1.Popliteal artery injury associated with severe trauma around the knee.
Sang Soo KIM ; Dae Moo SIM ; Hak Sun KIM ; Byoung Chang CHANG ; In Young CHOI
The Journal of the Korean Orthopaedic Association 1993;28(7):2380-2388
No abstract available.
Knee*
;
Popliteal Artery*
2.Clinical Characteristics of Primary Headache According to Age in Children and Adolescents.
Yeon Ju HONG ; Min Sung KIM ; Kyung Yeon LEE ; Chang Sun SIM
Journal of the Korean Child Neurology Society 2010;18(2):264-274
PURPOSE: Childhood headache is different from adulthood headache and according to their age in clinical aspects. This study investigated the clinical differences of primary headache according to ages of children and adolescents. METHODS: A 300 children who did not show abnormalities on neurologic examination or brain CT or MRI were classified into two groups according to their ages. RESULTS: The percentage of those in the migraine group (24.2% vs. 35.9% in Groups 1 and 2 respectively) was higher in Group 2, but it was not statistically significant. In relation to the duration of headache, pain lasting for less than one hour accounted for 59.8% and 40% in Groups 1 and 2, respectively (P=0.001). In relation to the location headaches developed, the frontal region (40.2%) and temporal region (48.1%) were the most common in Groups 1 and 2, respectively (P<0.001). In relation to the nature of the headaches, tightening sensation accounted for the highest percentage in both groups; however, pulsating sensation were more common in Group 2 than in Group 1 (16.2% vs. 8.3%, P=0.038). In relation to the severity of headaches, severe to profound headaches accounted for 35.5% and 61.1% in Groups 1 and 2, respectively (P<0.001). In relation to laterality, unilateral headaches accounted for 12.4% and 26.7% in Groups 1 and 2, respectively (P=0.002). In relation to accompanying symptoms, the incidence of photophobia was higher in Group 2 than in Group 1 (P=0.047). CONCLUSION: Age factors should be considered in the diagnosis of childhood headaches. Also, we consider that there may be a need to establish diagnostic criteria specifically for childhood headaches separately from those for adulthood headaches.
Adolescent
;
Age Factors
;
Brain
;
Child
;
Headache
;
Headache Disorders, Primary
;
Humans
;
Hydroxamic Acids
;
Incidence
;
Migraine Disorders
;
Neurologic Examination
;
Photophobia
;
Sensation
3.A clinical study of 218 cases of Tsutsugamushi disease.
Chang Hyun PARK ; Chan Woong PARK ; Seung Sig SIM ; Mann JUNG ; Young Mi LEE ; Hyung Sun RYEU ; Ji Woon KIM
Korean Journal of Medicine 1993;45(4):497-506
No abstract available.
Scrub Typhus*
4.Fine needle aspiration cytology of presacral chordoma-a case report-.
Su Kyeong YEON ; Mi Kyung JEE ; Chang Suk KANG ; Byoung Kee KIM ; Sun Moo KIM ; Sang In SIM
Korean Journal of Cytopathology 1993;4(2):133-139
No abstract available.
Biopsy, Fine-Needle*
5.Two Cases of Rickets that Developed as a Result of by Diet Restriction due to Atopic Dermatitis.
Hyoung Min CHO ; Chang Sun CHOI ; Gyu Keun SUN ; Eun Young KIM ; Kyoung Sim KIM ; Yong Wook KIM
Korean Journal of Pediatric Gastroenterology and Nutrition 2006;9(2):284-290
Nutritional rickets, which is caused by deficiency of calcium or vitamin D, is a rare disease in developed countries. However some cases have been reported recently, that developed as a result of a restricted and nutritionally imbalanced diet due to atopic dermatitis and related food allergy. We treated two infant cases of nutritional rickets. The infants had suffered from atopic dermatitis, and were fed "Sun-sik" (a powdery mixture of several grains and fruits) without receiving cow's milk or any milk products in their diet. After an adequate supply of calcium and nutritional management, they were markedly improved.
