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Annals of Clinical and Medical
Case Reports
Case Report
CT Diagnosis of Rare Case of Morgagni Hernia in an Adult
Gligorievski A1,*
1
Department of University Clinic of Surgery "St. Naum Ohridski" Skopje, North Macedonia
Volume 3 Issue 3- 2020
Received Date: 16 Feb 2020
Accepted Date: 10 Mar 2020
Published Date: 16 Mar 2020
2. Key words
Adult; Morgagni; Computed
Tomography; Congenital; Dia-
phragmatic; Hernia; Repair
*Corresponding Author (s): Antonio Gligorievski, University Clinic of Surgery “St. Naum Ohrid-
ski” Skopje, E-mail: atglmed@gmail.com
Citation: Gligorievski A, CT Diagnosis of Rare Case of Morgagni Hernia in an Adult. Annals of Clinical and
Medical Case Reports. 2020; 3(3): 1-4.
http://www.acmcasereport.com/
1. Abstract
1.1. Introduction: Morgagni’s hernia is the rarest of the congenital diaphragmatic defects with a re-
ported frequency of 1% to 5.1% Morgagni hernias are more commonly seen on the right side and it
occurs more commonly in females. However, most patients remain asymptomatic and the majority
of cases are discovered incidentally while investigating unrelated problems.
1.2. Aim: The aim of this paper is to present a rare case of Morgagni hernia in adults and to empha-
size the significant role of CT imaging in reaching the exact diagnosis of this condition.
1.3. Case report: We present a rare case of 46 years old female with an incidentally detected con-
genital diaphragmatic hernia on the right side. CT scan is the investigation of choice for diagnosis
of Morgagni’s hernia as it allows clear visualization of the defect, and its contents. The diagnosis is
established by the presence of a retrosternal mass of herniated omentum or by a transverse colon.
Surgical treatment options include a transabdominal or transthoracic repair, but in the case of larger
defects, a mesh may be necessary.
1.4. Conclusion: Most asymptomatic cases were found in adults by chest radiography for unrelated
problems. The diagnosis in the suspected case can be confirmed by a CT scan.
3. Introduction
Morgagni hernia was first described by Giovanni Battista
Morgagni, an Italian anatomist, and pathologist in 1769 [1]. The
foramen of Morgagni, also known as the sternocostal hiatus is
a triangular space caused by a congenital defect in the fusion of
septum transverses of the diaphragm and the costal arches [2].
Herniation of abdominal contents through this foramen is known
as the Morgagni hernia. The majority of theses hernias occur on
the right, but left-sided hernias have been reported. Morgagni
hernia is the rarest form of congenital hernia, representing 2 to 3%
of all case [3, 4].The majority of Morgagni hernias are diagnosed
late because most adults can be asymptomatic or present with
non-specific respiratory and gastrointestinal symptoms [5].
Diagnosis can be difficult and a missed diagnosis can lead to life-
threatening complications. In most adult cases these hernias are
noted incidentally on chest X-ray. Depending on the contents of
the hernia (omentum, stomach, small intestine, colon or liver)
it can appear differently on chest radiography and the diagnosis
can be missed. For example, if omentum is present in the sac, a
solid pericardiac shadow will appear on the chest radiographs [6].
Another option would be a barium enema for adults. CT with oral
contrast is the investigation of choice as it allows clear visualization
of the defect, and its contents [7]. When investigations are non-
diagnostic, confirmation by laparoscopy may be needed. Although
the majority of these hernias are asymptomatic, the repair is
recommended to avoid future complications. If the hernia is small
or if it contains omentum only, the operation is indicated when
symptoms are recurrent. Operation is indicated when the colon is
in the sac, as there is a high risk of obstruction. Treatment options
include transabdominal or transthoracic repair [8, 9].
4. Presentation of Case (Case Report)
The aim of this report is to highlights the importance of early CT
scanning in reaching the exact and early diagnosis of congenital
diaphragmatic hernia, particularly since a delay in diagnosis can
result in significant morbidity and mortality. Herein, we present
a rare case of 46 years old female with an incidentally detected
congenital diaphragmatic hernia on the right side and to emphasize
thesignificantroleofimagingforthediagnosisofthiscondition.She
complained about epigastric and abdominal pain for one week and
Volume 3 Issue 3 -2020 Case Report
Copyright ©2020 Gligorievski A et al. This is an open access article distributed under the terms of the Creative Commons Attribution
License, which permits unrestricted use, distribution, and build upon your work non-commercially.
