Báo cáo y học: Clear cell variant of diffuse large B-cell lymphoma: a case report.
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Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành y học dành cho các bạn tham khảo đề tài: Clear cell variant of diffuse large B-cell lymphoma: a case report...
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Báo cáo y học: "Clear cell variant of diffuse large B-cell lymphoma: a case report."Manxhuka-Kerliu et al. Journal of Medical Case Reports 2011, 5:182 JOURNAL OF MEDICALhttp://www.jmedicalcasereports.com/content/5/1/182 CASE REPORTS CASE REPORT Open AccessClear cell variant of diffuse large B-celllymphoma: a case reportSuzana Manxhuka-Kerliu1*, Gordana Petrusevska2, Irma Kerliu3, Emrush Kryeziu4, Fehmi Ahmeti6,Emine Devolli-Disha5, Vjollca Sahatciu-Meka6, Sadushe Loxha1 and Labinot Shahini1 Abstract Introduction: Diffuse large B-cell lymphoma is a diffuse proliferation of large neoplastic B lymphoid cells with a nuclear size equal to or exceeding the normal macrophage nuclei. We report a case of a clear cell variant of diffuse large B-cell lymphoma involving a lymph node in the neck, which was clinically suspected of being metastatic carcinoma. Case presentation: A 39-year-old Caucasian ethnic Albanian man from Kosovo presented with a rapidly enlarging lymph node in his neck, but he also disclosed B symptoms and fatigue. A cytological aspirate of the lymph node revealed pleomorphic features. Our patient underwent a cervical lymph node biopsy (large excision). The mass was homogeneously fish-flesh, pale white tissue replacing almost the whole structure of the lymph node. The lymph node biopsy showed a partial alveolar growth pattern, which raised clinical suspicion that it was an epithelial neoplasm. With regard to morphological and phenotypic features, we discovered large nodules in diffuse areas, comprising large cells with slightly irregular nuclei and clear cytoplasm admixed with a few mononuclear cells. In these areas, there was high mitotic activity, and in some areas there were macrophages with tangible bodies. Staining for cytokeratins was negative. These areas had the following phenotypes: cluster designation marker 20 (CD20) positive, B-cell lymphoma (Bcl)-2-positive, Bcl-6-, CD5-, CD3-, CD21+ (in alveolar patterns), prostate-specific antigen-negative, human melanoma black marker 45-negative, melanoma marker-negative, cytokeratin-7-negative and multiple myeloma marker 1-positive in about 30% of cells, and exhibited a high proliferation index marker (Ki- 67, 80%). Conclusion: According to the immunohistochemical findings, we concluded that this patient has a clear cell variant of diffuse large B-cell lymphoma of activated cell type, post-germinal center cell origin. Our patient is undergoing R-CHOP chemotherapy treatment.Introduction and the need for highly effective chemotherapy regimens [5]. These tumors are detected as primary or secondaryDiffuse large B-cell lymphoma (DLBCL) displays striking forms at both the nodal and extra-nodal levels inheterogeneity at the clinical, genetic and molecular levels immune-competent hosts as well as in patients with dif-[1]. DLBCL is the most common type of lymphoid tumor ferent types of immune-suppression. They display signifi-worldwide. This category was included in both the cant variability in terms of cell morphology and clinicalRevised European American Lymphoma (REAL) [2] clas- findings, which justifies the identification of variants andsification system and the World Health Organization subtypes [5]. DLBCL is a diffuse proliferation of large(WHO) classifications of 2001 [3] and 2008 [4], with the neoplastic B lymphoid cells with a nuclear size equal toaim of lumping together all malignant lymphomas char- or exceeding that of normal macrophage nuclei. How-acterized by the large size of the neoplastic cells of B-cell ever, even on the basis of simple histological examina-derivation as well as by an aggressive clinical presentation tion, considerable heterogeneity can be seen, and several morphological variants have been described [3].* Correspondence: skerliu@hotmail.com1 Immunophenotype, tissue microarray and molecular Faculty of Medicine, Institute of Pathology, University of Prishtina, MotherTheresa Street NN, 10 000, Prishtina, Kosovo studies underline the extreme heterogeneity of DLBCLsFull list of author information is available at the end of the article © 2011 Manxhuka-Kerliu et al; licensee BioMed Central Ltd. This is ...