Calcium
;
Edible Grain
;
Dermatitis, Atopic*
;
Developed Countries
;
Diet*
;
Food Hypersensitivity
;
Humans
;
Infant
;
Milk
;
Rare Diseases
;
Rickets*
;
Vitamin D
6.A case of acquired angioedema with C1 esterase inhibitor deficiency.
Chang Young HA ; Sun Sin KIM ; Hun Jong KIM ; Dong Suk HAN ; Jae Woong CHO ; Hyuck Jun CHUNG ; Hee Yeon KIM ; Dong Ho NAHM ; Hae Sim PARK
Journal of Asthma, Allergy and Clinical Immunology 1999;19(2):224-228
Angioedema is a well-demarcated localized edema involving the deeper layers of the skin, including the subcutaneous tissue. Angioedema occurs with Cl esterase inhibitor (Cl INH) deficiency that may be inborn as an autosomal dominant characteristic or may be acquired. Acquired angioedema (AAE) is a rare disorder characterized by adult onset and lack of evidence of inheritance of the disease. Two types of AAE are known today: type I in which there are lowering of functional Cl INH, an underlying disease such as a B-cell disease, and no detectable autoantibodies to Cl INH, type II with anti Cl INH autoantibodies in the circulation without detectable underlying disease and with depressed functional Cl INH levels. We experienced a case of angioedema in a 29-year old man. He had no family history of angioedema and laboratory data showed depressed Cl-INH levels. We diagnosed the case as acquired type of angioedema. Even though we could not measure anti-Cl INH auto-antibodies, we identified the case as type II because there was no evidence of underlying disease.
Adult
;
Angioedema*
;
Angioedemas, Hereditary*
;
Autoantibodies
;
B-Lymphocytes
;
Complement C1 Inhibitor Protein*
;
Complement C1s*
;
Edema
;
Humans
;
Skin
;
Subcutaneous Tissue
;
Wills
7.A case of Acute Arsine Poisoning with Hemolytic Anemia and Acute Renal Failure.
Kyoungsook JEONG ; Ji Ho LEE ; Chang Sun SIM ; Jong Soo LEE ; Hiroshi YAMAUCHI ; Yangho KIM
Korean Journal of Occupational and Environmental Medicine 2005;17(3):238-248
BACKGROUND: There has been no reported case of arsine poisoning in Korea so far. This article presents the first reported case of arsine poisoning with hemolytic anemia accompanied by acute renal failure. Initially we suspected an infectious agent to be the cause of this case but later discovered that it was arsine poisoning suffered while working at a zinc-smelting industry in the process of recovering the cadmium by-product. We report this case and discuss the arsine poisoning. CASE REPORT: A 27-year-old man employed at a zinc-smelting industry was exposed to arsine while working in the process to recover the cadmium by-product.On the 4th day at work, he had to redissolve defected by-product into a pot and began to experience febrile sensation, diarrhea, upper quadrant abdominal pain, jaundice, and anorexia.After he was admitted to a hospital, the laboratory results showed hemolytic anemia, acute renal failure and elevated concentration of arsenic. He was thus diagnosed as suffering from arsine-poisoning and underwent hem dialysisand supportive therapy.He recovered from the poisoning after51 days and was discharged from the hospital. DISCUSSION: When workers dealing with arsenic-containing material present with hematuria, nausea, vomiting, abdominal pain, and dyspnea followed by hemolysis with acute renal failure, arsine poisoning must be suspected and diagnosis followed by treatment must commence immediately. If any future cases occur, blood and urine samples should be kept in storage so any necessary analysis can be processed later.
Abdominal Pain
;
Acute Kidney Injury*
;
Adult
;
Anemia, Hemolytic*
;
Arsenic
;
Cadmium
;
Diagnosis
;
Diarrhea
;
Dyspnea
;
Hematuria
;
Hemolysis
;
Humans
;
Jaundice
;
Korea
;
Nausea
;
Poisoning*
;
Sensation
;
Vomiting
8.A Case of Sacral Tuberculosis Mimicking Metastatic Bone Tumor with Elevated CA 19-9.
