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Annalsof Clinicaland Medical
Case Reports
ISSN 2639-8109
Case Report
Superior MesentericArtery Syndrome Treated by Laparoscopic
Duodenojejunostomy
El-Khoury Elias1,*
, El-Darazi Elham2
and El-Attrache Najib3
1
Department of Surgery, Central Military Hospital, Beirut, Lebanon
2
Department of Nutrition, Faculty of Arts and Sciences, USEK, Lebanon
3
Department of Surgery, Lebanese University, Lebanon
1. Abstract
Superior Mesenteric Artery syndrome (SMA Sd) is a very rare disease. It is suspected in the case
of intestinal obstruction in severely underweight patients. When conservative management fails
surgery becomes needed, with laparoscopic duodenojejunostomy being the best approach.
2. Keywords:
Superior Mesenteric Artery; Duo-
denojejunostomy; Laparoscopy
3. Case report
A 22-year-old patient, with a BMI of 22 kg/m2, presented to us
with a history of intestinal obstruction for more than five days, and
a severely distended abdomen on physical exam. Abdominal CT
Scan confirmed the diagnosis of SMA sd with an aortomesenteric
angle of 20 degrees and a distance of 7 mm (Figure 1). He was
managed conservatively with nasojejunal feeding, with no relief in
his symptoms after five days. Laparoscopic duodenojejunostomy
was decided. Under general anesthesia, the patient waspositioned
in Trendelenbourg decubitus positon and the surgeon standed
between his legs. The Camera trocar was placed 2 cm below the
umbilicus and the two operating trocars at the midclavicular line
bilaterally on the same level. The transverse colon andmesocolon
were retracted superiorly till clear vision of the third part of the
duodenum (D3) (Figure 2-3). The retroperitoneum is entered by
incising the thin peritoneal layer below the middle of D3, the In-
ferior Vena Cava (IVC) became visualized. (Figure 4) Then, D3
was completely mobilised from the aorta and the IVC posteriorly
(Figure 5), and dissected from its junction with the secondduode-
num (D2) medially (Figure 6), from the Superior Mesenteric Vein
(SMV) laterally and from the transverse mesocolon anteriorly (Fi-
gure 7). Finally, the proximal Jejunum was anastomosed mechani-
cally to D3 laterolaterally (Figure 8). The post operative course was
uneventful. The patient was relieved from his obstructive symp-
toms and subsequently regained weight.
Figure 1: Aortomesenteric angle of 20 degrees compressing the distal D3 (arrow).
Severely distended stomach (Long arrow)
Figure 2: Third duodenum (Arrow) Retracted transverse colon with its mesentery
(grasper)
*Corresponding Author (s): El-Khoury Elias, Department of Surgery, Central Military Hospi-
tal, Beirut, Lebanon, E-mail : efkhoury@gmail.com
http://www.acmcasereport.com/
Citation: El-Khoury Elias, El-Darazi Elham and El-Attrache Najib.Superior Mesenteric Artery
Syndrome Treated by Laparoscopic Duodenojejunostomy. Annals of Clinical and Medical Case
Reports. 2020; 4(1): 1-4.
Volume 4 Issue 1- 2020
Received Date: 29 Apr 2020
Accepted Date: 08 May 2020
Published Date: 11 May 2020
Volume 4 Issue 1-2020 Case Report
Figure 3: Retraction of D3 (by the grasper) with identification of its inferior limit
(arrow)
Figure 4: Incision of the peritoneal layer inferior to D3 and entering the retroperi-
toneum with identification of the IVC (arrow)
Figure 5: Posterior mobilisation of D3 from the IVC (longer arrow) and aorta
(arrow)
Figure 6: Medial mobilisation of D3 (arrow) and identification of D2(longer
arrow)
Figure 7: Upper part of D3 ( arrow) dissected from the transverse mesocolon (lon-
ger arrow)
Figure 8: Mechanical duodenojejunal anastomosis
4. Discussion
SMA Sd was first reported by Von Rokitansky on an autopsy [1].
