下颌骨成釉细胞癌1例。

IF 2 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Satoru Ogane, Arisa Fujii, Taiki Suzuki, Kazuhiko Hashimoto, Sadamitsu Hashimoto, Masayuki Takano, Akira Katakura, Takeshi Nomura
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引用次数: 0

摘要

背景:成釉细胞癌是一种恶性成釉细胞瘤,是一种非常罕见的牙源性肿瘤。我们报告一个病例成釉细胞癌发生后,去除右侧下颌牙种植体。病例介绍:一名72岁的女性患者因37年前放置的右下种植体周围疼痛而去看家庭牙医。虽然诊断为种植体周围炎,将种植体取出,但患者感到下唇感觉迟钝,并由牙医随访,但没有改善。她被转介到一个高度专业化的机构,在那里她被诊断患有骨髓炎,并对病人进行了药物治疗;然而,没有任何改善。此外,在同一区域观察到肉芽,导致怀疑恶性肿瘤,并将患者转至我们的口腔癌中心。诊断为鳞状细胞癌后,在我们医院活检。在全身麻醉下,患者接受了下颌骨切除术、右侧颈部剥离术、用股前外侧皮瓣重建游离皮瓣、立即用金属板重建和气管切开术。苏木精和伊红染色的组织学分析显示,肿瘤中心的结构与牙釉质髓和鳞状上皮相似。肿瘤细胞高度不典型,核染色,肥大,核大小不规则,核形状不规则,均提示癌。免疫组化分析显示Ki-67在80%以上的靶区表达,最终诊断为原发性成釉细胞癌。结论:重建皮瓣移植后,采用颌面假体重建牙合。在1年3个月的随访中,患者保持无疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ameloblastic carcinoma of the mandible: a case report.

Ameloblastic carcinoma of the mandible: a case report.

Ameloblastic carcinoma of the mandible: a case report.

Ameloblastic carcinoma of the mandible: a case report.

Background: Ameloblastic carcinoma is a malignant form of ameloblastoma and a very rare odontogenic tumor. We report a case of ameloblastic carcinoma that occurred after removal of a right-sided mandibular dental implant.

Case presentation: A 72-year-old female patient visited her family dentist with a complaint of pain around a lower right implant placed 37 years previously. Although the dental implant was removed with the diagnosis of peri-implantitis, the patient experienced dullness of sensation in the lower lip and was followed up by her dentist, but after no improvement. She was referred to a highly specialized institution where she was diagnosed with osteomyelitis and treated the patient with medication; however, there was no improvement. In addition, granulation was observed in the same area leading to a suspicion of malignancy, and the patient was referred to our oral cancer center. The diagnosis of squamous cell carcinoma was made after a biopsy at our hospital. Under general anesthesia, the patient underwent mandibulectomy, right-sided neck dissection, free flap reconstruction with an anterolateral thigh flap, immediate reconstruction with a metal plate, and tracheostomy. Histological analysis of the resected specimen on hematoxylin and eosin staining showed structures reminiscent of enamel pulp and squamous epithelium in the center of the tumor. The tumor cells were highly atypical, with nuclear staining, hypertrophy, irregular nuclear size, and irregular nuclear shape, all of which were suggestive of cancer. Immunohistochemical analysis showed that Ki-67 was expressed in more than 80% of the targeted area, and the final diagnosis was primary ameloblastic carcinoma.

Conclusion: After reconstructive flap transplantation, occlusion was re-established using a maxillofacial prosthesis. The patient remained disease-free at the 1-year 3-month follow-up.

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来源期刊
Maxillofacial Plastic and Reconstructive Surgery
Maxillofacial Plastic and Reconstructive Surgery DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.30
自引率
13.00%
发文量
37
审稿时长
13 weeks
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