“…ARM is a rare disease with exceedingly poor prognosis, worse than cutaneous melanoma, with a median survival of one year and with five-year survival rate of 10% [12]. ARM could be located in the anal canal or at the anal verge (2/3), or in the distal rectum (1/3), and often presents with non-specific local symptoms such as rectal bleeding (55%), rectal masses (34%), anal pain (13%), and change in bowel habits (63%) [13,14]. However, women are more likely than men to be diagnosed with ARM (male to female ratio is 0.75) [15], and lesions are usually non-specific, amelanotic, and commonly mistaken for benign conditions such as hemorrhoids or rectal polyposis, which prolongs the establishment of the diagnosis [16,17].…”