ABSTRACT
Thin basement membrane nephropathy(TBMN) is defined histologically as follows: 1) By light rnicroscopy only minor abnormalities are detected in the glomeruli at most minor mesangial widening. 2) By electron microscopy, diffuse thinning of glomerular basement rnembrane is demonstrated. 3) By immunofluorescence, absence of immunoglobulins and complement components is demonstrated. 4) Alport's syndrome and systemic diseases that may affect the glomerular structure have been excluded. TBMN presented frequently with recurrent or persistent microscopic hematuria. Massive proteinuria such as in nephrotic syndrome rarely occurs in TBMN. We reported two cases of TBMN presented with typical minimal change nephrotic syndrome.
Subject(s)
Basement Membrane , Complement System Proteins , Fluorescent Antibody Technique , Hematuria , Immunoglobulins , Microscopy, Electron , Nephritis, Hereditary , Nephrosis, Lipoid , Nephrotic Syndrome , ProteinuriaABSTRACT
Renal abscess is rare in children and presents varying features which often lead to delay or error in diagnosis. Fever, lumbar pain, abdominal pain and occasional flank rnass are the usual presenting cornplaints but a high degree of suspicion is important for the early detection of renal abscess. Hematogenous seeding of the kidney or ascending infection from the urinary collecting system are two proposed mechanisms of renal abscess formation. Renal ultrasonography facilitates an earlier diagnosis and is also useful in establishing percutaneous drainage, which appears to be the treatment method of choice. We experienced a case of renal abscess which was treated by percutaneous aspiration and antibiotics without surgical intervention.
Subject(s)
Child , Humans , Abdominal Pain , Abscess , Anti-Bacterial Agents , Diagnosis , Drainage , Fever , Kidney , UltrasonographyABSTRACT
PURPOSE: This study was aimed at assessing the difference of the prevalence of iron deficiency and iron deficiency anemia among rural and urban middle school students in relation to dietary habit. METHODS: With a questionnaire, blood samples were obtained from 439 apparently healthy rural and urban middle school students residing in Ulsan. Anemia was defined as hemoglobin level of 12.6 g/dL or less for boys and 11.9 g/dL or less for girls. Iron deficiency was defined as serun ferritin level less than 12 micrograms/L or/and transferrin saturation less than 14%. Iron deficiency anemia was defined as iron deficiency plus low hemoglobin. RESULTS: 1) In boys, the prevalence rate of anemia was 17.2%. Among these anemias, 5.4% were found to be iron deficiency anemia. In girls, the prevalence of anemia increased with age. The prevalence of iron deficiency anemia was 6.9%. 2) In girls, the prevalence rate of anemia in rural area was higher than that of anemia in urban area (12.6% in rural, 6.1% in urban, P<0.01). 3) The prevalence of anemia and iron deficiency in the students with menstruation was 10.6% and 33.1%, which was higher than the prevalence of 2.5% and 7.5% in those who did not have the menarche (P<0.001 and P<0.001, respectively). 4) Dietary intake of rural and urban middle school students was estimated lower in energy, iron than the recommeded dietary allowance (RDA). In girls, dietary intake of rural middle school students was estimated lower in iron, niacin, and vitamin C than that of urban middle school students. 5) Nutritional factors such as energy, carbohydrate, protein, and phosphorus showed positive correlation with RBC, hemoglobin (P<0.05). CONCLUSION: It is recommended to enforce the nutritional education to take enough iron in middle school students to reduce the high prevalence rate of anemia among pubertal students.
Subject(s)
Female , Humans , Anemia , Anemia, Iron-Deficiency , Ascorbic Acid , Education , Ferritins , Feeding Behavior , Iron , Menarche , Menstruation , Niacin , Phosphorus , Prevalence , Surveys and Questionnaires , TransferrinABSTRACT
Joubert syndrome is an autosomal recessive disorder characterized by cerebellar vermis hypoplasia, hypotonia, developmental delay and either abnormal respiratory pattern(neonatal episodic tachypnea, or apnea), or altered eye movements. We describe a girl with Joubert syndrome associated with multicystic renal dysplasia and meningocele. The clinical and pathological findings of this patient included hypoplasia of the cerebella vermis, bilateral multicystic kidney, hepatic fibrosis, occipital meningocele, severe visual impairment from early infancy, profound psychomotor retartdation, hypotonia, nystagmus and progressive chronic renal insufficiency. Continuous peritoneal dialysis and medical control of azotemia, hyperkalemia and hypertension was instituted immediately. Concomitant malformation of these systems are likely based upon their common developmental and genetic features.
