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        find Keyword "肉瘤" 102 results
        • 胃濾泡樹突狀細胞肉瘤:2例報道并文獻復習

          目的總結胃濾泡樹突狀細胞肉瘤(follicular dendritic cell sarcoma,FDCS)的臨床病理特征。方法回顧性收集四川大學華西醫院(簡稱“我院” )收治的2例胃FDCS患者的臨床病理資料并回顧相關文獻進行分析。結果結合我院的2例及文獻收集的12例共14例胃FDCS患者的資料發現,胃FDCS好發于女性(男∶女=3∶11);發病年齡22~67歲、平均49歲、中位53歲;主要臨床癥狀為腹痛(7/14);胃FDCS最大徑2~23 cm、中位10 cm。鏡下可見腫瘤細胞多為梭形或卵圓形,呈束狀、漩渦狀、席紋狀、車輻狀、彌漫片狀或模糊的結節狀生長。腫瘤細胞中等大小,邊界不清;胞質嗜酸性;胞核橢圓形或梭形,通常呈泡狀,核仁明顯。部分區域瘤細胞異型性明顯,核大呈多邊形,雙核或多核常見,可觀察到瘤巨細胞或合體樣細胞存在,核分裂象易見(>5個/10 HPF)。腫瘤內常見小淋巴細胞浸潤,多聚集在血管周圍,可圍繞血管形成袖套狀結構;腫瘤周邊淋巴組織可呈透明血管Castleman病樣改變。此外,腫瘤內還可見擴張的假血管樣腔隙,內含嗜伊紅色的蛋白樣物,類似于胸腺瘤中的腔隙狀結構。部分病例可見明顯壞死及黏液變區域。大多數病例與周圍組織分界尚清楚,文獻報道中2例可見腫瘤浸潤性生長。免疫組織化學染色結果:本組資料中胃FDCS細胞多數表達CD21(13/14)、CD23(11/13)、CD35(11/14),部分表達CD68(6/9)、S100(4/9),不表達CD117(0/11)和DOG1(0/8)。胃FDCS應與多種發生于胃的腫瘤相鑒別,正確診斷的關鍵在于認識和熟悉FDCS的組織學形態特征,在鑒別診斷中納入濾泡樹突狀細胞免疫組織化學標志物。治療多采用手術切除(13/14)。本組胃FDCS中,4例累及網膜或橫結腸系膜,3例發生肝轉移,5例發生淋巴結轉移。有10例患者獲得隨訪資料,隨訪時間1~31個月,1例因肝轉移死亡,1例帶瘤生存,余均為無瘤生存。其中我院的病例1術后4個月發現肝多發轉移灶,進行特瑞普利單抗免疫治療和安羅替尼靶向治療并加用吉西他濱化療及局部放療,患者定期隨訪,目前病情穩定。結論胃FDCS好發于中年女性,臨床表現常為腹痛,其組織學特征與其他部位FDCS一致,但因它較罕見,易被誤診為消化道其他腫瘤,存在診斷陷阱。應廣泛取材并結合組織學特征以及免疫組織化學染色結果進行鑒別診斷,以提高對胃FDCS診斷的準確性,為患者后續治療提供支持。

          Release date:2024-06-20 05:33 Export PDF Favorites Scan
        • REPAIR OF LARGE UPPER THORACIC WALL DEFECT AFTER TUMORECTOMY