2
a moderate form of dyspnea. There was no history of any previous
abdominal or thoracic trauma. She had no other underlying
disease. Her physical examination revealed pain in the epigastric
area but did not reveal any significant abnormality. She was sent to
the Radiology Department for further evaluation. Postero Anterior
(PA) and Latero-Lateral (LL) chest X-ray revealed that the left
diaphragm was unexceptionally high. It was decided to perform
a CT scan of the chest and abdomen to clarify the changes seen
in the initial chest radiograph. CT scan of the chest and abdomen
revealed the presence of a left-sided anterolateral diaphragmatic
defect with herniation of the transverse colon including mesenteric
fat and omentum into the left hemithorax (Figure 1, 2, 3).
Intraperitoneal fat was responsible for the opacity seen in the x-ray.
The herniated omentum and transverse colon passes through the
defect, filling the chest cavity and causing the compression of the
lower lobe of the lung, and a shift of mediastinal structures to the
left side. (Figure 4) CT scan confirmed the diagnosis of left-sided
Morgagni hernia (Figure 5). The patient was counseled about the
possible complications of diaphragmatic hernia that might ocure
if left untreated. The patient was operated on and the diagnosis
of left-sided hernia was confirmed. Transabdominal operative
intervention for correction of the Morganic hernia has been
performed and the diaphragm defect is closed with a mesh. The
postoperative has no complications and the patient is discharged
in good general condition.
Figure 1: Noncontrast CT scans of the thorax and abdomen. A) Mediastinal
window; B) Lung window: At the level of Th7 axial CT images showed a large
Morgagni hernia containing omental fat (white arrow) and transverse colon loop
(black arrow). There were no signs of obstruction or strangulation.
Figure 2: Noncontrast axial CT scans of the thorax and abdomen. A) Medi-
astinal window; B) Lung window: At the level of Th10 axial CT images showed
an anterior defect (foramen of Morgagni) in the right and left hemidiaphragm,
with a large Morgagni hernia containing omental fat (white arrow) and transverse
colon loop (black arrow). There were no signs of obstruction or strangulation.
Figure 3: Contrast-enhanced axial CT scans of the thorax and abdomen at
the level of aorta ascendens (A); at the level of the right pulmonary artery (B):
Contrast-enhanced axial CT images show a large Morgagni hernia containing
omental fat (white arrow) and transverse colon loop (black arrow). There were
no signs of obstruction or strangulation.
Volume 3 Issue 3 -2020 Case Report
5. Discussion
Diaphragmatic hernias of Morgagni were first described in
1769 as anatomical defects in the anterior diaphragm that allow
herniation of abdominal viscera into the thorax [1]. The presence
of this hernia in adulthood is very rare and, when symptomatic, it
is usually associated with chronic respiratory symptoms (dyspnea,
fatigue, pain) or gastrointestinal involvement with occlusive
symptoms (constipation, occlusion) [10]. However, most patients
remain asymptomatic and the majority of cases are discovered
incidentally while investigating unrelated problems [11]. Despite
being a congenital condition, many cases present only later in life. It
is believed this is due to the presence of a sac that limits herniation.
Morgagni hernias are more commonly seen on the right side
despite protection from the liver. It has been suggested that this
happens because the presence of extensive pericardial attachments
on the left provides extra support [10]. It occurs more commonly
in females [9, 12]. Usually, the hernia sac contains the transverse
colon followed by omentum, stomach, and small intestine but
occasionally the liver may also protrude into the sac [13]. They are
the rarest of congenital diaphragmatic hernias, making up 2-3%
of cases [3, 4]. Incidental findings of this condition in adults are
less common with only 81 asymptomatic cases reported in a recent
review [3]. Symptomatic adult cases of Morgagni hernias are even
rarer with only 12 cases described.2 Almost 90% of Morgagni
hernias are reported to be on the right side, with 2% located on the
left and 8% bilateral [14].
