首页> 美国卫生研究院文献>SpringerPlus >An atypical lateral hernia and concomitant inguinal and umbilical hernias in a patient with polycystic kidney disease and an intracranial aneurysm – a combined approach of clinical and radiological investigation endoscopic hernia repair and anatomical cadaver model documentation and a systematic review of the literature
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An atypical lateral hernia and concomitant inguinal and umbilical hernias in a patient with polycystic kidney disease and an intracranial aneurysm – a combined approach of clinical and radiological investigation endoscopic hernia repair and anatomical cadaver model documentation and a systematic review of the literature

机译:多囊肾疾病和颅内动脉瘤患者的非典型性外侧疝以及伴随的腹股沟和脐疝–临床和放射学检查内窥镜疝修补和解剖尸体模型文献的结合方法以及对文献的系统评价

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摘要

Atypical hernias are difficult to diagnose due to their rarity and often unspecific symptoms. In the literature there exist hints to peri-inguinal hernias, i.e. direct lateral hernia, but most of them are forms of Spigelian hernias. Since the majority were described during the first half of the past century or even earlier, only very few cases have been documented using modern diagnostic techniques. We report a unique case of a 51 year old patient presenting with an atypical inguinal hernia with concomitant inguinal and umbilical hernias in combination with cystic kidney disease and intracranial aneurysm. The atypical position of the hernia was assumed from clinical inspection, ultrasound and CT scan and verified during pre-peritoneoscopy. Using an anatomical cadaver dissection approach, we followed the unusual position of the hernia through the abdominal wall below the aponeurosis of the external oblique muscle. After a thorough literature search, we assume that the present hernia containing a hernial sac has not been documented before, especially not in such a multidisciplinary approach comprising radiological, surgical and anatomical localisation and endoscopic treatment in a patient with a clinical situation being aggravated by large cystic kidneys leading to dialysis-dependency. Rare hernias have been described as being often associated with concomitant inguinal or other hernias, a predisposition for the male gender and a pathogenic mechanism related to other soft tissue defects such as cystic kidney disease or cranial aneurysm. Thus, we consider this a unique case that has not been documented in this constellation previously, which may increase the awareness for these rare hernias.
机译:非典型疝由于其稀有性和通常不明确的症状而难以诊断。在文献中存在提示周围神经疝的提示,即直接外侧疝,但其中大多数是斯皮杰尔疝的形式。由于大多数描述是在上个世纪上半叶或更早的时期进行的,因此使用现代诊断技术记录的病例很少。我们报告了一个独特的病例,其中一名51岁的患者表现为非典型的腹股沟疝,伴有腹股沟和脐疝,伴有囊性肾脏疾病和颅内动脉瘤。通过临床检查,超声检查和CT扫描确定疝的非典型位置,并在腹膜镜检查前对其进行验证。使用解剖尸体解剖方法,我们通过外部斜肌腱膜下方的腹壁跟踪疝的异常位置。经过全面的文献搜索后,我们认为以前没有记录包含疝囊的当前疝气,尤其是在临床情况严重恶化的患者中,这种包括放射学,手术和解剖学定位以及内窥镜治疗的多学科方法,尤其如此囊性肾脏导致透析依赖性。罕见的疝气被描述为常与腹股沟或其他疝气相关,是男性的易感性以及与其他软组织缺陷(如囊性肾病或颅内动脉瘤)有关的致病机制。因此,我们认为这是一个独特的病例,以前在这个星座中没有记录过,这可能会增加对这些罕见疝气的认识。

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