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Báo cáo y học: "Clear cell variant of diffuse large B-cell lymphoma: a case report."Manxhuka-Kerliu et al. Journal of Medical Case Reports 2011, 5:182 JOURNAL OF MEDICALhttp://www.jmedicalcasereports.com/content/5/1/182 CASE REPORTS CASE REPORT Open AccessClear cell variant of diffuse large B-celllymphoma: a case reportSuzana Manxhuka-Kerliu1*, Gordana Petrusevska2, Irma Kerliu3, Emrush Kryeziu4, Fehmi Ahmeti6,Emine Devolli-Disha5, Vjollca Sahatciu-Meka6, Sadushe Loxha1 and Labinot Shahini1 Abstract Introduction: Diffuse large B-cell lymphoma is a diffuse proliferation of large neoplastic B lymphoid cells with a nuclear size equal to or exceeding the normal macrophage nuclei. We report a case of a clear cell variant of diffuse large B-cell lymphoma involving a lymph node in the neck, which was clinically suspected of being metastatic carcinoma. Case presentation: A 39-year-old Caucasian ethnic Albanian man from Kosovo presented with a rapidly enlarging lymph node in his neck, but he also disclosed B symptoms and fatigue. A cytological aspirate of the lymph node revealed pleomorphic features. Our patient underwent a cervical lymph node biopsy (large excision). The mass was homogeneously fish-flesh, pale white tissue replacing almost the whole structure of the lymph node. The lymph node biopsy showed a partial alveolar growth pattern, which raised clinical suspicion that it was an epithelial neoplasm. With regard to morphological and phenotypic features, we discovered large nodules in diffuse areas, comprising large cells with slightly irregular nuclei and clear cytoplasm admixed with a few mononuclear cells. In these areas, there was high mitotic activity, and in some areas there were macrophages with tangible bodies. Staining for cytokeratins was negative. These areas had the following phenotypes: cluster designation marker 20 (CD20) positive, B-cell lymphoma (Bcl)-2-positive, Bcl-6-, CD5-, CD3-, CD21+ (in alveolar patterns), prostate-specific antigen-negative, human melanoma black marker 45-negative, melanoma marker-negative, cytokeratin-7-negative and multiple myeloma marker 1-positive in about 30% of cells, and exhibited a high proliferation index marker (Ki- 67, 80%). Conclusion: According to the immunohistochemical findings, we concluded that this patient has a clear cell variant of diffuse large B-cell lymphoma of activated cell type, post-germinal center cell origin. Our patient is undergoing R-CHOP chemotherapy treatment.Introduction and the need for highly effective chemotherapy regimens [5]. These tumors are detected as primary or secondaryDiffuse large B-cell lymphoma (DLBCL) displays striking forms at both the nodal and extra-nodal levels inheterogeneity at the clinical, genetic and molecular levels immune-competent hosts as well as in patients with dif-[1]. DLBCL is the most common type of lymphoid tumor ferent types of immune-suppression. They display signifi-worldwide. This category was included in both the cant variability in terms of cell morphology and clinicalRevised European American Lymphoma (REAL) [2] clas- findings, which justifies the identification of variants andsification system and the World Health Organization subtypes [5]. DLBCL is a diffuse proliferation of large(WHO) classifications of 2001 [3] and 2008 [4], with the neoplastic B lymphoid cells with a nuclear size equal toaim of lumping together all malignant lymphomas char- or exceeding that of normal macrophage nuclei. How-acterized by the large size of the neoplastic cells of B-cell ever, even on the basis of simple histological examina-derivation as well as by an aggressive clinical presentation tion, considerable heterogeneity can be seen, and several morphological variants have been described [3].* Correspondence: skerliu@hotmail.com1 Immunophenotype, tissue microarray and molecular Faculty of Medicine, Institute of Pathology, University of Prishtina, MotherTheresa Street NN, 10 000, Prishtina, Kosovo studies underline the extreme heterogeneity of DLBCLsFull list of author information is available at the end of the article © 2011 Manxhuka-Kerliu et al; licensee BioMed Central Ltd. This is ...
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