Depending on the contents of the hernia, the images in the chest
radiography may appear differently [10]. On a chest radiograph,
Morgagni hernias is frequently diagnosed incidentally as
homogeneous masses in the right cardio phrenic angle [6].
Most frequently, it will show a solid pericardiac shadow due to
the presence of omentum and the differential diagnosis should
include a pleuropericardial cyst, pericardial fat mass, lipoma or
liposarcoma, mesothelioma, diaphragmatic cyst, intrathoracic
tumors, and eventration of the diaphragm [15, 3, 7]. However, it
must be noted that plain radiography may be normal especially
in intermittent herniation [5]. Another diagnostic option would
be a barium enema, having the advantage of being less expensive.
Ultrasonography has been shown to be useful in assessing
diaphragmatic hernias but CT is the most sensitive an accurate
diagnostic metod as it gives excellent anatomical detail on the
contents of the hernia and its complications such as strangulation
[16,17]. CT scan is the investigation of choice for diagnosis of
Morgagni hernia. The diagnosis is established by the presence of
a retrosternal mass of fat density representing herniated omentum
Figure 4: Noncontrast Coronal reformatted CT image of the thorax and abdo-
men (A) and (B): Coronal reformatted CT image in 46 years old woman showed
an anterior defect (foramen of Morgagni) in the right and left cardiophrenic
angle, with a large Morgagni hernia containing omental fat (white arrow) and
transverse colon loop (black arrow). There were no signs of obstruction or
strangulation.
Figure 5: Noncontrast Sagittal reformatted CT image of the thorax and abdomen
(A) and (B): Sagital reformatted CT image shows anterior diaphragmatic defect
(foramen of Morgagni) and a large Morgagni hernia containing colon (black ar-
row) and omental fat (white arrow) There were no signs of obstruction or stran-
gulation.
http://www.acmcasereport.com/ 3
http://www.acmcasereport.com/ 4
or by a combination of omentum and a colon [12]. Magnetic
resonance imaging can distinguish Morgagni hernia from other
mediastinal masses. In our case, the diagnosis was made by CT.
Although the majority of patients are asymptomatic, the repair
is almost always recommended to avoid future complications,
especially when the colon is herniated due to the risk of obstruction
[8]. On the other hand, if it contains the only omentum, surgery is
only indicated in the presence of symptoms [18]. Surgical treatment
options include a transabdominal or transthoracic repair [19]. For
a smaller defect, primary closure is usually done, but in the case of
larger defects, a mesh may be necessary [18, 19].
6. Conclusions
In conclusion, Morgagni hernia is a rare type of congenital
diaphragmatic hernia in both adults and children and is more
common on the right side. A missed diagnosis can lead to life-
threatening complications such as obstruction or strangulation
which warrants early surgical intervention. Most asymptomatic
cases were found in adults by chest radiography for unrelated
problems. The diagnosis in the suspected case can be confirmed
by a CT scan. Surgery by abdominal approach is the management
of choice.
Volume 3 Issue 3 -2020 Case Report
References
1. Morgagni GB. The seats and causes of diseases investigated by anat-
omy. London: Millar and Cadell. 1769; 3: 205.
2. Eren S, Ciri F. Diaphragmatic hernia: diagnostic approaches with
review of the literature. Eur J Radiol. 2005; 54: 448-59.
3. Comer TP, Clagett OT. Surgical treatment of hernia of the foramen
of Morgagni. J Thorac Cardiovasc Surg. 1966; 52: 461-8.
4. Loong TP, Kocher HM. Clinical presentation and operative repair of
hernia of Morgagni. Postgrad Med J. 2005; 81: 41-4.
5. Marinceu D, Loubani M, O’Grady H. Late presentation of a large
Morgagni hernia in an adult. BMJ Case Rep. 2014;2014. pii:
bcr2013202440. doi: 10.1136/bcr-2013-202440.
6. Daneshvar S, Shriki J, Sohn H, Rahimtoola SH. Morgagni-type di-
aphragmatic hernia presenting as an abnormal cardiac silhouette.
Am J Med. 2010; 123: e11-2.
7. Arora S, Haji A. Adult Morgagni hernia: the need for clinical aware-
ness, early diagnosis and prompt surgical intervention. Ann R Coll
Surg Eng. 2008; 90: 694-5.
