Merkel Cell Carcinoma with Lymphoepithelioma-Like Pattern: A Case Report of an Exceedingly Rare Variant of Merkel Cell Carcinoma with Lymph Node Metastases at Presentation
Author(s) -
Soumaya Ben Abdelkrim,
Abdelmajid Dhouibi,
Adnène Moussa,
Rim Hadhri,
Leïla Njim,
Khalifa Mighri,
Abdelfatteh Zakhama
Publication year - 2011
Publication title -
case reports in pathology
Language(s) - English
Resource type - Journals
eISSN - 2090-6781
pISSN - 2090-679X
DOI - 10.1155/2011/840575
Subject(s) - merkel cell carcinoma , medicine , pathology , carcinoma , lymphoepithelioma like carcinoma , merkel cell , lymph node , differential diagnosis , immunohistochemistry , immunology , virus , epstein–barr virus
Merkel cell carcinoma (MCC) or primary neuroendocrine carcinoma of the skin is a rare neoplasm with aggressive behavior. Primary lymphoepithelioma-like (LEL) carcinoma of the skin is a recently described exceptional tumor, with a relatively good prognosis, and is characterized by a neoplastic epithelial component associated with a dense lymphoid stroma. Rarely, MCC shows a marked lymphocytic host response or can even mimic a LEL carcinoma. We report a new case of MCC mimicking an LEL carcinoma in a 72-year-old male; the diagnosis of MCC was made on the basis of the morphology and immunohistochemical findings. We present through this case an exceptional pattern of MCC which can be misleading, and we insist on differential diagnoses.
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