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Lower gastrointestinal bleeding (LGIB) in the pediatric population represents a frequently encountered clinical scenario that poses significant diagnostic and therapeutic challenges for gastroenterologists worldwide1. While many episodes of rectal bleeding in children are benign and self-limiting, persistent or recurrent hematochezia necessitates a rigorous and systematic diagnostic evaluation to identify the underlying etiology and prevent long-term sequelae2. Among the diverse causes of pediatric LGIB, colorectal polyps are identified as the most prevalent etiology, accounting for approximately 12% to 15% of all pediatric patients presenting with significant rectal bleeding in clinical settings3. Within the histological spectrum of pediatric polyps, juvenile polyps, also classified as retention polyps, represent the most frequent subtype, typically manifesting in children between the ages of 3–10 years4. These lesions are primarily characterized by cystic-dilated glands and an expanded, inflammatory stroma, often resulting from localized mucosal redundancy or chronic inflammatory stimuli5. Although juvenile polyps are traditionally regarded as benign inflammatory hamartomas, they are associated with several critical clinical risks that cannot be overlooked6. Chronic blood loss from the hyperemic and fragile surface of a polyp can lead to severe iron-deficiency anemia, which may negatively impact a child’s developmental milestones and cognitive progress7. Furthermore, large polyps can act as lead points for intussusception or cause intermittent bowel obstruction, leading to acute abdominal emergencies that require urgent surgical intervention8. Although considered rare in sporadic cases, isolated reports have also documented the potential for adenomatous transformation and subsequent malignant progression in long-standing or multiple juvenile polyps, reinforcing the clinical necessity of early and complete resection9.
A recurring difficulty in pediatric clinical practice is the subtle and often non-specific presentation of these polyps, which leads to a significant rate of misdiagnosis10. Because pediatric hematochezia is frequently painless, it is often erroneously attributed to more common benign anal conditions such as internal hemorrhoids or anal fissures by primary care providers11. This clinical misclassification frequently leads to prolonged periods of ineffective conservative management and parental anxiety12. As demonstrated in the present case, the patient suffered from intermittent bleeding for a full year before receiving a definitive diagnosis, a delay that is unfortunately common in regions where pediatric endoscopy is not routinely prioritized13. Such delays significantly exacerbate the physiological burden on the child, including the risk of chronic nutritional deficiencies and persistent psychological stress for the family unit14. Recent epidemiological investigations suggest that the detected incidence of pediatric colorectal polyps is increasing globally, a trend that may be attributed to improved diagnostic accessibility, such as high-resolution endoscopy, alongside shifts in environmental factors and Westernized dietary influences15. The exact pathophysiology of pediatric polyps remains a subject of ongoing research, with current theories pointing to a complex combination of genetic predisposition and localized inflammatory responses within the colonic mucosa16.
The anatomical distribution of pediatric polyps is another critical factor that clinicians must consider during the initial diagnostic workup17. While approximately 90% of these lesions are localized in the rectosigmoid region, a significant proportion of patients harbor proximal or multiple polyps that would be missed by simple digital rectal examinations or limited sigmoidoscopy18. This distribution pattern emphasizes the necessity of performing a full colonoscopy rather than a limited examination to ensure that synchronous lesions are not overlooked19. Historically, the management of large colorectal polyps in children often necessitated open surgical intervention or transanal excision, both of which carry inherent risks of postoperative adhesions, prolonged hospitalization, and significant physical trauma to the developing child20. The advent of therapeutic endoscopy has revolutionized this field, offering a safer and less invasive alternative that allows for simultaneous diagnosis and definitive treatment during a single procedure21. Endoscopic polypectomy, and more specifically Endoscopic Mucosal Resection (EMR), has emerged as the gold standard for managing colorectal lesions larger than 10 mm in diameter in both adult and pediatric populations22.
EMR offers several distinct technical and biomechanical advantages over traditional cold or hot snare polypectomy. By injecting a saline-based solution into the submucosal space, the clinician creates a protective fluid cushion that elevates the lesion and increases the safety margin between the mucosa and the muscularis propria. According to foundational pediatric outcome data, including the largest single-center pediatric EMR study to date, EMR is highly effective in children, achieving superior en bloc resection rates for large lesions while maintaining a low adverse event profile compared to conventional polypectomy23. Concrete practical selection boundaries for opting for EMR over conventional snare polypectomy in children include: (1) sessile or sub-pedunculated polyps measuring 15–20 mm; (2) lesions with a broad base where single-step conventional snare capture is technically difficult or margin clearance is uncertain; and (3) polyps located in anatomically precarious regions (such as the thin-walled right colon) where the risk of thermal injury is elevated24. The creation of a submucosal cushion effectively mitigates the risks of deep thermal injury and subsequent delayed perforation, which are the most feared complications of therapeutic endoscopy25. Despite these clear benefits, performing EMR for large polyps exceeding 20 mm remains technically demanding in young children due to the narrow caliber of the pediatric colon and the complexities associated with providing stable general anesthesia.
