No abstract available.
Child* ; Humans ; Tuberculosis, Renal*

No abstract available.
Alopecia* ; Scalp* ; Tissue Expansion*

No abstract available.
Abdominoplasty* ; Classification*

Most type I and II perforations are predominately caused by hydrophilic and stiff wires, often presented in the delayed form, and do not require pericardial drainage or surgical interventions. However, we report a type III delayed coronary artery perforation at the site of stent implantation after intervention without any evidence of immediate perforations. To the best of our knowledge, this is the first case report of angiographic documentation and treatment of delayed coronary perforation at the site of stent, presented as a cardiac arrest.
Angioplasty, Balloon, Coronary ; Cardiac Tamponade ; Coronary Vessels ; Drainage ; Drug-Eluting Stents ; Heart Arrest ; Stents

Mixed Connective Tissue Disease(MCTD) is an overlap syndrome characterized by a combination of clinical features similar to those of systemic lupus erythematosus(SLE), scleroderma, polymyositis, and rheumatoid arthritis and unusually high titers of circulating antibody to a nuclear ribonucleoprotein antigen. The mean age of presentation is 37 years and 80% of patients are female. Cardiac involvement is less common in adults but may be more frequent in children. Pericarditis is the most common finding,' other findings include mitral valve prolapse, myocarditis and congestive heart failure. We experienced a case of pericarditis and asymmetric LV hypertrophy in a 33-yr-old postpartum woman with mixed connective tissue disease, who admitted to our hospital because of fever, dyspnea and chest discomfort, which was diagnosed by echocardiography and selorogic study. She was treated with oral prednisolone and aspirin and presented symptoms improved and pericardial effusion was disappeared.
Adult ; Arthritis, Rheumatoid ; Aspirin ; Child ; Connective Tissue ; Dyspnea ; Echocardiography ; Female ; Fever ; Heart Failure ; Humans ; Hypertrophy ; Mitral Valve Prolapse ; Mixed Connective Tissue Disease* ; Myocarditis ; Pericardial Effusion ; Pericarditis ; Polymyositis ; Postpartum Period* ; Prednisolone ; Ribonucleoproteins ; Thorax

PURPOSE: The purpose of this study is to find out the relationship between clinical characteristics and pathologic findings of lacrimal sac in patients of primary acquired nasolacrimal duct obstruction. METHODS: This study reviewed medical records of 23 eyes of 21 patients who were received external dacryocystorhinostomy, and analyzed patients according to the obstruction patterns and locations on dacryocystography. The relationship between the pathologic degrees of lacrimal sac (inflammation, fibrosis, presence of goblet cells and squamous metaplasia) and clinical characteristics of the patients, was also evaluated. RESULTS: There were no significant relation between the pathologic degrees of lacrimal sac and clinical characteristics. From dacryocystography, the degree of fibrosis was 1.95 +/- 0.62 in complete obstruction, which was significantly higher than 1.00 +/- 0.82 in partial obstruction (p=0.015). In addition, the degree of fibrosis (2.20 +/- 0.63) was different depending on the location of the obstruction. In common canaliculus-obstruction group, it was 1.57 +/- 0.53 and in the nasolacrimal duct-obstruction group, it was 1.33 +/- 0.82 (p=0.041). However, there was no significant statistical difference between the patient's demographics and pathologic findings of lacrimal sac. CONCLUSIONS: The fibrosis of lacrimal sac mucosa is a major pathological finding of nasolacrimal duct obstruction and in particular, it is the characteristic of patients with lacrimal sac obstruction.
Dacryocystorhinostomy ; Demography ; Fibrosis ; Goblet Cells ; Humans ; Medical Records ; Mucous Membrane* ; Nasolacrimal Duct*

PURPOSE: Lacrimal gland duct cysts constitute a rare clinical entity and may be preceded by trauma, infection, or inflammation without antecedent history. The purpose of this study is to report one case of lacrimal gland duct cyst accompanied by a dacryolith. METHODS: A 41-year-old man presented with sudden enlarging mass in the left superotemporal conjunctival fornix 3 days ago. The lesion was about 10 X 10 mm in size. There was no tenderness or erythema in adjacent area. The CT scan was done and excisional biopsy was performed under local anesthesia. RESULTS: Specimen consisted of cystic membranous tissue in 9.0 X 7.0 mm in size and mucous material and a light brown dacryolith of 1mm in diameter within cyst. Specimen included normal lacrimal tissue. Microscopic examination found cyst was covered with stratified columnal epithelium accompanied by acute and chronic inflammation and eosinophilic acellular dacryolith mixed with inflammatory exudates. There was no bacterial colony and polarizing microscope found no birefringence. CONCLUSIONS: Such case of a eosinophilic dacryolith within lacrimal gland duct cyst has never been reported at home and abroad.
Adult ; Anesthesia, Local ; Biopsy ; Birefringence ; Eosinophils ; Epithelium ; Erythema ; Exudates and Transudates ; Humans ; Inflammation ; Lacrimal Apparatus ; Tomography, X-Ray Computed

