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Situs inversus totalis or situs inversus-dextroacardia is a rare congenital anomaly which is characterized by reverse position
of adnominal and thoracic viscera. This anomaly was detected in an eight- month-old female baby after a barium
enema examination which showed reversed position of colonic frame. The sigmoid and descending colons were located
in the right side of abdomen and ascending colon and cecum in the left side. Plain chest x-ray and abdominal ultrasonography
confirmed the anomaly by evidence of right side cardiac position and reversed location of abdominal organs,
respectively.
An-eight-month- female baby was referred to radiology department
of French Medical Institute for Children (FMIC) for
barium enema examination due to chronic constipation.
During the barium enema examination, reversed position of
colonic frame was detected which showed almost normal
caliber and haustrations of bowel loops. The sigmoid colon,
descending colon and splenic flexure were located in the right
side of abdomen while the hepatic flexure and ascending colon
were observed in the left side of abdomen (Figure 1).
For evaluation of cardiac position and axis, chest x-ray was
preformed which demonstrated right side position of the
heart (dextroacardia) with the location of liver in the left side
and stomach in the right side of abdomen (Figure 2) also in
trans-abdominal ultrasound spleen was seen in the right upper
abdomen (Figure 3) and liver in the left upper abdomen
(Figure 4) confirming presence of situs inversus dextrocardia.
Situs inversus is a term used when internal organs of the body
have reversed position or when mirror image of normal internal
organ is existed. The total transposition of all thoracic
and abdominal viscera is called situs inversus totalis.
Dextrocardia is a term used for the reversed position of the
heart. This occurs when the heart base to apex orientation
is pointed toward the right side of the chest rather than left
side (normal position). Situs inversus dextrocardia is a rare
congenital condition which is also called situs inversus totalis.
The occurrence of this congenital problem has been variously
expressed from 1/6000 to 1/ 35000 of live births. This is
an autosomal recessive genetic disorder which the defect occurs
in chromosome. The primitive loop during embryonic
developmental process traverses into the opposite direction
of normal position resulting to organ displacement. In situs
inversus totalis morphologically left atrium is located in the
right side and morphologically right atrium is in the left side,
also the lungs have changed their positions, as left lung has
three lobes and right lung contains two lobes. Abdominal
organs demonstrate reversed position, liver, gall bladder, ligament
of Treitz, ileum and ascending colon are in the left side
and spleen, stomach, jejunum and descending colon locate in
the right side. This congenital anomaly affects both males
and females equally. The affected individuals usually have an
asymptomatic life but in 3-5% of cases congenital heart diseases
can occur.
The atrioventricular discordance and transposition of great vessels are the commonest associated abnormalities
while the right sided aortic arch occurs in about
80% of cases. Some people with situs inversus suffer from
chronic sinusitis, bronchiectasis and nasal polyposis making
a syndrome called kartagener syndrome. A very rare type
of situs inversus is accompanied with normal left side cardiac
position, called situs inversus with levocardia. This anomaly is
highly seen with congenital heart diseases which make about
95% of cases. The affected population with Situs inversus dextroacardia
usually does not need any specific treatment except
when they are symptomatic or whenever any treatable
congenital heart anomaly is present. However the recognition
of this congenital condition is essential when any interventional
procedure or emergency surgery is going to be done in
order to avoid any mishaps.
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