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Rokitansky-Ashoff窦在胆囊疾病中病理学形态的改变——2586例胆囊的病理诊断复习与临床分析 被引量:1
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作者 李斌 张志强 盛黎黎 《海军医学杂志》 2012年第6期392-394,共3页
目的探讨Rokitansky-Ashoff窦在胆囊疾病中病理学形态改变。方法收集近年来我院手术切除胆囊标本的临床资料和病理切片,进行系统复习及分析。结果本组2586例胆囊炎中伴R-A窦形成431例,占16.67%;腺性胆囊炎357例,占13.81%;腺肌瘤211例,占... 目的探讨Rokitansky-Ashoff窦在胆囊疾病中病理学形态改变。方法收集近年来我院手术切除胆囊标本的临床资料和病理切片,进行系统复习及分析。结果本组2586例胆囊炎中伴R-A窦形成431例,占16.67%;腺性胆囊炎357例,占13.81%;腺肌瘤211例,占8.16%;腺肌瘤病259例,占10.02%;胆汁性腹膜炎3例,占0.11%;腹腔假粘液瘤1例,占0.04%;腺肌瘤恶变为胆囊癌2例,占0.08%;慢性胆囊炎急性发作167例,占6.46%;胆囊腺瘤9例,占0.35%;胆囊癌17例,占0.66%。结论 Rokitansky-Ashoff窦由于数量和伸入胆囊壁的深浅以及随之而改变的病理表现不同可有不同的诊断名称。 展开更多
关键词 rokitansky—Ashoff窦 胆囊 诊断复习 临床分析
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Vecchietti腹腔镜手术治疗Rokitansky综合征后新生阴道黏膜的结构和超微结构研究
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作者 Fedele L. Bianchi S. +1 位作者 Berlanda N. 张新艳 《世界核心医学期刊文摘(妇产科学分册)》 2006年第10期8-9,共2页
Objective: This study was undertaken to evaluate structural and ultrastructural characteristics of the mucosa of neovaginae created by Vecchietti’s laparoscopic operation for Rokitansky syndrome. Study design: Vagino... Objective: This study was undertaken to evaluate structural and ultrastructural characteristics of the mucosa of neovaginae created by Vecchietti’s laparoscopic operation for Rokitansky syndrome. Study design: Vaginoscopy and Schiller test were performed 3, 6, and 12 months after the operation in 106 patients. A biopsy specimen of the neovagina obtained 12 to 18 months after surgery in 19 patients was examined by light, scanning electron, and transmission electron microscopy. Results: At vaginoscopy, the neovaginal mucosa appeared smooth, lacking the folds that characterize the normal vagina; 12 months after the operation, an iodium-positive epithelium was present in all neovaginae. Mild ultrastructural modifications, as compared with normal vaginal mucosa, were reduced maturation, inflammatory infiltration, and tendency to superficial desquamation. Conclusion: At a 12-month follow-up, the mucosa of neovaginae created by the Vecchietti technique is comparable to the normal vaginal mucosa, with mild structural and ultrastructural modifications that we believe might be due to reduced vascularization. 展开更多
关键词 腹腔镜手术 rokitansky Vecchietti 超微结构研究 宫颈黏膜碘试验 阴道镜检查
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Mayer Rokitansky Küster Hauser Syndrome as a Cause of Infertility and Primary Amenorrhoea: A Case Report
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作者 Tidiani Traoré Hamidou Toungara +18 位作者 Famakan Kané Kassoum Sidibé Oumar S. Coulibaly Seydou Z. Dao Mamadou Touré Seydou Traoré Brahima Donigolo Babou Traoré Adama Coulibaly Abdourahamane Diarisso Birama Traoré Alima Sidibé Apha Sanogo Amadou Bocoum Seydou Fané Youssouf Traoré Ibrahim Teguété Niani Mounkoro Amadou Dolo 《Open Journal of Obstetrics and Gynecology》 2024年第12期1801-1806,共6页
