1.Analysis of clinical and pathological characteristics on henoch-schonlein purpura nephritis
Journal of Applied Clinical Pediatrics 2004;0(09):-
Objective To analyze the clinical and pathological characteristics and laboratory outcomes in henoch-schonlein purpura nephritis(HSPN) patients.Methods Twenty patients with HSPN were respectively studied. The clinical characteristics and laboratory outcomes were compared between patients with different glomerulus and renal tubule pathologic classification respectively. Results Patients with grade Ⅲ had a higher proteinuria rate than those with grade Ⅱ,and the glomerulus and renal tubule pathologic markedly changed in grade Ⅲ than that in grade Ⅱ.The HSPN patients had a higher concentration of IgA,C 3 in plasma and of minimal protein in urine than that in normal groups.Conclusions There are both glomerulus and renal tubule pathologic changes in HSPN patients. The basic pathologic changes are parallel and correlated with clinical manifestation.
2.Improved Staining Method for Permanent Specimen of Fasciolopsis buski
Chinese Journal of Parasitology and Parasitic Diseases 1987;0(03):-
Fasciolopsis buski speciemens were collected, fixed with neutral formalin fixative solution, stained with alum-carmine staining solution, discolored with 2% kalium alum. The fixed and stained specimen shows clear internal structure with bright color, and can be stored for long time.
3.The influence of glycemic control on bone turnover rate in type 2 diabetes mellitus
Chinese Journal of Diabetes 2000;8(4):198-200,214
ObjectiveTo investigate whether the good control of fasting plasma glucose(FPG) has any effects on bone turnover rate in type2 diabetes mellitus (DM).MethodsA series of markers,such as bone specific alkaline phosphatase (BAP),deoxypyridinoline (DPD),were assessed before and after glycemic control for more than 18 days in 43 poorly controlled type 2 DM patients with initial hemoglobin A1c over 8%.ResultsBy either oral hypoglycemic agent or insulin administration,or both, ideal control of FPG resulted in a reduction in the secretion of urinary calcium(Ca),phosphate(Pi) and magnesium(Mg),and an increase in serum Ca and Pi without obvious changes in serum Mg.The marker for bone resorption,urinary DPD and the marker for bone formation,BAP in serum were reduced significantly before and after the management.The results indicated that the decreases both in DPD and in BAP were not only correlated well with each other,but with the improvement in glycemic indices as well.ConclusionGood control of hyperglycemia in poorly controlled type 2 DM may have the high bone turnover rate back to normal and protect type 2 DM patients from bone loss.
4.Histologic evaluation of malignant lymphoma.
Chinese Journal of Pathology 2011;40(4):217-219
Dendritic Cells, Follicular
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pathology
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Diagnosis, Differential
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Humans
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Leukemia, Lymphocytic, Chronic, B-Cell
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pathology
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Lymphoma
;
pathology
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Lymphoma, Extranodal NK-T-Cell
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pathology
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Lymphoma, Follicular
;
pathology
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Lymphoma, Large B-Cell, Diffuse
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pathology
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Lymphoma, Large-Cell, Anaplastic
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pathology
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Lymphoma, Mantle-Cell
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pathology
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Lymphoma, T-Cell, Peripheral
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pathology
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Neoplasm Invasiveness
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Precursor Cell Lymphoblastic Leukemia-Lymphoma
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pathology
5.Study on Detection of Immunoglobulin and Glucocorticoid Administration in Children with Nephrotic Syndrome
Journal of Applied Clinical Pediatrics 1992;0(05):-
Objective To examine serum levels of IgG, IgA, IgM, IgE and C3 and explore sensitivity of glucocorticoid (prednisone) in primary nephropathyic children to study pathogenesis of primary nephropathy and direct clinical therapy. Methods Examine serum IgG, IgA, IgM and C3 by scattering turbidimetry and IgE by ELISA. Results Compared with healthy children, children suffering from primary nephropathy had lower IgG and higher IgM and IgE, but the same IgA and C3 Simple and nephritic nephropathy had very significant difference in sensitivity of glucocorticoid(x2=18.48 P
6.Pathologic diagnosis of renal neoplasm.
Chinese Journal of Pathology 2008;37(11):775-779
7.Research advance in tumors associated with microphthalmia-associated transcription factor gene family.
