“…The presence of rare melanocytes in the parotid gland is typically explained by its development from invaginating oral epithelium, which is known to contain melanoblasts (Greene and Bernier 1961;Takeda 1997). One requirement for the Table 2 Characteristics of cases of parotid melanoma of unknown primary from a comprehensive literature search Bahar et al (1990), Balm et al (1994), Barbieri et al (2002), Bussi et al (1999), Gao et al (2008), Greene and Bernier (1961), Jennings et al (1996), Jorgensen (1953, Karpowicz et al (2011), Laudadio et al (1984, Lussier et al (2000), Mesa et al (2009), Nichols et al (1980, Pain et al (1986), Prayson and Sebek (2000), Renaut (1996), Schroeder and Stahr (1998), Tsutsumida et al (2008), Wang et al (1999), Woodwards et al (1993) ND neck dissection, RT radiation therapy (2) Dead (3) diagnosis of a primary parotid melanoma states that the bulk of the tumor should be located in the parotid parenchyma and contains no identifiable LN tissue (Woodwards et al 1993). In our study, roughly half of all PMUP were histologically documented in the parotid parenchyma, suggesting that some cases may have represented primary parotid melanomas.…”