原发性下颌骨骨内腺样囊性癌1例。

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

摘要

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

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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