          Objective To observe an early result after the repair of the large upper thoracic wall defect by a combined use of the titaniumnet, reconstruction nickelclad, and latissimus dorsi myocutaneous flap in a patient who underwent a breast sarcomatoid caricinoma resection on the upper thoracic wall. Methods A breast sarcomatoid carcinoma in the upper thoracic wall was removed in 1 56yearold female patient in February 2006. After the tumorectomy, a large thoracic wall defect was left, which was 20cm×15cm in size. The defect was covered by the titanium net, the bilateral stumps of the clavicles were connected by the reconstruction nickelclad, and the soft tissue defect was repaired with the right latissimus dorsi myocutaneous flap(20cm×15cm). Results The patient depended on the breathing machine for 3 days after operation. When the breathing machine was discontinued, the patient developed a severe paradoxical breathing. Two weeks after operation when theblood circulation of the flap was stabilized, the paradoxical breathing disappeared with the help of the chest bandage for fixation of the chest cavity, and the blood supply of the flap was improved. The chest X-ray film showed that the titanium net and the reconstruction nickelclad were well positioned. The patient received chemotherapy 1 month after operation, The follow-up for 3 months revealed that the patient’s local condition and physical condition were good, and ROMof both the shoulders was improved, with AF 90° and ABD 90°. No recurrence ofthe tumor was found. Conclusion A large thoracic wall defect should be repaired with solid materials. The normal anatomic locations of the clavicles should be maintained with fixation by the reconstruction nickelclad for a good function of the shoulders. The latissimus dorsi myocutaneous flap can be properly enlarged.

          Release date:2016-09-01 09:22 Export PDF Favorites Scan
        • 乳腺葉狀囊肉瘤10例診治體會

          Release date:2016-08-29 09:16 Export PDF Favorites Scan
        • RECONSTRUCTION AND REPAIR AFTER RESECTION OF SOFT TISSUE SARCOMA

          OBJECTIVE To emphasize the importance of reconstruction and repair after resection of soft tissue sarcoma. METHODS From November 1990 to November 1996, in 107 cases of soft tissue sarcoma 32 cases had received various reconstructive or reparative operations. Among the 32 cases, 4 cases were primary sarcomas and 28 cases were recurrent sarcomas. In surgical grading, 3 cases were of I B, 3 cases of II A and 26 cases of II B. Radical resection was performed in 13 cases, widen local resection in 17 cases and local excision in 2 cases. After operation, 13 cases received chemotherapy and 7 cases received radiotherapy. Reconstruction of blood vessels was performed in 3 cases, reconstruction of kinetic function in 16 cases, and repair of defect was carried out in 23 cases. RESULTS Thirty patients were followed up for 4 months to 6 years and 6 months. The clinical results showed that the local control rate of sarcoma was 80%, limb-salvage rate after reconstruction of blood vessels was 100%, the excellent and good rate after reconstruction of kinetic function was 87.5%, and the survival rate of the tissue flap of transplantation and transposition was 96%. CONCLUSION It was concluded that the reconstruction and repair after resection of soft tissue sarcoma was the extension of operative treatment, and was very important in lowering the recurrence rate and improving the life quality of the sufferings.

          Release date:2016-09-01 11:04 Export PDF Favorites Scan
        • APOPTOSIS IN HUMAN OSTEOSARCOMA CELL LINE MG63 INDUCED BY PYROPHEOPHORBIDE-a METHYL ESTER-MEDIATED PHOTODYNAMIC THERAPY

