期刊文献+
共找到16篇文章
< 1 >
每页显示 20 50 100
1例睾丸未成熟型畸胎瘤伴精原细胞瘤的临床分析 被引量:5
1
作者 徐振群 田保玲 +2 位作者 詹运洪 霍军 吴斌 《中华男科学杂志》 CAS CSCD 北大核心 2011年第2期177-178,共2页
睾丸未成熟型畸胎瘤伴精原细胞瘤临床少见,2009年本院收治1例,现报告如下。 1临床资料患者,男,48岁,以左隐睾牵引固定术后41年,左睾丸不适半年,发现左睾丸增大2个月为主诉入院。
关键词 睾丸肿 混合肿 未成熟型畸胎瘤 精原细胞
下载PDF
关于卵巢成熟型畸胎瘤与未成熟型畸胎瘤的鉴别诊断(附27例病例分析) 被引量:4
2
作者 王学慧 于晓辉 +1 位作者 朱芳 卜秀华 《中国厂矿医学》 2003年第5期376-377,共2页
目的 :通过对 2 7例卵巢畸胎瘤病人 ,进行术前的影像学及肿瘤标志物检查 ,探讨鉴别诊断成熟型畸胎瘤与未成熟型畸胎瘤的可靠方法。方法 :成熟型畸胎瘤 2 0例 ,未成熟型畸胎瘤 7例。所有病人术前均行B超、CT及甲胎蛋白 (AFP)等检查。结... 目的 :通过对 2 7例卵巢畸胎瘤病人 ,进行术前的影像学及肿瘤标志物检查 ,探讨鉴别诊断成熟型畸胎瘤与未成熟型畸胎瘤的可靠方法。方法 :成熟型畸胎瘤 2 0例 ,未成熟型畸胎瘤 7例。所有病人术前均行B超、CT及甲胎蛋白 (AFP)等检查。结果 :所有畸胎瘤病人B超显示混合性影像 ,成熟型畸胎瘤边界光滑完整 ;但是未成熟型畸胎瘤多见形态不规则的实质光团。CT检查 ,未成熟型畸胎瘤都有散在钙化灶。以肿瘤影像中钙化灶总数与肿瘤最大径的平方之比为指标〔1〕,成熟型畸胎瘤 0 .64 0± 0 .0 5 0 ,未成熟型畸胎瘤 0 .170± 0 .0 84,两者比较差异具有显著性 (P <0 .0 0 1)。取AFP值的自然对数值 ,成熟型畸胎瘤 1.0 0± 0 .3 8,未成熟型畸胎瘤 3 .3 8± 2 .41,两者比较差异具有显著性 (P =0 .0 47)。结论 :卵巢畸胎瘤病人 ,术前综合检查、分析B超、CT以及AFP等 ,正确地鉴别成熟型畸胎瘤与未成熟型畸胎瘤 ,为选择最适宜的手术方式及治疗方法提供科学依据。 展开更多
关键词 卵巢成熟畸胎 卵巢未成熟型畸胎瘤 鉴别诊断 病例分析 标志物
下载PDF
儿童卵巢未成熟型畸胎瘤合并始基子宫1例
3
作者 吴晓华 程湘 《重庆医学》 CAS CSCD 北大核心 2010年第4期510-511,共2页
关键词 卵巢未成熟型畸胎瘤 始基子宫 儿童 尿路刺激症状 入院检查 抗感染治疗 下腹痛 临床资料
下载PDF
早孕合并巨大卵巢未成熟型畸胎瘤1例 被引量:2
4
作者 蔡少雨 《基层医学论坛》 2008年第11期384-384,共1页
1临床病例患者,女,30岁,因"停经9周,检查发现腹部巨大包块1d"入院。患者平素月经规则3/30d,量中,色鲜红,无痛经,本次月经2006年11月28日,性质同前,患者无腹痛、腹胀,无阴道流血、头晕、心悸、气促等不适。
关键词 卵巢未成熟型畸胎瘤 早孕 临床病例 阴道流血 月经
下载PDF
未成熟型畸胎瘤混有内胚窦瘤成份一例报道
5
作者 汪晓婷 郭盖章 詹荣举 《腹部外科》 2008年第3期147-147,共1页
关键词 未成熟型畸胎瘤 内胚窦 腹部包块 移动性浊音 排便异常 阴道出血 体格检查 腹部膨隆
下载PDF
腹膜后未成熟型畸胎瘤超声误诊为多囊肾1例
6
作者 陈彦红 许春梅 韦玲华 《中国超声诊断杂志》 2001年第9期61-62,共2页
胎儿,女性.当胎龄34周例行产前检查时,B超发现胎儿左肾增大,为40mm×31mm多囊状结构,内见多个小液性暗区,最大为11mm×13mm,暗区似相通.右肾大小36mm×18mm,未见异常.拟诊胎儿左侧多囊肾?肾积水?见图1.
