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Gallstone disease

Key points

Increasing obesity in children - primary gallstones (GS) now more common than haematological disease

Biliary dyskinesia now described in children


LITH, UGT1A1 genes predispose


Stone types

Mixed pigment - brown - due to sepsis, biliary obstruction

Black pigment - Calcium bilirubinate - due to haemolytic diseases

Cholesterol - often a single stone, more common in obese females

Calcium carbonate - associated with abdominal procedure as neonate, cystic duct obstruction


Conditions predisposing to GS

Congenital heart disease - calcium bilirubinate stones

Caused by chronic cyanosis and thrombocytopenia


Bone marrow + stem cell transplant

Graft vs host disease disrupts enterohepatic circulation

Chemo/radiotherapy also reisk factors


Cystic fibrosis

Mucus blocking of bile ducts causes biliary stasis and stone formation


Trisomy 21

Likely due to foetal hypercholesterolaemia


Parenteral nutrition

Due to disruption of enterohepatic circulation


Acalculous cholecystitis

Caused by trauma, sepsis, diabetes

Can do cholecystostomy in critically unwell patients. Cholecystectomy after stabilisation


Acalculous mucocoele (gallbladder hydrops)

Causes:

Kawasaki syndrome (i.e. mucocutaneous lymph node syndrome)

Streptococcal pharyngitis

Hepatitis

Familial Mediterranean fever

Nephrotic syndrome


Management

Define if symptoms are definitely related to GS

Bogue et al 2010 Asymptomatic GS can be managed conservatively - only 5% risk of complications

Infants can be managed conservatively - 25% resolve, 75% asymptomatic

Ursodeoxycholic acid helpful in dissolution of small stones in patients not fit for surgery


Offer laparoscopic cholecystectomy to patients who likely have symptomatic GS

Perform liver function tests prior - if elevated, get MRCP or do on-table cholangiogram as it may indicate ductal stones


Gallbladder duplications - no need to excise if not complicated


Complications of cholecystectomy

Retained stones - perform ERCP (in centre where this is available)

No lower age limit for ERCP - successful in 1 year olds

Can do ERCP in patients with pancreatitis


CBD injuries cause major morbidity - involve experienced hepatobilary (HPB) surgeon. If small, repair +/- T tube

If more extensive may need reconstruction e.g choledochojejunostomy

Large bile leak not responding to drainage - perform percutaneous transhepatic cholangiogram - then repair by experienced HPB surgeon



Gallbladder Polyps

Incidence

Uncommon findings, often discovered incidentally

Mostly benign and asymptomatic, malignant transformation is rare


Aetiology

Primary: occurring in isolation

Secondary:

Anomalous arrangement of the pancreatobiliary duct

Metachromatic leukodystrophy (an inherited lysosomal storage disorder)

Peutz-Jeghers syndrome

Gardner’s syndrome


Histological types

Cholesterol polyps (most common)

Hyperplastic polyps

Adenomatous polyps


Imaging

Ultrasound is the the modality of choice - polyps appear as intraluminal fixed, non-shadowing lesions

Distinguishable from gallstones (which are mobile with posterior acoustic shadow) and sludge (which is mobile but without shadow)


Management

Observation: for asymptomatic patients with small (<10 mm) isolated polyps AND no syndromic association.

Laparoscopic cholecystectomy if:

Polyps >10 mm with syndromic risk or >15 mm in patients without syndromic risk

Rapidly growing lesions on follow up USS

Multiple polyps

Associated with gallstones


Page edited by Mr Mahmoud Abdelbary MSc, MRCS August 2025


Page edited by Mrs Charnjit Seehra BSc August 2025



References

Gollin, Gerald, et al. "Gallbladder Disease." Pediatric Surgery NaT, American Pediatric Surgical Association, 2020. Pediatric Surgery Library, www.pedsurglibrary.com/apsa/view/Pediatric-Surgery-NaT/829468/all/Gallbladder_Disease.


Bogue CO, et al. Risk factors, complications, and outcomes of gallstones in children: a single-center review. J Pediatr Gastroenterol Nutr. 2010


Ballouhey Q, Binet A, Varlet F, Baudry M, Dubois R, Héry G, Podevin G, Abbo O, Arnaud A, Barras M, Guerin F. Management of Polypoid Gallbladder Lesions in Children: A Multicenter study. European Journal of Pediatric Surgery. 2018 Feb;28(01):006-11.


Ferzeliyev O, Oğuz B, Soyer T, Boybey Türer Ö, Haliloglu M, Tanyel FC. Clinical Features and Outcomes of Gallbladder Polyps in Children. Turk J Gastroenterol. 2022 Sep;33(9):803-807. doi: 10.5152/tjg.2022.21944. PMID: 35946883; PMCID: PMC9524491.


Stringer MD, Ceylan H, Ward K, Wyatt JI. Gallbladder polyps in children--classification and management. J Pediatr Surg. 2003 Nov;38(11):1680-4. doi: 10.1016/s0022-3468(03)00583-9. PMID: 14614726.


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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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