S4023 A Rare Case of Metastatic HPV-Associated Rectal Squamous Cell Carcinoma

Introduction: Squamous cell carcinoma (SCC) of the anus is strongly associated with high-risk human papillomavirus (HPV) types 16, 18, 31 and 33. However, the link between rectal SCC and HPV, along with its optimal management and prognosis, remains unclear. We present a case of a woman with previously unremarkable colonoscopies and no prior cervical HPV, who was found to have a 9 cm HPV-positive rectal SCC mass. Case Description/Methods: A 64-year-old woman with gastroesophageal reflux disease and Barrett’s esophagus presented to the Emergency Department for severe hypokalemia and leukocytosis. She reported 4 months of generalized weakness, poor appetite, 20 pounds unintentional weight loss, abdominal pain, vomiting, loose stools, intermittent constipation without hematochezia, and new-onset urinary retention requiring foley catheter placement. Her colonoscopy in 2019 showed diverticulosis and one benign polyp. She was afebrile, tachycardic, hypotensive and physical exam was unremarkable. Blood work revealed leukocytosis (27.4 × 103/uL), hemoglobin 8.6 g/dL, and hypokalemia (2.9 mmol/L). Computed tomography and Magnetic resonance imaging showed an 8.7 × 7.4 × 9.4 cm mass invading the sacrum and piriformis muscle, extending into the right sacral neural foramina. Flexible sigmoidoscopy revealed a rectal tumor with wall erosion. Pathology confirmed moderately differentiated invasive SCC, HPV (p16) positive. CA-125 was 51. Her Pap smear in 2021 was HPV negative. PET scan showed a 10 cm necrotic large low rectal mass with a left adrenal nodule concerning for metastasis. She underwent a diverting ostomy, radiation, and chemotherapy. Discussion: Primary rectal SCC is rare (0.1-0.25 per 1000 colorectal cancers), while adenocarcinoma (AC) accounts for approximately 90% of rectal cancers. Risk factors include chronic inflammation, radiation injury, and infections such as HIV. HPV is strongly linked to anal SCC though the role in rectal SCC remains uncertain. Audeau et al. studied 2351 colorectal cancer patients of which 20 had SCC, AC, or mixed tumors located above the dentate line. None tested positive for HPV, suggesting limited association between HPV and rectal SCC. This poses a diagnostic challenge as immunocompetent patients with regular, unremarkable colonoscopies and no prior HPV positivity require a high index of suspicion for HPV related rectal SCC. Weight loss and bowel habit changes should prompt earlier diagnostic evaluation with colonoscopy. Further studies are needed to clarify screening, management, and prognosis of HPV-associated rectal SCC.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001143552.94068.61
Primary Topic
Colorectal and Anal Carcinomas
Type
article
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article

S4023 A Rare Case of Metastatic HPV-Associated Rectal Squamous Cell Carcinoma

Karol Suchowiecki, Roopjeet K. Bath, Karthik Mathialagan, Danzhu Zhao
The American Journal of Gastroenterology
Colorectal and Anal Carcinomas
article

S4023 A Rare Case of Metastatic HPV-Associated Rectal Squamous Cell Carcinoma

Karol Suchowiecki, Roopjeet K. Bath, Karthik Mathialagan, Danzhu Zhao
article en

Abstract

Introduction: Squamous cell carcinoma (SCC) of the anus is strongly associated with high-risk human papillomavirus (HPV) types 16, 18, 31 and 33. However, the link between rectal SCC and HPV, along with its optimal management and prognosis, remains unclear. We present a case of a woman with previously unremarkable colonoscopies and no prior cervical HPV, who was found to have a 9 cm HPV-positive rectal SCC mass. Case Description/Methods: A 64-year-old woman with gastroesophageal reflux disease and Barrett’s esophagus presented to the Emergency Department for severe hypokalemia and leukocytosis. She reported 4 months of generalized weakness, poor appetite, 20 pounds unintentional weight loss, abdominal pain, vomiting, loose stools, intermittent constipation without hematochezia, and new-onset urinary retention requiring foley catheter placement. Her colonoscopy in 2019 showed diverticulosis and one benign polyp. She was afebrile, tachycardic, hypotensive and physical exam was unremarkable. Blood work revealed leukocytosis (27.4 × 103/uL), hemoglobin 8.6 g/dL, and hypokalemia (2.9 mmol/L). Computed tomography and Magnetic resonance imaging showed an 8.7 × 7.4 × 9.4 cm mass invading the sacrum and piriformis muscle, extending into the right sacral neural foramina. Flexible sigmoidoscopy revealed a rectal tumor with wall erosion. Pathology confirmed moderately differentiated invasive SCC, HPV (p16) positive. CA-125 was 51. Her Pap smear in 2021 was HPV negative. PET scan showed a 10 cm necrotic large low rectal mass with a left adrenal nodule concerning for metastasis. She underwent a diverting ostomy, radiation, and chemotherapy. Discussion: Primary rectal SCC is rare (0.1-0.25 per 1000 colorectal cancers), while adenocarcinoma (AC) accounts for approximately 90% of rectal cancers. Risk factors include chronic inflammation, radiation injury, and infections such as HIV. HPV is strongly linked to anal SCC though the role in rectal SCC remains uncertain. Audeau et al. studied 2351 colorectal cancer patients of which 20 had SCC, AC, or mixed tumors located above the dentate line. None tested positive for HPV, suggesting limited association between HPV and rectal SCC. This poses a diagnostic challenge as immunocompetent patients with regular, unremarkable colonoscopies and no prior HPV positivity require a high index of suspicion for HPV related rectal SCC. Weight loss and bowel habit changes should prompt earlier diagnostic evaluation with colonoscopy. Further studies are needed to clarify screening, management, and prognosis of HPV-associated rectal SCC.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 48%
Colorectal and Anal Carcinomas
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