Wilkie further detailed its pathophysiology and diagnostic findings
[2]. It is very rare with an incidence below 0.3%, [3, 4] affecting
mainly young adults and more commonly female patients [5]. SMA
Sd should be on the top of the differential diagnosis in severely
underweight patients with signs and symptoms of intestinal obs-
truction. In normal individuals, the angle created by the SMA and
the aorta is around 38 and 56 degrees while the normal distance is
10-20 mm [6, 7]. In SMA Sd the distal part of D3 becomes com-
pressed between the SMA and the aorta when the aortomesenteric
angle is less than 25% and the distance is shortened to < 8 mm [8-
11]. This is due in the majority of cases to the loss of the mesenteric
fat pad,[12] like in extreme weight loss, in some cases in bariatric
surgery, cancer, burns, and anorexia nervosa [13]. In a minorityof
cases, SMA Sd is caused by anatomic variants like short ligament
of Treitz, high insertion of duodenum at the ligament of Treitz, low
origin of SMA, lumbar hyperlordosis, where the aortomesenteric
angle is anatomically more acute or D3 is more cephalad than usual
and thus compression is more likely [14].SMA Sd can be a surgical
Copyright ©2020 El-Khoury et al. This is an open access article distributed under the terms of the Creative Commons Attribution Li- 2
cense, which permits unrestricted use, distribution, and build upon your work non-commercially.
Volume 4 Issue 1-2020 Case Report
http://www.acmcasereport.com/ 3
complication like in scoliosis surgery, [14, 15] ileoanal pouchsur-
gery, [16] abdominal aortic aneurysm repair [15]. SMA Sd may ra-
rely coexist with the Nutcracker syndrome when the left renal vein
becomes compressed [17, 18]. CT scan is the standard diagnostic
radiological tool as it allows the measurement of the aortomesen-
teric angle and distance. SMA Sd presents like any intestinal obs-
tructive disease. Relief occurs when the patient goes from supine
to prone position because gravity contributes to the duodenal
compression. Initially, SMA Sd should be treated conservatively,
and surgery is needed when medical treatment fails [19, 20]. The
surgical options include duodenojejunostomy, gastrojejunostomy
and duodenal derotation. Gastrojejunostomy does not relieve the
proximal duodenal obstruction and patients can continue to have
postoperative vomiting [21]. Duodenal derotation has the advan-
tages that it does not require an anastomosis, however it has a high
failure rate [9, 22, 23]. Laparoscopic duodenojejunostomy, first
performed in 1998, [24] is considered to be the best surgical treat-
ment for SMA Sd with the same outcome as open surgery but with
less morbidity with 90% success rate [6, 17, 22, 25-28].
References
1. Von Rokitansky C. In: Lehrbuch der pathologischen Anatomie. 3rd
ed. Vienna: Braumüller; 1861. Superior mesenteric artery syndrome;
p. 87.
2. Wilkie DPD. Chronic Duodenal Ileus. The American Journal of the
Medical Sciences. 1927; 173:643-48.
3. Ganss A, Rampado S, Savarino E, Bardini R. Superior Mesenteric
Artery Syndrome: a Prospective Study in a Single Institution. J Gas-
trointest Surg. 2019; 23:997-1005.
4. Shiu JR, Chao HC, Luo CC, Lai MW,Kong MS, Chen SY, et al. Clin-
ical and nutritional outcomes in children with idiopathic superior
mesenteric artery syndrome. J Pediatr Gastroenterol Nutr. 2010; 51:
177-82.
5. Smith BM, Zyromski NJ, Purtill MA. Superior mesenteric artery syn-
drome: an underrecognized entity in the trauma population. J Trau-
ma. 2008; 64: 827-30.
6. Valiathan G, Wani M, Lanker J, Reddy PK. A Case Series on Superior
Mesenteric Artery Syndrome Surgical Management, Single Institu-
tion Experience. J Clin Diagn Res. 2017; 11: 1-3.
7. Ozkurt H, Cenker MM, Bas N, Erturk SM, Basak M. Measurement
of the distance and angle between the aorta and superior mesenteric
artery: normal values in different BMI categories. Surg Radiol Anat.
2007; 29: 595-9.
8. Neri S, Signorelli SS, Mondati E, Pulvirenti D, Campanile E, Di Pino
L, et al. Ultrasound imaging in diagnosis of superior mesenteric ar-
tery syndrome. J Intern Med. 2005; 257: 346-51.
9. Merrett ND, Wilson RB, Cosman P,Biankin AV.Superior mesenteric
artery syndrome: diagnosis and treatment strategies. J Gastrointest
Surg. 2009; 13: 287-92.