8. Nasr A, Fecteau A. Foramen of Morgagni hernia: presentation and
treatment. Thorac Surg Clin. 2009; 19: 463-468.
9. Horton JD, Hofmann LJ, Hetz SP. Presentation and management
of Morgagni hernias in adults: a review of 298 cases. Surg Endosc.
2008; 22: 1413-1420.
10. Pfannschmidt J, Hoffmann H, Dienemann H. Morgagni hernia in
adults: results in 7 patients. Scand J of Surg. 2004; 93: 77-81.
11. Colakoglu O, Haciyanli M, Soyturk M, Colakoglu G, Simsek I. Mor-
gagni hernia in an adult: atypical presentation and diagnostic diffi-
culties. Turk J Gastroenterol. 2005; 16: 114-116.
12. Abraham V, Myla Y, Verghese S, Chandran BS. Morgagni-larrey her-
nia, a review of 20 cases. Indian J Surg. 2012; 74(5): 391-395.
13. Aghajanzadeh M, Khadem S, Khajeh Jahromi S, Gorabi HE, Ebra-
himi H, Maafi AA. Clinical presentation and operative repair of
Morgagni hernia. Interact Cardiovasc Thorac Surg. 2012; 15(4):
608-611.
14. Komatsu T, Takahashi Y. Is this a mediastinal tumor? A case of Mor-
gagni hernia complicated with intestinal incarceration mistaken for
the mediastinal lipoma previously. Int J Surg Case Rep 2013; 4: 302-
4.
15. Modi M, Dey AK, Mate A, and Rege S. Strangulated Morgagni’s Her-
nia: A Rare Diagnosis and Management. Case Rep Surgery. 2016;
2016: 2621383.
16. Kelly MD. Laparoscopic repair of strangulated Morgagni hernia. W
J Emergen Surg. 2007; 2: 1749-7922.
17. Durak E, Gur S, Cokmez A, Atahan K, Zahtz E, Tarcan E. Laparo-
scopic repair of Morgagni hernia. Hernia. 2007; 11(3): 265-270.
18. Harrington SW. Clinical manifestations and surgical treatment of
congenital types of diaphragmatic hernia. Rev Gastroenterol 1951;
18: 243.
19. Loong TP, Kocher HM. Clinical presentation and operative repair of
hernia of Morgagni. Postgrad Med J 2005; 81: 41-44.

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CT Diagnosis of Rare Case of Morgagni Hernia in an Adult

  • 1. Annals of Clinical and Medical Case Reports Case Report CT Diagnosis of Rare Case of Morgagni Hernia in an Adult Gligorievski A1,* 1 Department of University Clinic of Surgery "St. Naum Ohridski" Skopje, North Macedonia Volume 3 Issue 3- 2020 Received Date: 16 Feb 2020 Accepted Date: 10 Mar 2020 Published Date: 16 Mar 2020 2. Key words Adult; Morgagni; Computed Tomography; Congenital; Dia- phragmatic; Hernia; Repair *Corresponding Author (s): Antonio Gligorievski, University Clinic of Surgery “St. Naum Ohrid- ski” Skopje, E-mail: atglmed@gmail.com Citation: Gligorievski A, CT Diagnosis of Rare Case of Morgagni Hernia in an Adult. Annals of Clinical and Medical Case Reports. 2020; 3(3): 1-4. http://www.acmcasereport.com/ 1. Abstract 1.1. Introduction: Morgagni’s hernia is the rarest of the congenital diaphragmatic defects with a re- ported frequency of 1% to 5.1% Morgagni hernias are more commonly seen on the right side and it occurs more commonly in females. However, most patients remain asymptomatic and the majority of cases are discovered incidentally while investigating unrelated problems. 1.2. Aim: The aim of this paper is to present a rare case of Morgagni hernia in adults and to empha- size the significant role of CT imaging in reaching the exact diagnosis of this condition. 1.3. Case report: We present a rare case of 46 years old female with an incidentally detected con- genital diaphragmatic hernia on the right side. CT scan is the investigation of choice for diagnosis of Morgagni’s hernia as it allows clear visualization of the defect, and its contents. The diagnosis is established by the presence of a retrosternal mass of herniated omentum or by a transverse colon. Surgical treatment options include a transabdominal or transthoracic repair, but in the case of larger defects, a mesh may be necessary. 1.4. Conclusion: Most asymptomatic cases were found in adults by chest radiography for unrelated problems. The diagnosis in the suspected case can be confirmed by a CT scan. 3. Introduction Morgagni hernia was first described by Giovanni Battista Morgagni, an Italian anatomist, and pathologist in 1769 [1]. The foramen of Morgagni, also known as the sternocostal hiatus is a triangular space caused by a congenital defect in the fusion of septum transverses of the diaphragm and the costal arches [2]. Herniation of abdominal contents through this foramen is known as the Morgagni hernia. The majority of theses hernias occur on the right, but left-sided hernias have been reported. Morgagni hernia is the rarest form of congenital hernia, representing 2 to 3% of all case [3, 4].The majority of Morgagni hernias are diagnosed