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细针穿刺细胞学检查偶然诊断出颈动脉体瘤

Incidental Cytodiagnosis of Carotid Body Tumour on Fine Needle Aspiration Cytology.

作者信息

Mukherjee Sreetama, Bhake Arvind

机构信息

Pathology, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

出版信息

Cureus. 2024 Feb 24;16(2):e54817. doi: 10.7759/cureus.54817. eCollection 2024 Feb.

Abstract

A carotid body tumor is a rare form of neoplasm that arises near the carotid artery bifurcation and it has an incidence rate of less than 0.3 per 100,000 population. The low incidence rate of such tumors is due to their origination from the paraganglion cells which is relatively uncommon as compared to other forms of tumor. Here we present an incidental and unusual cytodiagnosis of carotid body tumors. A 45-year-old male presented to the surgery outpatient department with swelling in the left-sided anterior region of the neck. The swelling was gradually progressing over three years and was insidious. Clinically the swelling was 3 cm x 3 cm in size and the patient complained of pain in the last two months which was intermittent. The patient was sent to the cytopathology section for fine needle aspiration cytology with the clinical diagnosis of tubercular lymphadenopathy. The patient underwent fine needle aspiration cytology by 26 SW needle by standard institutional protocols. The cytodiagnosis of "Paraganglioma/ Carotid Body Tumour" was offered. Histomorphological features at excision were consistent with carotid body tumors (paraganglioma). The sections of the tumor immunohistochemically were positive for neuron-specific enolase. The incidental cytodiagnosis of carotid body tumors is reported in the literature sparsely. This case is presented for the cytomorphology of carotid body tumor which is unfamiliar to the reporting pathologist because of its rare occurrence.

摘要

颈动脉体瘤是一种罕见的肿瘤形式,起源于颈动脉分叉附近,发病率低于每10万人0.3例。此类肿瘤发病率低是因为其起源于副神经节细胞,与其他肿瘤形式相比相对少见。在此,我们报告一例偶然发现且不寻常的颈动脉体瘤细胞诊断病例。一名45岁男性因左侧颈部前区肿胀就诊于外科门诊。肿胀在三年间逐渐进展,较为隐匿。临床上肿胀大小为3厘米×3厘米,患者在过去两个月抱怨间歇性疼痛。患者因临床诊断为结核性淋巴结病被送往细胞病理学科室进行细针穿刺细胞学检查。按照标准的机构规程,使用26号SW针为患者进行了细针穿刺细胞学检查。给出了“副神经节瘤/颈动脉体瘤”的细胞诊断。切除标本的组织形态学特征与颈动脉体瘤(副神经节瘤)相符。肿瘤切片免疫组化显示神经元特异性烯醇化酶呈阳性。文献中关于颈动脉体瘤偶然细胞诊断的报道很少。由于其罕见性,本病例展示了报告病理学家不熟悉的颈动脉体瘤的细胞形态学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1519/10962302/10bf97401753/cureus-0016-00000054817-i01.jpg

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