1.A Case of Intradural Spinal Lipoma.
Byeong Kyu KIM ; Jae Young BAN ; Jowa Hyuk IHM ; Tae Hee RYU ; Bang Hyun NAM ; Suk Hoon YOON
Journal of Korean Neurosurgical Society 1996;25(9):1901-1904
Intradural spinal lipomas are rare, primary genign tumor of the spinal canal. A case of intradural spinal lipoma with intramedullary extension is presented. Clinical feature was slowly progressing paraparesis. A subtotal excision was performed, and pathological studies confirmed the diagnosis.
Diagnosis
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Lipoma*
;
Paraparesis
;
Spinal Canal
;
Spinal Cord Compression
;
Spinal Cord Neoplasms
2.Clinical Analysis of Chronic Subdural Hematomas: Review of 69 Operated Cases.
Byeong Kyu KIM ; Jae Yung BAN ; Jowa Hyuk IHM ; Tae Hee RYU ; Bang Hyun NAM ; Suk Hoon YOON
Journal of Korean Neurosurgical Society 1996;25(9):1820-1827
The authors analysed retrospectively, 69 cases of chronic subdural hematoma admitted to the Department of Neurological Surgery, from January 1992 to February 1995. All hematomas were operated on by one burr hole trephination and continuous closed-system cather drainage system. The results were as follows: 1) Male was more frequently involved than female with ratio of 5.3:1 and the incidence was prredominent in the patients whose ages were over 50. 2) History of head trauma was found in 52 cases(75.4%), among which habitual alcoholism was found in 6 cases(8.7%). 3) The major symptoms and signs at admission were headache(55.1%), hemiparesis(44.9%), and mental changes(30.4%). 4) On the brain CT scan, hematoma showed low, iso, mixed, and high in density, and the shapes of hematoma were crescenteric, biconvex, planoconvex, and concave in order of frequency. 5) We have found a significant relationship between the neurological grade at admission and the prognosis, and noted full recovery in 45 cases(65.2%) and no d eath as a result of 1-burr hole trephination.
Alcoholism
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Brain
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Craniocerebral Trauma
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Drainage
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Female
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Hematoma
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Hematoma, Subdural, Chronic*
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Humans
;
Incidence
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Male
;
Prognosis
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Retrospective Studies
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Tomography, X-Ray Computed
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Trephining
3.A Case of Acute Fulminant Fat Embolism Syndrome after Liposuction Surgery.
Seong Wook BYEON ; Tae Hyun BAN ; Chin Kook RHEE
Tuberculosis and Respiratory Diseases 2015;78(4):423-427
Fat embolism syndrome (FES) is a clinical manifestation that consists of multiple organ dysfunction due to fat emboli. FES occurs as a complication after trauma or procedures such as surgery. The diagnostic criteria of FES have not yet been established, so clinical criteria are used for its diagnosis. The clinical course of acute fulminant FES can be rapid. Liposuction surgery, in which adipocytes are mechanically disrupted, is one cause of FES. As the number of liposuction surgeries increases, clinicians should be aware of the possibility of FES. This was the first report of a case of acute fulminant FES with severe acute respiratory distress syndrome after liposuction surgery, in Korea.
Adipocytes
;
Diagnosis
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Embolism, Fat*
;
Korea
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Lipectomy*
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Respiratory Distress Syndrome, Adult
4.A Case of Toxic Megacolon Caused by Clostridium difficile Infection and Treated with Fecal Microbiota Transplantation.
Tae Geun GWEON ; Kyung Jin LEE ; Donghoon KANG ; Sung Soo PARK ; Kyung Hoon KIM ; Hyeonjin SEONG ; Tae Hyun BAN ; Sung Jin MOON ; Jin Su KIM ; Sang Woo KIM
Gut and Liver 2015;9(2):247-250
Toxic megacolon is a rare clinical complication of fulminant Clostridium difficile infection. The mortality rate of fulminant C. difficile infection is reported to be as high as 50%. Fecal microbiota transplantation is a highly effective treatment in patients with recurrent or refractory C. difficile infection. However, there are few published articles on the use of such transplantation for fulminant C. difficile infection. Here, we report on a patient with toxic megacolon complicated by C. difficile infection who was treated successfully with fecal microbiota transplantation.
