Haritha G H, Kushwaha Akshat, Lakshmanan Jijitha, Subhashini R, Raja Kalaiarasi
Department of Otorhinolaryngology, JIPMER, Puducherry, 06 India.
Department of Pathology, JIPMER, Puducherry, 06 India.
Indian J Otolaryngol Head Neck Surg. 2024 Feb;76(1):1126-1129. doi: 10.1007/s12070-023-04166-6. Epub 2023 Aug 26.
Neuroendocrine carcinoma originating from neuroendocrine cells is typically linked to unfavourable survival rates. We are introducing an exceptional case of neuroendocrine carcinoma occurring in the hypopharynx. To date, only a handful of instances involving primary neuroendocrine carcinoma of the hypopharynx have been documented. Advanced age, being male, a history of chronic alcoholism, smoking, and previous radiation are all risk factors associated with this condition. The majority of patients present with distant metastases and are not amenable to a complete cure. As there are no guidelines for the treatment of this rare tumour, various treatment modalities have been tried. Here, we are reporting one such case which was diagnosed as small-cell neuroendocrine carcinoma of the hypopharynx on the basis of histopathological cues and received concurrent chemoradiotherapy.
起源于神经内分泌细胞的神经内分泌癌通常与不良生存率相关。我们现介绍一例发生于下咽的神经内分泌癌特殊病例。迄今为止,仅有少数涉及下咽原发性神经内分泌癌的病例被记录。高龄、男性、慢性酒精中毒史、吸烟史以及既往放疗史均为与此病相关的危险因素。大多数患者出现远处转移,无法实现完全治愈。由于尚无针对这种罕见肿瘤的治疗指南,人们尝试了各种治疗方式。在此,我们报告这样一例病例,该病例根据组织病理学线索被诊断为下咽小细胞神经内分泌癌,并接受了同步放化疗。