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1.
The Korean Journal of Gastroenterology ; : 43-47, 2015.
Article in Korean | WPRIM | ID: wpr-208446

ABSTRACT

Spontaneous gastric perforation is a rare complication of gastric lymphoma that is potentially life threatening since it can progress to sepsis and multi-organ failure. Morbidity also increases due to prolonged hospitalization and delay in initiating chemotherapy. Therefore prompt diagnosis and appropriate treatment is critical to improve prognosis. A 64-year-old man presented to the emergency department with severe abdominal pain. Chest X-ray showed free air below the right diaphragm. Abdominal CT scan also demonstrated free air in the peritoneal cavity with large wall defect in the lesser curvature of gastric lower body. Therefore, the patient underwent emergency operation and primary closure was done. Pathologic specimen obtained during surgery was compatible to diffuse large B cell lymphoma. Fifteen days after primary closure, the patient received subtotal gastrectomy and chemotherapy was initiated after recovery. Patient is currently being followed-up at outpatient department without any particular complications. Herein, we report a rare case of gastric lymphoma that initially presented as peritonitis because of spontaneous gastric perforation.


Subject(s)
Humans , Male , Middle Aged , Abdominal Pain , Antigens, CD20/metabolism , Leukocyte Common Antigens/metabolism , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Gastrectomy , Intestinal Perforation/diagnostic imaging , Lymphoma, Large B-Cell, Diffuse/diagnosis , Lymphoma, Non-Hodgkin/diagnosis , Positron-Emission Tomography , Stomach Neoplasms/diagnosis , Tomography, X-Ray Computed
3.
Journal of Forensic Medicine ; (6): 1-11, 2012.
Article in Chinese | WPRIM | ID: wpr-983702

ABSTRACT

OBJECTION@#To investigate the time-dependent appearance of circulating fibrocytes of skeletal muscle in rats after contusion.@*METHODS@#The model of skeletal muscle wound was established in rat. The circulating fibrocytes in contused skeletal muscle were detected by CD45 and procollagen I double immunofluorescence staining method.@*RESULTS@#In the control group, CD45- and procollagen I-positive cells were not detected in skeletal muscle. A few CD45 cells were observed aged from 6 h to 1 d after contusion. A few CD45- and procollagen I-positive cells (fibrocytes) initially gathered in injury area 3d after injury. The ratio of positive fibrocytes significantly increased 5 d after injury. The ratio of fibrocytes was highest at 7 d after contusion and then decreased. The volume of fibrocytes showed bigger with injury time increase compared with 3 d group. The expression of procollagen I and CD45 were weakened at 14d after injury.@*CONCLUSION@#The circulating fibrocytes are detected in contused skeletal muscle in time-dependent pattern. Circulating fibrocytes may be a marker in the wound age determination for contused skeletal muscle.


Subject(s)
Animals , Male , Rats , Biomarkers/metabolism , Collagen Type I/metabolism , Contusions/pathology , Disease Models, Animal , Forensic Pathology , Immunohistochemistry , Leukocyte Common Antigens/metabolism , Mesenchymal Stem Cells/metabolism , Microscopy, Fluorescence , Muscle, Skeletal/pathology , Random Allocation , Rats, Sprague-Dawley , Time Factors , Wound Healing
4.
Journal of Korean Medical Science ; : 1009-1013, 2012.
Article in English | WPRIM | ID: wpr-154191

