S3993 Primary Anorectal Melanoma: An Unexpected Finding During Colorectal Cancer Surveillance

Introduction: Anorectal melanoma is a rare and aggressive cancer, comprising less than 1% of all melanomas and 0.4%–1.6% of anorectal malignancies. Its nonspecific symptoms often mimic benign conditions and delay diagnosis. The disease typically has a poor prognosis, with a median survival of 2 years. Herein, we present a case of asymptomatic anorectal melanoma identified during routine surveillance colonoscopy. Case Description/Methods: A 57-year-old man with a first-degree family history of colorectal cancer underwent screening colonoscopy in 2019, which revealed diverticulosis, non-bleeding hemorrhoids, and a small hyperplastic polyp. A 5-year follow-up was recommended. On repeat colonoscopy in April 2024, a 20 mm sessile polyp was noted at the anorectal junction and was removed. Histopathology revealed sheets of atypical melanocytic cells with prominent nucleoli and brisk mitosis. Immunohistochemical staining was positive for S100, SOX10, HMB-45, MART-1, CD10, and focal CD117, which is consistent with malignant melanoma. Glandular dysplasia was not observed. Computed tomography (CT) and magnetic resonance imaging revealed benign-appearing hepatic, splenic, and renal cysts, along with indeterminate lesions in the right kidney and liver, but no definitive metastatic disease. Positron emission tomography/CT showed physiological rectal uptake without distant malignancy. Physical examination results were unremarkable. The case was discussed by a multidisciplinary tumor board. The patient was referred for further evaluation of the indeterminate lesions and systemic chemotherapy. Discussion: Owing to its subtle presentation, anorectal melanoma is frequently diagnosed at advanced stages, with a 5-year survival rate below 20%. Diagnosis requires biopsy and confirmation of melanocytic markers. Historically managed with abdominoperineal resection, treatment has shifted toward wide local excision when feasible. Immunotherapy, particularly immune checkpoint inhibitors, is increasingly used in advanced or metastatic anorectal melanoma and may improve survival in select patients, but its benefit in the adjuvant or neoadjuvant setting for resected localized disease remains unproven and is an area of ongoing investigation.

Authors

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001143432.20646.12
Primary Topic
Cutaneous Melanoma Detection and Management
Type
article
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article

S3993 Primary Anorectal Melanoma: An Unexpected Finding During Colorectal Cancer Surveillance

Ruchir Paladiya, John Wysocki, Khushi Gadhia
The American Journal of Gastroenterology
Cutaneous Melanoma Detection and Management
article

S3993 Primary Anorectal Melanoma: An Unexpected Finding During Colorectal Cancer Surveillance

Ruchir Paladiya, John Wysocki, Khushi Gadhia
article en

Abstract

Introduction: Anorectal melanoma is a rare and aggressive cancer, comprising less than 1% of all melanomas and 0.4%–1.6% of anorectal malignancies. Its nonspecific symptoms often mimic benign conditions and delay diagnosis. The disease typically has a poor prognosis, with a median survival of 2 years. Herein, we present a case of asymptomatic anorectal melanoma identified during routine surveillance colonoscopy. Case Description/Methods: A 57-year-old man with a first-degree family history of colorectal cancer underwent screening colonoscopy in 2019, which revealed diverticulosis, non-bleeding hemorrhoids, and a small hyperplastic polyp. A 5-year follow-up was recommended. On repeat colonoscopy in April 2024, a 20 mm sessile polyp was noted at the anorectal junction and was removed. Histopathology revealed sheets of atypical melanocytic cells with prominent nucleoli and brisk mitosis. Immunohistochemical staining was positive for S100, SOX10, HMB-45, MART-1, CD10, and focal CD117, which is consistent with malignant melanoma. Glandular dysplasia was not observed. Computed tomography (CT) and magnetic resonance imaging revealed benign-appearing hepatic, splenic, and renal cysts, along with indeterminate lesions in the right kidney and liver, but no definitive metastatic disease. Positron emission tomography/CT showed physiological rectal uptake without distant malignancy. Physical examination results were unremarkable. The case was discussed by a multidisciplinary tumor board. The patient was referred for further evaluation of the indeterminate lesions and systemic chemotherapy. Discussion: Owing to its subtle presentation, anorectal melanoma is frequently diagnosed at advanced stages, with a 5-year survival rate below 20%. Diagnosis requires biopsy and confirmation of melanocytic markers. Historically managed with abdominoperineal resection, treatment has shifted toward wide local excision when feasible. Immunotherapy, particularly immune checkpoint inhibitors, is increasingly used in advanced or metastatic anorectal melanoma and may improve survival in select patients, but its benefit in the adjuvant or neoadjuvant setting for resected localized disease remains unproven and is an area of ongoing investigation.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 54%
Cutaneous Melanoma Detection and Management
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