          Objective To explore the effect of pyropheophorbide-a methyl ester-mediated photodynamic therapy (MPPa-PDT) on the apoptosis in human osteosarcoma cell line MG63 and the underlying mechanism. Methods Human osteosarcoma MG63 cells in logarithmic growth phase were divided into 4 groups: blank control group (control group), the MPPa treatment group (MPPa group), the light irradiation group (LED group), and MPPa-PDT treatment group (MPPa-PDT group). MPPa-PDT group and MPPa group were incubated with MPPa (0.75?μmol/ L) for 20 hours in dark condition; control group and LED group were incubated with equal volume of fresh medium for 20 hours in the same condition. After washing with PBS and replacement with fresh culture medium, LED group and MPPa-PDT group cells were exposed to light (4.8 J/cm2) for 120 seconds. After light exposure, all groups were cultured in dark condition again. Then cellular morphology changes were observed by an inverted phase contrast microscopy, endoplasmic reticulum morphology changes were observed by transmission electron microscopy, cellular apoptosis was detected by Hoechst33258 nuclear staining, cell apoptotic rate and the levels of Ca in cells were analyzed by flow cytometry, the expression of p-PERK, C/EBP homologous protein (CHOP), cleaved-Caspase-12 were assayed by Western blot. Results In MPPa-PDT group, the retracted and round cells were observed; Hoechst33258 nuclear staining showed nuclear condensation, fragmentation, and other typical apoptotic morphological changes; the cell apoptotic rate (48.76%±3.54%) was significantly higher than that of control group (5.04%±0.41%), MPPa group (5.33%±0.38%), and LED group (6.48%±0.46%) (P < 0.05); the levels of Ca2+ in cells (485.29±58.77) was also significantly higher than that of control group (97.24±4.77), MPPa group (97.95±6.30), and LED group (101.17±5.26) (P < 0.05); swelling endoplasmic reticulum was observed under transmission electron microscope; the expressions of p-PERK, CHOP, and cleaved-Caspase-12 gradually increased at 1, 3, and 6 hours after treatment respectively, which were significantly higher than those of the other groups (P < 0.05). There was no typical apoptotic morphological changes and endoplasmic reticulum morphological changes in control group, MPPa group, and LED group, and there was no significant difference in the above indexes among 3 groups (P > 0.05). Conclusion MPPa-PDT can significantly induce apoptosis in MG63 cells. The endoplasmic reticulum stress pathway is involved in the MPPa-PDT induced apoptosis.

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        • Clinical Analysis of Eight Patients with Pulmonary Artery Sarcoma

          Objective To improve the knowledge of pulmonary artery sarcoma ( PAS) and early diagnosis.Methods The clinical data of 8 patients with PAS confirmed by biopsy from April 2001 to April 2012 in Beijing Anzhen Hospital were retrospectively analyzed. Results There were 5 males and 3 females, with mean age of 46. 75 ±11. 47 years [ range: 32-67 years] . The main clinical manifestations were chest tightness, shortness of breath, intermittent syncope, heart palpitations at exertion, etc. Laboratory examinations showed the patients with PAS have no obvious hypoxemia and most of them have normal D-dimer level. Echocardiography revealed pulmonary hypertension, right ventricular enlargement, and echo of massive lumps in main pulmonary truck. Lower limb veins were normal in color doppler ultrasonography. Chest X-ray revealed prominent pulmonary artery segment, full segment of the right pulmonary artery, an increased hilum and pleural effusion. CT pulmonary angiography showed expansion of pulmonary artery, large filling defect in main pulmonary truck and left or right pulmonary artery, combined with pericardial effusion, pleural effusion. Lung ventilation/perfusion imaging did not match, showing radioactive sparse and defects in multiple lung segments and subsegments, involved 3 to 13 lung segments. Pulmonary angiography showed filling defects in the main pulmonary artery, left or right pulmonary artery. 8 patients were confirmed pathologically after operation. Pathological results showed leiomyosarcoma differentiation in 3 cases, undifferentiated sarcoma in2 cases, and undefined pathological type in 3 cases. All 8 patients were misdiagnosed as pulmonary embolism before surgery. The average days of misdiagnosis were 85. 6 ±21. 5 days. 7 cases were given simple surgical resection, one case underwent surgical resection combined with radiotherapy and chemotherapy. 7 cases were relieved and discharged, and one case died. Conclusion PAS is a rare disease clinically and is easily misdiagnosed as pulmonary embolism. Clinicians should enhance the recognition in order to diagnose early and treat comprehensively.

          Release date:2016-09-13 03:51 Export PDF Favorites Scan
        • Predictive factors for recurrence of retroperitoneal sarcoma

          ObjectiveTo summarize the predictive factors of recurrence of retroperitoneal sarcoma.MethodsThe literatures on the recurrence of retroperitoneal sarcoma at home and abroad were reviewed and analyzed.ResultsTumor size, margin negative resection, tumor grade, multifocal, and histological types were important predictors of the recurrence of retroperitoneal sarcoma. In addition, combined organ resection, diversity of tumor growth patterns, and tumor-free surgical techniques could also affect the recurrence of retroperitoneal sarcoma.ConclusionUnderstanding the predictive factors of the recurrence of retroperitoneal sarcoma is of great significance to guide surgeons to understand and recognize the disease, to reduce the recurrence of retroperitoneal sarcoma.

