1.Cytopathological characterization of ascites for the diagnosis of serous ovarian carcinoma.
Yan Hua CHANG ; Bing Qing ZOU ; Ying CAI ; Shu Dong YANG ; Yang ZHANG ; Jia Bei LIANG ; Cong LI
Chinese Journal of Oncology 2023;45(5):424-432
Objective: To investigate the cytomorphological and immunocytochemical features of tumor cells in the ascites of ovarian plasmacytoma (SOC). Methods: Specimens of serous cavity effusions were collected from 61 tumor patients admitted to the Affiliated Wuxi People's Hospital of Nanjing Medical University from January 2015 to July 2021, including ascites from 32 SOC, 10 gastrointestinal adenocarcinomas, 5 pancreatic ductal adenocarcinomas, 6 lung adenocarcinomas, 4 benign mesothelial hyperplasia and 1 malignant mesothelioma patients, pleural effusions from 2 malignant mesothelioma patients and pericardial effusion from 1 malignant mesothelioma. Serous cavity effusion samples of all patients were collected, conventional smears were made through centrifugation, and cell paraffin blocks were made through centrifugation of remaining effusion samples. Conventional HE staining and immunocytochemical staining were applied to observe and summarize cytomorphological characteristics and immunocytochemical characteristics. The levels of serum tumor markers carbohydrate antigen 125 (CA125), carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9) were detected. Results: Of the 32 SOC patients, 5 had low-grade serous ovarian carcinoma (LGSOC) and 27 had high-grade serous ovarian carcinoma (HGSOC). 29 (90.6%) SOC patients had elevated serum CA125, but the difference was not statistically significant between them and patients with non-ovarian primary lesions included in the study (P>0.05); The serum CEA was positive in 9 patients with gastrointestinal adenocarcinoma and 5 patients with lung adenocarcinoma, and the positive rate was higher than that in SOC patients (P<0.001); The serum CA19-9 was positive in 5 patients with gastrointestinal adenocarcinoma and 5 patients with pancreatic ductal adenocarcinoma, and the positive rate was higher than that in SOC patients (P<0.05). The serum CA125, CEA and CA19-9 were within the normal range in 4 patients with benign mesothelial hyperplasia. LGSOC tumor cells were less heterogeneous and aggregated into small clusters or papillary pattern, and psammoma bodies could be observed in some LGSOC cases. The background cells were fewer and lymphocytes were predominant; the papillary structure was more obvious after making cell wax blocks. HGSOC tumor cells were highly heterogeneous, with significantly enlarged nuclei and varying sizes, which could be more than 3-fold different, and nucleoli and nuclear schizophrenia could be observed in some cases; tumor cells were mostly clustered into nested clusters, papillae and prune shapes; there were more background cells, mainly histiocytes. Immunocytochemical staining showed that AE1/AE3, CK7, PAX-8, CA125, and WT1 were diffusely positively expressed in 32 SOC cases. P53 was focally positive in all 5 LGSOCs, diffusely positive in 23 HGSOCs, and negative in the other 4 HGSOCs. Most of adenocarcinomas of the gastrointestinal tract and lung had a history of surgery, and tumor cells of pancreatic ductal adenocarcinoma tend to form small cell nests. Immunocytochemistry can assist in the differential diagnosis of mesothelial-derived lesions with characteristic "open window" phenomenon. Conclusion: Combining the clinical manifestations of the patient, the morphological characteristics of the cells in the smear and cell block of the ascites can provide important clues for the diagnosis of SOC, and the immunocytochemical tests can further improve the accuracy of the diagnosis.
Female
;
Humans
;
Carcinoembryonic Antigen
;
Ascites
;
CA-19-9 Antigen
;
Mesothelioma, Malignant/diagnosis*
;
Hyperplasia
;
Adenocarcinoma/pathology*
;
Cystadenocarcinoma, Serous/diagnosis*
;
Biomarkers, Tumor
;
Carcinoma, Ovarian Epithelial
;
Diagnosis, Differential
;
Ovarian Neoplasms/pathology*
;
Carbohydrates
6.A Case of Peritoneal Sarcomatoid Mesothelioma with Absence of Occupationl Exposure to Asbestos
Seung Hoon YOO ; Hee Man KIM ; Jea Kun PARK ; Mi Sung KIM ; Sang Yeop YI
Kosin Medical Journal 2019;34(2):146-151
Sarcomatoid mesothelioma is not very common, mesothelioma is directly attributable to occupational asbestos exposure, with 90% of cases showing a history of exposure. A 66-year-old male was admitted with an abdominal pain that persisted for 3 weeks. He had no abdominal mass. Computed tomography showed soft tissue thickening in perihepatic space and nodularities in omentum and peritoneum with ascites. There was no absolute diagnosis evidence in ascites analysis. Although the pathology of ascites was free for malignancy, the patient underwent omentum biopsy for definitive diagnosis. In laproscopic exploration, there was omental cake, peritoneal nodular seeding. It was suspected cancer carcinomatosis. Immunohistochemical findings suggested that it was sarcomatoid masothelioma. This is the rare case of a peritoneal sarcomatoid mesothelioma, without any exposure to asbestos.