Subject(s)
Female , Humans , Azotemia , Eye Movements , Fibrosis , Hyperkalemia , Hypertension , Meningocele , Multicystic Dysplastic Kidney , Muscle Hypotonia , Peritoneal Dialysis , Renal Insufficiency, Chronic , Tachypnea , Vision DisordersABSTRACT
No abstract available.
Subject(s)
Protein C Deficiency , Protein C , Purpura Fulminans , PurpuraABSTRACT
No abstract available.
Subject(s)
Child , Humans , Infant , Urinary Tract Infections , Urinary TractABSTRACT
Clinical and bacteriologicaql studies on 133 cases of urinary tract infection who were admitted to the Dept. of Pediatrics, NMC during the period of Jan. 1974 to Jan. 1979 were subjected in this study. The resultes were as follows : 1. Among the total 133 cases, 100 cases(75.2%) were male and 33 cases(24.8%) were female with sex ratio of 3:1. 2. The highest incidence(42.1%) was in children below the age of one year. The rate then decreased with age. 3. Seasonal incidence was relatively high in summer months, but seasonal difference was not significant. 4. Edema, signs of URI, vomiting, hematuria, failure to thrive and feeding problem were common clinical features. 5. Urinalysis disclosed proteinuria in 43 cases(32.3%), hematuria in 36 cases(27.1%) and pyuria in 26 cases(19.6%). 6. Hematological findings showed low hemoglobin in 40 cases(30.0%), leucocytosis in 31 cases(23.3%) and elevated ESR in 42 cases(31.6%). 7. IVP was performed in 13 cases, and 3 cases of them showed abnormal findings. 8. Nephrotic syndrome, acute glomerulonephritis, hyperbilirubinemia and sepsis were the common concurrent illnesses. 9. E. coli predominated as the infecting organisms(36.8%). It was most sensitive to ;gentamycin(83.7%) and cefamezine(77.8%)
Subject(s)
Child , Female , Humans , Male , Edema , Failure to Thrive , Glomerulonephritis , Hematuria , Hyperbilirubinemia , Incidence , Nephrotic Syndrome , Pediatrics , Proteinuria , Pyuria , Seasons , Sepsis , Sex Ratio , Urinalysis , Urinary Tract Infections , Urinary Tract , VomitingABSTRACT
Clinical and bacteriologicaql studies on 133 cases of urinary tract infection who were admitted to the Dept. of Pediatrics, NMC during the period of Jan. 1974 to Jan. 1979 were subjected in this study. The resultes were as follows : 1. Among the total 133 cases, 100 cases(75.2%) were male and 33 cases(24.8%) were female with sex ratio of 3:1. 2. The highest incidence(42.1%) was in children below the age of one year. The rate then decreased with age. 3. Seasonal incidence was relatively high in summer months, but seasonal difference was not significant. 4. Edema, signs of URI, vomiting, hematuria, failure to thrive and feeding problem were common clinical features. 5. Urinalysis disclosed proteinuria in 43 cases(32.3%), hematuria in 36 cases(27.1%) and pyuria in 26 cases(19.6%). 6. Hematological findings showed low hemoglobin in 40 cases(30.0%), leucocytosis in 31 cases(23.3%) and elevated ESR in 42 cases(31.6%). 7. IVP was performed in 13 cases, and 3 cases of them showed abnormal findings. 8. Nephrotic syndrome, acute glomerulonephritis, hyperbilirubinemia and sepsis were the common concurrent illnesses. 9. E. coli predominated as the infecting organisms(36.8%). It was most sensitive to ;gentamycin(83.7%) and cefamezine(77.8%)
