下咽原发性低分化小细胞型神经内分泌癌

Primary poorly differentiated small cell type neuroendocrine carcinoma of the hypopharynx.

作者信息

Ao Yin-Jie, Zhou Shui-Hong

机构信息

Department of Otolaryngology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Zhejiang Province 310003, China,

出版信息

Onco Targets Ther. 2019 Feb 27;12:1593-1601. doi: 10.2147/OTT.S189241. eCollection 2019.

Abstract

The incidence of primary poorly differentiated neuroendocrine carcinoma (PDNC) of the hypopharynx iŝ4%. However, the disease pathogenesis, natural history, and prognostic factors remain poorly understood. We report the case of a 66-year-old man who presented with multiple metastases from primary PDNC of the hypopharynx. Physical examination revealed ã3×4 cm left cervical mass located at the level III, with tenderness and an unclear boundary. Laryngoscopy revealed a large mass arising from the posterior hypopharynx; glottis and vocal cord movements were invisible. After consultation with our head and neck oncological multidisciplinary team, diagnosis and specific treatment plan were made. Under general anesthesia, a biopsy sample was obtained via suspension laryngoscopy. Routine pathology revealed small cell carcinoma. Immunohistochemical staining identified neoplastic cells that were positive for cytokeratins, CD56, chromogranin A, and synaptophysin. The Ki-67 mitotic index approached 80%. These findings confirmed hypopharyngeal PDNC, and chemotherapy was prescribed. After 7 months, the tumor metastasized to the left side of the anterior chest wall, bilateral lungs, left liver, and skeleton. The soft tissue of the chest wall was biopsied, and pathology revealed PDNC. Subsequent examinations over the next 4 months confirmed multiple liver metastatic lesions. The patient succumbed to the cancer progression a month later. Here, we systematically review the clinical manifestations, pathogenesis, prognostic factors, and treatment of the disease. In conclusion, patients always have a poor prognosis due to a lack of optimal treatment.

摘要

下咽原发性低分化神经内分泌癌(PDNC)的发病率为4%。然而,该病的发病机制、自然史和预后因素仍知之甚少。我们报告了一例66岁男性患者,其患有下咽原发性PDNC的多处转移。体格检查发现左颈部III级水平有一个3×4厘米的肿块,有压痛且边界不清。喉镜检查发现下咽后部有一个大肿块;声门和声带动度不可见。在与我们的头颈肿瘤多学科团队会诊后,做出了诊断并制定了具体治疗方案。在全身麻醉下,通过悬吊喉镜获取了活检样本。常规病理显示为小细胞癌。免疫组化染色显示肿瘤细胞细胞角蛋白、CD56、嗜铬粒蛋白A和突触素呈阳性。Ki-67有丝分裂指数接近80%。这些发现证实为下咽PDNC,并开具了化疗药物。7个月后,肿瘤转移至前胸壁左侧、双侧肺、左肝和骨骼。对胸壁软组织进行活检,病理显示为PDNC。随后在接下来的4个月里进行的检查证实有多处肝转移病灶。1个月后,患者因癌症进展死亡。在此,我们系统回顾了该病的临床表现、发病机制、预后因素和治疗方法。总之,由于缺乏最佳治疗方法,患者的预后总是很差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cdf/6398402/fd9f8a5e50dc/ott-12-1593Fig1.jpg

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