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Interval Squamous Cell Carcinoma of the Rectum
Daryl Ramai1, Kinesh Changela2, Jonathan Lai1
1Department of Anatomical Sciences, St. George's University, True Blue, Grenada.
This case report details a rare instance of rectal squamous cell carcinoma (SCC) in an 82-year-old female. Diagnosis was confirmed via biopsy of a rectal mass presenting with abdominal pain and lymphadenopathy.
Area of Science:
- Gastroenterology
- Oncology
Background:
- Rectal squamous cell carcinoma (SCC) is a rare malignancy with unclear etiology, though chronic inflammation and infections are suspected contributing factors.
- The incidence of rectal SCC is estimated at 0.1-0.25% per 1,000 cases, highlighting its infrequent occurrence.
Observation:
- An 82-year-old female presented with a two-month history of abdominal pain, hematochezia, and inguinal lymphadenopathy with purulent discharge.
- Imaging revealed an irregular rectal mass with significant pelvic and retroperitoneal adenopathy.
- Colonoscopy identified a large, circumferential, nonobstructing rectal lesion, further characterized by endoscopic ultrasound.
Findings:
- Histopathological analysis of a cold biopsy confirmed the rectal mass as squamous cell carcinoma (SCC).
- The findings underscore the importance of considering rare diagnoses even after unremarkable prior screenings.
Implications:
- This case highlights the diagnostic challenges and clinical presentation of rare rectal SCC.
- Further research into the pathogenesis of rectal SCC is warranted to improve early detection and treatment strategies.
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