Mayer Rokitansky Küster Hauser (MRKH) syndrome is a rare congenital disorder that occurs during foetal development. MRKH is characterised by agenesis of the uterus and part of the vagina. Its exact aetiology is s... Mayer Rokitansky Küster Hauser (MRKH) syndrome is a rare congenital disorder that occurs during foetal development. MRKH is characterised by agenesis of the uterus and part of the vagina. Its exact aetiology is still unknown due to the complexity of the genetic pathways involved in the embryogenetic development of the Müllerian ducts. Although these women have a female phenotype and functional ovaries, they do not have menstrual cycles. We report the rare case of a 23-year-old married woman who consulted us for primary amenorrhoea and desire for pregnancy. On assessment and investigation, it was confirmed that the patient had no uterus and a poorly developed vagina. However, she had normal functioning ovaries, and no abnormalities in other organs were detected. A multidisciplinary team provided advice on the nature of the anomaly, its implications for sex life, infertility and possible child adoption alternatives. 展开更多
关键词 rokitansky Syndrome Müllerian Ducts Uterine Agenesis
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Esophageal diverticulum:New perspectives in the era of minimally invasive endoscopic treatment 被引量:5
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作者 Hiroki Sato Manabu Takeuchi +5 位作者 Satoru Hashimoto Ken-ichi Mizuno Koichi Furukawa Akito Sato Junji Yokoyama Shuji Terai 《World Journal of Gastroenterology》 SCIE CAS 2019年第12期1457-1464,共8页
Esophageal diverticula are rare conditions that cause esophageal symptoms,such as dysphagia,regurgitation,and chest pain.They are classified according to their location and characteristic pathophysiology into three ty... Esophageal diverticula are rare conditions that cause esophageal symptoms,such as dysphagia,regurgitation,and chest pain.They are classified according to their location and characteristic pathophysiology into three types:epiphrenic diverticulum,Zenker's diverticulum,and Rokitansky diverticulum.The former two disorders take the form of protrusions,and symptomatic cases require interventional treatment.However,the esophageal anatomy presents distinct challenges to surgical resection of the diverticulum,particularly when it is located closer to the oral orifice.Since the condition itself is not malignant,minimally invasive endoscopic approaches have been developed with a focus on alleviation of symptoms.Several