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一例罕见的多房性宫颈胸腺囊肿伪装成结核性腺炎病例。

A Rare Case of Multiloculated Cervical Thymic Cyst Masquerading as Tuberculous Adenitis.

作者信息

Krishnamurthy Arvind, Murhekar Kanchan, Majhi Urmila

机构信息

Surgical Oncology, Cancer Institute (WIA), 38, Sardar Patel Rd, Adyar, Chennai, 600036 India.

Department of Pathology, Cancer Institute (WIA), 38, Sardar Patel Rd, Adyar, Chennai, 600036 India.

出版信息

J Maxillofac Oral Surg. 2016 Jul;15(Suppl 2):375-7. doi: 10.1007/s12663-016-0905-7. Epub 2016 Apr 21.

Abstract

Cervical thymic cysts are among the rarest cysts found in the neck. They usually occur during infancy and childhood, and they are extremely rare in adults. They may be found at any level of the pathway of normal thymic descent, from the angle of the mandible to the superior mediastinum. Being uncommon, they are rarely included in the clinical diagnosis of lateral neck masses and are commonly misdiagnosed as branchial cysts, lymphatic malformations, epidermoid cysts, dermoid cysts, lymphadenitis or neoplastic masses. The diagnosis of cervical thymic cyst is rarely made preoperatively and histopathological examination of the excised specimen is the only definitive means of diagnosis in a majority of the reported cases. We report the clinical presentation and therapeutic management of a rare case of multiloculated cervical thymic cyst in a 24-year-old adult which masqueraded as a tuberculous lympadenitis along with a review of literature.

摘要

颈胸腺囊肿是颈部发现的最罕见囊肿之一。它们通常在婴儿期和儿童期出现,在成人中极为罕见。它们可能出现在正常胸腺下降路径的任何水平,从下颌角到上纵隔。由于不常见,它们很少被纳入侧颈部肿块的临床诊断,并且常被误诊为鳃裂囊肿、淋巴管畸形、表皮样囊肿、皮样囊肿、淋巴结炎或肿瘤性肿块。颈胸腺囊肿术前很少能确诊,在大多数报道的病例中,切除标本的组织病理学检查是唯一确定的诊断方法。我们报告了一例24岁成人罕见的多房性颈胸腺囊肿的临床表现及治疗处理,该囊肿伪装成结核性淋巴结炎,并对相关文献进行了综述。

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