10. Oliva-Fonte C, Fernández Rey C, Pereda Rodríguez J, González-
Fernández AM. Wilkie´s syndrome. Rev Esp Enferm Dig. 2017;
109: 62-3.
11. Cardarelli-Leite L, Velloni FG, Salvadori PS, Lemos MD, D’Ippolito
G. Abdominal vascular syndromes: characteristic imaging findings.
Radiol Bras. 2016; 49: 257-63.
12. Biank V,Werlin S. Superior mesenteric artery syndrome in children:
a 20-year experience. J Pediatr Gastroenterol Nutr. 2006 ;42: 522-5.
13. Mascolo M, Dee E, Townsend R, Brinton JT, Mehler PS. Severe gas-
tric dilatation due to superior mesenteric artery syndrome in anorex-
ia nervosa. Int J Eat Disord. 2015; 48: 532-4.
14. Iwaoka Y,Yamada M, Takehira Y,Hanajima K, Nakamura T, Muro-
hisa G, et al. Superior mesenteric artery syndrome in identical twin
brothers. Intern Med. 2001; 40:713-5.
15. Zaraket V,Deeb L. Wilkie’s Syndrome or Superior Mesenteric Artery
Syndrome: Fact or Fantasy? Case Rep Gastroenterol. 2015; 9: 194-9.
16. Matheus Cde O, Waisberg J, Zewer MH, Godoy AC. Syndrome of
duodenal compression by the superior mesenteric artery following
restorative proctocolectomy: a case report and review of literature.
Sao Paulo Med J. 2005; 123: 151-3.
17. Shi Y, Shi G, Li Z, Chen Y, Tang S, Huang W. Superior mesenteric
artery syndrome coexists with Nutcracker syndrome in a female: a
case report. BMC Gastroenterol. 2019; 19: 15.
18. Barsoum MK, Shepherd RF, Welch TJ. Patient with both Wilkie syn-
drome and nutcracker syndrome. Vasc Med. 2008; 13: 247-50.
19. Rodriguez EJ, Hernandez-Villegas AC, Serralde-Zuniga AE, Reyes-
Ramirez A. The two sides of superior mesenteric artery syndrome
treatment: conservative or surgical management? Nutr Hosp. 2017;
34: 997-1000.
20. Bohanon FJ, Nunez Lopez O, Graham BM, Griffin LW,Radhakrish-
nan RS. A Case Series of Laparoscopic Duodenojejunostomy for the
Treatment of Pediatric Superior Mesenteric Artery Syndrome. Int J
Surg Res. 2016; 2016:1-5.
21. Pottorf BJ, Husain FA, Hollis HW Jr, Lin E. Laparoscopic manage-
ment of duodenal obstruction resulting from superior mesenteric
artery syndrome. JAMA Surg. 2014; 149: 1319-22.
Volume 4 Issue 1-2020 Case Report
http://www.acmcasereport.com/ 4
22. Lorentziadis ML. Wilke’s syndrome: A rare cause of duodenal ob-
struction. Ann Gastroenterol. 2011; 24:59-61.
23. Reece K, Day R, Welch J. Superior Mesenteric Artery Syndrome
with Abdominal Compartment Syndrome. Case Rep Emerg Med.
2016; 2016: 7809281.
24. Gersin KS, Heniford BT. Laparoscopic duodenojejunostomy for
treatment of superior mesenteric artery syndrome. JSLS. 1998; 2:
281-4.
25. Wang T,Wang ZX, Wang HJ. Clinical Insights into Superior Mesen-
teric Artery Syndrome with Multiple Diseases: A Case Report. Dig.
Dis. Sci. 2019; 64:1711-4.
26. Kirby GC, Faulconer ER, Robinson SJ, Perry A, Downing R. Su-
perior mesenteric artery syndrome: a single Centre experience of
laparoscopic duodenojejunostomy as the operation of choice. Ann
R Coll Surg Engl. 2017; 99: 472-5.
27. Wyten R, Kelty CJ, Falk GL. Laparoscopic duodenojejunostomy for
the treatment of superior mesenteric artery (SMA) Syndrome:case
series. J Laparoendosc Adv Surg Tech A. 2010; 20: 173-6.
28. BarchiLC, Alves AM, Jacob CE,Bresciani CJC, YagiOK,Nogueira
TG, et al. Favorable minimal invasive surgery in the treatment of
superior mesenteric artery syndrome: Case report. Int J Surg Case
Rep. 2016; 29: 223-6.