关键词 腹膜后肿 未成熟型畸胎瘤 超声诊断 误诊 多囊肾
下载PDF
胎儿骶尾部巨大未成熟型畸胎瘤1例
7
作者 韦景平 《浙江预防医学》 2002年第9期55-55,共1页
关键词 胎儿 骶尾部巨大未成熟型畸胎瘤 病例报告 诊断 骶尾部肿
下载PDF
单纯性卵巢未成熟型畸胎瘤33例临床病理分析
8
作者 乔国霞 《河南外科学杂志》 2009年第5期74-75,共2页
关键词 卵巢未成熟型畸胎瘤 单纯性 病理分级Ⅰ级 神经上皮 感觉上皮 附件切除 转移 癌转移 原发肿 复发 临床分期 连利娟 子宫 女生殖器
下载PDF
婴幼儿四脑室未成熟型畸胎瘤1例
9
作者 高进喜 陈乃洁 +1 位作者 郑兆聪 王守森 《福州总医院学报》 2011年第B09期328-329,共2页
畸胎瘤是由一个以上胚层来源的含多种组织的异位瘤.颅内畸胎瘤较为少见,占婴幼儿畸胎瘤的2%-5%,约占所有颅内肿瘤的0.3%~0.6%,多发生在中线部位。常见于松果体区及鞍上区,第四脑室畸胎瘤少见。我科于2011年1月收治婴幼儿第... 畸胎瘤是由一个以上胚层来源的含多种组织的异位瘤.颅内畸胎瘤较为少见,占婴幼儿畸胎瘤的2%-5%,约占所有颅内肿瘤的0.3%~0.6%,多发生在中线部位。常见于松果体区及鞍上区,第四脑室畸胎瘤少见。我科于2011年1月收治婴幼儿第四脑室巨大型未成熟型畸胎瘤1例。治疗效果良好,结合相关文献分析如下。 展开更多
关键词 未成熟型畸胎瘤 幼儿四脑室 颅内畸胎 脑室畸胎 颅内肿 松果体区 第四脑室 治疗效果
原文传递
卵巢未成熟型畸胎瘤肝转移超声表现一例
10
作者 陈凤玲 王建敏 饶忠云 《中华医学超声杂志(电子版)》 2012年第4期29-29,共1页
患者女,33岁,自幼生活在牧区,3年前行左侧附件肿块切除,病理诊断为未成熟型畸胎瘤,术后化疗3次,近日转我院检查。超声检查示:肝右叶近膈顶处可探及一范围71mm×65mm异常回声团块(图1),边界清楚,由多个大小不等的强回声... 患者女,33岁,自幼生活在牧区,3年前行左侧附件肿块切除,病理诊断为未成熟型畸胎瘤,术后化疗3次,近日转我院检查。超声检查示:肝右叶近膈顶处可探及一范围71mm×65mm异常回声团块(图1),边界清楚,由多个大小不等的强回声团组成,且强回声区呈厚壁不规整,其内可见斑片状钙化灶。 展开更多
关键词 卵巢未成熟型畸胎瘤 超声表现 肝转移 超声检查 肿块切除 病理诊断 术后化疗 异常回声
原文传递
胰腺成熟型囊性畸胎瘤一例并文献回顾
11
作者 胡昊 何天霖 +1 位作者 程鹏 王斐 《中华胰腺病杂志》 CAS 2017年第5期338-339,共2页
胰腺成熟型囊性畸胎瘤,或者叫胰腺皮样囊肿,是一种极为罕见的胰腺肿瘤。自1918年Kerr首次报道以来,目前全世界仅有30余例报道。畸胎瘤来源于生殖细胞,是生殖细胞肿瘤中常见的一种,根据病理学可以分为成熟型畸胎瘤、未成熟型畸胎瘤... 胰腺成熟型囊性畸胎瘤,或者叫胰腺皮样囊肿,是一种极为罕见的胰腺肿瘤。自1918年Kerr首次报道以来,目前全世界仅有30余例报道。畸胎瘤来源于生殖细胞,是生殖细胞肿瘤中常见的一种,根据病理学可以分为成熟型畸胎瘤、未成熟型畸胎瘤和特殊类型畸胎瘤。其中成熟型畸胎瘤又分为实性或囊性,可含有多种组织成分,如毛发、牙齿、汗腺、神经等。成熟型囊性畸胎瘤最好发于卵巢,也可以发生于外胚层细胞迁移的任何部位,如睾丸、颅骨、脑、纵隔、大网膜、腹膜后和骶尾区,尤以身体中线附近为主,以胰腺来源的成熟型囊性畸胎瘤最为罕见。上海长海医院收治了1例胰腺成熟型囊性畸胎瘤患者,并结合文献进行回顾性分析,现报道如下。 展开更多
关键词 成熟囊性畸胎 胰腺肿 文献回顾 未成熟型畸胎瘤 生殖细胞肿 上海长海医院 皮样囊肿 组织成分
原文传递
CEA、CA125、CA199、HE4和AFP在185例卵巢畸胎瘤的表达分析 被引量:8
12
作者 段拽林 赵瑞霞 +5 位作者 魏丽军 郭勇峰 张瑶 路娜 王洁 唐松梅 《肿瘤学杂志》 CAS 2021年第8期686-689,共4页
[目的]分析CEA、CA125、CA199、HE4、AFP在成熟型畸胎瘤与未成熟型畸胎瘤患者中的表达,探讨鉴别两者的有效肿瘤学标志物。[方法]收集2016年1月至2021年3月山西省肿瘤医院妇科收治的134例卵巢成熟型畸胎瘤和51例未成熟型畸胎瘤患者的临... [目的]分析CEA、CA125、CA199、HE4、AFP在成熟型畸胎瘤与未成熟型畸胎瘤患者中的表达,探讨鉴别两者的有效肿瘤学标志物。[方法]收集2016年1月至2021年3月山西省肿瘤医院妇科收治的134例卵巢成熟型畸胎瘤和51例未成熟型畸胎瘤患者的临床资料,分析CEA、CA125、CA199、HE4、AFP在两组间的阳性表达率,计算各指标分别及联合诊断未成熟组的灵敏度、特异性,并绘制ROC曲线。[结果]血清CEA、CA125、AFP阳性表达率在两组间差异有统计学意义(P<0.05),CA199、HE4阳性表达率在两组间差异无统计学意义(P>0.05)。CEA、CA125、HE4、AFP在未成熟组中表达的灵敏度均<50%。CA125诊断未成熟型畸胎瘤的特异性为87.5%,其余3项均为100%。CA199在未成熟组表达的灵敏度为64.7%,但特异性只有24.7%。联合检测在未成熟组中表达的灵敏度高达92%,特异性为100%。CEA、CA125、CA199、HE4、AFP单独及联合诊断未成熟畸胎瘤的ROC曲线下面积(AUC值)分别为0.764、0.791、0.692、0.678、0.687、0.898。[结论]联合检测5种标志物在术前诊断卵巢未成熟型畸胎瘤具有一定的准确性。 展开更多
关键词 学标志物 卵巢未成熟型畸胎瘤 卵巢成熟畸胎 鉴别诊断
原文传递
新生儿畸胎瘤2例并文献复习 被引量:2
13
作者 郝磊 吴秋珍 +3 位作者 刘晓涛 韩茉 卢书信 王桂芝 《中国临床研究》 CAS 2022年第1期97-100,共4页
