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        west china medical publishers
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        find Keyword "淋巴瘤" 139 results
        • Radiologic-Pathologic Study on Primary Pulmonary Non-Hodgkin’s Lymphoma

          Objective To investigate the relevance of primary pulmonary non-Hodgkin’s lymphoma ( PPNHL) imaging with pathology features, so as to improve the diagnostic accuracy. Methods Twenty-two patients of PPNHL were scanned by chest computed tomography, and the results of clinical and pathology features were analyzed. Results The resulting pathologic examination showed that all patients in 12 cases of low-grade lymphoma had MALT lymphoma( 54. 5% ) , histologically with slightly atypical small lymphocyte proliferated. The radiological findings indicated unilateral peripheral lesion which extended along mucous membrane in 11 patients ( 91. 7% ) and multilateral lesion in only 1 patients ( 8. 3% ) . CT features were illdefined nodule or mass with halo sign ( n =8, 66. 7%) , patchy infiltrate ( n = 4, 33. 3% ) , and ill-defined consolidations with air-bronchograms ( n =7, 58. 3% ) . The resulting pathologic examination showed that 10 patients were high and middle-grade lymphoma ( 45. 5% ) . The radiological findings indicated unilateral lesion in4 patients ( 40%) and multilateral lesion in 6 patients( 60% ) . CT features were ill-defined noduleor mass ( n =4, 40% ) , patchy infiltrate ( n = 1, 10% ) , mixed manifestation ( n =5, 50% ) , pleural effusion ( n =5, 50% ) , hilar and mediastinal lymph node enlargement ( n =2, 20% ) , atelectasis ( n =3, 30%) , and pulmonary interstitial with interlobular septal thickening ( n=2, 20% ) . Conclusions The imaging features of PPNHL rely on its’ basic pathology. Low-grade lymphoma is characterized by peripheral focal consolidation with air-bronchograms. High and middle-grade lymphoma is characterized by mixed manifestation of interstitial change and nodular focus. Analyzing CT features seriously may be helpful for diagnosis of PPNHL.

          Release date:2016-09-13 04:06 Export PDF Favorites Scan
        • 脈絡膜黏膜相關淋巴組織淋巴瘤一例

          Release date:2020-11-19 09:16 Export PDF Favorites Scan
        • Analysis of 21 Cases of Acute Abdomen Misdiagnosed as Acute Appendicitis

          目的 分析其他疾病誤診為急性闌尾炎的原因。方法 結合相關文獻資料,對2004年2月至2008年12月期間本院21例其他疾病被誤診為急性闌尾炎的過程進行回顧性分析。結果 除了膽囊結石、胃穿孔、腸結核、異位妊娠等常見病可能被誤診為急性闌尾炎外,肝包蟲、膽管癌、癔病、惡性淋巴瘤等也有可能被誤診為急性闌尾炎。誤診的主要原因是經治醫生經驗不足、思維局限、知識面狹窄,更重要的則是重視不足,檢查不仔細、不全面。結論 系統和全面仔細地問診、查體,努力提高輔助檢查診斷水平等是減少誤診的關鍵。

          Release date:2016-09-08 10:54 Export PDF Favorites Scan
        • The Clinico-pathological Features of Malignant Breast Lymphoma

          【摘要】 目的 探討乳腺惡性淋巴瘤的臨床病理特征、治療方式及其與預后關系。 方法 1980年1月-2007年12月對收治的21例乳腺惡性淋巴瘤患者的臨床病理特點、診斷和治療方法進行回顧性分析。 結果 21例乳腺惡性淋巴瘤患者均為女性,中位年齡47歲;其中原發性乳腺惡性淋巴瘤18例,繼發性惡性淋巴瘤3例。原發性乳腺惡性淋巴瘤均為非霍奇金淋巴瘤,B細胞來源為主,大多為術后診斷,治療均采用手術+化學療法。 結論 乳腺惡性淋巴瘤治療應強調手術,化學療法和放射治療的綜合治療。【Abstract】 Objective To study the clinico-pathological features and treatment modality of malignant breast lymphoma, and their relationships with the prognosis of the disease. Methods The clinico-pathological features, diagnosis and treatment methods of 21 cases of malignant breast lymphoma diagnosed between January 1980 and December 2007 were analyzed retrospectively and related domestic and overseas literature was reviewed. Results Among the 21 female patients, 18 had primary breast lymphoma (PBL), 3 had secondary breast lymphoma. All cases of PBL were non-Hodgkin’s lymphoma with mainly B cells as the origin. The median age of the patients was 46.5 years old. Most of the cases were diagnosed postoperatively and all patients were treated by operation combined with chemotherapy. Related literature reviewing showed that clinical staging and treatment modality were important factors of prognosis. Conclusion In treating malignant breast lymphoma, operation and chemoradiotherapy should be combined together to get a better result.

