A rare case of intracytoplasmic mucin‐rich nasopharyngeal carcinoma

Nasopharyngeal carcinoma (NPC) is an Epstein–Barr virus (EBV)‐associated tumor with a high incidence in Asian countries. NPC is a type of squamous cell carcinoma originating from the nasopharyngeal mucosa. Although rare, NPCs show some uncommon histologic variants; these variations remain to be unde...

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Veröffentlicht in:Diagnostic cytopathology 2022-06, Vol.50 (6), p.E151-E155
Hauptverfasser: Yamaguchi, Yohei, Odate, Toru, Nakazawa, Kumiko, Oishi, Naoki, Mochizuki, Kunio, Shimizu, Tatsuya, Horiuchi, Kiwako, Ishii, Hiroki, Sakurai, Daiju, Kondo, Tetsuo
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container_end_page E155
container_issue 6
container_start_page E151
container_title Diagnostic cytopathology
container_volume 50
creator Yamaguchi, Yohei
Odate, Toru
Nakazawa, Kumiko
Oishi, Naoki
Mochizuki, Kunio
Shimizu, Tatsuya
Horiuchi, Kiwako
Ishii, Hiroki
Sakurai, Daiju
Kondo, Tetsuo
description Nasopharyngeal carcinoma (NPC) is an Epstein–Barr virus (EBV)‐associated tumor with a high incidence in Asian countries. NPC is a type of squamous cell carcinoma originating from the nasopharyngeal mucosa. Although rare, NPCs show some uncommon histologic variants; these variations remain to be understood. We described the cytologic characteristics of a rare NPC variant with abundant intracytoplasmic mucin. A 37‐year‐old Japanese man presented to our hospital with bilateral ear discomfort and palpable lymph nodes. Nasopharyngeal biopsy showed tumor cells with abundant intracytoplasmic, Alcian blue‐PAS‐positive mucin. Immunohistochemical analysis demonstrated that the tumor cells were positive for p40 and p53. Epstein–Barr encoding region (EBER) in situ hybridization (ISH) showed EBV infection of the tumor cells. Fluorescence in situ hybridization (FISH) using MAML2 break‐apart probes did not show split signals. Fine needle aspiration biopsy (FNAB) cytology of the metastatic lymph nodes was also performed. Smear samples had a necrotic and inflammatory background with both lymphocyte and neutrophil infiltration. Highly cellular tumor clusters and dispersed cells with naked nuclei were observed. The tumor cells showed a clear cytoplasm with distinct cell borders. Intracytoplasmic mucin pushing the nucleus to the periphery was observed in the scattered tumor cells in a liquid‐based cytology sample. Given these findings, the final diagnosis was advanced nasopharyngeal carcinoma; cisplatin‐based chemoradiation therapy was performed as the first‐line treatment. The tumor recurred 8 months after completing the treatment. The recurrent nasopharyngeal tumor was a typical non‐keratinizing NPC and lacked intracytoplasmic mucin.
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NPC is a type of squamous cell carcinoma originating from the nasopharyngeal mucosa. Although rare, NPCs show some uncommon histologic variants; these variations remain to be understood. We described the cytologic characteristics of a rare NPC variant with abundant intracytoplasmic mucin. A 37‐year‐old Japanese man presented to our hospital with bilateral ear discomfort and palpable lymph nodes. Nasopharyngeal biopsy showed tumor cells with abundant intracytoplasmic, Alcian blue‐PAS‐positive mucin. Immunohistochemical analysis demonstrated that the tumor cells were positive for p40 and p53. Epstein–Barr encoding region (EBER) in situ hybridization (ISH) showed EBV infection of the tumor cells. Fluorescence in situ hybridization (FISH) using MAML2 break‐apart probes did not show split signals. Fine needle aspiration biopsy (FNAB) cytology of the metastatic lymph nodes was also performed. Smear samples had a necrotic and inflammatory background with both lymphocyte and neutrophil infiltration. Highly cellular tumor clusters and dispersed cells with naked nuclei were observed. The tumor cells showed a clear cytoplasm with distinct cell borders. Intracytoplasmic mucin pushing the nucleus to the periphery was observed in the scattered tumor cells in a liquid‐based cytology sample. Given these findings, the final diagnosis was advanced nasopharyngeal carcinoma; cisplatin‐based chemoradiation therapy was performed as the first‐line treatment. The tumor recurred 8 months after completing the treatment. 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Smear samples had a necrotic and inflammatory background with both lymphocyte and neutrophil infiltration. Highly cellular tumor clusters and dispersed cells with naked nuclei were observed. The tumor cells showed a clear cytoplasm with distinct cell borders. Intracytoplasmic mucin pushing the nucleus to the periphery was observed in the scattered tumor cells in a liquid‐based cytology sample. Given these findings, the final diagnosis was advanced nasopharyngeal carcinoma; cisplatin‐based chemoradiation therapy was performed as the first‐line treatment. The tumor recurred 8 months after completing the treatment. 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subjects Biopsy
Cancer
Cellular biology
cytology
Epstein-Barr virus
lymph node
Lymphatic system
mucin
nasopharyngeal carcinoma
Throat cancer
title A rare case of intracytoplasmic mucin‐rich nasopharyngeal carcinoma
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