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Primary neuroendocrine carcinoma with ganglion cell differentiation in a crural lymph node

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Abstract.

A primary neuroendocrine carcinoma with ganglion cell differentiation is described in a crural lymph node. The patient, a 48-year-old woman, presented a palpable lymph node of the crural region in March 1994. Histologically, the lesion was composed mostly of small cells immunoreactive for cytokeratins, neuron specific enolase and synaptophysin. The small cells merged gradually with areas containing ganglion cells immersed in a fibrillar matrix resembling neuropil. Ganglion cells expressed neuron-specific enolase, synaptophysin, neurofilament proteins and S-100 protein. Moreover, a minority of them featured cytokeratin expression. Electron microscopy was performed in the small cell component. These cells featured attenuated desmosomes and electron dense granules with an average size of 120 nm within bundles of intermediate filaments. Clinically, no tumour was found elsewhere despite extensive work-up over the 76-month follow-up period. Although similarities with previous cases of primary neuroendocrine carcinoma of lymph node, ganglion cell differentiation has never been described.

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Roncaroli, F., Mauri, F. & Pasquinelli, G. Primary neuroendocrine carcinoma with ganglion cell differentiation in a crural lymph node. Virchows Arch 437, 675–679 (2000). https://doi.org/10.1007/s004280000288

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  • DOI: https://doi.org/10.1007/s004280000288

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