S3867 Uncommon Pathology in Uncommon Age: Colitis Cystica Profunda in the Youngest Pediatric Case to Date

Introduction: Colitis cystica profunda (CCP), a benign condition primarily affects the submucosal layer of the colon. Histologically, characterized by mucosal cysts that extend deep into the colonic wall, often causing distension of the colonic mucosa. While CCP is commonly seen in adults, there are very few pediatric cases. Here we present an extremely rare case of CCP in an 8-year-old child, who represents the youngest patient in available literature to date. Case Description/Methods: An 8-year-old boy presented with 3 months of rectal bleeding and intermittent left lower quadrant pain, with no relevant medical, family, or genetic history. He was well nourished with lower abdominal tenderness; vitals and digital rectal exam were normal. Labs showed mild anemia (Hb 10.2 g/dL); C-reactive protein and coagulation were normal. Abdo-USG showed no abnormalities. Colonoscopy revealed a 4 cm pedunculated sigmoid polyp, removed via detachable end loop and snare. Post-procedure check showed no residual lesion or bleeding. Histology confirmed CCP with submucosal cysts lined by benign epithelium. Discussion: CCP is a rare benign condition, histologically characterized by mucus filled cyst in the submucosa, often mimic malignant lesions like mucinous adenocarcinomas, mostly in rectum and sigmoid. The localized form usually presents as solitary polyp, while diffuse form usually occurs in inflammatory bowel disease. In Pediatric cases, symptoms vary from rectal bleeding, mucorrhea, diarrhea, and colonic obstruction to indeed a pure incidental finding at imaging or colonoscopy. Pathogenesis of CCP includes combination of congenital muscularis mucosa weakness, continuous inflammation, ischemia or trauma causing epithelial herniation. It is important to diagnose and differentiate HPE from malignancies like mucinous adenocarcinomas. Computed tomography and magnetic resonance imaging are considered for D/D by identifying cystic, non-invasive submucosal lesions. Endoscopic findings often include nodular or polypoid lesions with normal or edematous mucosa. Here, colonoscopy demonstrated a pedunculated polyp histologically confirmed as CCP. Treatment varies according to the size and symptomatology of the lesion. Localized CCP is treated conservatively, whereas CBT shows further evidence of endoscopic removal. Radicals are indicated for cases with complications like obstruction or suspicion of malignant disease. In cases of recurrence monitoring is done through follow-up colonoscopy, but it would generally mean an excellent prognosis with proper management of the condition.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001142928.53296.7b
Primary Topic
Microscopic Colitis
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article
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article

S3867 Uncommon Pathology in Uncommon Age: Colitis Cystica Profunda in the Youngest Pediatric Case to Date

Pradip Vekariya, Rajesh Patel, Ishika A. Golakiya, Yash M. Hapani et al.
The American Journal of Gastroenterology
Microscopic Colitis
article

S3867 Uncommon Pathology in Uncommon Age: Colitis Cystica Profunda in the Youngest Pediatric Case to Date

Pradip Vekariya, Rajesh Patel, Ishika A. Golakiya, Yash M. Hapani, Niralkumar L. Ghevariya
article en

Abstract

Introduction: Colitis cystica profunda (CCP), a benign condition primarily affects the submucosal layer of the colon. Histologically, characterized by mucosal cysts that extend deep into the colonic wall, often causing distension of the colonic mucosa. While CCP is commonly seen in adults, there are very few pediatric cases. Here we present an extremely rare case of CCP in an 8-year-old child, who represents the youngest patient in available literature to date. Case Description/Methods: An 8-year-old boy presented with 3 months of rectal bleeding and intermittent left lower quadrant pain, with no relevant medical, family, or genetic history. He was well nourished with lower abdominal tenderness; vitals and digital rectal exam were normal. Labs showed mild anemia (Hb 10.2 g/dL); C-reactive protein and coagulation were normal. Abdo-USG showed no abnormalities. Colonoscopy revealed a 4 cm pedunculated sigmoid polyp, removed via detachable end loop and snare. Post-procedure check showed no residual lesion or bleeding. Histology confirmed CCP with submucosal cysts lined by benign epithelium. Discussion: CCP is a rare benign condition, histologically characterized by mucus filled cyst in the submucosa, often mimic malignant lesions like mucinous adenocarcinomas, mostly in rectum and sigmoid. The localized form usually presents as solitary polyp, while diffuse form usually occurs in inflammatory bowel disease. In Pediatric cases, symptoms vary from rectal bleeding, mucorrhea, diarrhea, and colonic obstruction to indeed a pure incidental finding at imaging or colonoscopy. Pathogenesis of CCP includes combination of congenital muscularis mucosa weakness, continuous inflammation, ischemia or trauma causing epithelial herniation. It is important to diagnose and differentiate HPE from malignancies like mucinous adenocarcinomas. Computed tomography and magnetic resonance imaging are considered for D/D by identifying cystic, non-invasive submucosal lesions. Endoscopic findings often include nodular or polypoid lesions with normal or edematous mucosa. Here, colonoscopy demonstrated a pedunculated polyp histologically confirmed as CCP. Treatment varies according to the size and symptomatology of the lesion. Localized CCP is treated conservatively, whereas CBT shows further evidence of endoscopic removal. Radicals are indicated for cases with complications like obstruction or suspicion of malignant disease. In cases of recurrence monitoring is done through follow-up colonoscopy, but it would generally mean an excellent prognosis with proper management of the condition.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 59%
Microscopic Colitis
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