Aged
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*Clostridium difficile
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Enterocolitis, Pseudomembranous/*complications
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Fecal Microbiota Transplantation/*methods
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Feces/*microbiology
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Humans
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Male
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Megacolon, Toxic/*microbiology/*therapy
5.Arthroscope-guided Closed Reduction and Internal Fixation of the Lateral Malleolar Fracture.
Sung Il SHIN ; Gab Lae KIM ; Yoon Suk HYUN ; Tae Seo BAN ; Tae Hwa KIM
Journal of Korean Foot and Ankle Society 2008;12(1):74-79
PURPOSE: In this study, we introduced an newly developed technique of operation for fracture of lateral malleolus of the ankle. We treated the fracture by close reduction and internal fixation using arthroscopy. MATERIALS AND METHODS: From July 2006 to June 2007, we had treated 23 cases of lateral malleolar fracture (SER type) by closed reduction and internal fixation with arthroscopy and followed them up more six month. Operation time, union time, clinical and functional result were evaluated. RESULTS: After the final follow-up, all the fractures were healed with satisfactory bony union. The subjective result was excellent in 15 cases (65%), good in 8 cases (35%), the objective result was excellent in 13 cases (57%), good in 10 cases (43%), and the roentgenographic result was excellent in 17 cases (74%), good in 6 cases (26%). CONCLUSION: Closed reduction and internal fixation with arthroscopy technique is an effective treatment method in treating lateral malleolar fracture of the ankle since it offers advantages including corrective anatomical reduction and minimizing complication associated with injury of soft tissue.
Animals
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Ankle
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Arthroscopy
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Follow-Up Studies
6.A Case of Descending Thoracic and Abdominal Aortic Aneurysm with Ankylosing Spondylitis.
Yeo Ree YANG ; Rae Seok LEE ; Tae Hyun BAN ; Jae Hyun SEO ; Dae Jun KIM ; Seung Min JUNG ; Sung Hwan PARK
Journal of Rheumatic Diseases 2014;21(1):43-45
Ankylosing spondylitis (AS) is a systemic inflammatory disorder that affects the axial skeleton. It often involves the extra-articular organs. Cardiovascular involvement is one of the extra-articular manifestations, which is mostly represented by aortic root, valvular heart disease, and conduction disturbances. An aortic sclerosing inflammatory process induces aortic root thickening and rigidity. An aortic aneurysmal change is a rare complication that often leads to life threatening conditions. A few cases regarding aortic aneurysm have been reported, but there are no reported cases in Korea. We report the first case of descending thoracic and abdominal aortic aneurysm in a patient with ankylosing spondylitis.
Aortic Aneurysm
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Aortic Aneurysm, Abdominal*
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Heart Valve Diseases
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Humans
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Korea
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Skeleton
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Spondylitis, Ankylosing*
7.A Case of Squamoid Cyst of Pancreatic Ducts Shown Malignant Behavior.
Yoon Seok CHOI ; Tae hyun BAN ; Ik Hyun JO ; Ji Young MOK ; Sang Bin LEE ; Won Jik LEE ; Sung Hoon JUNG ; Jung Hwan OH
Korean Journal of Pancreas and Biliary Tract 2014;19(2):84-89
Detection of cystic lesions in the pancreas has increased because of the widespread use of high-resolution diagnostic imaging techniques. Therefore, cystic lesions of the pancreas constitute an increasingly important category with a challenging differential diagnosis. Squamoid cyst of pancreatic ducts is a recently recognized type of cystic lesion in the pancreas in which cystically dilated ducts are lined by non-keratinized squamous epithelium. Although it is clinically known as benign cystic lesion, we experienced its malignant behavior and report here with review of the international literatures.
Diagnosis, Differential
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Diagnostic Imaging
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Epithelium
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Pancreas
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Pancreatic Cyst
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Pancreatic Ducts*
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Pancreatic Neoplasms
8.Case of Multiple Cranial Diabetic Neuropathies Involving the Third, Fourth and Sixth Cranial Nerves.