新生儿成熟型畸胎瘤好发部位在骶尾部,大多为良性,但不及时手术存在恶变的风险。鼻咽部未成熟畸胎瘤较少见,病因可能与胚胎期的发育障碍或异常、遗传和环境的因素有关。通过实验室及影像学检查、临床表现等不难做出早期诊断,行手术或联... 新生儿成熟型畸胎瘤好发部位在骶尾部,大多为良性,但不及时手术存在恶变的风险。鼻咽部未成熟畸胎瘤较少见,病因可能与胚胎期的发育障碍或异常、遗传和环境的因素有关。通过实验室及影像学检查、临床表现等不难做出早期诊断,行手术或联合化疗要考虑新生儿的生理、代谢状况及对以后生长发育的影响。2019年至2020年河南省省立医院诊治2例新生儿畸胎瘤患儿,其中1例足月儿骶尾部畸胎瘤(sacrococcygeal teratoma,SCT),另1例早产儿鼻咽部畸胎瘤(nasopharyngeal teratoma,NPT)。 展开更多
关键词 畸胎 成熟 成熟 骶尾部 鼻咽部 新生儿 甲胎蛋白
原文传递
Characteristics, diagnosis and treatment of hepatic metastasis of pure immature ovarian teratoma 被引量:1
14
作者 樊庆泊 黄惠芳 +1 位作者 连利娟 郎景和 《Chinese Medical Journal》 SCIE CAS CSCD 2001年第5期58-61,107,共5页
Objective To analyze the characteristics of hepatic metastasis of pure immature ovarian teratoma and explore its proper diagnosis and treatment.Methods Eighteen cases of hepatic metastasis of pure immature ovarian ter... Objective To analyze the characteristics of hepatic metastasis of pure immature ovarian teratoma and explore its proper diagnosis and treatment.Methods Eighteen cases of hepatic metastasis of pure immature ovarian teratoma were included in this study. The clinical stage, operation, chemotherapy and histopathology of primary and secondary tumors as well as the data from long term follow-ups were analyzed retrospectively,Results All of the hepatic metastatic tumors were located on the surface of the liver. 61.1% (11/18) of them were clinical stage Ⅲ and 44.4% (8/18) were grade 1 at first operation. The hepatic metastatic rate was 16.7% (3/18) in the standard adjuvant chemotherapy group but increased markedly to 31.2% (15/48) in the irregular chemotherapy group. Auxiliary diagnostic methods could not indicate the correct results. The surgical resection rate of hepatic metastasis of pure immature ovarian teratoma was 94.4% (17/18). There were less complications in the group with tumor diameter less than 15 cm. The follow-up time ranged from 3 to 205 months with a mean of 20.9 months. The 3-year-survival rate was 77.8% (14/ 18), and mortality rate was 22.2%. The 5- and 10-year-survival rate was 55.6% (10/18) and 38.9% (7/18), respectively. The rate of loss in follow-up was 22.2% (4/18) and 38.9% (7/18), respectively, and one patient has survived for more than 17 years.Conclusions The hepatic metastatic rate of pure immature ovarian teratoma could be decreased using standard adjuvant chemotherapy. Suitable surgical treatment could reduce complications and improve the prognosis for patients. 展开更多
关键词 immature ovarian teratoma · hepatic metastasis
原文传递