Abdominal Pain
;
Aged
;
Asbestos
;
Ascites
;
Biopsy
;
Carcinoma
;
Diagnosis
;
Humans
;
Male
;
Mesothelioma
;
Omentum
;
Pathology
;
Peritoneum
;
Sarcoma
7.Detection of p16 by fluorescence in-situ hybridization and immunohistochemistry in malignant mesothelioma.
Ying LIU ; E-mail: XKLY13@126.COM. ; Xiaoling CHEN ; Ningning DING ; Wenxiang XU ; Hong YANG ; Xuechen CHEN
Chinese Journal of Pathology 2015;44(4):262-265
OBJECTIVETo study the role of p16 gene mutation status as detected by fluorescence in-situ hybridization (FISH) and p16 protein expression as detected by immunohistochemistry in differential diagnosis of malignant mesothelioma and benign mesothelial hyperplasia.
METHODSp16 gene mutation status and protein expression were detected by FISH and immunohistochemistry respectively in 55 cases of pleural malignant mesothelioma and 30 cases of benign mesothelial hyperplasia.
RESULTSFISH study showed that the rate of p16 deletion in malignant mesothelioma (81.8%,45/55) was higher than that in benign mesothelial hyperplasia (3.3%,1/30). The difference was statistically significant (P<0.05). Immunohistochemical study showed that the rate of p16 protein expression in malignant mesothelioma (23.6%) was lower than that in benign mesothelial hyperplasia (76.7%). The difference was also statistically significant. The sensitivity and specificity of FISH in distinguishing between mesothelioma and reactive mesothelial hyperplasia were higher than those of immunohistochemistry.
CONCLUSIONSIn contrast to reactive mesothelial hyperplasia, p16 gene is deleted and p16 protein is not expressed in malignant mesothelioma. The sensitivity and specificity of FISH are higher than those of immunohistochemistry in the distinction.
Cyclin-Dependent Kinase Inhibitor p16 ; metabolism ; Diagnosis, Differential ; Epithelium ; pathology ; Genes, p16 ; Humans ; Hyperplasia ; diagnosis ; genetics ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Mesothelioma ; diagnosis ; genetics ; metabolism ; Mutation ; Pleura ; pathology ; Pleural Neoplasms ; diagnosis ; genetics ; metabolism ; Sensitivity and Specificity
8.Clinical features of patients with malignant peritoneal mesothelioma initially presenting as a local inflammation.
Hui SONG ; Guoqi ZHENG ; Sichen WEI ; Yuxin YANG ; Xinliang WEI
Chinese Journal of Oncology 2014;36(4):312-313
Aged
;
Antineoplastic Combined Chemotherapy Protocols
;
therapeutic use
;
Calbindin 2
;
metabolism
;
Cholecystitis
;
pathology
;
Cisplatin
;
administration & dosage
;
Cystitis
;
pathology
;
Diagnosis, Differential
;
Female
;
Glutamates
;
administration & dosage
;
Guanine
;
administration & dosage
;
analogs & derivatives
;
Humans
;
Inflammation
;
pathology
;
Keratins
;
metabolism
;
Lung Neoplasms
;
drug therapy
;
metabolism
;
pathology
;
surgery
;
Male
;
Mesothelioma
;
drug therapy
;
metabolism
;
pathology
;
surgery
;
Middle Aged
;
Pemetrexed
;
Peritoneal Neoplasms
;
drug therapy
;
metabolism
;
pathology
;
surgery
;
Survival Rate
;
Vimentin
;
metabolism
9.Knockdown of Bcl-xL Enhances Growth-Inhibiting and Apoptosis-Inducing Effects of Resveratrol and Clofarabine in Malignant Mesothelioma H-2452 Cells.
