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DOI 10.1177/2036361320973526

Медицинская библиотека · Rare tumors · 2020

Primary squamous cell carcinoma of major salivary gland: "Sapienza Head and Neck Unit" clinical recommendations.

Mezi Silvia, Pomati Giulia, Botticelli Andrea, De Felice Francesca, Musio Daniela, Della Monaca Marco, Amirhassankhani Sasan, Vullo Francesco, Cerbelli Bruna, Carletti Raffaella, Di Gioia Cira, Catalano Carlo, Valentini Valentino, Tombolini Vincenzo, Della Rocca Carlo, Marchetti Paolo

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Аннотация

Primary squamous cell carcinoma of salivary gland (SCG) is an extremely rare type of malignant salivary gland tumor, which in turn results in scarcity of data available regarding both its treatment and associated genetic alterations. A retrospective analysis of 12 patients with primary SCG was conducted, along with analysis of the association between treatment, clinical/pathological characteristics, and outcomes. Most patients (8) were staged IVa, with the majority of them (10) having G3 fast growing cancer. Local and systemic recurrence were reported in only three out of nine parotid cases (0 out of 2 submandibular SCGs). In two out of eight patients local relapse occurred after integrated treatment, while recurrence occurred in two out of three patients undergoing exclusive surgery. Five patients eventually died. Treatment of resectable disease must be aggressive and multimodal, with achievement of loco-regional control in order to reduce rate of recurrence and improve outcomes. Metastatic disease would require a therapeutic strategy tailored to the molecular profile in order to improve the currently disappointing results.

Для цитирования: Mezi Silvia, Pomati Giulia, Botticelli Andrea, De Felice Francesca, Musio Daniela, Della Monaca Marco, Amirhassankhani Sasan, Vullo Francesco, Cerbelli Bruna, Carletti Raffaella, Di Gioia Cira, Catalano Carlo, Valentini Valentino, Tombolini Vincenzo, Della Rocca Carlo, Marchetti Paolo. Primary squamous cell carcinoma of major salivary gland: "Sapienza Head and Neck Unit" clinical recommendations.. Rare tumors. 2020. DOI: 10.1177/2036361320973526.
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