Retrospective analysis of 67 consecutive cases of pure ovarian immature teratoma 被引量:1
15
作者 李洪君 洪婉君 +3 位作者 张蓉 吴令英 刘丽影 章文华 《Chinese Medical Journal》 SCIE CAS CSCD 2002年第10期1496-1500,共5页
OBJECTIVE: To investigate the development regularity, treatment methods and prognosis of ovary immature teratoma (POIT). METHODS: Sixty-seven patients with POIT, admitted from 1958 to 1998, were retrospectively analyz... OBJECTIVE: To investigate the development regularity, treatment methods and prognosis of ovary immature teratoma (POIT). METHODS: Sixty-seven patients with POIT, admitted from 1958 to 1998, were retrospectively analyzed. There were 31 patients with stage I, 4 with stage II, 2 with stage III and 1 with stage IV lesions. Twenty-seven patients had recurrences and 2 had distant metastases. Unilateral adnexectomy was performed for stage I lesions. From the 1980s, this was followed by four-cycles of combination chemotherapy (VAC, PVB or BEP x 3 cycles) as post-operative adjuvant therapy. Combined chemotherapy and multiple operations were performed for advanced and recurrent lesions. RESULTS: The overall survival rate was 75% (50/67). However, there was a remarkable difference in the results from the various periods. From 1958 to 1983, the 5-year survival rate was 40% (6/15), and it was raised to 79% (26/33) from 1984 to 1993. In the period 1994 to 1998, 95% (18/19)of patients were rescued. Thirty-five patients who had early lesions (stage I and II) had a 5-year survival rate of 91.4% (32/35). Thirty-two patients with recurrent or advanced lesions had a 5-years survival rate of 56% (18/32). There were 8 patients with grade III tumors and their 5-year survival rate was only 25% (2/8). The chief prognostic factors for this disease are clinical stage, pathological grade and adequate treatment. CONCLUSION: POIT is a potentially curable disease in today's practice. It is characterized by the fact that recurrent tumors may be converted back to mature ones as time goes on. With chemotherapy, these is a good opportunity to rescue those patients with recurrent tumors. At present, treatment of POIT gives the most satisfactory results among all malignant ovarian germ cell tumor types. Tests of serum specific tumor markers (CA19-9, AFP, CA125, CEA) performed preoperatively or before chemotherapy and during follow-up have been found helpful in the evaluation of prognosis. 展开更多
关键词 ADOLESCENT Adult CHILD Child Preschool Female Humans Neoplasm Staging Ovarian Neoplasms Prognosis Retrospective Studies Survival Rate TERATOMA Tumor Markers Biological
