Neuroendocrine Neoplasms of the Larynx: A Clinicopathologic Analysis of 27 Neuroendocrine Tumors and Neuroendocrine Carcinomas.

IF 4.1
Head and neck pathology Pub Date : 2022-06-01 Epub Date: 2021-08-16 DOI:10.1007/s12105-021-01367-9
Munita Bal, Aishwarya Sharma, Swapnil Ulhas Rane, Neha Mittal, Devendra Chaukar, Kumar Prabhash, Asawari Patil
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引用次数: 8

Abstract

Laryngeal neuroendocrine neoplasms (NENs) are rare and heterogeneous, encompassing well-differentiated neuroendocrine tumors (NETs; grade 1, 2, and 3), neuroendocrine carcinomas (NECs, small cell and large cell types), and mixed neuroendocrine non-neuroendocrine neoplasms (MiNEN). We aimed to study the clinicopathologic spectrum of these neoplasms. A retrospective review of all primary laryngeal NENs diagnosed from 2005 to 2017 was undertaken. Mitotic index was divided into < 2, ≥ 2-10, and > 10 mitoses/2 mm2, with a Ki-67 labelling index of < 2%, ≥ 2-20%, and > 20% for the NET grade 1, 2 and 3 categories, respectively. A total of 27 patients were included. The median age at presentation was 60 years; the male-to-female ratio was 8:1. Supraglottis (n = 22) was the most frequently affected subsite. There were 9 NETs grade 2 (G2), and 18 NECs cases. There were no NET grade 1 or 3 cases in our cohort. Among the NETs G2, the morphology was epithelioid (2), plasmacytoid (3), clear (2), oncocytic (1), and rhabdoid (1). Unique 'glomeruloid structures' (n = 5), calcification (n = 3), lymphoid aggregates (n = 5), intranuclear inclusions (n = 2), hyaline globules (n = 3), and Leisegang rings (n = 2) were identified. NECs comprised 16 small cell neuroendocrine carcinoma and 2 large cell neuroendocrine carcinoma. On immunohistochemistry, tumor cells expressed AE1/AE3 (86%), synaptophysin (100%), chromogranin (100%), INSM1 (100%), calcitonin (33.3%). In the NEC group, p53 aberrant expression (87.5%), Retinoblastoma (Rb) loss (88.2%), and diffuse p16 immunoreactivity (66.7%) were additionally observed. Lymph-node metastasis was detected in 62.5% and 85.7%, while distant metastasis in 55.6% and 76.9%, respectively in NET G2 and NEC. Laryngeal NENs are aggressive neoplasms with a high rate of nodal and distant metastasis. Awareness of the wide pathologic spectrum of laryngeal NENs and appropriate use of IHC is needed to render an accurate diagnosis. Ki67 assessment is strongly recommended for laryngeal NEN prognostication.

喉神经内分泌肿瘤:27例神经内分泌肿瘤和神经内分泌癌的临床病理分析。
喉神经内分泌肿瘤(NENs)罕见且异质性,包括分化良好的神经内分泌肿瘤(NETs;1级、2级和3级)、神经内分泌癌(nec、小细胞和大细胞类型)和混合神经内分泌非神经内分泌肿瘤(MiNEN)。我们的目的是研究这些肿瘤的临床病理谱。回顾性分析了2005年至2017年诊断的所有原发性喉部NENs。有丝分裂指数分为10个有丝分裂/2 mm2, NET分级1、2和3级Ki-67标记指数分别为20%。共纳入27例患者。发病时的中位年龄为60岁;男女比例为8:1。声门上(n = 22)是最常受影响的亚部位。NETs 2级(G2) 9例,nec 18例。在我们的队列中没有NET 1级或3级病例。NETs G2的形态为上皮样(2例)、浆细胞样(3例)、透明(2例)、嗜瘤细胞样(1例)和横纹肌样(1例)。发现独特的“肾小球样结构”(n = 5)、钙化(n = 3)、淋巴样聚集物(n = 5)、核内包涵体(n = 2)、透明小球(n = 3)和雷钢环(n = 2)。nec包括16例小细胞神经内分泌癌和2例大细胞神经内分泌癌。免疫组化结果显示,肿瘤细胞表达AE1/AE3(86%)、synaptophysin(100%)、chromogranin(100%)、INSM1(100%)、降钙素(33.3%)。在NEC组中,p53异常表达(87.5%),视网膜母细胞瘤(Rb)丢失(88.2%),弥漫性p16免疫反应(66.7%)。淋巴结转移率分别为62.5%和85.7%,远处转移率分别为55.6%和76.9%。喉内隐细胞瘤是一种侵袭性肿瘤,具有较高的淋巴结和远处转移率。意识到喉内耳炎的广泛病理谱和适当的使用免疫显像是需要做出准确的诊断。Ki67评估被强烈推荐用于喉部NEN的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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