;
Hematoma
;
Humans
;
Hyperplasia
;
Hypertension*
;
Laparotomy
;
Mortality
;
Pregnancy
;
Renal Artery*
;
Rupture, Spontaneous*
;
Ultrasonography
;
Vasculitis
8.A Case of Acute Cholecystitis Caused by Plasmodium vivax Infection.
Bo Kyung YANG ; Jin Gu KANG ; Hye Mi OH ; Hee Su PARK ; Kyung Up KIM ; Seong Jin CHO ; Hyun Jung CHO ; Jin Heon LEE
Korean Journal of Pancreas and Biliary Tract 2015;20(3):162-167
Acute cholecystitis as a complication of malarial disease is a rare condition, especially with Plasmodium vivax infection. A 62 year-old-female was admitted via emergency room (ER) due to high fever (40.3degrees C) and epigastric pain. Initial abdominal ultrasound and computed tomography (CT) scan showed edematous gallbladder with stone, which suggested acute calculous cholecystitis. Emergency percutaneous transhepatic gallbladder drainage (PTGBD) was done with systemic antibiotic therapy. The clinical course, however, unusually worsened with hypotension and intensive care unit (ICU) management was done. Four days after admission multi-focal splenic infarction was developed and Plasmodium vivax infection was diagnosed afterward. The clinical symptoms and laboratory results, including fever and epigastric pain, improved dramatically after anti-malarial treatment and cholecystectomy was done. The resected gallbladder (GB) specimen shows vasculitis pattern with capillary red blood cell (RBC) engorgement, which suggests the cause of cholecystitis was due to Plasmodium vivax rather than GB stone.
Capillaries
;
Cholecystectomy
;
Cholecystitis
;
Cholecystitis, Acute*
;
Drainage
;
Emergencies
;
Emergency Service, Hospital
;
Erythrocytes
;
Fever
;
Gallbladder
;
Hypotension
;
Intensive Care Units
;
Plasmodium vivax*
;
Plasmodium*
;
Splenic Infarction
;
Ultrasonography
;
Vasculitis
9.Clinical Significance of Gastrointestinal Symptoms and Abdominal Ultrasonographic Findings in Henoch-Schonlein Purpura.
Eun Jung CHOI ; Chang Woo LEE ; Du Young CHOI
Korean Journal of Pediatrics 2005;48(1):63-67
PURPOSE: Henoch-Schonlein purpura(HSP) is a systemic vasculitis, characterized by cutaneous palpable purpura, gastrointestinal(GI) symptoms, arthritis and renal involvement. In general, the prognosis is determined by GI complication as well as the severity of nephritis. In this study, we analyzed the statistical relationship between the GI symptom and other clinical findings for assessing the prognosis, and evaluated abdominal ultrasonographic findings for early diagnosis of this disease with atypical clinical presentation and early detection of serious GI complications. METHODS: One hundred seventy seven patients with HSP in the Department of Pediatrics, Wonkwang University Hospital from January 1994 to June 2004, were enrolled. We retrospectively analyzed charts about clinical and abdominal ultrasonographic findings, and classified our patients into two groups(GI-Sx(-), GI-Sx(+)) for statistical analysis. RESULTS: The ratio of female to male is 1.5:1. The peak age incidence was five to eight years in 95 cases(53%). The GI symptoms appeared in 117 cases(66%), which include abdominal pain 115 (98 %), tenderness 45(38%), nausea and vomiting 35(30%), bloody stool 10(8.5%), diarrhea four(3.4%), rebound tenderness four(3.4%), and also intussusception and appendicitis were complicated in five and two cases respectively. GI-Sx(+) group had an increased risk of renal involvement and relapse than the GI-Sx(-) group. But there were no relationships about sex and age incidence, or other clinical and laboratory findings between two groups. Ultrasonographic findings in 98 patients with GI symptoms included small bowel thickening in 70 cases(71%) in which duodenum, jejunum and ileum were involved in 71%, 45.7%, 40% respectively, small bowel dilatation in 41 cases(42%), lymph node swelling in 46 cases(47%), and ascites in 25 cases(25.5%). CONCLUSION: GI symptoms in patients with HSP suggested increased risk of renal involvement and relapse. Abdominal ultrasonography could be helpful in the early diagnosis on atypical clinical presentation and early detection of serious GI complication in these patients.
Abdominal Pain
;
Appendicitis
;
Arthritis
;
Ascites
;
Diarrhea
;
Dilatation
;
Duodenum
;
Early Diagnosis
;
Female
;
Humans
;
Ileum
;
Incidence
;
Intussusception
;
Jejunum
;
Lymph Nodes
;
Male
;
Nausea
;
Nephritis
;
Pediatrics
;
Prognosis
;
Purpura
;
Purpura, Schoenlein-Henoch*
;
Recurrence
;
Retrospective Studies
;
Systemic Vasculitis
;
Ultrasonography
;
Vomiting
10.A Case of Hemobilia Associated with Spontaneous Gallbladder Hemorrhage.
Eul Soon IM ; Seok Ho DONG ; Kun Woo LIM ; Sang Hwa KIM ; Hyo Jong KIM ; Byung Ho KIM ; Jung Il LEE ; Young Woom CHANG ; Rin CHANG ; Sang Mok LEE
Korean Journal of Gastrointestinal Endoscopy 1999;19(6):1005-1010
Hemobilia is a hemorrhage into the biliary tract that may follow trauma (including surgical and percutaneous techniques in hepatobiliary system), aneurysms of the hepatic artery (and its branch), tumors of the biliary tract, hepatoma, inflammation, liver abscess, and gallstone disease. But, a case has not been reported involving of hemobilia associated with gallbladder hemorrhage without obvious predisposing factors or causes. A 62-year-old woman was admitted to Kyunghee Medical Center due to intermittent nausea, and right upper quadrant pain for 2 days before admission. She had no history of abdominal trauma. On the second and third day of her stay, she experienced melena of which the amount was about 300 ml. Abdominal ultrasonography revealed a gallbladder with a 8 mm sized cystic lesion attached to the fundus. Computed tomographic (CT) evaluation of the abdomen demonstrated a highly enhanced 7~8 mm sized nodular mass in the lumen of the gallbladder. The gallbladder, cystic duct, and CBD were dilated due to the filling of blood clots or sludge material. An ERCP was performed and bleeding from the papilla of Vater was confirmed. Subsequently, emergent laparoscopic cholecystectomy was conducted. Pathologic evaluation revealed a grayish-red gallbladder that had a ruptured vessel. The ruptured vessel showed a severe hypertrophic state but there was no evidence of vasculitis, aneurysm, arterio-venous malformation, or malignancy. The case is here in reported of hemobilia associated with spontaneous gallbladder hemorrhage.
Abdomen
;
Aneurysm
;
Biliary Tract
;
Carcinoma, Hepatocellular
;
Causality
;
Cholangiopancreatography, Endoscopic Retrograde
;
Cholecystectomy, Laparoscopic
;
Cystic Duct
;
Female
;
Gallbladder*
;
Gallstones
;
Hemobilia*
;
Hemorrhage*
;
Hepatic Artery
;
Humans
;
Inflammation
;
Liver Abscess
;
Melena
;
Middle Aged
;
Nausea
;
Sewage
;
Ultrasonography
;
Vasculitis