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1.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 2422-2426,后插3, 2017.
Article in Chinese | WPRIM | ID: wpr-617785

ABSTRACT

Objective To explore the role and mechanism of Toll-like receptor 4(TLR4)and chemokine receptor 7(CXCR7)in the pathogenesis and development of Helicobacter pylori(HP)positive gastric cancer.Methods Tissues of 147 cases with gastric carcinoma and 60 normal control were collected.The protein expression of TLR4,CXCR7 was detected by immunohistochemical staining.HP infection in these samples were detected by immunohistochemistry and Gram staining.Results The positive rates of TLR4 and CXCR7 in gastric cancer tissues were 63.9% and 62.6%,respectively,which were significantly higher than those in normal control group(15.0% and 5.0%,respectively;X2=40.832,56.901,all P<0.01).The positive rates of TLR4 and CXCR7 in patients with lymph node metastasis were significantly higher than those without lymph node metastasis(X2=9.809,11.444,all P<0.01).The positive rates of TLR4 and CXCR7 in patients with stage Ⅲ and Ⅳ were significantly higher than those of stageⅠand Ⅱ(X2=24.927,27.642,all P<0.01).The expression of TLR4 and CXCR7 in gastric carcinoma was significantly related to HP infection.Kaplan-Meier survival analysis showed that the survival rates in TLR4 and CXCR7 positive group were significantly lower than those in TLR4 and CXCR7 negative groups(F=4.053,4.091,all P<0.05).COX regression analysis indicated that the TNM stage,the expression of TLR4 and CXCR7 were independent prognosis factors of gastric carcinoma.Conclusion TLR4 and CXCR7 are closely related to the occurrence and development of gastric cancer,and may play an important role in HP carcinogenesis.It may be involved in the invasion and metastasis of gastric cancer cells via LPS/TLR4 signaling pathway.

2.
Chinese Journal of Pathology ; (12): 256-259, 2014.
Article in Chinese | WPRIM | ID: wpr-292315

ABSTRACT

<p><b>OBJECTIVE</b>To analyze the clinicopathologic and immunohistochemical features of nodular histiocytic/mesothelial hyperplasia (NHMH) and to improve the knowledge of this disease.</p><p><b>METHODS</b>Seven cases of NHMH were collected and the clinicopathologic and immunohistochemical data were analyzed with review of the literature.</p><p><b>RESULTS</b>Seven male patients aged from 1.5 to 5.0 years (mean 2.8). The main clinical symptom was an inguinal mass.Grossly, main pathological changes were the mural nodule or free nodule in lumen, with diameter of 0.1-0.5 cm.Histologically, the tumor cell morphology was relatively single, cohesive polygonal or oval cells which were arranged in solid sheets or nests, usually with ovoid or deeply grooved nuclei and a moderate amount of pale pink cytoplasm in the nodular collection area. The nuclei had delicate chromatin and no obvious atypia, and mitosis was incidentally found. A few scattered lymphocytes were found in the stroma. The cyst wall was lined by a single layer of mesothelial cells.Immunohistochemically, the most cells in nodular lesion were strongly positive for the histiocytic marker CD68, vimentin and α1-antichymotrypsin, while lining mesothelial cells on the wall were positive for calretinin, MC, WT1, CK5/6, CKpan and EMA.</p><p><b>CONCLUSIONS</b>NHMH is a rare and benign tumor-like lesion, and easy to be misdiagnozed, which should be distinguished from neuroendocrine tumors, Langerhans cell histiocytosis, seminoma, mesothelioma and so on. The correct diagnosis of this lesion depends on the clinical characteristics, morphology and immunohistochemistry.</p>


Subject(s)
Child, Preschool , Humans , Infant , Male , Antigens, CD , Metabolism , Antigens, Differentiation, Myelomonocytic , Metabolism , Calbindin 2 , Metabolism , Diagnosis, Differential , Epithelium , Metabolism , Pathology , General Surgery , Histiocytes , Metabolism , Pathology , Histiocytosis, Langerhans-Cell , Metabolism , Pathology , Hyperplasia , Metabolism , Pathology , General Surgery , Leukocyte Common Antigens , Metabolism , Mesothelioma , Metabolism , Pathology , Mucin-1 , Metabolism , Neuroendocrine Tumors , Metabolism , Pathology , Seminoma , Metabolism , Pathology , Vimentin , Metabolism , WT1 Proteins , Metabolism , alpha 1-Antichymotrypsin , Metabolism
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