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ACMCR-v4-1379.pdf

  • 1. Annalsof Clinicaland Medical Case Reports ISSN 2639-8109 Case Report Superior MesentericArtery Syndrome Treated by Laparoscopic Duodenojejunostomy El-Khoury Elias1,* , El-Darazi Elham2 and El-Attrache Najib3 1 Department of Surgery, Central Military Hospital, Beirut, Lebanon 2 Department of Nutrition, Faculty of Arts and Sciences, USEK, Lebanon 3 Department of Surgery, Lebanese University, Lebanon 1. Abstract Superior Mesenteric Artery syndrome (SMA Sd) is a very rare disease. It is suspected in the case of intestinal obstruction in severely underweight patients. When conservative management fails surgery becomes needed, with laparoscopic duodenojejunostomy being the best approach. 2. Keywords: Superior Mesenteric Artery; Duo- denojejunostomy; Laparoscopy 3. Case report A 22-year-old patient, with a BMI of 22 kg/m2, presented to us with a history of intestinal obstruction for more than five days, and a severely distended abdomen on physical exam. Abdominal CT Scan confirmed the diagnosis of SMA sd with an aortomesenteric angle of 20 degrees and a distance of 7 mm (Figure 1). He was managed conservatively with nasojejunal feeding, with no relief in his symptoms after five days. Laparoscopic duodenojejunostomy was decided. Under general anesthesia, the patient waspositioned in Trendelenbourg decubitus positon and the surgeon standed between his legs. The Camera trocar was placed 2 cm below the umbilicus and the two operating trocars at the midclavicular line bilaterally on the same level. The transverse colon andmesocolon were retracted superiorly till clear vision of the third part of the duodenum (D3) (Figure 2-3). The retroperitoneum is entered by incising the thin peritoneal layer below the middle of D3, the In- ferior Vena Cava (IVC) became visualized. (Figure 4) Then, D3 was completely mobilised from the aorta and the IVC posteriorly (Figure 5), and dissected from its junction with the secondduode- num (D2) medially (Figure 6), from the Superior Mesenteric Vein (SMV) laterally and from the transverse mesocolon anteriorly (Fi- gure 7). Finally, the proximal Jejunum was anastomosed mechani- cally to D3 laterolaterally (Figure 8). The post operative course was uneventful. The patient was relieved from his obstructive symp- toms and subsequently regained weight. Figure 1: Aortomesenteric angle of 20 degrees compressing the distal D3 (arrow). Severely distended stomach (Long arrow) Figure 2: Third duodenum (Arrow) Retracted transverse colon with its mesentery (grasper) *Corresponding Author (s): El-Khoury Elias, Department of Surgery, Central Military Hospi- tal, Beirut, Lebanon, E-mail : efkhoury@gmail.com http://www.acmcasereport.com/ Citation: El-Khoury Elias, El-Darazi Elham and El-Attrache Najib.Superior Mesenteric Artery Syndrome Treated by Laparoscopic Duodenojejunostomy. Annals of Clinical and Medical Case Reports. 2020; 4(1): 1-4. Volume 4 Issue 1- 2020 Received Date: 29 Apr 2020 Accepted Date: 08 May 2020 Published Date: 11 May 2020
  • 2. Volume 4 Issue 1-2020 Case Report Figure 3: Retraction of D3 (by the grasper) with identification of its inferior limit (arrow) Figure 4: Incision of the peritoneal layer inferior to D3 and entering the retroperi- toneum with identification of the IVC (arrow) Figure 5: Posterior mobilisation of D3 from the IVC (longer arrow) and aorta (arrow) Figure 6: Medial mobilisation of D3 (arrow) and identification of D2(longer arrow) Figure 7: Upper part of D3 ( arrow) dissected from the transverse mesocolon (lon- ger arrow) Figure 8: Mechanical duodenojejunal anastomosis 4. Discussion SMA Sd was first reported by Von Rokitansky on an autopsy [1]. Wilkie further detailed its pathophysiology and diagnostic findings [2]. It is very rare with an incidence below 0.3%, [3, 4] affecting mainly young adults and more commonly female patients [5]. SMA Sd should be on the top of the differential diagnosis in severely underweight patients with signs and symptoms of intestinal obs- truction. In normal individuals, the angle created by the SMA and the aorta is around 38 and 56 degrees while the normal distance is 10-20 mm [6, 7]. In SMA Sd the distal part of D3 becomes com- pressed between the SMA and the aorta when the aortomesenteric angle is less than 25% and the distance is shortened to < 8 mm [8- 11]. This is due in the majority of cases to the loss of the mesenteric fat pad,[12] like in extreme weight loss, in some cases in bariatric surgery, cancer, burns, and anorexia nervosa [13]. In a minorityof cases, SMA Sd is caused by anatomic variants like short ligament of Treitz, high insertion of duodenum at the ligament of Treitz, low origin of SMA, lumbar hyperlordosis, where the aortomesenteric angle is anatomically more acute or D3 is more cephalad than usual and thus compression is more likely [14].SMA Sd can be a surgical Copyright ©2020 El-Khoury et al. This is an open access article distributed under the terms of the Creative Commons Attribution Li- 2 cense, which permits unrestricted use, distribution, and build upon your work non-commercially.
