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下颌骨中央腺泡细胞癌误诊为良性牙源性病变:一例报告

Central Acinic Cell Carcinoma of the Mandible Simulating as Benign Odontogenic Lesion: A Case Report.

作者信息

Bajpai Manas, Pardhe Nilesh, Chandolia Betina, Arora Manika

机构信息

Department of Oral and maxillofacial Pathology, NIMS Dental College, Jaipur, India.

出版信息

Iran J Med Sci. 2018 Mar;43(2):223-226.

Abstract

Centrally occurring salivary gland tumors are rare. Because of a considerable overlap between the clinical and histopathological features, this group of tumors often produces a diagnostic difficulty to the clinicians and oral pathologists. Acinic cell carcinoma (ACC) is an unusual, low-grade, malignant salivary gland tumor that represents approximately 2% of the salivary gland tumors with almost 90% arising in the parotid gland. The rest involve the submandibular and the minor salivary gland. ACC of the jaw is extremely rare and, to our knowledge, only 8 cases have been reported in the English literature. Herein, a case of primary intraosseous ACC of the mandible in a 31-year-old woman is presented. The present case is unique, as the central ACC has never been reported in a patient in the third decade of life. The complete surgical removal of the tumor was carried out under general anesthesia along with the extraction of teeth #31, #32, #41, and #42. The follow-up period of 1-year was uneventful.

摘要

发生于中枢的涎腺肿瘤较为罕见。由于临床和组织病理学特征存在相当大的重叠,这组肿瘤常常给临床医生和口腔病理学家带来诊断困难。腺泡细胞癌(ACC)是一种不常见的、低级别恶性涎腺肿瘤,约占涎腺肿瘤的2%,其中近90%发生于腮腺。其余的发生于下颌下腺和小涎腺。颌骨的ACC极其罕见,据我们所知,英文文献中仅报道过8例。在此,本文报告了一名31岁女性下颌骨原发性骨内ACC病例。本病例很独特,因为中枢性ACC从未在30岁患者中报道过。在全身麻醉下对肿瘤进行了完整的手术切除,并拔除了31、32、41和42号牙。1年的随访期无异常情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc23/5936856/133c7d4cf89d/IJMS-43-223-g001.jpg

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