Vulvar Merkel Cell Carcinoma – Case Report (CROSBI ID 260975)
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Podaci o odgovornosti
Butorac, Dražan ; Djaković, Ivka ; Kruljac, Ivan ; Kuna, Krunoslav
engleski
Vulvar Merkel Cell Carcinoma – Case Report
Merkel cell carcinoma is a rare neuroendocrine tumour. Predisposing factors for its development are age, immunosuppression, ultraviolet light exposure, and exposure to the polyoma virus. It is usually localized in the head region, neck, and extremities. Primary neuroendocrine tumours of the vulva are extremely rare and so far there have been only 20 cases reported in the English language literature. Tumors at this location have a more aggressive clinical course than neuroendocrine tumours at other sites. The majority of patients present with metastases in regional lymph nodes at the time of diagnosis. Due to the low incidence there is no algorithm for diagnostic and therapeutic procedures. We present a case of a 79-year-old patient with a primary vulvar neuroendocrine tumor with metastases in the regional lymph nodes. Diagnostic and therapeutic measures are described
merkel cell carcinoma ; neuroendocrine tumor ; surgical management ; vulva
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