Yoon Jin LEE ; In Sung HWANG ; Yong Jin LEE ; Chang Ho LEE ; Sung Ho KIM ; Hae Saeon NAM ; Young Jin CHOI ; Sang Han LEE
Journal of Korean Medical Science 2014;29(11):1464-1472
Mcl-1 and Bcl-xL, key anti-apoptotic proteins of the Bcl-2 family, have attracted attention as important molecules in the cell survival and drug resistance. In this study, we investigated whether inhibition of Bcl-xL influences cell growth and apoptosis against simultaneous treatment of resveratrol and clofarabine in the human malignant mesothelioma H-2452 cells. Resveratrol and clofarabine decreased Mcl-1 protein levels but had little effect on Bcl-xL levels. In the presence of two compounds, any detectable change in the Mcl-1 mRNA levels was not observed in RT-PCR analysis, whereas pretreatment with the proteasome inhibitor MG132 led to its accumulation to levels far above basal levels. The knockdown of Bcl-xL inhibited cell proliferation with cell accumulation at G2/M phase and the appearance of sub-G0/G1 peak in DNA flow cytometric assay. The suppression of cell growth was accompanied by an increase in the caspase-3/7 activity with the resultant cleavages of procaspase-3 and its substrate poly (ADP-ribose) polymerase, and increased percentage of apoptotic propensities in annexin V binding assay. Collectively, our data represent that the efficacy of resveratrol and clofarabine for apoptosis induction was substantially enhanced by Bcl-xL-lowering strategy in which the simultaneous targeting of Mcl-1 and Bcl-xL could be a more effective strategy for treating malignant mesothelioma.
Adenine Nucleotides/*pharmacology
;
Antimetabolites, Antineoplastic/*pharmacology
;
Apoptosis/*drug effects
;
Arabinonucleosides/*pharmacology
;
Caspase 3/metabolism
;
Caspase 7/metabolism
;
Cell Line, Tumor
;
Cell Proliferation/drug effects
;
G2 Phase Cell Cycle Checkpoints/drug effects
;
Gene Knockdown Techniques
;
Humans
;
Leupeptins/pharmacology
;
Lung Neoplasms/metabolism/pathology
;
M Phase Cell Cycle Checkpoints/drug effects
;
Mesothelioma/metabolism/pathology
;
Myeloid Cell Leukemia Sequence 1 Protein/antagonists & inhibitors/genetics/metabolism
;
RNA Interference
;
RNA, Messenger/metabolism
;
RNA, Small Interfering/metabolism
;
Stilbenes/*pharmacology
;
bcl-X Protein/antagonists & inhibitors/*genetics/*metabolism
10.Sarcomatoid malignant mesothelioma: a clinicopathologic and immunohistochemical analysis of 22 cases.
Iweng LAO ; Qingming CHEN ; Lin YU ; Jian WANG ; E-mail: SOFTTISSUETUMOR@163.COM.
Chinese Journal of Pathology 2014;43(6):364-369
OBJECTIVETo elaborate on the clinical and pathologic features of sarcomatoid malignant mesothelioma (SMM), its diagnostic criteria and differential diagnoses.
METHODSTwenty-two cases of SMM retrieved from in-house and consultation files (between January 2009 to September 2013) were reviewed with emphasis on the clinicopathologic characteristics, immunophenotypes and the prognostic impact.
RESULTSThe mean age of the patients was 54 years (ranged from 24-73 years). There was no sexual predilection and the majority of the patients did not have history of asbestos exposure. Overall, 14 tumors developed in the pleura and 8 cases arose from the peritoneal cavity. Clinically, patients presented signs and symptoms in accord with the location of the tumors, notably coughing, shortness of breath, and chest pain for patients with pleural origin, and nausea, abdominal distention and abdominal pain for those with peritoneal primary. In most cases, CT and MRI scan demonstrated lobulated masses (8/11). However, diffuse infiltrative growth patterns were observed exclusively in a minority of pleural cases (3/11). No visceral lesion was observed in any case. Histologically, 19 cases had either fibrosarcomatous or undifferentiated pleomorphic sarcoma-like appearance. Two cases were consistent with desmoplastic mesothelioma. One case contained osteosarcomatous element. All cases expressed pan-cytokeratin (AE1/AE3), and most cases were also positive for D2-40 (15/20). The staining of calretinin (9/21) and WT1 (10/14) was generally weak and focal. They were all negative for TTF-1, napsin A, SP-A, p63 and CD34. Follow-up information (range from 1 to 36 months) was available in 11 cases, 6 of which were alive with unresectable tumor, 1 patient with recurrent disease and 4 patients succumbed to disease. The overall survival was 5 months (mean 8 months).
CONCLUSIONSThe diagnosis of SMM is achieved by comprehensive evaluation of medical history, imageological and pathological findings. Since calretinin immunoreactivity is infrequently observed in SMM, application of pan-cytokeratin and D2-40 immunostains offers a reasonable alternative for diagnosis. Diagnosis of SMM can be made by excluding a variety of spindle cell neoplasms with overlapping features, such as sarcomatoid carcinoma, synovial sarcoma, solitary fibrous tumor and fibrous pleuritis.
Adult ; Aged ; Biomarkers, Tumor ; metabolism ; Carcinoma ; diagnosis ; pathology ; Diagnosis, Differential ; Humans ; Lung Neoplasms ; diagnosis ; pathology ; Mesothelioma ; diagnosis ; pathology ; Middle Aged ; Prognosis ; Sarcoma ; diagnosis ; pathology ; Solitary Fibrous Tumors ; diagnosis ; pathology

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