Mascitti M, Luconi E, Togni L, Rubini C
Department of Clinical Specialistic and Dental Sciences, Marche Polytechnic University, Ancona, Italy.
Department of Biomedical Sciences and Public Health, Marche Polytechnic University, Ancona, Italy.
Pathologica. 2019 Jun;111(2):70-75. doi: 10.32074/1591-951X-13-19.
Neuroendocrine tumors (NET) are a heterogeneous group of malignancies with a broad spectrum of histomorphologies, tissue origins, and clinical outcomes, which arise from neural crest cells with neuroendocrine differentiation. Salivary gland tumors account for 3-6% of all head and neck neoplasms, while large cell neuroendocrine carcinomas (LCNEC) of the salivary gland are extremely rare, with few cases reported in literature, and only 5 cases involving submandibular gland. The rarity of these tumors in salivary glands is probably related to the scarcity of neuroendocrine cells in this tissue, whose presence is still a matter of debate. Regardless of their low frequency, it is imperative to differentiate these tumors from the much more common squamous cell carcinomas and metastatic NETs, due to different therapeutic approach and prognosis. In this paper, we report the case of a 21-year-old man, with a LCNEC involving a submandibular gland followed by several recurrences over the years. In addition, we include a comprehensive review of the available literature on this topic.
神经内分泌肿瘤(NET)是一组异质性恶性肿瘤,具有广泛的组织形态学、组织起源和临床结局,起源于具有神经内分泌分化的神经嵴细胞。涎腺肿瘤占所有头颈肿瘤的3%至6%,而涎腺大细胞神经内分泌癌(LCNEC)极为罕见,文献报道的病例很少,仅有5例累及下颌下腺。这些肿瘤在涎腺中罕见可能与该组织中神经内分泌细胞稀少有关,其存在仍存在争议。尽管其发病率低,但由于治疗方法和预后不同,将这些肿瘤与更为常见的鳞状细胞癌和转移性NET区分开来至关重要。在本文中,我们报告了一例21岁男性病例,其下颌下腺发生LCNEC,多年来多次复发。此外,我们还对该主题的现有文献进行了全面综述。