late because most adults can be asymptomatic or present with non-specific respiratory and gastrointestinal symptoms [5]. Diagnosis can be difficult and a missed diagnosis can lead to life- threatening complications. In most adult cases these hernias are noted incidentally on chest X-ray. Depending on the contents of the hernia (omentum, stomach, small intestine, colon or liver) it can appear differently on chest radiography and the diagnosis can be missed. For example, if omentum is present in the sac, a solid pericardiac shadow will appear on the chest radiographs [6]. Another option would be a barium enema for adults. CT with oral contrast is the investigation of choice as it allows clear visualization of the defect, and its contents [7]. When investigations are non- diagnostic, confirmation by laparoscopy may be needed. Although the majority of these hernias are asymptomatic, the repair is recommended to avoid future complications. If the hernia is small or if it contains omentum only, the operation is indicated when symptoms are recurrent. Operation is indicated when the colon is in the sac, as there is a high risk of obstruction. Treatment options include transabdominal or transthoracic repair [8, 9]. 4. Presentation of Case (Case Report) The aim of this report is to highlights the importance of early CT scanning in reaching the exact and early diagnosis of congenital diaphragmatic hernia, particularly since a delay in diagnosis can result in significant morbidity and mortality. Herein, we present a rare case of 46 years old female with an incidentally detected congenital diaphragmatic hernia on the right side and to emphasize thesignificantroleofimagingforthediagnosisofthiscondition.She complained about epigastric and abdominal pain for one week and
  • 2. Volume 3 Issue 3 -2020 Case Report Copyright ©2020 Gligorievski A et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and build upon your work non-commercially. 2 a moderate form of dyspnea. There was no history of any previous abdominal or thoracic trauma. She had no other underlying disease. Her physical examination revealed pain in the epigastric area but did not reveal any significant abnormality. She was sent to the Radiology Department for further evaluation. Postero Anterior (PA) and Latero-Lateral (LL) chest X-ray revealed that the left diaphragm was unexceptionally high. It was decided to perform a CT scan of the chest and abdomen to clarify the changes seen in the initial chest radiograph. CT scan of the chest and abdomen revealed the presence of a left-sided anterolateral diaphragmatic defect with herniation of the transverse colon including mesenteric fat and omentum into the left hemithorax (Figure 1, 2, 3). Intraperitoneal fat was responsible for the opacity seen in the x-ray. The herniated omentum and transverse colon passes through the defect, filling the chest cavity and causing the compression of the lower lobe of the lung, and a shift of mediastinal structures to the left side. (Figure 4) CT scan confirmed the diagnosis of left-sided Morgagni hernia (Figure 5). The patient was counseled about the possible complications of diaphragmatic hernia that might ocure if left untreated. The patient was operated on and the diagnosis of left-sided hernia was confirmed. Transabdominal operative intervention for correction of the Morganic hernia has been performed and the diaphragm defect is closed with a mesh. The postoperative has no complications and the patient is discharged in good general condition. Figure 1: Noncontrast CT scans of the thorax and abdomen. A) Mediastinal window; B) Lung window: At the level of Th7 axial CT images showed a large Morgagni hernia containing omental fat (white arrow) and transverse colon loop (black arrow). There were no signs of obstruction or strangulation. Figure 2: Noncontrast axial CT scans of the thorax and abdomen. A) Medi- astinal window; B) Lung window: At the level of Th10 axial CT images showed an anterior defect (foramen of Morgagni) in the right and left hemidiaphragm, with a large Morgagni hernia containing omental fat (white arrow) and transverse colon loop (black arrow). There were no signs of obstruction or strangulation. Figure 3: Contrast-enhanced axial CT scans of the thorax and abdomen at the level of aorta ascendens (A); at the level of the right pulmonary artery (B): Contrast-enhanced axial CT images show a large Morgagni hernia containing omental fat (white arrow) and transverse colon loop (black arrow). There were no signs of obstruction or strangulation.
