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Title: A Case Report On Left-Sided Appendicitis
Title: A Case Report On Left-Sided Appendicitis
First author
Himal Kharel, Tribhuvan University Teaching Hospital, Maharajgunj, POB #1524, Kathmandu,
Nepal
Email: pigzeni@gmail.com
Second author
Druva Shah, Tribhuvan University Teaching Hospital, Maharajgunj, POB #1524, Kathmandu,
Nepal
Email : drshah_dn@live.com
Third author
Kathmandu, Nepal
Email : dr.namratakhadka@gmail.com
Fourth author
Email: zenikharel11@gmail.com
Correspondence
Himal Kharel
Email : pigzeni@gmail.com
1
Abstract
genitourinary pathologies. The diagnosis becomes more challenging when it is associated with
intestinal malrotation. A rare case of acute appendicitis with intestinal malrotation is reported
below.
Case presentation : A 32 year old male presented with left-sided abdominal pain. CT and USG of
abdomen showed intestinal malrotation with acute appendicitis. Exploratory laparotomy and
appendectomy via midline incision was performed and the patient had no issues on follow-up.
Conclusion : Given the rarity of acute appendicitis associated with intestinal malrotation, the
Introduction
incomplete rotation, over rotation and malfixation. The incidence of intestinal malrotation is
around 1 in 6000 live births1. Its manifestation varies greatly in different subjects. Infants
usually present acutely with volvulus whereas adults experience chronic abdominal pain. A vast
majority of adult patients are asymptomatic, and malrotation is usually an incidental finding 2. In
contrast to intestinal malrotation, acute appendicitis is a relatively common disease with overall
lifetime risks for male and female being 8.6 and 6.7%, respectively 3. It is a mimicker of wide
Case presentation
2
A 32-year old gentleman without known co-morbidities presented to emergency department of
progressive, constant pain in his left iliac fossa without radiation, nausea, vomiting and anorexia
for 2 days. There was no history of per rectal bleed, melena, fever or surgical intervention and
his bowel and bladder habits were normal. On examination, the patient was found to be
iliac fossa with bowel sounds and normal digital rectal examination.
Routine investigations were normal except for leukocytosis (11,800 with 90% neutrophils).
USG showed non-compressible, blind ending, tubular structure with surrounding hyperechoic
mesentery with probe tenderness in left iliac fossa without any free fluid (Figure 1). The chest X-
showed large bowel predominantly on the left side and small bowel predominantly on the right
side. Superior mesenteric artery (SMA) and superior mesenteric vein (SMV) relation was
inverted with SMA on the right and SMV on the left side. Duodenum was absent in between the
SMA and aorta and was entirely on the right side (Figure 2). Appendix arising from cecum was
noted in the left iliac fossa (LIF) with thickened wall and periappendiceal fat stranding with two
Thus, the diagnosis of acute appendicitis with complete nonrotation of midgut was made.
anatomy and anticipation of bands which may have been missed by imaging, laparoscopic
procedure was not used and surgery via midline incision was deemed appropriate. The intra
operative findings were inflamed appendix with appendiculolith with healthy base arising from
cecum which was fixed in left lower quadrant with minimal free fluid. Duodeno-jejunal flexure
3
with whole small bowel was seen on right side and the large bowel was seen on left side (Figure
5). The postoperative period was uneventful and the diagnosis was correlated with
histopathological examination of appendix. Patient didn't have any issues during first follow up
visit. Patient was lost to further follow up which was later found out to be due to geographical
Discussion
Embryological development of the gut is a complex process in which tubular structure undergoes
rotation and fixation. There is total of 270° counterclockwise rotation of midgut around the
superior mesenteric artery axis with 90° when the midgut herniates out and 180° when the
midgut reduces. If this process fails to occur normally, the result is midgut malrotation.
Acute appendicitis is a fairly common condition caused due to obstruction of lumen and
subsequent bacterial infection.3 It can co-exist with midgut malrotation which can sometimes
lead to a confusing clinical picture like in this case. A significant minority of left sided
appendicitis leads to presentation similar to that of right sided appendicitis with pain on right
iliac fossa.5
Midgut malrotation is associated with heterotaxy syndromes, other anomalies like annular
hernia, imperforate anus, Meckel's diverticulum, biliary atresia and omphalocele. It is especially
important to obtain Chest X-ray to rule out situs inversus totalis which may be confused with
intestinal malrotation. More than two-thirds of the left sided appendicitis are due to situs inversus
4
The incidence of midgut volvulus in symptomatic malrotation was 42.1% in the neonatal
period, and 50% beyond the neonatal period.6 Midgut volvulus presents as abdominal pain and
bilious vomiting. But this is less common than more chronic presentations of abdominal pain,
There are different methods to diagnose midgut malrotation with appendicitis which includes
abdominal X-ray, Upper gastrointestinal (UGI) contrast studies, USG abdomen and CECT
abdomen. Abdominal X-ray shows paucity of small bowel air or may be completely normal. UGI
contrast studies shows abnormal position of duodenojejunal junction which is normally situated
to the left of the left sided pedicles of vertebral bodies. The sensitivity of the upper GI series for
the diagnosis of malrotation has been reported as 95%. 8 USG is considered to be the best initial
imaging modality especially for children. USG may show inversion of SMA and SMV
relationship with blind non-compressible aperistaltic tube on the left side. CECT abdomen may
also show inversion of SMA and SMV9 along with large bowel predominantly on left, small
bowel predominantly on right side and concomitant feature of acute appendicitis. Abnormalities
of the SMA and SMV relationship is not entirely diagnostic of intestinal malrotation.
When it presents as volvulus, Ladds procedure is generally performed with derotation of gut,
broadening of mesenteric base, division of Ladds bands, appendicectomy, fixing small bowel on
the right side and large bowel on the left side. It can be performed as open or laparoscopic
surgery.
pathology like acute appendicitis then Ladds procedure becomes optional. Laparoscopic
unlike open procedures, laparoscopic procedures have a steep learning curve and are not well
5
established in low resource settings like ours. Some recommend only correction of intestinal
pathology without Ladds procedure as the risk of complications following Ladds procedure
outweighs the risk of developing volvulus. While others recommend a more aggressive approach
to treat the asymptomatic malrotation as the consequences of volvulus are usually disastrous
including short gut syndrome and perforation peritonitis. But there is a lack of quality data to
Conclusion
present, consensus among experts regarding the management of incidental malrotation is lacking.
List of abbreviations
CT = Computerised tomography
USG = Ultrasonography
Declaration
Ethics approval and consent to participate
Need for ethical approval waived. Consent from the patient deemed to be enough.
Consent for publication
Written informed consent was obtained from the patient for publication of this case report and
any accompanying images. A copy of the written consent is available for review by the Editor-
in-Chief of this journal.
Availability of data and material
6
Data mentioned in the case report are available to the reviewers if required.
Competing interests
The authors declare that they have no competing interests
Funding
None
Authors' contributions
HK gathered the data and wrote the parts of discussion section. DS and NK performed the
surgery and proof read the manuscript. ZK also wrote part of discussion.
Acknowledgements
None
References
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gastrointestinal imaging and Intervention, 2nd ed. London: B.C. Decker Inc; 2000. p. 311–
475.
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1;50(10):1783-90. doi:10.1016/j.jpedsurg.2015.06.019
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