Diagnostic strategies have also evolved to include non-invasive imaging modalities as essential supportive tools for preoperative planning. While colonoscopy remains the definitive gold standard, multi-modal imaging such as three-dimensional computed tomography (3D CT) and high-frequency ultrasound can provide valuable preliminary data regarding lesion size, vascularity, and exact anatomical location, especially in emergency settings to rule out other acute pathologies26. While EMR is well-established for large polyps, its granular technical application in the pediatric demographic warrants further documentation. This illustrative case adds meaningfully to the existing pediatric EMR literature by detailing the specific technical nuances, equipment settings, and multi-step clinical decision-making required to safely manage a delayed-diagnosis, large rectal polyp initially presenting as an acute pediatric emergency27.
Case presentation:
A 7-year-old female presented to the Emergency Department with acute lower gastrointestinal bleeding and was subsequently admitted to the Department of Gastroenterology in October 2025 with a significant one-year history of intermittent hematochezia. The symptoms initially manifested as small amounts of bright red blood streaking the end of the stool, occurring approximately once every 1–2 weeks. The bleeding was occasionally accompanied by mild anal pain. Before admission, the patient had sought medical consultation at a general surgery clinic where she was empirically diagnosed with internal hemorrhoids. Management at that time consisted of conservative dietary modifications, including increased intake of fiber and fluids to maintain soft stools; however, no formal endoscopic evaluation was performed. Despite adherence to these recommendations, the hematochezia persisted and worsened over the week leading up to admission, characterized by bright red blood dripping after defecation, prompting an immediate emergency medical evaluation. The patient also reported occasional difficulty in defecation and dry stools. There were no associated symptoms of abdominal pain, vomiting, diarrhea, dizziness, fatigue, or significant weight loss.
The patient had no notable past medical history, with a normal growth and developmental trajectory. Family history was non-contributory for gastrointestinal malignancies or hereditary polyposis syndromes. Upon physical examination, the patient was alert and hemodynamically stable. Her conjunctivae and sclerae showed no signs of anemia or jaundice. Superficial lymph nodes were not palpable. Abdominal examination revealed a soft, non-tender abdomen with no palpable masses, organomegaly, or signs of peritoneal irritation. Laboratory investigations, including a complete blood count (CBC), liver and renal function tests, electrolytes, ultra-sensitive C-reactive protein (CRP < 0.5 mg/L), procalcitonin (PCT 0.04 ng/mL), and coagulation profiles, were all within normal reference ranges. A fecal occult blood test (FOBT) was positive. Chest radiography and electrocardiography showed no clinically significant abnormalities, although a minor sinus arrhythmia and short PR interval were noted.
Diagnosis, assessment, and plan:
Diagnosis: Large rectal retention polyp (juvenile polyp) with chronic intermittent hematochezia.
Assessment: Upon admission, the clinical focus was to identify the source of the prolonged lower gastrointestinal bleeding. Given the acute exacerbation of symptoms leading up to admission, an abdominal contrast-enhanced 3D CT was strictly prioritized as an initial screening tool to rapidly rule out life-threatening acute surgical abdomens common in children, such as intussusception or bleeding from a Meckel’s diverticulum. The CT identified a nodular, high-density protrusion in the rectum measuring approximately 15 mm × 12 mm, suggesting a polypoid lesion rather than vascular congestion. Subsequent diagnostic colonoscopy was performed, revealing a large sub-pedunculated polyp on the left rectal wall, measuring 20 mm × 25 mm. The polyp exhibited a hyperemic, “strawberry-like” surface with punctate white sediment. The “hemorrhoid trap” was thus definitively ruled out. Differential diagnoses considered included inflammatory bowel disease (IBD)-associated polyps and Peutz-Jeghers syndrome; however, the solitary nature and characteristic morphology were highly suggestive of a sporadic juvenile (retention) polyp. The size of the lesion (>20 mm) presented a high risk for spontaneous torsion, ongoing hemorrhage, or neoplastic transformation, providing a clear indication for therapeutic intervention.
Plan: Following a multidisciplinary discussion and obtaining informed consent from the legal guardian, the patient was scheduled for Endoscopic Mucosal Resection (EMR). Immediate conventional snare polypectomy during the initial diagnostic colonoscopy was deemed unsafe due to the lesion’s magnitude and the unacceptably high risk of severe bleeding in a pediatric patient. Therefore, the procedure was purposefully deferred to a scheduled EMR session under deeper endotracheal general anesthesia, ensuring the availability of specialized electrosurgical and hemostatic equipment. The EMR technique was selected over simple snare polypectomy to ensure a safer, deeper resection margin and to protect the relatively thin pediatric rectal wall. The plan included submucosal injection to create a fluid cushion, followed by high-frequency snare resection. To mitigate the risk of delayed postoperative hemorrhage or perforation, mechanical closure of the mucosal defect with endoclips was planned. Postoperative management included fasting, parenteral nutritional support, and a conservative inpatient observation period to monitor for delayed complications.