          Release date:2016-09-08 09:24 Export PDF Favorites Scan
        • 原發乳腺淋巴瘤的診療現狀及進展

          原發乳腺淋巴瘤(primary breast lymphoma,PBL)是一種罕見的結外型非霍奇金淋巴瘤,定義為原發于乳腺,伴或不伴區域淋巴結轉移,但無胸外浸潤的淋巴瘤。由于乳腺組織正常情況下無淋巴組織,所以其發病率較低,約占結外型非霍奇金淋巴瘤的 2%,在乳腺惡性腫瘤中約占 0.5%。PBL 無典型臨床表現,診斷依賴于病理學。其主要病理學類型為彌漫大 B 淋巴細胞瘤。中樞神經系統為 PBL 治療后常見的復發部位。目前關于 PBL 的報道少見,且多為小樣本回顧性分析,尚無統一治療規范。文獻報道 PBL 治療多以系統化學療法聯合放射治療及免疫治療為主,手術僅適用于明確病理學診斷,對生存獲益有限。國際預后指數為 PBL 主要預后因素。對于復發/難治的 PBL,靶向治療將是一個新的突破點,有望為臨床治療提供更多選擇。該文就 PBL 的診斷,臨床特征,治療策略及研究進展等方面加以綜述,旨在加深對 PBL 的認識,指導臨床治療。

          Release date:2017-12-25 06:02 Export PDF Favorites Scan
        • Economic evaluation of ALK-TKIs in ALK-positive non-small cell lung cancer: a systematic review

          ObjectiveTo systematically review the economic evaluations of anaplastic lymphoma kinase (ALK)-tyrosine kinase inhibitors (TKIs) in the treatment of ALK-positive non-small cell lung cancer (NSCLC). MethodsPubMed, Web of Science, The Cochrane Library, CNKI, VIP and WanFang Data databases were electronically searched to collect economic evaluations of ALK-TKIs in the treatment of ALK-positive NSCLC from inception to July 2022. Two reviewers independently screened literature, extracted data and assessed the risk of bias of included studies; then, a systematic review was performed. ResultsA total of 20 studies were included. 18 of the included studies were cost-utility analyses based on the models. The method of survival data extrapolation involved the standard parameter model and the standard parameter model with a hazard ratio adjusting. 10 studies considered or included the disutility value of adverse events. 18 studies performed cost estimation on direct costs. In China, 45% of the included studies were first-line treatment, the results showed that ALK-TKIs were less economical than chemotherapy, and second-/third-generation ALK-TKIs were less economical than crizotinib. Only 1 studies were second-line treatment, the result showed that crizotinib was more economical than chemotherapy. ConclusionThe economic evaluation results of ALK-TKIs in ALK-positive NSCLC vary according to treatment stage and national scenario, and there is also room for optimization of methodological application in this field.

          Release date:2023-01-16 02:58 Export PDF Favorites Scan
        • 易誤診的皮下脂膜炎樣T細胞淋巴瘤一例

          Release date:2016-09-07 02:37 Export PDF Favorites Scan
        • 霍奇金淋巴瘤并發眼部偽裝綜合征一例

          Release date:2019-03-18 02:49 Export PDF Favorites Scan
        • MDT discussion of a case of primary diffuse large B cell lymphoma of liver

          ObjectiveTo investigate the clinical manifestations, imaging manifestations, etiology, histological origin, pathological characteristics, diagnosis and differential diagnosis, selection of treatment methods, and prognosis of primary diffuse large B cell lymphoma of livers (PDLBCLL), so as to improve understanding and reasonable diagnosis and treatment of this kind of disease.MethodThe clinicopathologic data of a case of PDLBCLL diagnosed in the West China Hospital of Sichuan University in June 2019 were analyzed retrospectively.ResultsIt was very difficult to diagnose PDLBCLL preoperatively and to distinguish PDLBCLL from primary liver cancer and other liver space occupying lesions. It was also easy to ignore the possibility of invasion of liver by lymphopoietic tissue tumor, which was often diagnosed by postoperative pathological diagnosis or puncture biopsy, and after the elimination of hematological diseases by various examinations. This patient was admitted to the hospital as a space occupying in right liver. Preoperative imaging examination considered that may be a tumor. After MDT discussion, considering that the nature of the tumor should be confirmed by surgical resection, and then go to the Department of Oncology. Irregular right hemihepatectomy + cholecystectomy + hilar lymphadenectomy + diaphragmatic repair was performed after MDT discussion. The diagnosis of PDLBCLL was confirmed by postoperative pathological examination. The operation duration was about 230 min, and the intraoperative blood loss was about 200 mL. The patient recovered well without complications and was discharged on the 10th day after operation. The patient was followed up for 9 months. The liver and kidney function, electrolytes and abdominal Doppler ultrasound examination were regularly reviewed every month. No obvious abnormality was found in these results.ConclusionsAt present, there is no unified treatment principle, most of them will undergo surgery, chemotherapy, radiotherapy or combined treatment. Due to its unknown etiology and unclear mechanism, clinicians can only implement individualized treatment according to the characteristics of patients’ conditions.

          Release date:2021-02-08 07:10 Export PDF Favorites Scan
        • 復發難治性套細胞淋巴瘤的治療進展

          套細胞淋巴瘤(MCL)是一組以t(11;14)和細胞周期蛋白D1陽性過度表達為特征的侵襲性非霍奇金淋巴瘤(NHL),約占NHL發病的3%~10%,預后較差,生存期僅為3~5年。復發難治性MCL預后極差,第1次復發后,中位生存期僅1~2年,現有治療方法仍不能治愈MCL,許多新的作用于細胞周期和凋亡通路的藥物,如蛋白酶體抑制劑、免疫調節劑、雷帕霉素靶蛋白抑制劑、組蛋白去乙酰化酶抑制劑取得了令人鼓舞的療效,為復發難治性MCL患者帶來新的希望。現就近年國際上復發難治性MCL的治療進展作一綜述。

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