          Release date:2019-09-26 10:54 Export PDF Favorites Scan
        • EXTENDIBLE REPLACEMENT OF THE DISTAL FEMUR IN THE TREATMENT OF OSTEOSARCOMA IN GROWING INDIVIDUALS

          Objective To investigate the possibility of using extendible distal femoral replacements in the treatment of osteosarcoma in growing individuals. Methods From December 1999 to March 2003, 3 cases (2 were typeⅡB, 1 was type ⅡA) with osteosarcoma were treated byextendible distal femoral replacements. Of the 3 cases, 2 underwent prosthesis extention operation, 1 was not operated. Results After the removal of tumor, the extremities of 2 patients were shortened by 4 to 5 cm within 2 to 3 years. After the lengthening procedure, the affected extremities were of equal length to the unaffected extremities and no drag symptoms of blood vessel and nerves were observed. Follow-up was done for 2 months to 3 years. There was no aseptic loosening. The function of joints was fairly good. Conclusion Extendible distal femoral replacements is an easy, convenient, and effective way to treat osteosarcoma. 

          Release date:2016-09-01 09:29 Export PDF Favorites Scan
        • Clinical Analysis of Thyroid Carcinoma in 5 Cases

          目的探討甲狀腺肉瘤的診斷與治療。 方法回顧性分析2008年1月至2013年8月期間貴陽醫學院附屬醫院甲狀腺外科和貴州腫瘤醫院甲狀腺外科收治的5例甲狀腺肉瘤患者的臨床資料。 結果5例患者均行根治性手術,3例行術后化療及放療。術后均未發生聲音嘶啞、呼吸困難、嗆咳、肺部感染等并發癥,切口均甲級愈合。經病理學免疫組化檢查,具體分型為甲狀腺組織細胞肉瘤1例,甲狀腺血管肉瘤2例,甲狀腺平滑肌肉瘤1例,甲狀腺未分化肉瘤1例;波形蛋白(Vimentin)陽性5例,角蛋白(CK)陽性2例,平滑肌肌動蛋白(SMA)、結蛋白(Des)及S-100各陽性1例,甲狀腺球蛋白(TG)、上皮膜抗原(EMA)、甲狀腺轉錄因子(TTF)及降鈣素均為陰性。術后5例患者均經電話隨訪,隨訪時間3~9個月,中位數為6個月。隨訪期間,3例患者因復發和轉移而死亡;余2例仍在化療及放療中,無復發及轉移。 結論甲狀腺肉瘤的惡性程度高,宜采用以手術為主的綜合治療方案。

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        • 1例誤診為非哺乳期乳腺炎的原發性乳腺血管肉瘤并文獻復習

          目的通過回顧分析1例被誤診為非哺乳期乳腺炎的原發性乳腺血管肉瘤患者資料,結合國內外文獻,對乳腺血管肉瘤疾病特征及診治要點進行總結,提供臨床診治參考,避免誤診。方法回顧性分析該例患者的臨床表現、診療經過、輔助檢查及病理特點;檢索相關中英文文獻資料,綜合分析文獻報道病例特點。結果該例患者初始表現為乳房脹痛,查體可見乳房腫脹,彩超及鉬靶檢查考慮乳腺炎性病變,前2次病理活檢未提示惡性病變。腫瘤明顯長大突出皮膚表面后行第3次活檢確診。總結文獻報道病例資料,乳腺原發性血管肉瘤為罕見的乳腺惡性病變,手術為主要治療方式,無標準化療、放療及靶向治療方案。結論乳腺血管肉瘤惡性程度高,遠期生存率低,模仿了乳腺多種良性疾病的生長模式。乳腺彩超及鉬靶X線攝片無特征性改變,易延誤診治,病理活檢為確診依據。結合臨床表現及輔助檢查確診后應盡早治療,可改善預后。

          Release date:2023-12-26 06:00 Export PDF Favorites Scan
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