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find Keyword "肉瘤样癌" 6 results
  • Effects of Gefitinib in Treatment of Sarcomatoid Carcinoma of Lung:A Case Report and Literature Review

    Objective To investigate the effects of gefitinib in the treatment of sarcomatoid carcinoma. Methods Clinical data of a case of sarcomatoid carcinoma was analyzed and related literatures were reviewed.Results A patient with sarcomatoid carcinoma was admitted with progressive dry cough,chest pain and dyspnea for 3 months. The patient was diagnosed as lung sarcomatoid carcinoma by thoracoscopy and treated with gefitinib. After 2 weeks treatment, symptoms disappeared and tumor was stable for 4 months. Literatures review suggested that sarcomatoid carcinoma is a rare malignant tumor. Treatment of sarcomatoid carcinoma includes surgery, chemotherapy and radiotherapy, but these methods show little effect in advanced patients. In our case, the patient with sarcomatoid carcinoma in stage Ⅳ was treated by gefitinib and showed favourable effect. Conclusions Advanced sarcomatoid carcinoma patients have a short life span and poor life quality. Gefitinib may provide these patients a feasible therapeutic approach.

    Release date:2016-09-13 04:00 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
  • 气管、肺、食管多原发肿瘤一例

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  • 肺肉瘤样癌10例临床分析

    目的通过分析肺肉瘤样癌的临床表现、影像学和病理特点及治疗转归, 增加对其认识, 提高对它的诊断和治疗。 方法回顾性分析我院2011年6月至2013年10月经住院治疗并得到病理诊断的10例肺肉瘤样癌患者的临床资料。 结果10例患者中男6例, 女4例。发病年龄40~73(57.1±11.0)岁。6例有吸烟史。临床症状与其他类型非小细胞肺癌无明显差别。经组织病理均诊断为肺肉瘤样癌。8例接受手术治疗, 2例因不能手术直接行化疗。10例患者中ⅠA期4例, ⅠB期1例, ⅡA期1例, ⅡB期1例, ⅢA期1例, Ⅳ期2例。8例术后患者4例行化疗, 现今存活; 4例未化疗, 2例术后半年死亡, 2例IA期患者观察3个月和1年后未出现复发及转移征象。2例因转移未能手术患者中, 1例化疗2年后死亡, 1例化疗半年后存活。 结论肺肉瘤样癌是一种罕见疾病, 多发于老年吸烟男性。诊断主要依靠病理和免疫组化染色明确诊断。手术是其主要的诊断和治疗方法, 但预后较差。

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  • 食管肉瘤样癌诊治现状

    食管肉瘤样癌是一种十分罕见的食管恶性肿瘤,无特异性临床症状及体征,主要表现为吞咽梗阻、胸骨后疼痛等;其生长速度较快,常呈息肉样生长;具有上皮性癌和梭性肉瘤样细胞 2 种成分,并以肉瘤样成分占优势,其发病原因及病理组织起源目前尚未明确;免疫组织化学检测癌成分常见细胞角蛋白及上皮膜抗原表达,肉瘤样成分常见波形纤维蛋白表达;治疗方式以手术为主,对放射治疗、化学疗法(化疗)较敏感,常用化疗方案为铂类联合氟尿嘧啶类或紫杉类的双药联合方案,其早期预后较食管鳞状细胞癌好。

    Release date:2017-11-24 10:58 Export PDF Favorites Scan
  • 肺梗死样梭形细胞癌一例并文献复习

    目的 探讨肺梗死样梭形细胞癌(ISCCL)的临床病理特征、诊断及鉴别诊断。方法 分析2020年10月会诊的1例ISCCL患者的临床信息、病理组织形态以及免疫组织化学染色结果,并复习相关文献。结果 患者为49岁男性。胸部CT示右肺下叶结节,于外院行右肺下叶肿块切除术。右肺下叶肿块术后病检结果显示大片梗死样区域,其间可见短梭形异型细胞,围绕血管生长,部分区域胶原纤维增生,核分裂象少见;免疫组织化学结果显示肿瘤细胞表达广谱细胞角蛋白、上皮膜抗原、波形蛋白。病理诊断为ISCCL,行肺叶切除术辅以紫杉醇联合卡铂进行化学治疗,但效果不佳,患者拒绝进一步治疗,于术后8个月因肺癌多发骨转移死亡。结论 ISCCL是一种罕见的侵袭性恶性肿瘤,形态学特征与多种肺良恶性病变容易混淆,极易误诊、漏诊,需综合分析相鉴别。

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