ABSTRACT

Recently, subpopulations of regulatory T (Treg) cells, resting Treg (rTreg) and activated Treg (aTreg), have been discovered. The authors investigated the relationship between the change of Treg, aTreg and rTreg and autoimmune diseases. Treg cells and those subpopulations were analyzed by using the human regulatory T cell staining kit and CD45RA surface marker for 42 rheumatoid arthritis (RA), 13 systemic lupus sclerosis (SLE), 7 Behcet's disease (BD), and 22 healthy controls. The proportion of Treg cells was significantly lower in RA (3.8% +/- 1.0%) (P < 0.001) and BD (3.3% +/- 0.5%) (P < 0.01) compared to healthy controls (5.0% +/- 1.3%). The proportion of aTreg cells was also significantly lower in RA (0.4% +/- 0.2%) (P = 0.008) and BD (0.3% +/- 0.1%) (P = 0.013) compared to healthy controls (0.6% +/- 0.3%). The rTreg cells showed no significant differences. The ratio of aTreg to rTreg was lower in RA patients (0.4% +/- 0.2%) than that in healthy controls (0.7% +/- 0.4%) (P = 0.002). This study suggests that the decrement of aTreg not rTreg cells contributes the decrement of total Treg cells in peripheral blood of RA and BD autoimmune diseases. Detailed analysis of Treg subpopulations would be more informative than total Treg cells in investigating mechanism of autoimmune disease.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , CD4 Antigens/metabolism , Leukocyte Common Antigens/metabolism , Arthritis, Rheumatoid/immunology , Behcet Syndrome/immunology , Forkhead Transcription Factors/metabolism , Interleukin-2 Receptor alpha Subunit/metabolism , Leukocyte Count , Lupus Erythematosus, Systemic/immunology , T-Lymphocytes, Regulatory/cytology
5.
Journal of Forensic Medicine ; (6): 246-249, 2011.
Article in Chinese | WPRIM | ID: wpr-983657

ABSTRACT

OBJECTIVE@#To investigate the time-dependent recruitment and differentiation of fibrocytes in skin wound healing.@*METHODS@#Fibrocytes (expressing CD45 and procollagen I ) and myofibroblasts (expressing CD45 and alpha-SMA) were co-localized by immunofluorescent staining. The number of fibrocytes and myofibroblasts was counted at different post-wounding interval.@*RESULTS@#At 3 d after injury, fibrocytes started to recruit at the margin of the wounds. At 5 d after injury, myofibroblasts started to appear in new formed granulation tissue. The number of fibrocytes and myofibroblasts peaked at 7 d post-wounding.@*CONCLUSION@#During skin wound healing, myofibroblasts in granulation tissue originated at least partly from fibrocytic differentiation. The time-dependent recruitment and differentiation of fibrocytes may provide new information for wound age determination.


Subject(s)
Animals , Male , Mice , Cell Count , Cell Differentiation , Disease Models, Animal , Fibroblasts/metabolism , Leukocyte Common Antigens/metabolism , Mice, Inbred BALB C , Myofibroblasts/metabolism , Skin/pathology , Staining and Labeling , Time Factors , Wound Healing
6.
The Korean Journal of Laboratory Medicine ; : 97-104, 2010.
Article in English | WPRIM | ID: wpr-151635

ABSTRACT

BACKGROUND: Despite the diagnostic utility of immunophenotyping for myelodysplastic syndromes (MDS), it has not been widely performed, and reports on this are absent in Korea. We aimed to evaluate the immunophenotypic features of non-blastic granulocytes, monocytes, and blasts in patients with MDS and non-clonal disorders using routine flow cytometry (FCM). Moreover, we evaluated the phenotypic abnormalities of mature cells in leukemic patients. METHODS: Marrow aspirates from 60 patients, including 18 with MDS, 18 with leukemia, and 24 with non-clonal disorders (control group), were analyzed using FCM. Blasts, non-blast myeloid cells, and monocytes were gated based on CD45 expression and side scatter (SSC). The phenotypes were then compared among the 3 groups. RESULTS: Compared to non-clonal disorders, the granulocytic lineages of MDS showed decreased SSC (P=0.005), increased CD45 intensity (P=0.020), decreased CD10-positive granulocytes (P= 0.030), and a higher CD56-positive rate (P=0.005). It is noteworthy that similar results were obtained in the leukemia group, and these findings were not related to the phenotypes of the leukemic cells. Using blast and monocytic gating, useful parameters for generating a differential diagnosis were not found. CONCLUSIONS: Gating the granulocytic region is a relatively easy method for MDS immunophenotyping. Among the parameters studied, SSC, CD10, and CD56 were the most useful for differentiating MDS from non-clonal disorders. While immunophenotypic changes in MDS appear to be useful for differentiating MDS from non-clonal disorders, these changes were also noted in the mature cells of leukemic patients.


