1.Histomorphological study on folk medicine Lysimachia fortunei.
Zhi-gui WU ; Xiao-mei FU ; Sheng-fu HU ; Jian-guo PEI ; Fei GE ; Xiao-lan CHU ; Cui-sheng FAN
China Journal of Chinese Materia Medica 2015;40(4):639-642
To set standards for histomorphological studies on Lysimachia fortunei, an efficacious and widely applied folk medicine in this study, in order to develop its resources. Its species were identified by observing plant morphology and herbs appearance characters, preparing slices with routine methods and defining structural characters. According to the results of morphologic observation, leaves, stamen and pistil of this plant were different from the descriptions in Flora of China. The whole herb can be used in medicines, mainly including rhizomes, stems and leaves. According to the findings in the first study on microscopic structures, its rhizomes, stems and leaves were characteristic and worth identifying. The transaction tissue structures of rhizomes and stems were under developed and contained endodermis, secretory structures; Stems had sclerenchymata of different shapes of sclereids; Leaves were bifacial and had vascular bundles under midribs, which were surrounded by parenchymal sheathes. On the surface of leaves, stomata, glandular hairs and keratin lines were morphologically different in upper and lower epidermis. The herbal power had glandular hairs, sclereids and vessels. In conclusion, herbs of L. fortunei can be identified by the above histomorphological characteristics, which lays a foundation for further development and application of L. fortunei.
Medicine, Traditional
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Plant Leaves
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anatomy & histology
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growth & development
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Plant Stems
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anatomy & histology
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growth & development
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Plants, Medicinal
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anatomy & histology
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growth & development
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Primulaceae
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anatomy & histology
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growth & development
2.Analysis and identification of B cell epitopes of the OMP18 from Campy lobacter jejuni
Hongqiang LOU ; Ye HU ; Lan WANG ; Xiaoyun SHAN ; Xiusheng SHENG ; Suhua GAO
Chinese Journal of Zoonoses 2014;(7):739-742
In this study ,we aimed to understand the sequence characteristics ,transmembrane structures ,line B cell epitopes present in the OMP18 from Campylobacter jejuni ,and provide candidate antigens for the antibody detection and vac-cine development .NCBI/Blast ,TMHMM Server V2 and DNA Star softwares were used for the OMP18 sequence analysis . Based on the ELISA ,the whole bacterial antibody IgG of Campylobacter jejuni was used for the identification of the predicted line B cell epitopes .The OMP18 gene was found conserved in different Campylobacter jejuni strains .The OMP18 was predic-ted to be located on the outer surface of the bacteria .And three line B cell epitopes were determined to be present in the OMP18 protein .As a conclusion ,the OMP18 protein was confirmed to be an important outer membrane protein ;three line B cell epitopes were identified in the OMP18 ,which could be further used for Campylobacter jejuni antibody detection and vaccine development .
3.Nephroblastomatosis and nephroblastoma: report of a case.
Xiao-li HU ; Lan-yun SONG ; Lin-sheng ZHAO ; Pei-ru NING ; Li ZHAO
Chinese Journal of Pathology 2013;42(12):841-842
Humans
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Infant
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Kidney Neoplasms
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metabolism
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pathology
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surgery
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Male
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Mucin-1
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metabolism
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Nephrectomy
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Precancerous Conditions
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metabolism
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pathology
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surgery
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Vimentin
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metabolism
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WT1 Proteins
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metabolism
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Wilms Tumor
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metabolism
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pathology
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surgery
4.Epigastric heteropagus twins: report of a case.
Xiao-li HU ; Lan-yun SONG ; Lin-sheng ZHAO ; Pei-ru NING
Chinese Journal of Pathology 2009;38(7):491-492
Abnormalities, Multiple
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pathology
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surgery
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Humans
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Infant, Newborn
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Male
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Twins, Conjoined
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pathology
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surgery
5.Carcinoid tumor of common bile duct: report of a case in pediatric patient.
