Journal of Cutaneous Pathology · 2017 · 52 citations · 53 references
MedicineOncologyPathologyMolecular OncologyNeoplasiaTumor PathologyEndocrine TumorsEwing SarcomaMerkel Cell CarcinomaNeuroendocrine TumorsTumor ClassificationTumor HistopathologyEndocrine Tumor ImmunohistochemistryHistologic Differential DiagnosisMerkel Cell Carcinoma HistopathologyNeuroendocrine Skin TumorsNeuroendocrine Tumor ClassificationNeuroendocrine Tumor HistologyTumor Differentiation Assessment
Merkel cell carcinoma (MCC) is a rare, clinically aggressive, cutaneous neuroendocrine (NE) neoplasm. As a tumor with small, round, blue cells, the histologic differential diagnosis for MCC can include melanoma, metastatic small cell carcinoma (SCC), nodular hematopoietic tumors, basal cell carcinoma (BCC), atypical variants of squamous carcinoma and the uncommon occurrence of primary cutaneous Ewing sarcoma. In cases with atypical histology or without the classic immunophenotype, the diagnosis can be challenging. Ultimately, immunohistochemistry (IHC) is essential to the definitive diagnosis of MCC and in difficult cases, the diagnosis may hinge entirely on the immunophenotype of the tumor cells. Insulinoma-associated 1 (INSM1) is a transcription factor expressed in tissues undergoing terminal NE differentiation. As a nuclear protein tied to both differentiation and the cell cycle, INSM1 may offer additional utility in comparison to traditional, cytoplasmic markers of NE differentiation.
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