Tae Hyun BAN ; Sang Ah CHANG ; Jung Min LEE ; Ji Hyun KIM ; Ji Hye KIM ; Ji Woong ROH ; Kyung Hoon KIM
Korean Journal of Medicine 2014;87(1):92-95
Multiple simultaneous cranial neuropathies occur rarely in diabetes patients. In general, diabetic cranial neuropathy presents in an isolated form and frequently involves oculomotor or facial nerves. We report a 73-year-old man with known type 2 diabetes mellitus who presented with severe dizziness, diplopia and third, fourth and sixth nerve ophthalmoplegia of both eyes. Radiological, laboratory and ophthalmic work-up including magnetic resonance imaging and angiography (MRI and MRA) revealed no specific tumor, aneurysm, or inflammation findings, except for a previous cerebral infarction and atherosclerotic changes in the internal carotid and vertebral arteries. After strict blood glucose control, the multiple cranial nerve palsies spontaneously resolved in 12 weeks. We report the case with a review of the literature.
Abducens Nerve*
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Aged
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Aneurysm
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Angiography
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Blood Glucose
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Cerebral Infarction
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Cranial Nerve Diseases
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Diabetes Mellitus
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Diabetes Mellitus, Type 2
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Diabetic Neuropathies*
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Diplopia
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Dizziness
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Facial Nerve
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Humans
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Inflammation
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Magnetic Resonance Imaging
;
Ophthalmoplegia
;
Vertebral Artery
9.A Case of Relapsing Granulomatosis with Polyangiitis Treated Successfully with Rituximab.
Ji Won HAN ; Kwi Young KANG ; Tae Hyun BAN ; Ik Hyun JO ; Sung Hwan PARK
Journal of Rheumatic Diseases 2014;21(5):257-260
Granulomatosis with polyangiitis (GPA) is a rare antineutrophil cytoplasmic antibody associated with systemic disease characterized by granulomas and vasculitis affecting small and medium vessels. Neurological manifestations in GPA are less frequent than classical manifestations, such as lung and kidney involvement, and cranial nerve palsies are much rarer. Cyclophosphamide and glucocorticoids have been conventionally administered as an initial induction immunosuppressive therapy for GPA. However, increasing evidence has demonstrated the efficacy and safety of rituximab, an anti-B cell monoclonal antibody, for the treatment of GPA. Herein, we describe a successful treatment of relapsing GPA with cranial nerve involvement using rituximab in a 56-year-old male patient who was previously treated with cyclophosphamide plus glucocorticoids.
Antibodies, Antineutrophil Cytoplasmic
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Cranial Nerve Diseases
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Cranial Nerves
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Cyclophosphamide
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Glucocorticoids
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Granuloma
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Humans
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Kidney
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Lung
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Male
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Middle Aged
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Neurologic Manifestations
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Vasculitis
;
Rituximab
10.Development of End Stage Renal Disease after Long-Term Ingestion of Chaga Mushroom: Case Report and Review of Literature
Sua LEE ; Hwa Young LEE ; Yohan PARK ; Eun Jeong KO ; Tae Hyun BAN ; Byung Ha CHUNG ; Hyun Soon LEE ; Chul Woo YANG
Journal of Korean Medical Science 2020;35(19):e122-
Chaga mushrooms are widely used in folk remedies and in alternative medicine. Contrary to many beneficial effects, its adverse effect is rarely reported. We here report a case of end-stage renal disease after long-term taking Chaga mushroom. A 49-year-old Korean man with end stage renal disease (ESRD) was transferred to our hospital. Review of kidney biopsy finding was consistent with chronic tubulointerstitial nephritis with oxalate crystal deposits and drug history revealed long-term exposure to Chaga mushroom powder due to intractable atopic dermatitis. We suspected the association between Chaga mushroom and oxalate nephropathy, and measured the oxalate content of remained Chaga mushroom. The Chaga mushroom had extremely high oxalate content (14.2/100 g). Estimated daily oxalate intake of our case was 2 times for four years and 5 times for one year higher than that of usual diet. Chaga mushroom is a potential risk factor of chronic kidney disease considering high oxalate content. Nephrologist should consider oxalate nephropathy in ESRD patients exposed to Chaga mushrooms.