  • 3. Volume 4 Issue 1-2020 Case Report http://www.acmcasereport.com/ 3 complication like in scoliosis surgery, [14, 15] ileoanal pouchsur- gery, [16] abdominal aortic aneurysm repair [15]. SMA Sd may ra- rely coexist with the Nutcracker syndrome when the left renal vein becomes compressed [17, 18]. CT scan is the standard diagnostic radiological tool as it allows the measurement of the aortomesen- teric angle and distance. SMA Sd presents like any intestinal obs- tructive disease. Relief occurs when the patient goes from supine to prone position because gravity contributes to the duodenal compression. Initially, SMA Sd should be treated conservatively, and surgery is needed when medical treatment fails [19, 20]. The surgical options include duodenojejunostomy, gastrojejunostomy and duodenal derotation. Gastrojejunostomy does not relieve the proximal duodenal obstruction and patients can continue to have postoperative vomiting [21]. Duodenal derotation has the advan- tages that it does not require an anastomosis, however it has a high failure rate [9, 22, 23]. Laparoscopic duodenojejunostomy, first performed in 1998, [24] is considered to be the best surgical treat- ment for SMA Sd with the same outcome as open surgery but with less morbidity with 90% success rate [6, 17, 22, 25-28]. References 1. Von Rokitansky C. In: Lehrbuch der pathologischen Anatomie. 3rd ed. Vienna: Braumüller; 1861. Superior mesenteric artery syndrome; p. 87. 2. Wilkie DPD. Chronic Duodenal Ileus. The American Journal of the Medical Sciences. 1927; 173:643-48. 3. Ganss A, Rampado S, Savarino E, Bardini R. Superior Mesenteric Artery Syndrome: a Prospective Study in a Single Institution. J Gas- trointest Surg. 2019; 23:997-1005. 4. Shiu JR, Chao HC, Luo CC, Lai MW,Kong MS, Chen SY, et al. Clin- ical and nutritional outcomes in children with idiopathic superior mesenteric artery syndrome. J Pediatr Gastroenterol Nutr. 2010; 51: 177-82. 5. Smith BM, Zyromski NJ, Purtill MA. Superior mesenteric artery syn- drome: an underrecognized entity in the trauma population. J Trau- ma. 2008; 64: 827-30. 6. Valiathan G, Wani M, Lanker J, Reddy PK. A Case Series on Superior Mesenteric Artery Syndrome Surgical Management, Single Institu- tion Experience. J Clin Diagn Res. 2017; 11: 1-3. 7. Ozkurt H, Cenker MM, Bas N, Erturk SM, Basak M. Measurement of the distance and angle between the aorta and superior mesenteric artery: normal values in different BMI categories. Surg Radiol Anat. 2007; 29: 595-9. 8. Neri S, Signorelli SS, Mondati E, Pulvirenti D, Campanile E, Di Pino L, et al. Ultrasound imaging in diagnosis of superior mesenteric ar- tery syndrome. J Intern Med. 2005; 257: 346-51. 9. Merrett ND, Wilson RB, Cosman P,Biankin AV.Superior mesenteric artery syndrome: diagnosis and treatment strategies. J Gastrointest Surg. 2009; 13: 287-92. 10. Oliva-Fonte C, Fernández Rey C, Pereda Rodríguez J, González- Fernández AM. Wilkie´s syndrome. Rev Esp Enferm Dig. 2017; 109: 62-3. 11. Cardarelli-Leite L, Velloni FG, Salvadori PS, Lemos MD, D’Ippolito G. Abdominal vascular syndromes: characteristic imaging findings. Radiol Bras. 2016; 49: 257-63. 