原文传递
Retrospective analysis of 67 consecutive cases of pure ovarian immature teratoma
16
作者 李洪君 洪婉君 +3 位作者 张蓉 吴令英 刘丽影 章文华 《Chinese Medical Journal》 SCIE CAS CSCD 2002年第10期56-60,148,共6页
To investigate the development regularity, treatment methods and prognosis of ovary immature teratoma (POIT) Methods Sixty seven patients with POIT, admitted from 1958 to 1998, were retrospectively analyzed There... To investigate the development regularity, treatment methods and prognosis of ovary immature teratoma (POIT) Methods Sixty seven patients with POIT, admitted from 1958 to 1998, were retrospectively analyzed There were 31 patients with stage Ⅰ, 4 with stage Ⅱ, 2 with stage Ⅲ and 1 with stage Ⅳ lesions Twenty seven patients had recurrences and 2 had distant metastases Unilateral adnexectomy was performed for stage Ⅰ lesions From the 1980s, this was followed by four cycles of combination chemotherapy (VAC, PVB or BEP×3 cycles) as post operative adjuvant therapy Combined chemotherapy and multiple operations were performed for advanced and recurrent lesions Results The overall survival rate was 75% (50/67) However, there was a remarkable difference in the results from the various periods From 1958 to 1983, the 5 year survival rate was 40% (6/15), and it was raised to 79% (26/33) from 1984 to 1993 In the period 1994 to 1998, 95% (18/19)of patients were rescued Thirty five patients who had early lesions (stage Ⅰ and Ⅱ) had a 5 year survival rate of 91 4% (32/35) Thirty two patients with recurrent or advanced lesions had a 5 years survival rate of 56% (18/32) There were 8 patients with grade Ⅲ tumors and their 5 year survival rate was only 25% (2/8) The chief prognostic factors for this disease are clinical stage, pathological grade and adequate treatment Conclusion POIT is a potentially curable disease in today’s practice It is characterized by the fact that recurrent tumors may be converted back to mature ones as time goes on With chemotherapy, these is a good opportunity to rescue those patients with recurrent tumors At present, treatment of POIT gives the most satisfactory results among all malignant ovarian germ cell tumor types Tests of serum specific tumor markers (CA19 9, AFP, CA125, CEA) performed preoperatively or before chemotherapy and during follow up have been found helpful in the evaluation of prognosis 展开更多
关键词 pure ovarian immature teratoma · surgery · chemotherapy · prognostic factors · combination treatment
全文增补中
上一页 1 下一页 到第
使用帮助 返回顶部