Korean J Otorhinolaryngol-Head Neck Surg.  2018 Oct;61(10):546-551. 10.3342/kjorl-hns.2017.00164.

Merkel Cell Carcinoma of Cheek: 2 Case Reports

Affiliations
  • 1Department of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Korea University, Seoul, Korea. diakonos@korea.ac.kr

Abstract

Merkel cell carcinoma (MCC) is a rare aggressive skin cancer with the mortality rate of 33%. MCC was first described by Toker in 1972 as a trabecular cell carcinoma and is classified as a neuroendocrine tumor similar to small cell lung carcinoma and melanoma. The pathogenesis of MCC remains largely unknown. However, ultraviolet radiation and immunosuppression are likely to play a significant pathogenic role. The primary skin lesion is usually asymptomatic and it typically presents as a red or purple dome-shaped nodule. The management of MCC is controversial, however, local wide excision followed by radiotherapy is accepted as the primary treatment modality. The regional draining nodal basin is the most common site for recurrence. Therefore, sentinel lymph node biopsy is recommended in all cases, except for the clinically node-negative cases. We herein report two cases of MCC on the left cheek with different clinical manifestations.

Keyword

Cheek; Merkel cell carcinoma; Neoplasms

MeSH Terms

Carcinoma, Merkel Cell*
Cheek*
Immunosuppression
Melanoma
Mortality
Neuroendocrine Tumors
Radiotherapy
Recurrence
Sentinel Lymph Node Biopsy
Skin
Skin Neoplasms
Small Cell Lung Carcinoma
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