PURPOSE:Present evidences suggest that Ureaplasma urealyticum is a cause of pneumonia, septicemia, and bronchopulmonary dysplasia (BPD) in newborn infants, particularly those born prematurely. The purpose of this work was to examine the relationship between Ureaplasma urealyticum in the tracheal aspirates and adverse outcomes, such as BPD and early onset neonatal sepsis in premature infants. METHODS:A polymerase chain reaction (PCR) was performed on tracheal aspirates collected within 24 hour after birth in 176 premature infants less than 35 weeks of gestation and admitted to the neonatal intensive care unit of Bundang CHA Hospital. RESULTS:U. urealyticum was detected in 37 of 176 preterm infants (21.0%). Gestational age (29+5+/-2+5 wk vs. 30+6+/-2+5 wk, P=0.013) and birth weight (1.39+/-0.44 kg vs. 1.59+/-0.55 kg, P=0.037) were lower in the U. urealyticum-positive group compared to the control group. The incidence of early onset neonatal sepsis (16.2% vs. 6.5%, P=0.045) and BPD (45.9% vs. 29.5%, P=0.047) was higher in the U. urealyticum-positive group compared to the control group, but the severity of BPD was not different between two groups. However, multiple logistic regression analysis revealed that the presence of U. urealyticum was not independently related to the development of early onset neonatal sepsis and BPD. CONCLUSION:The results suggest that colonization of the lower respiratory tract by U. urealyticum might not be related to the development of neonatal sepsis and BPD directly in preterm infants.
Birth Weight ; Bronchopulmonary Dysplasia ; Colon ; Gestational Age ; Humans ; Incidence ; Infant, Newborn ; Infant, Premature ; Intensive Care, Neonatal ; Logistic Models ; Parturition ; Pneumonia ; Polymerase Chain Reaction ; Pregnancy ; Respiratory System ; Sepsis ; Ureaplasma ; Ureaplasma urealyticum

It is difficult to identify the exact cause of ocular motility disturbances in orbital wall fracture patients. By performing CT and ocular motility tests before and after surgery, this study analyzes the functions of the extraocular muscles and determines correlations between the results. Between February 2001 and January 2003, 45 eyes of 45 patients with orbital wall fractures, whose medical records could be traced back at least 6 months, underwent surgical repair in our hospital. All variables were analyzed using the independent t-test, paired t-test, and Chi-square test. There was no significant difference in the location and degree of fracture and the incarceration pattern of 6 patients who had moderate or severe diplopia, and of the remaining patients 6 months after surgery. However, in the case of diplopia, the sum of ocular motility limitation was 5.67 +/- 4.18, and the degree of extraocular motility disturbance was 3.67 +/- 2.42 before surgery. When there was no diplopia, the sum of ocular motility limitation was 1.13 +/- 1.38, and the degree of extraocular motility disturbance was 1.08 +/- 1.16 (p < 0.005, independent t-test). Ocular movement was successfully recovered by surgical reduction within 3 weeks from trauma. Postoperative ocular motility disturbance was more related to various ocular motility test results than CT findings. Ocular motility disturbances can remain after surgery if ocular motility limitation and extraocular motility disturbance are significant after trauma. Additional studies on the various tests to examine functions of extraocular muscles are required to identify and analyze the exact cause of ocular motility disturbance.
Adult ; Child ; Diagnostic Techniques, Ophthalmological ; Diplopia/*etiology/radiography ; Humans ; Middle Aged ; Ocular Motility Disorders/*etiology/radiography ; Orbital Fractures/*complications/radiography ; Tomography, X-Ray Computed

PURPOSE: To report one case of lymphoproliferative disorder on the upper eyelid. METHODS: Primary CD30+ lymphoproliferative disorder on the skin is very rare. A 31-year-old female patient visited our clinic complaining of red, erosive papules on the right upper eyelid and on the left flank for two weeks. A 2.0 cm erythematous papule showed central ulceration. A 1.5 cm lymph node enlargement was palpated on the left groin. There was no abnormal finding on the slit-lamp test. Computed tomography showed a subcutaneous nodule on the anterolateral aspect of the flank and a lymph node enlargement on the left inguinal area. There was no evidence of other visceral involvement. Histopathologic finding showed diffuse infiltration of atypical cells with lobated nuclei showing multifocal positivity to CD30; a finding consistent with primary cutaneous CD30+ T-cell lymphoproliferative disorder and borderline lesion. RESULTS: This case seems to be a borderline case between CD30+ T-cell large cell lymphoma and lymphoid papulodesis. We are conducting conservative care and observing the progress on the skin lesion for further evaluation.
Female ; Humans