Perianal Merkel cell carcinoma - a rare case report

INTRODUCTION Merkel cell carcinoma is a rare, aggressive neuroendocrine skin cancer that primarily affects elderly men in sun-exposed areas such as the extremities. To the best of our knowledge, this is the first case of a perianal MCC. OBJECTIVE We present a young male with perianal Merkel cell...

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Main Authors: B A, Arifin, Sainal, Mohd. Yusof, Elagili, Faisal, Md Nor, Azmi
Format: Conference or Workshop Item
Language:English
English
Published: 2022
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Online Access:http://irep.iium.edu.my/97083/2/MuhyuddinArifinPoster106.pdf
http://irep.iium.edu.my/97083/1/Coloproctology2022_SPAB.pdf
http://irep.iium.edu.my/97083/
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Institution: Universiti Islam Antarabangsa Malaysia
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spelling my.iium.irep.970832022-03-08T00:48:59Z http://irep.iium.edu.my/97083/ Perianal Merkel cell carcinoma - a rare case report B A, Arifin Sainal, Mohd. Yusof Elagili, Faisal Md Nor, Azmi RD Surgery INTRODUCTION Merkel cell carcinoma is a rare, aggressive neuroendocrine skin cancer that primarily affects elderly men in sun-exposed areas such as the extremities. To the best of our knowledge, this is the first case of a perianal MCC. OBJECTIVE We present a young male with perianal Merkel cell carcinoma. CASE REPORT A previously healthy 35-year-old man presented with left perianal a mass. Initially, his symptoms were attributed to a cold perianal abscess. He was referred to our center due to persistent swelling. The mass was 4x4cm in size and 3cm away from the anal verge; it was firm, nontender and not mobile in relation to the underlying musculature; it grew rapidly and ulcerated in a few weeks. Following biopsies of the lesion, it was discovered to be a neuroendocrine carcinoma that stained CK20- positive, indicating it was a Merkel cell carcinoma. A thorough metastatic work-up, which included a chest x-ray, CT scan, and MRI, revealed evidence of widespread metastatic disease. A multidisciplinary team meeting was held to discuss the case, and palliative chemoradiotherapy was scheduled for the patient. However, he died before receiving palliative care. CONCLUSION MCC is a rare, aggressive carcinoma that typically appears in areas that are exposed to the sun. A colorectal surgeon should consider MCC as a differential diagnosis when faced with a rapidly growing, painless lesion in the perianal region. Early detection and treatment may lead to a higher rate of patient survival. However, because MCC is uncommon, more research is required to develop treatment protocols for metastatic disease. 2022-03-04 Conference or Workshop Item NonPeerReviewed application/pdf en http://irep.iium.edu.my/97083/2/MuhyuddinArifinPoster106.pdf application/pdf en http://irep.iium.edu.my/97083/1/Coloproctology2022_SPAB.pdf B A, Arifin and Sainal, Mohd. Yusof and Elagili, Faisal and Md Nor, Azmi (2022) Perianal Merkel cell carcinoma - a rare case report. In: Coloproctology 2022, 4-6 Mar 2022, Virtual. (Unpublished)
institution Universiti Islam Antarabangsa Malaysia
building IIUM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider International Islamic University Malaysia
content_source IIUM Repository (IREP)
url_provider http://irep.iium.edu.my/
language English
English
topic RD Surgery
spellingShingle RD Surgery
B A, Arifin
Sainal, Mohd. Yusof
Elagili, Faisal
Md Nor, Azmi
Perianal Merkel cell carcinoma - a rare case report
description INTRODUCTION Merkel cell carcinoma is a rare, aggressive neuroendocrine skin cancer that primarily affects elderly men in sun-exposed areas such as the extremities. To the best of our knowledge, this is the first case of a perianal MCC. OBJECTIVE We present a young male with perianal Merkel cell carcinoma. CASE REPORT A previously healthy 35-year-old man presented with left perianal a mass. Initially, his symptoms were attributed to a cold perianal abscess. He was referred to our center due to persistent swelling. The mass was 4x4cm in size and 3cm away from the anal verge; it was firm, nontender and not mobile in relation to the underlying musculature; it grew rapidly and ulcerated in a few weeks. Following biopsies of the lesion, it was discovered to be a neuroendocrine carcinoma that stained CK20- positive, indicating it was a Merkel cell carcinoma. A thorough metastatic work-up, which included a chest x-ray, CT scan, and MRI, revealed evidence of widespread metastatic disease. A multidisciplinary team meeting was held to discuss the case, and palliative chemoradiotherapy was scheduled for the patient. However, he died before receiving palliative care. CONCLUSION MCC is a rare, aggressive carcinoma that typically appears in areas that are exposed to the sun. A colorectal surgeon should consider MCC as a differential diagnosis when faced with a rapidly growing, painless lesion in the perianal region. Early detection and treatment may lead to a higher rate of patient survival. However, because MCC is uncommon, more research is required to develop treatment protocols for metastatic disease.
format Conference or Workshop Item
author B A, Arifin
Sainal, Mohd. Yusof
Elagili, Faisal
Md Nor, Azmi
author_facet B A, Arifin
Sainal, Mohd. Yusof
Elagili, Faisal
Md Nor, Azmi
author_sort B A, Arifin
title Perianal Merkel cell carcinoma - a rare case report
title_short Perianal Merkel cell carcinoma - a rare case report
title_full Perianal Merkel cell carcinoma - a rare case report
title_fullStr Perianal Merkel cell carcinoma - a rare case report
title_full_unstemmed Perianal Merkel cell carcinoma - a rare case report
title_sort perianal merkel cell carcinoma - a rare case report
publishDate 2022
url http://irep.iium.edu.my/97083/2/MuhyuddinArifinPoster106.pdf
http://irep.iium.edu.my/97083/1/Coloproctology2022_SPAB.pdf
http://irep.iium.edu.my/97083/
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