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    find Keyword "淋巴瘤" 139 results
    • 原發性肺淋巴瘤兩例并文獻復習

      目的探討原發性肺淋巴瘤的臨床特點、診斷和治療方法。 方法回顧性總結原發性肺淋巴瘤2 例,并結合文獻對其臨床表現、影像學特點、診斷及治療方法進行分析。 結果原發性肺淋巴瘤的臨床表現無特異性,影像學改變易誤診為支氣管肺癌。確診主要依靠開胸手術,纖維支氣管鏡檢查病理陽性率低。 結論及時進行有創檢查有利于早期診斷原發性肺淋巴瘤。

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    • 原發性眼內淋巴瘤一例

      Release date:2016-09-02 05:46 Export PDF Favorites Scan
    • Diagnosis and Treatment of Primary Pancreatic Lymphoma

      【摘要】 目的 探討原發性胰腺淋巴瘤( PPL) 的臨床特點及治療方法。方法 回顧性分析我院2002~2006年期間收治的6 例PPL 的臨床資料。結果 本組6 例患者中3 例病灶位于胰頭,3 例位于胰體尾。臨床癥狀以上腹不適、黃疸為主。術前僅1 例通過影像學檢查獲得診斷。2 例行胰十二指腸切除術,3 例行胰體尾聯合脾切除術,1 例行剖腹探查、組織活檢術。術后病理診斷均為胰腺非霍奇金淋巴瘤。患者術后均行化療,除1 例失訪以外,其余5 例均存活。結論 PPL 的臨床癥狀、影像學表現及實驗室檢查結果不具特異性,與胰腺癌難以區分,明確診斷有賴于病理組織學檢查。對術前未能確診的胰腺淋巴瘤患者,外科手術治療結合術后化療、放療安全有效。

      Release date:2016-09-08 11:45 Export PDF Favorites Scan
    • 原發性頸面部惡性淋巴瘤化學治療的臨床分析

      【摘要】目的 觀察原發性頸面部惡性淋巴瘤手術前后化學治療(化療)的治療效果。方法 回顧性分析18例頸面部惡性淋巴瘤患者的發病年齡和臨床表現。結果 18例患者中,2例1.5、2.0年死亡,隨訪失訪1例。存活的15例患者中,2、3年的4例,3、4年的4例,4年以上的7例。結論 惡性淋巴瘤的治療主要以化療為主,且以聯合化療效果最佳;手術前后化療對惡性淋巴瘤的近期臨床療效滿意。

      Release date:2016-09-08 09:45 Export PDF Favorites Scan
    • 咳嗽, 活動后氣促, 左肺大片致密影

      Release date:2016-09-13 04:00 Export PDF Favorites Scan
    • 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
    • 自然殺傷/T細胞淋巴瘤的生物學行為和臨床及診斷研究進展

      自然殺傷(NK)/T細胞淋巴瘤(NKTCL)作為非霍奇金淋巴瘤(NHL)的獨立類型,在亞洲、拉丁美洲地區發病率明顯高于西方國家。其發病與EB病毒(EBV)感染關系密切,而遺傳因素、農藥、化學溶劑等與其發病有一定相關性。病理組織學上以血管中心和多形淋巴網狀內皮細胞的破壞性浸潤為特征,表達T或NK細胞抗原,以及T細胞內抗原-1、粒酶B、穿孔素等細胞毒顆粒相關蛋白,組織標本中絕大部分EBV編碼的小分子RNA檢測陽性。臨床上以中軸區受累為多見,早期病變常局限,進展期則呈侵襲性生長、少數可發生遠處轉移。目前診斷主要依靠組織標本的病理學檢查,CD2+、CD3ε+及CD56+可作為診斷該腫瘤較特異的免疫組織化學標記;同時,EBV相關成分及白介素-9、白介素-10和γ-干擾素等相關細胞因子和蛋白的檢出對診斷具有積極幫助,卟啉鈣黏蛋白15則可望成為診斷NK細胞來源腫瘤的新的重要標記。近年來,影像學檢查、尤其18氟標記脫氧葡萄糖正電子發射型計算機斷層掃描顯像儀對診斷的價值更加受到重視,有利于與B細胞來源淋巴瘤鑒別,并對NKTCL的分期及預后判斷有一定價值。

      Release date:2016-09-08 09:13 Export PDF Favorites Scan
    • Ultrasonography Features of Primary Thyroid Non-Hodgkin Lymphoma

      Objective To investigate ultrasonography features of primary thyroid non-Hodgkin lymphoma (PT-NHL). Methods Ultrasonographic data of patients with PT-NHL(PT-NHL group) and non-Hodgkin lymphoma (control group) who were treated in our hospital from May. 2002 to Jul. 2014 were collected and analyzed. Results Compared with control group, enhancement of posterior echoes was more common in PT-NHL group (P=0.000), and difference values of transverse diameters, anteroposterior diameters, and sagittal diameters of more involved lobe to another lobe were bigger(P < 0.05), but echo pattern of gland, ultrasonographic classification of lesions, classification of vascularity, and condition of cervical lymph nodes were found no statistical difference(P > 0.05). In patients with nodular-type lesions(37 patients in PT-NHL group and 12 patients in control group), length of nodule lesions was larger in PT-NHL group (P=0.000), but there was no statistical difference in shape, boundary, orientation, and echoes of nodules between 2 groups(P > 0.05). In Pulsed-Wave(PW) Doppler between 2 groups(17 patients in PT-NHL group and 4 patients in control group), vascular resistance index(RI) was higher in PT-NHL group than those of control group (P=0.024). Conclusion The enhancement of posterior echoes was a feature in ultrasonography images of PT-NHL. Asymmetrical volume, high value of RI, and big nodule might link to PT-NHL, but diffuse heterogeneous echo with hypoechoic lesions might result in wrong diagnosis as PT-NHL.

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    • 原發肺部非霍奇金淋巴瘤一例

      Release date:2016-08-26 02:09 Export PDF Favorites Scan
    • 原發性甲狀腺淋巴瘤4例臨床分析

      目的總結原發性甲狀腺淋巴瘤的臨床表現、診斷方法、治療及預后。 方法回顧性分析我院2015年收治的4例原發性甲狀腺淋巴瘤的相關資料并結合國內外相關文獻進行分析。 結果4例患者術前行細針穿刺吸取細胞學檢查未能明確診斷,均診斷為橋本甲狀腺炎,術后通過免疫組織化學診斷為淋巴瘤,其中黏膜相關淋巴組織淋巴瘤及彌漫性大B細胞淋巴瘤各2例。 結論原發性甲狀腺淋巴瘤的治療以綜合治療為主,術前確診率低,手術只為明確診斷及緩解癥狀,確定其組織學分型后采用相應的放化療,患者的分期、組織學分型及采用合適的治療方式與預后都是相關的。

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