“Upside Down Stomach”: Rare Form of Diaphragmatic Hernia

1952 ◽  
Vol 21 (2) ◽  
pp. 300-303 ◽  
Author(s):  
Raymond A. Gagliardi
2020 ◽  
Vol 99 (7) ◽  

Morgagni hernia is a rare form of diaphragmatic hernia. It is a congenital defect of the diaphragm, often asymptomatic in adulthood and thus usually found only incidentally. Its treatment is predominantly surgical. This article presents three case reports of patients operated in our department.


1939 ◽  
Vol 26 (103) ◽  
pp. 632-642 ◽  
Author(s):  
W. C. Osman Hill ◽  
Milroy Paul

2021 ◽  
Vol 27 (1) ◽  
pp. 42-45
Author(s):  
Nur Shafinaz Rusli ◽  
Syed Abdul Khaliq Syed Abdul Hamid ◽  
Norhafiza Ab. Rahman ◽  
Azian Abd. Aziz ◽  
Ahmad Fadzil Abdullah

Congenital chest wall deformities occurred in roughly 1% of children and if asymptomatic are often overlooked and taken lightly. This results in a progressive deformity of the chest and delays in diagnosis of the underlying causes. Complications can also develop from the underlying condition. Chest wall deformities are associated with a number of syndromes and other anomalies including abnormalities of the diaphragm. Congenital Diaphragmatic Hernia (CDH) is one of the underlying causes of chest deformity. Congenital Morgagni Hernia (CMH) is a rare form of CDH and consists of 3-5% in all CDH. Many cases were delayed in diagnosis due to the subtle presentation or were incidental findings. The consequence of delay in diagnosis can lead to the onset of complications which carries morbidities and even mortality. We report a case of a child with missed diagnosis of a rare condition Morgagni Diaphragmatic Hernia presenting with chest deformity.


2021 ◽  
pp. 36-38
Author(s):  
Ankur Akela ◽  
Prashant Kumar Singh

Morgagni hernia occurs after a congenital retrosternal diaphragmatic defect; it is a rare form of diaphragmatic hernia (1-3% of cases). In general, this pathology is diagnosed in children; in adults it is frequently discovered in emergency or incidentally. Methods: We prospectively evaluated a series of 6 patients admitted to department of surgery IGIMS. Results: Out of 6 patients the laparoscopic approach was used in all cases: one conversion was recorded due to the tight adherences of the herniated viscera (gastric, colon, epiplon). In 4 cases, the surgical cure of hernia was performed by suture and in 2 cases with prosthesis: dual mesh in one case and polypropylene mesh in another case. We did not register morbidity and the mean postoperative stay was 4 days (range 2-6 days). Conclusions: Hernia Morgagni betrays a rare pathology. The most common is asymptomatic but in complicated cases it is a cause of acute surgical abdomen. Surgical treatment is indicated even for asymptomatic cases due to serious complications Morgagni hernia may develop. The laparoscopic approach is ideal, as reduction of viscera in the abdomen is easy and the defect will be repaired by suturing or using a prosthesis, depending on its size.


2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Gholamali Godazandeh ◽  
Farzad Mokhtari-esbuie

Introduction. Morgagni hernia is a rare form of congenital diaphragmatic hernia.Case Presentation. We present three cases of Morgagni hernia with GI symptoms treated by laparoscopic surgery.Discussion. Hernial sac was excised in two cases and left in situ in one case. There was no recurrence in symptoms after 30 months from surgery.


Author(s):  
Wafaa Alrawi ◽  
Ashraf Abuobayda ◽  
Nabil Elmansoury ◽  
Abhijeet Lonikar ◽  
Anas Alshorman ◽  
...  

In 2020, we had reported one of the few cases of trisomy 13 with ectrodactyly, a rare form of limb deformity. Herein, we report another newborn who suffered from trisomy 13 and ectrodactyly. The patient also possessed another unusual manifestation of trisomy 13, congenital diaphragmatic hernia, a life- threatening pathology.


1951 ◽  
Vol 18 (3) ◽  
pp. 448-450
Author(s):  
John R. Ross ◽  
Allen C. Johnson

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