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[Colitis cystica profunda. A case report]

E Villanueva Sáenz1, J P Peña, J L Rocha Ramírez

  • 1Departamento de cirugía de colon y recto, Hospital de Oncología, México, D.F.

Revista De Gastroenterologia De Mexico
|January 1, 1997
PubMed
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Colitis cystica profunda (CCP), a rare rectal condition, was successfully treated with surgery in a localized case presenting with mucous discharge. Surgical resection is the optimal treatment for CCP, offering better outcomes than medical management.

Area of Science:

  • Gastroenterology
  • Colorectal Surgery
  • Pathology

Background:

  • Colitis cystica profunda (CCP) is a rare, benign condition of unknown etiology, characterized by submucous cysts.
  • Histologically, CCP involves lamina propria obliteration by fibroblasts and submucous cysts, presenting in localized, segmental, or diffuse forms.
  • CCP can be associated with conditions like solitary rectal ulcer, rectal prolapse, and pelvic floor alterations.

Observation:

  • A localized case of Colitis cystica profunda (CCP) presented with transanal mucous secretion.
  • Physical examination revealed a sessile, mucous polypoid formation 8 cm from the anal verge.
  • The patient underwent surgical resection for the observed CCP lesion.

Findings:

  • Surgical resection of the localized Colitis cystica profunda (CCP) resulted in a satisfactory outcome.

Related Experiment Videos

  • The presented case highlights transanal mucous secretion as a key symptom of CCP.
  • Histopathological confirmation of CCP was established.

    • Implications:

    • Colitis cystica profunda (CCP) should be suspected in patients with pelvic floor dysfunction or sigmoidorectal intussusception.
    • Surgical treatment is considered optimal for Colitis cystica profunda (CCP), with medical management having a high failure rate.
    • This case contributes to the national literature on Colitis cystica profunda (CCP) management and presentation.