CASE REPORT
Dextrocardia associated with Left
hemidiaphragmatic Eventration
Tahir
Saeed, Tariq Saeed Mufti*
Department
of Paediatrics and *Department of Surgery,
Ayub Medical College, Abbottabad
A rare case of dextrcardia in association
with eventration of left hemidiaphragm
who failed to thrive is
presented. Growth retardation could not be attributed to these congenital
anomalies.
Introduction
Dextrocardia is the condition where heart is
positioned on right side and apex beat is also palpable on the right. It may
present as isolated entity or as combination of asplenia/polysplenia syndromes
or situs inversus. The first case of
dextrocardia was reported in a male in 1906.1 Dextrocardia in
association with diaphragmatic eventration
and other anomalies e.g. hypoplasia of right lung has also been documented.
Here we report a case of dextrocardia associated with left hemidiaphragmatic
eventration.
Case report
A six years old male
presented with failure to thrive. He was born as first of the twins while the other,
a female, grew healthy and normal. His birth size was reported as small. His
weight remained static at 13 kg for the last two years. He measured 105.5 cm
high with head circumference of 46.5 cm and mid arm circumference of 12.5 cm. His
cognitive functions were adequate for age and did not show any other
neurological deficit. Rest of systemic examination was unremarkable except that
his apex beat felt on the right side. Routine chest X-ray (Fig. 1) showed
cardiac shadow on the right and elevated left diaphragm with prominent gas
shadow underneath it. A diagnosis of dextrocardia associated with eventration
of left hemidiaphragm was confirmed on barium meal x-ray (Fig. 2) and
echocardiogram. Further enquiry revealed
that an earlier sibling suffered from Arthrogryposis Multiplex Congenita and
died at the age of four years. There was no history of congenital anomalies in rest
of the kins.
Discussion
Dextrocardia with
isolated hemidiaphragmatic eventration is rarely encountered in literature.
Jroundi et al described a case of
dextrocardia with localized right diaphragmatic eventration.2
Dextrocardia
with other anamolies of diaphragm e.g diaphragmatic hernia has been reported in
literature causing symptoms due to diaphragmatic condition. However,
eventration of diaphragm is usually an asymptomatic condition.3
In
this case presenting complaints were failure to thrive and the congenital
anomalies of dextrocadia and eventration of left hemidiaphragm were discovered
incidentally. Malone et al have also reported cases with diaphragmatic
eventration presenting with failure to thrive.4 The reason for
failure to thrive have not been explained in documented cases. The same is true
in this case as well.
Figure-1: Chest X-ray
Figure-2: Barium Meal X-ray
References
1. Behrman
RE, Kleigman RM, Jenson HB. Nelson text book of paediatrics, 16thed.
Philadelphia, WB Saunders;2000:p 1345
2. Itoh
M, Yada Y, Hashimoto U, Sasaki Y, Ohga K, Oka T. A case of intralobar pulmonary
sequesteration associated with ASD, dextrocardia, hypoplasia of the right lung
& eventration of the diaphragm. Kyoba geka 1987;40(13):1099-103.
3. Jroundi
L, Cherkasni MM, Dafrin R, Imani F. Localized right diaphragmatic eventration
associated with dextrocardia. J Radiol 2001;82(5):593-5
4. Malone
PS, Brain AJ, Kiely EM, Spitz L. Congenital diaphragmatic defects that present late. Arch Dis Child 1989; 64(11):
1542-4.
Address for Correspondence: Prof. Tariq Saeed Mufti,
Professor & Head of Surgery, Ayub Medical College, Abbottabad. Phone:
(0992) 381907-3222 Email: tariqmufti@hotmail.com