Cystic intra-abdominal masses in children
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Updated: Feb 19, 2026

Laparoscopic Choledochal Cyst Excision and Roux-en-Y Choledochojejunostomy in Adults
Published on: February 28, 2025
Luisa Ferrero1, Riccardo Guanà1, Giulia Carbonaro1
1Division of Pediatric General, Thoracic and Minimally Invasive Surgery, AOU Città della Salute e della Scienza, Regina Margherita Children's Hospital, Torino, Italy.
Insights
Benign pediatric intra-abdominal cystic masses are rare but can cause significant pain. Surgical excision is effective for diagnosis and treatment, with no recurrences observed in this study.
Area of Science:
- Pediatric Surgery
- Surgical Pathology
- Abdominal Imaging
Background:
- Benign intra-abdominal cystic masses in children are uncommon.
- Their etiopathogenesis, histology, and clinical presentation vary significantly.
- Prompt diagnosis and appropriate management are crucial.
Purpose of the Study:
- To report the experience in treating pediatric intra-abdominal cystic masses.
- To discuss optimal diagnostic and treatment modalities.
- To highlight the importance of considering these masses in differential diagnosis.
Main Methods:
- Retrospective review of 5 pediatric patients with cystic intra-abdominal masses.
- Inclusion of data on clinical presentation, diagnostic tools, surgical approach, and histopathology.
- Analysis of surgical outcomes and follow-up.
Main Results:
- Five patients (2 male, 3 female) aged 8 months to 9 years were treated.
- Diagnoses included hepatobiliary cystadenoma, hepatic hamartoma, and cystic lymphangiomas.
- All patients underwent successful open surgery with no major complications or recurrences.
Conclusions:
- Benign cystic abdominal masses in children, though rare, should be considered in cases of acute abdominal pain.
- Preoperative differential diagnosis can be challenging.
- Radical excision allows for definitive histological diagnosis and prevents recurrence.
Abstract:
Benign intra-abdominal cystic masses in infancy are fairly uncommon and their etiopathogenesis, histology and clinical presentation differ significantly. Our aim is to report our experience in their treatment in order to discuss the best diagnostic and treatment modality. The medical records of 5 children (2M, 3F) with cystic intraabdominal masses referred to our hospital between November 2012 and September 2016, were retrospectively reviewed. All patients underwent open surgery and subsequent histopathologic analysis. Different clinical presentations, localizations of the masses, diagnostic tools, surgical approaches, histological examinations and outcomes were reviewed. Patients mean age was 5.4 years (range: 8 months-9 years). Two patients presented recurrent abdominal pain and abdominal distension; 1 patient had a palpable mass discovered incidentally and 2 complained acute abdominal pain. Routine laboratory tests, tumor markers and abdominal ultrasound were immediately done in all patients. Three patients underwent MRI and 1 abdominal CT. At laparotomy 2 hepatic cysts, 2 mesenteric cyst and 1 retroperitoneal cyst were discovered. Histology reports described: 1 hepatobiliary cystadenoma, 1 benign hepatic hamartoma and 3 cystic lymphangiomas (1 retroperitoneal and 2 mesenteric). There were no major postoperative complications, deaths, or recurrences in our series (follow-up 3-24 months). Despite the rarity of these lesions, benign cystic abdominal masses in children are not so uncommon and should be considered as causes of acute abdominal pain. The differential diagnosis is not always possible preoperatively. In our series, radical excision of the lesions was possible in all cases, allowing reliable histological results and avoiding recurrences.
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