Lan-yun SONG ; Xiao-li HU ; Lin-sheng ZHAO ; Pei-ru NING
Chinese Journal of Pathology 2011;40(1):54-55
Adenocarcinoma
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metabolism
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pathology
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Carcinoid Tumor
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metabolism
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pathology
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surgery
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Child
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Chromogranin A
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metabolism
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Common Bile Duct
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pathology
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surgery
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Common Bile Duct Neoplasms
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metabolism
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pathology
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surgery
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Diagnosis, Differential
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Duodenum
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pathology
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surgery
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Gallbladder
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pathology
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surgery
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Humans
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Keratins
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metabolism
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Lymphoma
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metabolism
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pathology
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Male
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Mucin-1
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metabolism
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Neoplasm Invasiveness
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Rhabdomyosarcoma
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metabolism
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pathology
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Stomach
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pathology
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surgery
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Synaptophysin
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metabolism
6.Significance of COX2 and beta-catenin expression in nephroblastoma.
Xiao-Li HU ; Lin-Sheng ZHAO ; Lan-Yun SONG ; Pei-Ru NING
Chinese Journal of Pathology 2008;37(10):698-699
Child
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Child, Preschool
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Female
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Gene Expression Regulation, Neoplastic
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Humans
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Infant
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Male
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Wilms Tumor
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genetics
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metabolism
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Wnt Proteins
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genetics
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metabolism
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beta Catenin
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genetics
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metabolism
8.Clinical study of ESHAP regimen for relapsed or refractory aggressive non-Hodgkin lymphoma
Sheng LUO ; Xu-Dong HU ; Zhi-Jian SHEN ; Jun-Li ZHANG ; Lan SUN ; Yi CHEN ;
Cancer Research and Clinic 2006;0(11):-
Objective To evaluate the efficacy and safety of ESHAP regimen,as a salvage regimen, in treating patients with relapsed or refractory aggressive NHL.Methods 38 patients with relapsed or refrac- tory aggressive NHL were selected to be treated by ESHAP regimen.Results The 38 patients received ES- HAP regimen with a range of 2~6 cycles. The total RR was 55.3 % with complete response(CR)rate of 26.3 %.The major toxicity was myelosuppression with infection,which was tolerable.Conclusion ESHAP regimen is one of safe and effective salvage regimens for the patients with relapsed or refractory aggressive NHL.
9.Clinical analysis of four patients with Schwartz-Jampel syndrome.
Shen ZHANG ; Hu-sheng WU ; Jun-lan LÜ
Chinese Journal of Pediatrics 2012;50(3):231-234
OBJECTIVETo analyze the clinical manifestation, diagnosis and treatment of Schwartz-Jampel syndrome (SJS).
METHODThe clinical data, including demographic, laboratory tests (creatase, creatine kinase, etc.) and electromyography of 4 children with SJS were analyzed.
RESULTAll the 4 patients were male. The age of onset was from 0.5 to 1.25 years (average 0.83 years). The onset of 4 patients was insidious, the age to see doctor was from 2.17 to 10 years (average 5.92 years), body height was less than the third percentile rank in the children of same age and gender, they presented with facial expression stiffness, microstomia, difficult in opening mouth, blepharophimosis, limbs stiffness and, so formed a characteristic phenotype. Investigations showed the creatase in serum increased, creatine kinase (CK): 229 - 1039 U/L (normal value < 200 U/L), Creatine Kinase MB (CK-MB): 30 - 45 U/L (normal value < 25 U/L), lactate dehydrogenase (LDH): 455 - 716 U/L (normal value < 240 U/L). General myotonia potential was found in electromyography, osteoarticular deformities in medical imaging, and muscle biopsy in 2 patients showed type I muscle fibers differed in size and were disproportionate. All the patients took oral vitamin B, and received rehabilitation training, 1 patient took carbamazepine for 1 month, blepharophimosis and limbs stiffness was improved.
CONCLUSIONSJS is a rare autosomal recessive inherited disease. Clinical manifestations of SJS are characteristic facies, skeletal abnormalities, generous myotonia and short stature. Carbamazepine is effective for treatment.
Child ; Child, Preschool ; Humans ; Male ; Osteochondrodysplasias ; diagnosis ; pathology