Kyung Yoon CHANG ; Kyung Sun HA ; Kyung Seon PARK ; Eun Hui SIM ; Jae Ho BYUN
Yeungnam University Journal of Medicine 2011;28(2):196-201
A 73-year-old male presented a six-month history of buttock pain radiating into his thigh. The MRI revealed a large enhancing mass lesion involving the sacrum, with extension into the sacral canal. The tumor markers were measured to distinguish skeletal metastasis of carcinoma from primary bone tumor. The CA 19-9 was elevated. Despite the investigation, the primary site of cancer could not be found. Sacral bone biopsy was done. The pathologic examination revealed necrosis, chronic granulomatous inflammation, and multinucleated giant cells, consistent with tuberculosis. Sacral tuberculosis is rare in patients with no history of tuberculosis. Such solitary osteolytic lesions involving the subarticular region of large joints may mimic bone neoplasms and may be called "tuberculous pseudotumors." This case report intends to emphasize that bone tuberculosis should be a differential diagnosis in the presence of atypical clinical and radiological features. As tuberculous lesions may be mistaken for neoplasms, a small amount of fresh tissue should be sent for culture even if clinical diagnosis of a tumor seems likely. Described herein is a case of sacral tuberculosis mimicking metastatic bone tumor with elevated CA 19-9.
Aged
;
Biopsy
;
Bone Neoplasms
;
Buttocks
;
Diagnosis, Differential
;
Giant Cells
;
Humans
;
Hydrazines
;
Inflammation
;
Joints
;
Male
;
Necrosis
;
Neoplasm Metastasis
;
Sacrum
;
Thigh
;
Tuberculosis
;
Tuberculosis, Osteoarticular
;
Biomarkers, Tumor
9.Dumbbell Glossopharyngeal Schwannoma at Jugular Foramen with Intrapetrosal Extension.
Chang Jin KIM ; Hee Won JUNG ; Sun Ho LEE ; Byung Kyu CHO ; Bo Sung SIM ; Je G CHI
Journal of Korean Neurosurgical Society 1984;13(1):167-174
Schwannomas arising from the cranial nerves of the jugular foramen are rare, only 50 cases including 15 glossopharyngeal schwannomas have been reported. They may be confused with the far more common acoustic schwannoma because of the presenting symptom of hearing loss. With the symptoms and signs of the lower cranial nerve involvement, the characteristic radiographic findings of enlarged jugular foramen and normal internal acoustic meatus can make the diagnosis. The authors review the literature and present a unique case of glossopharyngeal schwannoma which had intra-and extracranial growth with intrapetrosal extension.
Acoustics
;
Cranial Nerves
;
Diagnosis
;
Hearing Loss
;
Neurilemmoma*
;
Neuroma, Acoustic
10.Treatment with intravenous immunoglobulin in a case of adult onset Still's disease.
Sun Sin KIM ; Hae Sim PARK ; Dong Ho NAM ; Soo Keol LEE ; Jae Woong CHO ; Hyeon Kyeong CHO ; Chang Young HA
Journal of Asthma, Allergy and Clinical Immunology 1999;19(6):985-990
Adult onset Stills Disease (AOSD) is a systemic inflammatory disease characterized by spiking high fevers, arthritis, and an evanescent rash. Although many patients respond to nonsteroidal anti-inflammatory drugs (NSAIDs) and corticosteroid, some patients fail to do so or are found to be resistant and require high doses of corticosteroid which induce severe side effects. Recently, treatment with intravenous immunoglobulin (IVIG) has been reported to be effective in patients with AOSD who were refractory to NSAIDs. Here, we report a case of AOSD treated with IVIG with a review of the literature.
Adult*
;
Anti-Inflammatory Agents, Non-Steroidal
;
Arthritis
;
Exanthema
;
Fever
;
Humans
;
Immunoglobulins*
;
Immunoglobulins, Intravenous
;
Still's Disease, Adult-Onset*