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食管裂孔疝

Hiatal Hernia

作者信息

Smith Ryan E., Sharma Sanjeev, Shahjehan Rai Dilawar

机构信息

University of Tennessee

Conemaugh Memorial Medical Center

Abstract

A hiatal hernia is a medical condition characterized by the abnormal protrusion of the upper part of the stomach or other internal organs through the diaphragm's hiatus. The diaphragm is a muscular structure that assists in respiration. The diaphragm has a small opening, a hiatus, through which the esophagus passes before connecting to the stomach. The region where the esophagus joins the stomach is called the "gastroesophageal junction" (GEJ). In a hiatal hernia, the stomach pushes through the diaphragmatic opening into the chest, compromising the lower esophageal sphincter (LES). This laxity of the LES may allow gastric contents and acid to back up into the esophagus, leading to gastroesophageal reflux disease (GERD). Small hiatal hernias are often asymptomatic and typically managed medically. Large hiatal hernias usually require surgery (see  Massive Hiatal Hernia). Hiatal hernias can cause symptoms such as heartburn, regurgitation, and difficulty swallowing. The condition is more common in adults than children and rarely results in life-threatening complications. However, severe hiatal hernias are typically repaired surgically through various procedures, often in conjunction with laparoscopic Nissen fundoplication. Hiatal hernias are classified into 4 types: Type I: The sliding type, representing more than 95% of hiatal hernias. This type occurs when the GEJ is displaced toward the hiatus. Type II: A paraesophageal hiatal hernia, which occurs when part of the stomach migrates into the mediastinum parallel to the esophagus. Type III: A paraesophageal hernia combined with a sliding hernia, where both the GEJ and a portion of the stomach have migrated into the mediastinum. Type IV: The stomach and an additional organ, such as the colon, small intestine, or spleen, herniate into the chest. Proper classification of this condition guides short- and long-term treatment.

摘要

食管裂孔疝是一种医学病症,其特征为胃上部或其他内部器官通过膈肌裂孔异常突出。膈肌是协助呼吸的肌肉结构。膈肌有一个小开口,即裂孔,食管在与胃相连之前穿过该裂孔。食管与胃相连的区域称为“胃食管交界”(GEJ)。在食管裂孔疝中,胃通过膈肌开口进入胸腔,使食管下括约肌(LES)受损。LES的这种松弛可能会使胃内容物和胃酸反流至食管,导致胃食管反流病(GERD)。小型食管裂孔疝通常无症状,一般通过药物治疗。大型食管裂孔疝通常需要手术治疗(见巨大食管裂孔疝)。食管裂孔疝可引起烧心、反流和吞咽困难等症状。这种病症在成年人中比儿童更常见,很少导致危及生命的并发症。然而,严重的食管裂孔疝通常通过各种手术进行修复,通常与腹腔镜尼氏胃底折叠术联合进行。食管裂孔疝分为4种类型:I型:滑动型,占食管裂孔疝的95%以上。当GEJ向裂孔移位时发生这种类型。II型:食管旁裂孔疝,当胃的一部分平行于食管移入纵隔时发生。III型:食管旁疝合并滑动疝,GEJ和部分胃均已移入纵隔。IV型:胃和另一个器官,如结肠、小肠或脾脏,疝入胸腔。对这种病症进行正确分类有助于指导短期和长期治疗。

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