Intestinal malrotation |
Classification and external resources |
ICD-10 |
Q43.3 |
ICD-9 |
751.4 |
OMIM |
193250 |
eMedicine |
ped/1200 |
Intestinal malrotation is a congenital anomaly of rotation of the midgut (embryologically, the gut undergoes a complex rotation outside the abdomen). As a result:
- the small bowel is found predominantly on the right side of the abdomen
- the cecum is displaced (from its usual position in the right lower quadrant) into the epigastrium - right hypochondrium
- the ligament of Treitz is displaced inferiorly and rightward
- fibrous bands (of Ladd) course over the horizontal part of the duodenum (DII), causing intestinal obstruction.
- the small intestine has an unusually narrow base, and therefore the midgut is prone to volvulus (a twisting that can obstruct the mesenteric blood vessels and cause intestinal ischemia).
Contents
- 1 Associated conditions
- 2 Causes
- 3 Presentation
- 4 Diagnosis
- 5 Treatment
- 6 See also
- 7 References
- 8 External links
Associated conditions
This can lead to a number of disease manifestations such as:
- Acute midgut volvulus
- Chronic midgut volvulus
- Acute duodenal obstruction
- Chronic duodenal obstruction
- Internal herniation
- Superior mesenteric artery syndrome
Causes
The exact causes are not known. It is not associated with a particular gene, but there is some evidence of recurrence in families.[1]
Presentation
Patients (often infants) present acutely with midgut volvulus, manifested by bilious vomiting, crampy abdominal pain, abdominal distention, and the passage of blood and mucus in their stool. Patients with chronic, uncorrected malrotation can have recurrent abdominal pain and vomiting.
Malrotation can also be entirely asymptomatic.
Diagnosis
With acutely ill patients, consider emergency surgery laparotomy if there is a high index of suspicion.
Plain radiography may demonstrate signs of duodenal obstruction with dilatation of the proximal duodenum and stomach but it is often non-specific. Upper gastrointestinal series is the modality of choice for the evaluation of malrotation as it will show an abnormal position of the duodeno-jejunal flexure (ligament of Treitz). In cases of malrotation complicated with volvulus, it demonstrates a corkscrew appearance of the distal duodenum and jejunum. In cases of obstructing Ladd bands, it will reveal a duodenal obstruction.
In equivocal cases, contrast enema, may be helpful by showing the caecum at an abnormal location.
It is usually discovered near birth, but in some cases is not discovered until adulthood.[2] In adults, the "whirlpool sign" of the superior mesenteric artery can be useful in identifying malrotation.[3]
Treatment
Treatment is possible and these are the steps taken: Resuscitate the patient with fluids to stabilize them before surgically
- correcting the malrotation (counterclockwise rotation of the bowel)
- cutting the fibrous bands over the duodenum.
- widening the mesenteric pedicle by separation of the duodenum and cecum
With this condition the appendix is often on the wrong side of the body and therefore removed as a precautionary measure during the surgical procedure.
One surgical technique is known as "Ladd's procedure", after Dr. William Ladd.[4][5]
Long term research on the Ladd procedure shows that even after the procedure, patients are susceptible to have complaints and might need further surgery. [6]
See also
- Normal rotation of the gut
- Situs inversus, a congenital condition in which the major visceral organs are reversed or mirrored from their normal positions.
Scientific article with literature review on the topic published in 2011[7]
References
- ^ Stalker HJ, Chitayat D (1992). "Familial intestinal malrotation with midgut volvulus and facial anomalies: a disorder involving a gene controlling the normal gut rotation?". Am. J. Med. Genet. 44 (1): 46–7. doi:10.1002/ajmg.1320440111. PMID 1519649.
- ^ Dietz DW, Walsh RM, Grundfest-Broniatowski S, Lavery IC, Fazio VW, Vogt DP (2002). "Intestinal malrotation: a rare but important cause of bowel obstruction in adults". Dis. Colon Rectum 45 (10): 1381–6. doi:10.1007/s10350-004-6429-0. PMID 12394439.
- ^ Yeh WC, Wang HP, Chen C, Wang HH, Wu MS, Lin JT (1999). "Preoperative sonographic diagnosis of midgut malrotation with volvulus in adults: the "whirlpool" sign". Journal of Clinical Ultrasound 27 (5): 279–83. doi:10.1002/(SICI)1097-0096(199906)27:5<279::AID-JCU8>3.0.CO;2-G. PMID 10355892.
- ^ Ladd WE (1936). "Surgical Diseases of the Alimentary Tract in Infants". N Engl J Med 215: 705–8. doi:10.1056/NEJM193610152151604.
- ^ Bass KD, Rothenberg SS, Chang JH (1998). "Laparoscopic Ladd's procedure in infants with malrotation". J. Pediatr. Surg. 33 (2): 279–81. doi:10.1016/S0022-3468(98)90447-X. PMID 9498402.
- ^ Murphy FL, Sparnon AL (2006-04-01). "Long-term complications following intestinal malrotation and the Ladd’s procedure: a 15 year review". Pediatric Surgery International 22 (4): 326–329. doi:10.1007/s00383-006-1653-4.
- ^ Emanuwa et al. (2011). "Midgut malrotation first presenting as acute bowel obstruction in adulthood: a case report and literature review". World Journal of Emergency Surgery 6 (22). doi:10.1186/1749-7922-6-22.
External links
- Macrorad Teleradiology Intestinal Malrotation of Adults
Congenital malformations and deformations of digestive system (Q35–Q45, 749–751)
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Upper GI tract |
Tongue, mouth and pharynx |
- Cleft lip and palate
- Van der Woude syndrome
- tongue
- Ankyloglossia
- Macroglossia
- Hypoglossia
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Esophagus |
- EA/TEF
- Esophageal atresia: types A, B, C, and D
- Tracheoesophageal fistula: types B, C, D and E
- esophageal rings
- Esophageal web (upper)
- Schatzki ring (lower)
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Stomach |
- Pyloric stenosis
- Hiatus hernia
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Lower GI tract |
Intestines |
- Intestinal atresia
- Meckel's diverticulum
- Hirschsprung's disease
- Intestinal malrotation
- Dolichocolon
- Enteric duplication cyst
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Rectum/anal canal |
- Imperforate anus
- Vestibular fistula
- Persistent cloaca
- Rectal atresia
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Accessory |
Pancreas |
- Annular pancreas
- Accessory pancreas
- Johanson–Blizzard syndrome
- Pancreas divisum
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Bile duct |
- Choledochal cysts
- Biliary atresia
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Liver |
- Alagille syndrome
- Polycystic liver disease
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noco/cofa (c)/cogi/tumr, sysi
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anat (t, g, p)/phys/devp/enzy
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noco/cong/tumr, sysi/epon
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proc, drug (A2A/2B/3/4/5/6/7/14/16), blte
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