Subject(s)
Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Leukocyte Common Antigens/metabolism , CD56 Antigen/metabolism , Bone Marrow Cells/cytology , Cell Lineage , Diagnosis, Differential , Flow Cytometry , Granulocytes/classification , Immunophenotyping , Leukemia/diagnosis , Monocytes/classification , Myelodysplastic Syndromes/diagnosis , Neprilysin/metabolism , Phenotype
7.
The Korean Journal of Gastroenterology ; : 127-132, 2010.
Article in Korean | WPRIM | ID: wpr-37308

ABSTRACT

Histiocytic sarcoma is a rare malignant neoplasm that originates from a histiocytic hematopoietic lineage characterized by histiocytic differentiation and its corresponding immunophenotypic features. Patients with histiocytic sarcoma usually have a poor prognosis due to its aggressive clinical behavior. Here we report a rare case of extranodal histiocytic sarcoma of the stomach which was confirmed through immunohistochemical staining. A 71-yearold man was presented with epigastric pain. Gastroscopy, abdominal CT, and EUS revealed a mass located on the posterior wall of upper body and fundus of the stomach. Grossly, grayish white solid masses were seen extending down to the submucosal layer. Microscopically, the tumor cells had eosinophilic cytoplasm, abundant vacuole, and mitosis. Immunohistochemical staining revealed that the tumor cells were positive for LCA, CD68, and lysozyme. Early detection and accurate diagnosis of this rare neoplasm is important because it can make a great difference in prognostic outcomes. To make an accurate and definitive diagnosis, immunohistochemical staining is essential in the confimation of histiocytic orign.


Subject(s)
Aged , Humans , Male , Adenocarcinoma/diagnosis , Antigens, CD/metabolism , Leukocyte Common Antigens/metabolism , Antigens, Differentiation, Myelomonocytic/metabolism , Diagnosis, Differential , Gastroscopy , Histiocytic Sarcoma/diagnosis , Muramidase/metabolism , Stomach Neoplasms/diagnosis , Tomography, X-Ray Computed
8.
The Korean Journal of Laboratory Medicine ; : 194-198, 2009.
Article in English | WPRIM | ID: wpr-208986

ABSTRACT

Natural killer (NK) cell neoplasms are a group of rare but highly malignant tumors. We report here one case of NK cell leukemia. A 54-yr-old woman presented with a 2-month history of progressive left neck mass. Based on the positive result of tissue PCR for Mycobacterium tuberculosis, she was at first diagnosed with tuberculous lymphadenopathy. After two weeks, she developed generalized lymphadenopathy, hepatosplenomegaly, fever and anemia. Subsequent evaluation was performed including bone marrow aspiration and biopsy. Peripheral blood smear showed leukoerythroblastic features with 31% blasts. Bone marrow was packed with agranular blastoid cells, which were periodic acid-Schiff (PAS) positive and myeloperoxidase (MPO) negative. Immunophenotyping showed that these cells were positive for CD45 and HLA-DR, whereas negative for CD3, CD5, CD7, CD10, CD13, CD14, CD19, CD20, CD22, CD33, CD34, and CD61. Because of the absence of the markers of T-cell, B-cell, and myeloid lineage-specific antigens, we added CD16/56 for the immunophenotyping and the blasts were positive (94%). The tumor cells of biopsied lymph node were only positive for CD56, consistent with NK cell lymphoma. Epstein-Barr virus (EBV) was not detected by RNA in situ hybridization. Culture for M. tuberculosis was negative. Thus this patient was diagnosed with blastic NK cell lymphoma/leukemia involving bone marrow and lymph node.