  • 3. Volume 3 Issue 3 -2020 Case Report 5. Discussion Diaphragmatic hernias of Morgagni were first described in 1769 as anatomical defects in the anterior diaphragm that allow herniation of abdominal viscera into the thorax [1]. The presence of this hernia in adulthood is very rare and, when symptomatic, it is usually associated with chronic respiratory symptoms (dyspnea, fatigue, pain) or gastrointestinal involvement with occlusive symptoms (constipation, occlusion) [10]. However, most patients remain asymptomatic and the majority of cases are discovered incidentally while investigating unrelated problems [11]. Despite being a congenital condition, many cases present only later in life. It is believed this is due to the presence of a sac that limits herniation. Morgagni hernias are more commonly seen on the right side despite protection from the liver. It has been suggested that this happens because the presence of extensive pericardial attachments on the left provides extra support [10]. It occurs more commonly in females [9, 12]. Usually, the hernia sac contains the transverse colon followed by omentum, stomach, and small intestine but occasionally the liver may also protrude into the sac [13]. They are the rarest of congenital diaphragmatic hernias, making up 2-3% of cases [3, 4]. Incidental findings of this condition in adults are less common with only 81 asymptomatic cases reported in a recent review [3]. Symptomatic adult cases of Morgagni hernias are even rarer with only 12 cases described.2 Almost 90% of Morgagni hernias are reported to be on the right side, with 2% located on the left and 8% bilateral [14]. Depending on the contents of the hernia, the images in the chest radiography may appear differently [10]. On a chest radiograph, Morgagni hernias is frequently diagnosed incidentally as homogeneous masses in the right cardio phrenic angle [6]. Most frequently, it will show a solid pericardiac shadow due to the presence of omentum and the differential diagnosis should include a pleuropericardial cyst, pericardial fat mass, lipoma or liposarcoma, mesothelioma, diaphragmatic cyst, intrathoracic tumors, and eventration of the diaphragm [15, 3, 7]. However, it must be noted that plain radiography may be normal especially in intermittent herniation [5]. Another diagnostic option would be a barium enema, having the advantage of being less expensive. Ultrasonography has been shown to be useful in assessing diaphragmatic hernias but CT is the most sensitive an accurate diagnostic metod as it gives excellent anatomical detail on the contents of the hernia and its complications such as strangulation [16,17]. CT scan is the investigation of choice for diagnosis of Morgagni hernia. The diagnosis is established by the presence of a retrosternal mass of fat density representing herniated omentum Figure 4: Noncontrast Coronal reformatted CT image of the thorax and abdo- men (A) and (B): Coronal reformatted CT image in 46 years old woman showed an anterior defect (foramen of Morgagni) in the right and left cardiophrenic angle, with a large Morgagni hernia containing omental fat (white arrow) and transverse colon loop (black arrow). There were no signs of obstruction or strangulation. Figure 5: Noncontrast Sagittal reformatted CT image of the thorax and abdomen (A) and (B): Sagital reformatted CT image shows anterior diaphragmatic defect (foramen of Morgagni) and a large Morgagni hernia containing colon (black ar- row) and omental fat (white arrow) There were no signs of obstruction or stran- gulation. http://www.acmcasereport.com/ 3
