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成年男性患者偶然诊断出的大型无症状莫尔加尼疝

Incidentally Diagnosed Large Asymptomatic Morgagni Hernia in Adult Male Patient.

作者信息

Misimi Shqipe, Shurlani Arben, Nikolovski Andrej

机构信息

Ss. Cyril and Methodius University in Skopje, Medical Faculty, Skopje, North Macedonia.

Department of Visceral Surgery, University Surgery Hospital "St. Naum Ohridski", Skopje, North Macedonia.

出版信息

Eur J Case Rep Intern Med. 2023 Aug 31;10(10):004047. doi: 10.12890/2023_004047. eCollection 2023.

Abstract

BACKGROUND

Congenital diaphragmatic hernias are rare congenital defects resulting in abdominal organ protrusion into the thoracic cavity; they mainly present with pulmonary or gastrointestinal symptoms. Although congenital and discovered in utero or in early childhood, they can be asymptomatic for a long time and even remain asymptomatic despite the growing hernia sac dimensions and the hernia sac contents.

CASE DESCRIPTION

We present a case of a 58-year-old patient with incidentally diagnosed Morgagni hernia during the COVID-19 pandemic following a computerised tomography (CT) scan of the chest. He presented without any symptoms related to the existence of the hernia. Another CT scan was performed 20 months after the initial diagnosis to evaluate the progression of the hernia. The patient refused the offered surgery due to the absence of symptoms.

DISCUSSION

A Morgagni hernia is usually discovered during pregnancy or in early childhood, but sometimes can be asymptomatic for years. Main symptoms originate from the respiratory and gastrointestinal system.

CONCLUSION

Due to the refusal of surgery, we were able to follow the CT scan enlargement progression of patients' hernia over a 20-month period.

LEARNING POINTS

Congenital diaphragmatic Morgagni hernias can remain undiscovered for a long period of time.Despite the usual clinical presentation with pulmonary and/or gastrointestinal symptoms, it can be asymptomatic in some patients.Surgery is the recommended treatment for a Morgagni hernia (via the thoracic or abdominal access).

摘要

背景

先天性膈疝是一种罕见的先天性缺陷,导致腹腔脏器突入胸腔;主要表现为肺部或胃肠道症状。虽然先天性膈疝在子宫内或儿童早期就已发现,但它们可能长期无症状,即使疝囊尺寸增大且疝囊内容物增多,仍可能保持无症状状态。

病例描述

我们报告一例58岁患者,在COVID-19大流行期间进行胸部计算机断层扫描(CT)时偶然诊断出莫尔加尼疝。他没有出现与疝存在相关的任何症状。在初次诊断20个月后进行了另一次CT扫描,以评估疝的进展情况。由于没有症状,患者拒绝了提供的手术。

讨论

莫尔加尼疝通常在孕期或儿童早期被发现,但有时可能多年无症状。主要症状源于呼吸和胃肠道系统。

结论

由于患者拒绝手术,我们得以在20个月的时间里跟踪患者疝的CT扫描扩大进展情况。

学习要点

先天性膈莫尔加尼疝可能长时间未被发现。尽管通常临床表现为肺部和/或胃肠道症状,但在某些患者中可能无症状。手术是莫尔加尼疝的推荐治疗方法(通过胸部或腹部入路)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d505/10545154/498fadc578c8/4047_Fig1.jpg

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Incidentally Diagnosed Large Asymptomatic Morgagni Hernia in Adult Male Patient.成年男性患者偶然诊断出的大型无症状莫尔加尼疝
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本文引用的文献

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Prenatal diagnosis, imaging, and prognosis in Congenital Diaphragmatic Hernia.先天性膈疝的产前诊断、影像学表现和预后。
Semin Perinatol. 2020 Feb;44(1):51163. doi: 10.1053/j.semperi.2019.07.002. Epub 2019 Jul 30.
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Update on Congenital Diaphragmatic Hernia.先天性膈疝更新。
Anesth Analg. 2020 Sep;131(3):808-821. doi: 10.1213/ANE.0000000000004324.

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