1. Intestinal Obstruction
Malrotation
&
Hirschsprung disease
Supervised by:- Dr/AAyed Al-Qahtany
Presented by:- Maram Al-Zain

2. Malrotation
Embryology :-
-Disproportional growth& elongation of the midgut beginning in the 5th gestational week results in :-
* Herniation of the 1ry midgut loop ( base of umbilical cord,10th week) .
*Reduction of the extracoelomic gut (10th-12th weeks,180 degree ) .
* Fixatation of the intestine into the posterior wall of the body after the 12th gestational week .

5. Cont….. -Malrotation classified into:- 1- Non-rotation .
2- Mixed OR Incomplete rotation .
3- Mesocolic hernias .

6. Cont……. Non-rotation :- Commonest abnormality.
Chch. By inadequate counterclockwise rotation of the midgut loop around SMA,(absent or arrested before exceeding 90 degrees).
Colon resides in Lt. abdomen, Cecum is near in the midline, SI is to the right of midline.
MidgutVOLVULUS & Duodenal OBSTRUCTION are significant .

7. Cont…… Mixed OR Incomplete rotation :-
2nd common rotational abnormalities .
Chch. By arrest of normal rotational process or at near 180 degree
Prearterial segment has failed to complete its rotation post. & Lt. of the SMA .
Cecum resides in the upper abdomen (usually Lt. to the SMApertoneal band ) .
Midgut volvulus & dudenal obstruction are relatively common from extrinsic compression.

8. Cont….. Mesocolic hernias:-
Result from failure of fixation of either the RT. Or Lt. mesocolon to the post. Body wall .
Rare BUT surgically important anomaly .
The resulting potential cavities may allow entrapment of small intestine on either side of the abdomen.
As with any hernia Obstruction, Incarceration & Strangulation are potential risk .

9. Clinical presentation
Incidense :- As high as 1% of the total population .
Sex :- M:F :1 (neonate),But no sexual predilection in pt. older than 1yr .
40% in the 1st week of life .
75% of the pt. diagnosed by the age of 1yr.
The remaining 25% present after age of 1yr & late adulthood
Presentation :- 1- Asymptomatic .
2- Duodenal obstruction .
3- Midgut volvulus .
Older children & adults may present :-
1- Acute volvulus .
2- Episodic obstructive symptoms .
3- Chronic abdominal pain .
the absence of symptoms in many pt. yields in much lower clinical incidense.

11. Diagnosis History Maternal Neonatal Examination General Specific
Investigation Lab
Radiological

12. History & Examination
Most of the infant present with Acute duodenal obstructionforceful vomiting, may/may NOT bilious .
Chronic duodenal obstructionintermittent abdominal pain, failure to thrive, bilious vomiting .
Abdominal distention .
Bloody stool .
Tachycardia .
Tachypnea .
Shock .

13. Radiological Investigation
Plain abdominal x-ray .
Contrast study .
Barium swallow .
Barium enema .

14. Management -General :- -Specific :- NPO . IV. Fluid . Antibiotics .
Pre-operative preparation .
-Specific :-
NO role of non-operative management of malrotation .
Operative repair of malrotation is nearly achieved by LADD procedure .

15. Cont…..
Surgical repair is performed, the bowel is untwisted & checked carefully for damage .
Exploratory laparotomy (1st) .
If the intestine is healthy, an operation called LADD’s procedure to prevent another volvulus .
Appendectomy usually done .
?? Bowel viability Abdomen will be left open & 2nd look procedure will be planned within hrs .
If there is a section of necrotic bowel colostomy may be needed temporarily .

17. Hirschsprung disease
Def. :- It is a congenital agangliosis of the intestine which result of disordered emberyogenesis involving the myenteric nervous system .
Etiology :- Lack of migratory nerve cells to develop .
Esophagus th week .
Transverse colon th week .
Rectum th week .
Incidence :- 1 per 5000 live births .
Sex :- M:F :1
Most cases are sporadic, but long segment or total colonic agangliosis & female gender are strongly associated with familial disease

18. Clinical presentation
50% of pt. present in the neonatal age .
Most infant Don’t have normal passage of meconium in the 1st hrs .
They maybe discovered during the evaluation of chronic constipation .
Abdominal distention .
Bilious vomiting .
Malnutrition .
Failure to thrive .

19. Physical examination Physical examination NOT diagnostic .
PR. Examination shows spasm of the rectum, empty rectum .
Gush of stool or Forceful decompression of gray liquid ,?? Bloody stool at the time of the rectal examination ??Enterocolitis.

20. Diagnosis History & physical examination . Investigation :- Lab test
Radiology Plain abdominal x-ray .
2- Contrast enema .
RECTAL BIOBSY .
Anorectal manometry .

21. Management 1 - General : NPO . NGT IV. Fluid . Antibiotic .
2- Specific :
All operations depend on resection or bypass of distal aganglionic rectum in conjunction with a low rectal anastomosis to normally innervated pulled-through proximal intestine.

22. 1st stage Rlieve obstruction
Laparotomy
Identify transition zone between dilated upstream normal bowel and non-peristaltic,aganglionic distal bowel .
Colostomy above transition zone .
2nd stage
Swenson :- Proctocolectomy .
Duhamel :- Post. Pull-through with side to side anastomosis to a ganglionic rectum .
Soave :- Pull ganglionated bowel through sleeve of rectum.
Rectal myomectomy

23. & All the best Maram Al-Zain