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      2. west china medical publishers
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        find Author "沈旦" 2 results
        • Lymphoma manifested firstly as symptoms in respiratory system: nine cases report and literature review

          Objective To explore the clinical characteristics of patients with lymphoma firstly manifested as symptoms in respiratory system. Methods The clinical data of 9 patients with lymphoma were analyzed retrospectively and discussed with literature review. Results There were 7 males and 2 females with an average age of 48.2 years and a median disease course of 20 days. All patients were diagnosed by pathology while specimens were obtained by cervical lymph node biopsies in 2 cases, by CT-guided percutaneous lung biopsies in 2 cases, by bronchoscope mucosal biopsies in 2 cases, by transbronchial needle aspiration biopsies in 1 case, by thoracoscope lung biopsies in 1 case, and by ascites cell block inspection in 1 case. The main symptoms were cough (7/9), expectoration (3/9), fever (3/9) and wheeze (2/9). Chest CT showed tumors (3/9, multiple in 1 case), enlarged mediastinal lymph nodes (6/9), enlarged hilar lymph nodes (3/9), pulmonary consolidation (3/9), pleural effusion (6/9, bilateral in 3 cases), pleural thickening (2/9), pulmonary atelectasis (2/9), patchy shadow (7/9), pericardial effusion (1/9). Laboratory examination demonstrated elevated cancer antigen 125 (CA125) in 7 cases while elevated lactic acid dehydrogenase (LDH) in 4 cases. One patient died during hospitalization in the respiratory department, 1 patient auto-discharged without further treatment, 1 patient died in follow-up period. Five patients remain alive up to now. Conclusions The symptoms of patients with lymphoma are atypical while the chest radiological findings are varied. CA125 and LDH play important role in evaluating disease and predicting prognosis in patients with lymphoma.

          Release date:2017-04-01 08:56 Export PDF Favorites Scan
        • 肺朗格漢斯細胞組織細胞增生癥誤診為肺腫瘤四例報告并文獻復習

          目的探討誤診為肺部腫瘤的肺朗格漢斯細胞組織細胞增生癥(pulmonary Langerhans cell histiocytosis,PLCH)的臨床特點,提高該疾病的診治能力。方法收集本院4例初診誤診為肺部腫瘤后經病理診斷的PLCH患者的臨床資料,并回顧復習相關文獻資料進行分析。結果4例PLCH中,男1例,女3例,年齡45~78歲。吸煙2例,不吸煙2例。臨床表現2例為體檢發現,1例發熱,1例淺表淋巴結腫大起病。胸部CT表現為2例多發的肺囊腫、肺大皰改變,4例均出現結節影,其中3例為單發,1例雙肺多發圓形小結節影,部分見空洞。3例行正電子發射計算機斷層顯像(positron emission computed tomography/X-ray computed tomography,PET/CT)檢查的患者均提示肺部及淋巴結等病灶標準攝取值增高。4例患者均被誤診為肺部腫瘤,經外科手術、肺穿刺及氣管鏡等檢查,病理見朗格漢斯組織細胞增生,結合S100、CD1a、Langerin等特征性免疫組織化學標志物,最終確診PLCH。結論 PLCH臨床表現不典型,影像學表現為肺結節及多發囊氣腔改變需考慮PLCH診斷可能,PET/CT易誤診,通過活檢行常規及特征性免疫組織化學病理檢查可明確診斷。

          Release date:2023-04-28 02:38 Export PDF Favorites Scan
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          2. 射丝袜