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里氏型复发性间接腹股沟疝,极为罕见病例报告

Richter's Type Recurrent Indirect Inguinal Hernia, an Extremely Rare Occurrence: A Case Report.

作者信息

Bayeh Agegnehu, Limenh Simachew

机构信息

Department of Surgery, College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, Ethiopia.

Department of Midwifery, College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, Ethiopia.

出版信息

Open Access Emerg Med. 2022 Jul 8;14:323-326. doi: 10.2147/OAEM.S363212. eCollection 2022.

Abstract

BACKGROUND

Richter's type recurrent indirect inguinal hernia remains to be an extremely rare entity reported scarcely. It may present with grave complications in the absence of symptoms and signs of intestinal obstruction. The aim of this study is to report a rare case of Richter's hernia after a previously repaired indirect inguinal hernia.

CASE PRESENTATION

A 31-year-old male farmer came up with complaints of colicky abdominal pain and two episodes of vomiting. He had a previous right inguinal surgery. A physical examination revealed a full abdomen with right inguinal tenderness and oblique surgical scar. Abdominal ultrasound showed a bowel segment entrapped in the deep inguinal ring of the inguinal canal. Right inguinal exploration was done, and the finding was a gangrenous Richter's type recurrent indirect inguinal hernia. The patient was discharged and improved on the seventh post-operative day after resection and anastomosis.

DISCUSSION

Richter's hernia is a rare form of hernia that occurs when the anti-mesenteric border of the bowel is partly trapped in a tight hernial ring. Its rarity, combined with the fact that it may present in the absence of typical symptoms and signs of intestinal obstruction and local physical findings, poses a diagnostic challenge which often end up with complications like gangrenous bowel at the time of diagnosis.

CONCLUSION

Richter's hernia can occur in an extremely rare form as Richter's type recurrent indirect inguinal hernia. A high degree of suspicion, an early referral and timely imaging on the provider's side may prevent mortality and morbidity.

摘要

背景

里氏型复发性腹股沟斜疝仍然是一种极为罕见的疾病,鲜有报道。在没有肠梗阻症状和体征的情况下,它可能会出现严重并发症。本研究的目的是报告一例既往修补过腹股沟斜疝后发生的罕见里氏疝病例。

病例介绍

一名31岁男性农民,主诉有绞痛性腹痛和两次呕吐。他曾接受过右侧腹股沟手术。体格检查发现全腹,右侧腹股沟压痛,有斜行手术瘢痕。腹部超声显示一段肠管被困在腹股沟管的深环处。进行了右侧腹股沟探查,发现是坏疽性里氏型复发性腹股沟斜疝。患者在切除吻合术后第七天出院,情况好转。

讨论

里氏疝是一种罕见的疝类型,当肠管的对系膜缘部分被困在紧密的疝环中时发生。其罕见性,再加上它可能在没有典型肠梗阻症状和体征以及局部体格检查结果的情况下出现,构成了诊断挑战,常常在诊断时导致如肠坏疽等并发症。

结论

里氏疝可极为罕见地以里氏型复发性腹股沟斜疝的形式出现。医疗人员高度怀疑、早期转诊和及时进行影像学检查可预防死亡和发病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a6d/9275495/92b3d079907a/OAEM-14-323-g0001.jpg

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