Subject(s)
Female , Humans , Middle Aged , Leukocyte Common Antigens/metabolism , Bone Marrow/pathology , HLA-DR Antigens/metabolism , Killer Cells, Natural/immunology , Leukemia/diagnosis , Tuberculosis, Lymph Node/diagnosis
9.
Indian J Cancer ; 2008 Jul-Sep; 45(3): 112-8
Article in English | IMSEAR | ID: sea-50586

ABSTRACT

Primary central nervous system lymphomas (PCNSLs) are a rare form of non-Hodgkin's lymphoma which arise within and remain confined primarily to the central nervous system (CNS). They generally account for 1-2% of all primary brain tumors and are reported to be on the rise due to the Acquired Immune Deficiency Syndrome (AIDS) epidemic. AIMS AND OBJECTIVES: To study the clinicopathological and immunophenotypic characteristics of PCNSLs and look for any differences in PCNSLs reported in India from those in other countries. MATERIALS AND METHODS: All cases of PCNSLs between January 1998 and December 2006 were reviewed. Presence of lymphadenopathy, organomegaly and bone marrow study was done to exclude the possibility of secondary involvement by lymphoma. The diagnosis was confirmed by histopathology with Hematoxylin and Eosin and reticulin stains. Immunohistochemistry (IHC) with leucocyte common antigen (LCA), CD 20 and CD 3 was performed on available blocks. The immune status was evaluated by clinical examination and human immunodeficiency virus (HIV) serology (since 1996). RESULTS: In a 19-year study period, there were 56 patients of PCNSLs, accounting for 1.07% of all intracranial neoplasms. The patients ranged from 10-75 years of age with a median age of 42 years. Barring one patient who was HIV positive, all the others were immunocompetent. All cases were diffuse large cell lymphomas on histopathology. IHC with LCA and CD 20 revealed positivity in 100% and 86.4% cases respectively. There was a single case of CD 3 positive T-cell lymphoma. In the present study, PCNSLs occurred in young immunocompetent patients and majority were diffuse large B cell lymphomas.


Subject(s)
Adolescent , Adult , Aged , Antigens, CD20/metabolism , CD3 Complex/metabolism , Leukocyte Common Antigens/metabolism , Brain Neoplasms/epidemiology , Child , Female , Humans , Immunocompetence , Immunoenzyme Techniques , India/epidemiology , Lymphoma, Large B-Cell, Diffuse/epidemiology , Male , Middle Aged , Young Adult
10.
Asian Pac J Allergy Immunol ; 2006 Mar; 24(1): 65-71
Article in English | IMSEAR | ID: sea-36429

ABSTRACT

The immunomagnetic beads method for isolation of fetal nucleated red blood cells (FNRBCs) from peripheral blood of 78 pregnant women for prenatal diagnosis was developed. The study subjects were classified into 8-10 and 11-14 weeks of gestation (n = 39 each). Peripheral blood cells were divided into two for the FNRBCs isolation using two protocols, one with anti-CD45 depletion followed by anti-CD71 and anti-GPA monoclonal antibodies and another without CD45 depletion. The use of CD45 depletion gave a slightly higher number of sorted cells but not significantly different (p > 0.05). The percentage of CD71+ and GPA+ cells obtained from 8-10 weeks and 11-14 weeks of gestation was not different (p > 0.05). The sensitivity in determining the sorted FNRBCs for male fetal sex by PCR using 8-10 and 11-14 weeks of gestation was generally 50 and 69%, respectively. The method so developed is simple and cost effective and may thus be applied for prenatal diagnosis.


Subject(s)
Antigens, CD/metabolism , Leukocyte Common Antigens/metabolism , Erythrocytes , Female , Fetus , Flow Cytometry , Glycophorins/metabolism , Humans , Immunohistochemistry , Immunomagnetic Separation , Leukocyte Reduction Procedures , Polymerase Chain Reaction , Pregnancy , Prenatal Diagnosis/methods , Receptors, Transferrin/metabolism , Sensitivity and Specificity , Sex Determination Analysis/methods
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