  • 4. http://www.acmcasereport.com/ 4 or by a combination of omentum and a colon [12]. Magnetic resonance imaging can distinguish Morgagni hernia from other mediastinal masses. In our case, the diagnosis was made by CT. Although the majority of patients are asymptomatic, the repair is almost always recommended to avoid future complications, especially when the colon is herniated due to the risk of obstruction [8]. On the other hand, if it contains the only omentum, surgery is only indicated in the presence of symptoms [18]. Surgical treatment options include a transabdominal or transthoracic repair [19]. For a smaller defect, primary closure is usually done, but in the case of larger defects, a mesh may be necessary [18, 19]. 6. Conclusions In conclusion, Morgagni hernia is a rare type of congenital diaphragmatic hernia in both adults and children and is more common on the right side. A missed diagnosis can lead to life- threatening complications such as obstruction or strangulation which warrants early surgical intervention. Most asymptomatic cases were found in adults by chest radiography for unrelated problems. The diagnosis in the suspected case can be confirmed by a CT scan. Surgery by abdominal approach is the management of choice. Volume 3 Issue 3 -2020 Case Report References 1. Morgagni GB. The seats and causes of diseases investigated by anat- omy. London: Millar and Cadell. 1769; 3: 205. 2. Eren S, Ciri F. Diaphragmatic hernia: diagnostic approaches with review of the literature. Eur J Radiol. 2005; 54: 448-59. 3. Comer TP, Clagett OT. Surgical treatment of hernia of the foramen of Morgagni. J Thorac Cardiovasc Surg. 1966; 52: 461-8. 4. Loong TP, Kocher HM. Clinical presentation and operative repair of hernia of Morgagni. Postgrad Med J. 2005; 81: 41-4. 5. Marinceu D, Loubani M, O’Grady H. Late presentation of a large Morgagni hernia in an adult. BMJ Case Rep. 2014;2014. pii: bcr2013202440. doi: 10.1136/bcr-2013-202440. 6. Daneshvar S, Shriki J, Sohn H, Rahimtoola SH. Morgagni-type di- aphragmatic hernia presenting as an abnormal cardiac silhouette. Am J Med. 2010; 123: e11-2. 7. Arora S, Haji A. Adult Morgagni hernia: the need for clinical aware- ness, early diagnosis and prompt surgical intervention. Ann R Coll Surg Eng. 2008; 90: 694-5. 8. Nasr A, Fecteau A. Foramen of Morgagni hernia: presentation and treatment. Thorac Surg Clin. 2009; 19: 463-468. 9. Horton JD, Hofmann LJ, Hetz SP. Presentation and management of Morgagni hernias in adults: a review of 298 cases. Surg Endosc. 2008; 22: 1413-1420. 10. Pfannschmidt J, Hoffmann H, Dienemann H. Morgagni hernia in adults: results in 7 patients. Scand J of Surg. 2004; 93: 77-81. 11. Colakoglu O, Haciyanli M, Soyturk M, Colakoglu G, Simsek I. Mor- gagni hernia in an adult: atypical presentation and diagnostic diffi- culties. Turk J Gastroenterol. 2005; 16: 114-116. 12. Abraham V, Myla Y, Verghese S, Chandran BS. Morgagni-larrey her- nia, a review of 20 cases. Indian J Surg. 2012; 74(5): 391-395. 13. Aghajanzadeh M, Khadem S, Khajeh Jahromi S, Gorabi HE, Ebra- himi H, Maafi AA. Clinical presentation and operative repair of Morgagni hernia. Interact Cardiovasc Thorac Surg. 2012; 15(4): 608-611. 14. Komatsu T, Takahashi Y. Is this a mediastinal tumor? A case of Mor- gagni hernia complicated with intestinal incarceration mistaken for the mediastinal lipoma previously. Int J Surg Case Rep 2013; 4: 302- 4. 15. Modi M, Dey AK, Mate A, and Rege S. Strangulated Morgagni’s Her- nia: A Rare Diagnosis and Management. Case Rep Surgery. 2016; 2016: 2621383. 16. Kelly MD. Laparoscopic repair of strangulated Morgagni hernia. W J Emergen Surg. 2007; 2: 1749-7922. 17. Durak E, Gur S, Cokmez A, Atahan K, Zahtz E, Tarcan E. Laparo- scopic repair of Morgagni hernia. Hernia. 2007; 11(3): 265-270. 18. Harrington SW. Clinical manifestations and surgical treatment of congenital types of diaphragmatic hernia. Rev Gastroenterol 1951; 18: 243. 19. Loong TP, Kocher HM. Clinical presentation and operative repair of hernia of Morgagni. Postgrad Med J 2005; 81: 41-44.