A Case of Primary Intraosseous Adenoid Cystic Carcinoma of the Mandible.

Pub Date : 2023-01-01 DOI:10.1155/2023/2422086
Erika Sasaki, Kenji Yamagata, Takayuki Hagiwara, Ryo Takasaki, Satoshi Fukuzawa, Fumihiko Uchida, Naomi Ishibashi-Kanno, Hiroki Bukawa
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引用次数: 1

Abstract

Primary intraosseous adenoid cystic carcinoma (PIACC) of the jaw is rare. To our knowledge, only 51 cases have been reported in the English literature. We present a rare case of PIACC arising in the mandible with multiple bone metastases and review the previous articles. A 70-year-old woman presented with paresthesia of the right chin and lower gingiva for 4 months. Radiography revealed an irregular radiolucent region on the right side of the ramus, infiltrating to the mandibular canal. Biopsy revealed a pathological diagnosis of adenoid cystic carcinoma. Multiple bone metastases were present in the sternum, scapula, and thighs. The treatment effect was progressive disease for chemotherapy; therefore, best supportive care was provided for 3 years.

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原发性下颌骨骨内腺样囊性癌1例。
摘要原发性颌骨骨内腺样囊性癌(PIACC)非常罕见。据我们所知,在英语文献中仅报道了51例。我们报告一例罕见的PIACC发生在下颌骨并伴有多发性骨转移,并回顾以往的文章。一位70岁女性,以右下巴及下牙龈感觉异常4个月为主诉。x线片示支右侧不规则透光区,浸润至下颌管。活检病理诊断为腺样囊性癌。胸骨、肩胛骨和大腿有多发骨转移灶。化疗治疗效果为进展性疾病;因此,最好的支持治疗提供了3年。
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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