Chinese Journal of Pathology 2011;40(7):496-498
Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
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genetics
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metabolism
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Carcinoma, Renal Cell
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genetics
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metabolism
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Cell Cycle Proteins
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genetics
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metabolism
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Humans
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Melanoma
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genetics
;
metabolism
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Microphthalmia-Associated Transcription Factor
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genetics
;
metabolism
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Neoplasm Proteins
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genetics
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metabolism
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Oncogene Proteins, Fusion
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genetics
;
metabolism
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Perivascular Epithelioid Cell Neoplasms
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genetics
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metabolism
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Sarcoma, Clear Cell
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genetics
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metabolism
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Translocation, Genetic
8.Application of immunohistology in the diagnosis of kidney tumor.
Chinese Journal of Pathology 2006;35(4):244-247
Adenoma, Oxyphilic
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diagnosis
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metabolism
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Carcinoma, Renal Cell
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diagnosis
;
metabolism
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Humans
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Immunohistochemistry
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methods
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Keratins
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analysis
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Kidney Neoplasms
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diagnosis
;
metabolism
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Proto-Oncogene Proteins c-kit
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analysis
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Sensitivity and Specificity
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WT1 Proteins
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analysis
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Wilms Tumor
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diagnosis
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metabolism
9.Comparison of Nutritional Status before and after Treatment with Pre diasure on Children with Anorexia
xiao-shan, QIU ; zhi-feng, CHEN ; xiao-hua, HE
Journal of Applied Clinical Pediatrics 2004;0(09):-
Objective To evaluate the clinical effect of the enteral nutrient(Pediasure) on making improvements in nutritional status of children with anorexia.Methods Thirty children were treated with pediasure for 2 months, twice a day, and height(Ht),weight(Wt),AG,TSF,SSF,ASF,RBC,Hb were measured before and after treatment and their appetites,alimentary canal reactions were recorded.Results Compared with the effects after 2 months, the average Ht,Wt,AG,SF all increased, and there was significant difference between pretreatment and after treatment(P0.05). All of the 30 children had no adverse reactions during treatment.Twenty-two children (73.33%) had better appetites and increased the amount of eating after treatment.Conclusion The study suggests that pediasure may be safely used in the treatment of children′s anorexia and effectively improve patients′ nutrition without adverse reactions.
10. The aberrant sugar chains of amylase and different TCM syndrome patterns in primary hepatic cancer as well as the related mechanism
Tumor 2008;28(4):322-325
Objective: To investigate the changes of sugar chain structures of serum amylase and difference in TCM syndrome patterns in primary hepatic cancer (PHC) patients and their relation with free radicals. Methods: Agglutinin precipitation assay was used to detect the binding ratios of serum amylase with various kinds of agglutinin in PHC, hepatocirrhosis, and hepatitis patients. The serum amylase activity and malindialdehyde (MDA) level were determined simultaneously. The association of the binding ratios of amylase with free radicals was analyzed. The difference mentioned above in PHC patients with different TCM syndromes was analyzed. Results: The binding ratios of serum amylase to ConA, PSA, PNA, and LCA were significantly higher in PHC and hepatocirrhosis patients than hepatitis patients and normal controls. The binding ratios of serum amylase to PSA and LCA were significantly higher in PHC patients with spleen deficiency and liver stagnation than those with liver and kidney Yin deficiency. PHC patients with spleen deficiency and liver stagnation had higher ConA-binding ratio compared with those with QI and blood stasis. A positive correlation was found between PSA-, LCA-, and PNA-binding ratios of serum amylase and MDA. Conclusion: For PHC and hepatocirrhosis patients, core-fucosylated high-mannose-type and hybrid-type sugar chains of serum amylase increased. The reduced terminal sialic acid and fucose on the sugar chain caused the exposure of the terminal galactose residues. In addition, the exposure of the terminal GlcNAc residues was induced by decreased terminal galactose on the sugar chain of serum amylase from HPC patients. These changes of serum amylase were also observed in hepatocirrhosis patients. It may be related with the damage of sugar chains induced by free radicals. In spleen deficiency and liver stagnation group, core-fucosylated high-mannose-type and hybrid-type sugar chains of serum amylase increased, and the terminal galactose on the sugar chain decreased, resulting in the exposure of the terminal GlcNAc residues. The changes were not observed in QI and blood stasis or liver and kidney Yin deficiency patients. It indicated that spleen deficiency and liver stagnation played an important role in generation of aberrant sugar chains of serum amylase for PHC patients.