types of endoscopic devices and techniques are currently employed,including peroral endoscopic myotomy(POEM).However,the use of minimally invasive endoscopic approaches,like POEM,has allowed the development of new disorder called iatrogenic esophageal diverticula.In this paper,we review the pathophysiology of each type of diverticulum and the current state-of-the-art treatment based on our experience. 展开更多
关键词 DIVERTICULUM ESOPHAGUS Epiphrenic diverticulum Zenker’s diverticulum rokitansky diverticulum Iatrogenic disease Esophageal achalasia Peroral endoscopic myotomy DIVERTICULECTOMY
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胆囊腺肌增生症的多排螺旋CT的诊断特点 被引量:2
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作者 袁学文 吕敏文 +1 位作者 黄伟康 唐志伟 《实用医技杂志》 2009年第4期254-256,共3页
目的探讨胆囊腺肌增生症的CT表现特点,提高对其诊断的准确性。方法收集2005年1月至2007年12月经CT诊断并经手术和病理证实的13例胆囊腺肌增生症患者。采用16层螺旋CT作平扫及多时相增强扫描,胆囊区作2.0mm薄层重建,显示囊壁情况。结果1... 目的探讨胆囊腺肌增生症的CT表现特点,提高对其诊断的准确性。方法收集2005年1月至2007年12月经CT诊断并经手术和病理证实的13例胆囊腺肌增生症患者。采用16层螺旋CT作平扫及多时相增强扫描,胆囊区作2.0mm薄层重建,显示囊壁情况。结果13例中有2例在强化灶中可见小囊状低密影,即Rokitan-sky-Aschoff窦。依据病理,结合CT表现可分3型:①弥漫型5例;②节段型1例;③局限型7例。弥漫型及节段型CT表现:平扫胆囊壁呈明显增厚的软组织影,增强后出现"环样"强化灶。局限型表现为胆囊体部或底部呈局部增厚的软组织影,增强后出现"舌样"强化灶。结论采用多排螺旋CT多时相扫描后薄层重建,能较好地显示"二环征"、"三环征"及"舌样"强化征,这是CT诊断胆囊腺肌增生症的重要依据。 展开更多
关键词 胆囊腺肌增生症 rokitansky—Aschoff窦 CT/诊断 薄层重建
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MRKH综合征伴一侧子宫腺肌病1例并文献复习 被引量:5
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作者 董喆 冷金花 +1 位作者 戴毅 郎景和 《中国实用妇科与产科杂志》 CAS CSCD 北大核心 2009年第12期936-937,共2页
目的探讨Mayer-Rokitansky-Kuster-Hauser综合征(MRKH综合征)合并子宫腺肌病发生的可能机制及诊治方法。方法回顾性分析北京协和医院2009年4月收治的1例47岁MRKH综合征合并子宫腺肌病患者的诊治经过,并复习相关文献。结果患者表现为周... 目的探讨Mayer-Rokitansky-Kuster-Hauser综合征(MRKH综合征)合并子宫腺肌病发生的可能机制及诊治方法。方法回顾性分析北京协和医院2009年4月收治的1例47岁MRKH综合征合并子宫腺肌病患者的诊治经过,并复习相关文献。结果患者表现为周期性下腹痛10年,妇科检查发现阴道成盲端,长度6cm,无子宫。MRI检查提示盆腔实性包块。血CA125明显增高。腹腔镜探查见无正常发育子宫,右侧始基子宫,左侧子宫腺肌病孕10周左右大小。双侧卵巢输卵管正常。腹腔镜下切除左侧子宫,子宫标本切面为腺肌病改变,无内膜结构,病理提示子宫腺肌病,无内膜,雌激素受体(+)、孕激素受体(+)。结论MRKH综合征可以合并子宫腺肌病,提示子宫腺肌病的发生可能与苗勒管的残余化生有关。 展开更多
关键词 Mayer—rokitansky—Kuster—Hauser综合征 子宫腺肌病
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急性非结石性胆囊炎伴罗-阿氏窦穿孔5例误诊分析 被引量:2
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作者 邓海山 徐小平 +1 位作者 冯跃 马吉泉 《中华全科医学》 2014年第5期829-829,831,共2页
目的提高急性非结石性胆囊炎伴罗-阿氏窦穿孔术前确诊率和治愈率。方法回顾性分析5例误诊的急性非结石性胆囊炎伴罗-阿氏窦穿孔病例的临床资料。误诊为十二指肠穿孔2例,胃穿孔1例,急性胰腺炎1例,急性阑尾炎1例,2例先保守治疗后再手术探... 目的提高急性非结石性胆囊炎伴罗-阿氏窦穿孔术前确诊率和治愈率。方法回顾性分析5例误诊的急性非结石性胆囊炎伴罗-阿氏窦穿孔病例的临床资料。误诊为十二指肠穿孔2例,胃穿孔1例,急性胰腺炎1例,急性阑尾炎1例,2例先保守治疗后再手术探查,3例入院后急诊手术。术中均发现胆囊水肿及胆囊附近区域有胆汁积聚,未见胆囊坏疽及穿孔,胆囊内无结石。4例行一期胆囊切除术;1例行一期胆囊造瘘,二期胆囊切除术。结果 5例患者均治愈。结论对于不明原因的急性腹膜炎积极行超声检查和腹腔穿刺能提高急性非结石性胆囊炎伴罗-阿氏窦穿孔的确诊率。积极剖腹探查和术中选择个体化的手术方式能提高其治愈率。 展开更多
关键词 非结石性 胆囊穿孔 误诊 胆囊罗-阿氏窦(rokitansky—Aschof)
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