Merkel Cell Carcinoma – Clinical Presentation and Treatment

Author(s):  
Ingrid Moll
2014 ◽  
Vol 104 (4) ◽  
pp. 422-425 ◽  
Author(s):  
Dominic J. Roda ◽  
Brian Albano ◽  
Bharti Rathore ◽  
Linda Zhou

Merkel cell carcinoma is a rare, often fatal, neuroendocrine cutaneous malignancy with a highly variable clinical presentation. Due to the rapid progression of the disease, early detection and treatment is vital to survival. Here, we report the case of a 45-year-old woman whose podiatrist noticed an unusual lesion on her lower left leg and referred her to a dermatologist for work-up. A diagnostic excisional biopsy confirmed the diagnosis and was followed by treatment that included wide local excision of the primary lesion with subsequent chemotherapy and radiation. At the time of diagnosis, sentinel lymph node biopsy was positive. Due to the increasing prevalence of Merkel cell carcinoma in the past decade and its propensity to present on the lower extremity, podiatric physicians need to be aware of the clinical presentation and treatment guidelines for this elusive disease.


2015 ◽  
Vol 33 (5) ◽  
pp. e22-e24 ◽  
Author(s):  
Francesca R. Grippaudo ◽  
Brando Costantino ◽  
Fabio Santanelli

2010 ◽  
Vol 2010 ◽  
pp. 1-3 ◽  
Author(s):  
Deba P. Sarma ◽  
Dawn E. Heagley ◽  
Julianne Chalupa ◽  
Meredith Cox ◽  
James M. Shehan

Introduction. Merkel cell carcinoma is a rare, aggressive neuroendocrine cell carcinoma arising in the sun-exposed skin of elderly patients. Most of these tumors are located in the dermis. An unusual clinical presentation of such a tumor in the subcutis, if not biopsied, may be easily mistaken as a benign lesion.Case Presentation. An 83-year-old white woman presented with a several-month history of a painless 7 mm subcutaneous mass that was initially thought to be a lipoma. A conservative follow-up was planned. At the insistence of the patient, an excisional biopsy of the mass was performed revealing a subcutaneous Merkel cell carcinoma. The tumor cells stained positively for CK 20, chromogranin, and synaptophysin. No other primary or metastatic tumors found after a thorough work-up. The patient was treated with local irradiation. She remains disease free at her six-month follow-up visit.Conclusion. When a new growth is encountered in the sun-exposed skin of elderly patients, a biopsy is warranted even if the lesion clinically appears benign.


2013 ◽  
Vol 58 (3) ◽  
pp. 243 ◽  
Author(s):  
Enzo Errichetti ◽  
Angelo Piccirillo ◽  
Federico Ricciuti ◽  
Francesco Ricciuti

2020 ◽  
Vol 6 (4) ◽  
pp. 100197
Author(s):  
Fawaz H. Alotaibi ◽  
Ricardo Lugo ◽  
Stavan Y. Patel ◽  
Jehan Abdulsattar ◽  
G.E. Ghali

2011 ◽  
Vol 2011 ◽  
pp. 1-2 ◽  
Author(s):  
C. Iavazzo ◽  
M. Terzi ◽  
P. Arapantoni-Dadioti ◽  
V. Dertimas ◽  
G. Vorgias

This is a new case of Merkel cell carcinoma of the vulva. It is a rare neuroendocrine carcinoma with an aggressive behavior. Because of its rarity in this location, it is not clear whether it behaves differently from the usual neuroendocrine carcinomas of the skin. A case of a 63-year-old patient with vulvar Merkel carcinoma is presented. The clinical presentation, microscopic and immunohistochemical features, and treatment are discussed.


2013 ◽  
Vol 03 (01) ◽  
pp. 16-18
Author(s):  
Manpreet Singh ◽  
Swati Singh ◽  
Usha Singh ◽  
Zoramthara Zadeng

2019 ◽  
Vol 26 (5) ◽  
pp. 1033-1034
Author(s):  
Lea Korsa ◽  
Lucija Kovacevic ◽  
Sanja Barsic Ostojic ◽  
Maja Prutki ◽  
Zlatko Marusic

2016 ◽  
Vol 20 (6) ◽  
pp. 563-566 ◽  
Author(s):  
Maria A. McGowan ◽  
Matthew F. Helm ◽  
Michelle B. Tarbox

Background:Merkel cell carcinoma (MCC) is a rare and aggressive cutaneous neoplasm that has exhibited an exponential increase in incidence in the past 3 decades. Combined MCC and cutaneous squamous cell carcinoma (SCC/MCC) is an uncommon variant of MCC that exhibits worse prognosis than pure MCC.Objective:To describe the clinical presentation, dermoscopy, and histology of an unusual subtype of combined SCC/MCC.Methods and Results:A 73-year-old white woman presented with an ulcerated and violaceous 10-mm plaque on her right jawline that had been present for 2 to 3 months. On dermoscopy, the lesion was predominantly milky pink to red with peripheral crusting and large-caliber polymorphous vessels. Histology revealed SCC in situ above and adjacent to MCC. The tumor was excised with clear margins, and sentinel lymph node scintography was negative for nodal involvement.


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