scholarly journals Merkel cell carcinoma: a case report and literature review

Author(s):  
Soulé-Martínez Christian Enrique ◽  
Monroy-Ramírez Miguel Angel ◽  
Jaimes-Durán Edwing Michel ◽  
Castellanos-Aguilar Leonel ◽  
Ricarte-Almeida Eros Rafael ◽  
...  

Merkel cell carcinoma (MCC) is a rare, but highly aggressive, malignant neuroendocrine tumor, with a higher prevalence in men, Caucasians, and the elderly. It is usually identified in photo-exposed areas such as the head, trunk, and extremities. It is related to locoregional recurrences and metastases, which conditions a high mortality rate. Currently, the pathogenesis is unclear, but it is related to ultraviolet radiation, immunosuppression, and polyomavirus infection. Prompt diagnosis and treatment are essential to improve the survival rate.

Author(s):  
◽  

Few cases of anal canal Merkel cell Carcinoma have been reported in the literature. Merkel Cell Carcinoma is rare neuroendocrine tumor which commonly found in sun-exposed areas such as extremities. We describe a case of 74-year-old male with anal canal Merkel Cell Carcinoma. He presented with peri-anal pain, tenesmus and itching. Besides, he was found to have chronic anemia. An anal nodule was found during per-rectum physical examination that was excised during endoscopy. Histological examination of the nodule confirmed the diagnosis of Merkel Cell Carcinoma. Thenceforward, patient died 7 months after diagnosis with marked metastatic disease despite initiation of Pembrolizumab therapy.


2000 ◽  
Vol 10 (2) ◽  
pp. 173-176 ◽  
Author(s):  
L. Collaço ◽  
J.P. Silva ◽  
M. Gonçalves ◽  
P. Abrantes

A 22-year-old woman who presented with a tumour of the upper eyelid with clinical, histological, immunohistochemical and ultrastructural features of a Merkel cell carcinoma is reported. This is a unique case of Merkel cell carcinoma in such a young patient. This neuroendocrine tumour is typically found in the elderly. It can grow rapidly, has the potential for local recurrence and early metastatic spread. The authors recommend wide resection of the primary site, which proved effective in this case.


2016 ◽  
Vol 19 ◽  
pp. 21-24 ◽  
Author(s):  
Osvaldo A. Quiroz-Sandoval ◽  
Mario Cuellar-Hubbe ◽  
Leonardo S. Lino-Silva ◽  
Rosa A. Salcedo-Hernández ◽  
Horacio N. López-Basave ◽  
...  

2013 ◽  
Vol 84 (5) ◽  
Author(s):  
Joanna Jońska-Gmyrek ◽  
Piotr Bobkiewicz ◽  
Leszek Gmyrek ◽  
Agnieszka Żółciak-Siwińska ◽  
Bogusław Lindner ◽  
...  

2019 ◽  
Vol 2019 (11) ◽  
Author(s):  
Nicholas Mulchan ◽  
Alberto Cayton ◽  
Armand Asarian ◽  
Philip Xiao

Abstract Merkel cell carcinoma (MCC) is an aggressive cutaneous malignancy of neuroendocrine origin presenting as a painless, rapidly growing nodule. MCC often presents in elderly, fair-skinned individuals in sun-exposed areas. Diagnosis is often overlooked at time of presentation due to its rarity, but MCC is twice as deadly as malignant melanoma. There has been bigger interest in the disease due to increasing incidence and an association with the prevalent virus Merkel cell polyomavirus. This study describes an uncommon presentation of MCC as a right gluteal lesion in an Afro-Panamanian patient. The tumor was suspected to be fibrolipoma, but Immunohistochemistry revealed the diagnosis of MCC, as stains for CD56 and CK20 were positive. In addition to surgical excision, the patient was referred for adjuvant radiotherapy. This case report and literature review elucidates the clinical, histopathologic and management aspects of MCC, which will help in recognizing and treating these tumors.


2019 ◽  
Vol 23 (3) ◽  
pp. 365-373 ◽  
Author(s):  
Claudio Caldarelli ◽  
Umberto Autorino ◽  
Caterina Iaquinta ◽  
Andrea De Marchi

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