Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia

Anorectal melanomas are exceptionally uncommon and only 30% of anorectal melanomas are amelanotic. We report here a case of an anorectal amelanotic melanoma in a female patient. An 84-year-old patient complained of anal mass for 3 months. On examination, there was a 7.0 cm mass prolapsing through th...

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Main Authors: Khaled Ali Baniyaseen, Muhammad Saeed, Ahmed Omar Albonni, Bothaina Mohammed Abdulshakour, Ghida Dairi, Faisal A. Al-Allaf, Mohiuddin M. Taher
Format: Article
Language:English
Published: Iranian Association of Gastroenterology and Hepatology, Shiraz University of Medical Sciences 2019-07-01
Series:Middle East Journal of Digestive Diseases
Subjects:
Online Access:http://www.mejdd.org/index.php/mejdd/article/view/2066
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author Khaled Ali Baniyaseen
Muhammad Saeed
Ahmed Omar Albonni
Bothaina Mohammed Abdulshakour
Ghida Dairi
Faisal A. Al-Allaf
Mohiuddin M. Taher
author_facet Khaled Ali Baniyaseen
Muhammad Saeed
Ahmed Omar Albonni
Bothaina Mohammed Abdulshakour
Ghida Dairi
Faisal A. Al-Allaf
Mohiuddin M. Taher
author_sort Khaled Ali Baniyaseen
collection DOAJ
description Anorectal melanomas are exceptionally uncommon and only 30% of anorectal melanomas are amelanotic. We report here a case of an anorectal amelanotic melanoma in a female patient. An 84-year-old patient complained of anal mass for 3 months. On examination, there was a 7.0 cm mass prolapsing through the anus that was pale-pink in color. Abdominal, pelvic, and chest computed tomography (CT) showed rectal wall thickening with an eccentric polypoid soft tissue density mass, and left inguinal and presacral lymph node enlargement along with a small nodule in the lower lobe of the left lung, likely representing metastatic deposit. Microscopic examination revealed a piece of skin with hyperplastic squamous epithelium with surface ulceration. The dermis and underlining tissue were showing infiltration by malignant sheets and nests of ovoid and spindle shape cells with prominent nucleolus and high mitotic s. Immuno-staining for HMB-45, S-100, and Melan-A was positive, and it was negative for P63, CK 5/6, and Pan-CK, thus confirming it as an anorectal amelanotic melanoma, and not an epithelial tumor. This is the first case of an amelanotic anorectal melanoma reported from Saudi Arabia.
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spelling doaj.art-f71f787b6ef647c2a6c78eae4d42df642022-12-21T23:57:56ZengIranian Association of Gastroenterology and Hepatology, Shiraz University of Medical SciencesMiddle East Journal of Digestive Diseases2008-52302008-52492019-07-0111316617310.15171/mejdd.2019.144Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi ArabiaKhaled Ali Baniyaseen0Muhammad Saeed1Ahmed Omar Albonni2Bothaina Mohammed Abdulshakour3Ghida Dairi4Faisal A. Al-Allaf5Mohiuddin M. Taher6Histopathology Division, Al-Noor Specialist Hospital, Makkah, Saudi ArabiaFaculty of Medicine, Umm-Al-Qura University, Makkah, Saudi ArabiaHistopathology Division, King Fahad Central Hospital, Jazan, Saudi ArabiaDepartment of Radiology, Al-Noor Specialty Hospital, Makkah, Saudi ArabiaMedicine and Medical Sciences Research Center, Deanship of Scientific Research, Umm-Al-Qura University, Makkah, Saudi ArabiaDepartment of Medical Genetics, Umm-Al-Qura University, Saudi ArabiaScience and Technology Unit, Umm- Al-Qura University, Makkah, Saudi ArabiaAnorectal melanomas are exceptionally uncommon and only 30% of anorectal melanomas are amelanotic. We report here a case of an anorectal amelanotic melanoma in a female patient. An 84-year-old patient complained of anal mass for 3 months. On examination, there was a 7.0 cm mass prolapsing through the anus that was pale-pink in color. Abdominal, pelvic, and chest computed tomography (CT) showed rectal wall thickening with an eccentric polypoid soft tissue density mass, and left inguinal and presacral lymph node enlargement along with a small nodule in the lower lobe of the left lung, likely representing metastatic deposit. Microscopic examination revealed a piece of skin with hyperplastic squamous epithelium with surface ulceration. The dermis and underlining tissue were showing infiltration by malignant sheets and nests of ovoid and spindle shape cells with prominent nucleolus and high mitotic s. Immuno-staining for HMB-45, S-100, and Melan-A was positive, and it was negative for P63, CK 5/6, and Pan-CK, thus confirming it as an anorectal amelanotic melanoma, and not an epithelial tumor. This is the first case of an amelanotic anorectal melanoma reported from Saudi Arabia.http://www.mejdd.org/index.php/mejdd/article/view/2066Anorectal cancerAnorectal melanomaAmelanotic melanomaLung metastasis
spellingShingle Khaled Ali Baniyaseen
Muhammad Saeed
Ahmed Omar Albonni
Bothaina Mohammed Abdulshakour
Ghida Dairi
Faisal A. Al-Allaf
Mohiuddin M. Taher
Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia
Middle East Journal of Digestive Diseases
Anorectal cancer
Anorectal melanoma
Amelanotic melanoma
Lung metastasis
title Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia
title_full Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia
title_fullStr Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia
title_full_unstemmed Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia
title_short Primary Anorectal Amelanotic Melanoma: The First Case Report from Saudi Arabia
title_sort primary anorectal amelanotic melanoma the first case report from saudi arabia
topic Anorectal cancer
Anorectal melanoma
Amelanotic melanoma
Lung metastasis
url http://www.mejdd.org/index.php/mejdd/article/view/2066
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