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Gastric pathology

Key points


Gastric anatomy and physiology


Muscularis propria has three layers - innermost oblique layer, middle circular layer and outer longitudinal layer


Gastro-oesophageal junction - lies at T10

Transplyoric plane - L1


Fundus + body - oxyntic gland - mucus cells, parietal (oxyntic - HCl) cells and chief cells (pepsinogen)

Antrum - pyloric glands - neck mucus cells + G-cells (gastrin) + some chief cells


Enterochromaffin-like cells (ECL) stimulated by acetylcholine, gastrin and adrenaline - produce histamine


Acid production inhibited by somatostatin - released from D-cells in the fundus and antrum in response to gastrin and acid luminal contents. Directly inhibits release of gastrin from G-cells and histamine from ECL cells


H+/K+-ATPase pump in the parietal cell inhibited by PPI


Zollinger-Ellison syndrome - gastrin from G-cell neuroendocrine tumours (gastrinoma)


Neonatal gastric perforation


Aetiology -

Possible gaps in neonatal circular muscle

NG tube perforation

Can be due to NSAID/Steroid use

Tracheo-oesophageal fistula + ventilation

NEC


Most commonly fundus + greater curvature


Presents with sudden deterioration with large volume pneumoperitoneum. As opposed to slow deterioration (NEC), or well patient with pneumoperitoneum (SIP)


Operation

2 layer closure

Should make sure stomach is decompressed - use malecot catheter. If unwell, can close and use NG to save time, but NG can get blocked


Pyloric atresia


1:100,000


Polyhydramnios + distended stomach my be seen on antenatal scans


50% have associated anomalies - malrotation, cardiac defects, OA/TOF, other atresias in 10%

25% have Epidermolysis Bullosa - presents in 48 hours - possible autosomal recessive


Different to gastric antral web -which is normal tissues built up around pylorus


Types:

A: Thin pyloric membrane

B: Complete stenosis

C: Stomach and duodenum not connected


Treat A + B with resection of diaphragm and pyloroplasty - possibly endoscopy

C with anastomosis


Gastric heterotopic pancreas


Usually in submucosa

Secretion of enzymes causes bleeding

All diseases of normal pancreas also possible

Manage with endoscopy - if fails, needs resection


Congenital Microgastria


Very rare - less than 100 cases worldwide

Small stomach with normal mucosa


Presents with diarrhoea, oesophagitis and dilated oesophagus

Polyhydramnios and small stomach on antenatal scans


Can be isolated or associated with:

VACTERL association

Tracheo-oesophageal cleft

Malrotation/heterotaxy

Asplenia


UGI contrast shows small saccular/tubular structure where stomach should be


Management:

Start with continuous NG feeds

If fails - Hunt-Lawrence pouch - Roux-en-Y with J pouch anastomosed to oesophagus

Divide jejunum 30cm from DJ. Y anastomosis 20cm away from pouch

Start PN, contrast in 7 days

Dumping syndrome/Afferent loop syndrome are complication


Gastric diverticula


Symptoms of gastritis and peptic ulcer

Visible on lateral UGI contrast views

Can be excised if symptomatic


Gastroparesis


Causes: Idiopathic, autonomic neuropathy, diabetes in older children


Gastric pacemaker if medical management fails

Laparoscopy or laparotomy - place 2 leads in seromuscular layer between antrum and body

Tunnel into subcutaneous pouch with generator


Gastric volvulus


Primary: Laxity of the gastric ligaments

Secondary: Diaphragmatic hernia, splenic disorder

Right atrial isomerism (Ivemark syndrome): Asplenia, heterotaxy, cardiac abnormalities


Organoaxial: Rotation on the longitudinal axis through the pylorus and gastro-oesophageal junction (GOJ)

Mesenteroaxial: Rotation on an imaginary line through the lesser and greater curvatures


Presentation with Borchardt’s triad:

  1. Inability to vomit

  2. Severe epigastric distension

  3. Inability to pass a nasogastric tube


Investigations


XR signs: Mesenteroaxial - pylorus/antrum higher than GOJ

Organoaxial - greater curvature lies higher than the lesser curvature

CT to confirm


Management

Resuscitation

Decompression of stomach if possible

Laparotomy and gastropexy or gastrostomy insertion


References


Vacek, Jonathan, and Mary E Fallat. "Congenital Gastric Anomalies." Pediatric Surgery NaT, American Pediatric Surgical Association, 2020. Pediatric Surgery Library, www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829497/all/Congenital_Gastric_Anomalies.


Brahmamdam, Pavan, et al. "Gastric Disorders." Pediatric Surgery NaT, American Pediatric Surgical Association, 2021. Pediatric Surgery Library, www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829525/all/Gastric_Disorders.


Lopez PP, Megha R. Gastric Volvulus. [Updated 2022 Nov 7]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK507886/

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Please note that all information on this site is for professional educational purposes only, it does not constitute medical advice

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