12. Biank V,Werlin S. Superior mesenteric artery syndrome in children: a 20-year experience. J Pediatr Gastroenterol Nutr. 2006 ;42: 522-5. 13. Mascolo M, Dee E, Townsend R, Brinton JT, Mehler PS. Severe gas- tric dilatation due to superior mesenteric artery syndrome in anorex- ia nervosa. Int J Eat Disord. 2015; 48: 532-4. 14. Iwaoka Y,Yamada M, Takehira Y,Hanajima K, Nakamura T, Muro- hisa G, et al. Superior mesenteric artery syndrome in identical twin brothers. Intern Med. 2001; 40:713-5. 15. Zaraket V,Deeb L. Wilkie’s Syndrome or Superior Mesenteric Artery Syndrome: Fact or Fantasy? Case Rep Gastroenterol. 2015; 9: 194-9. 16. Matheus Cde O, Waisberg J, Zewer MH, Godoy AC. Syndrome of duodenal compression by the superior mesenteric artery following restorative proctocolectomy: a case report and review of literature. Sao Paulo Med J. 2005; 123: 151-3. 17. Shi Y, Shi G, Li Z, Chen Y, Tang S, Huang W. Superior mesenteric artery syndrome coexists with Nutcracker syndrome in a female: a case report. BMC Gastroenterol. 2019; 19: 15. 18. Barsoum MK, Shepherd RF, Welch TJ. Patient with both Wilkie syn- drome and nutcracker syndrome. Vasc Med. 2008; 13: 247-50. 19. Rodriguez EJ, Hernandez-Villegas AC, Serralde-Zuniga AE, Reyes- Ramirez A. The two sides of superior mesenteric artery syndrome treatment: conservative or surgical management? Nutr Hosp. 2017; 34: 997-1000. 20. Bohanon FJ, Nunez Lopez O, Graham BM, Griffin LW,Radhakrish- nan RS. A Case Series of Laparoscopic Duodenojejunostomy for the Treatment of Pediatric Superior Mesenteric Artery Syndrome. Int J Surg Res. 2016; 2016:1-5. 21. Pottorf BJ, Husain FA, Hollis HW Jr, Lin E. Laparoscopic manage- ment of duodenal obstruction resulting from superior mesenteric artery syndrome. JAMA Surg. 2014; 149: 1319-22.
  • 4. Volume 4 Issue 1-2020 Case Report http://www.acmcasereport.com/ 4 22. Lorentziadis ML. Wilke’s syndrome: A rare cause of duodenal ob- struction. Ann Gastroenterol. 2011; 24:59-61. 23. Reece K, Day R, Welch J. Superior Mesenteric Artery Syndrome with Abdominal Compartment Syndrome. Case Rep Emerg Med. 2016; 2016: 7809281. 24. Gersin KS, Heniford BT. Laparoscopic duodenojejunostomy for treatment of superior mesenteric artery syndrome. JSLS. 1998; 2: 281-4. 25. Wang T,Wang ZX, Wang HJ. Clinical Insights into Superior Mesen- teric Artery Syndrome with Multiple Diseases: A Case Report. Dig. Dis. Sci. 2019; 64:1711-4. 26. Kirby GC, Faulconer ER, Robinson SJ, Perry A, Downing R. Su- perior mesenteric artery syndrome: a single Centre experience of laparoscopic duodenojejunostomy as the operation of choice. Ann R Coll Surg Engl. 2017; 99: 472-5. 27. Wyten R, Kelty CJ, Falk GL. Laparoscopic duodenojejunostomy for the treatment of superior mesenteric artery (SMA) Syndrome:case series. J Laparoendosc Adv Surg Tech A. 2010; 20: 173-6. 28. BarchiLC, Alves AM, Jacob CE,Bresciani CJC, YagiOK,Nogueira TG, et al. Favorable minimal invasive surgery in the treatment of superior mesenteric artery syndrome: Case report. Int J Surg Case Rep. 2016; 29: 223-6.