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一名阿赞德部落青少年的巨大单囊性成釉细胞瘤:一例临床病例报告

Giant Unicystic Ameloblastoma in a Teenager of Azande Tribe: A Clinical Case Report.

作者信息

Posite Charles Malisaba, Faustin Tatana Museketwa, Woldemichael Mihret Adane, Vargas Escalante Elizabeth, Mohamud Snr Mohamed Abdirahman, Laetitia Fazila Malengera, Moses Acan, Santos Mirna Batista, Samuel Tumwesigire, Ali Zeinab Ibrahim, Olive Mughanda Mugheni, Maha Alain Bakwanamaha, Baanitse Jeannot, Said Mahad, Wabinga Henry, Rosales Yanurkis Duranones

机构信息

Department of Pathology, Kampala International University, Ishaka, Uganda.

Department of Pathology, Université Catholique du Graben, Butembo, Democratic Republic of the Congo.

出版信息

Int Med Case Rep J. 2025 Aug 10;18:1003-1010. doi: 10.2147/IMCRJ.S538385. eCollection 2025.

Abstract

Ameloblastoma, a locally aggressive benign odontogenic tumor, represents about 1% of jaw tumors. While typically affecting adults aged 30-60, this case highlights its occurrence in a 17-year-old. Incidence varies globally, with lower rates in non-African populations (around 0.5 per million annually) compared to higher prevalence in Nigeria and South Africa, where Black populations show increased susceptibility. Limited epidemiological data from sub-Saharan Africa, including Uganda, likely underestimates the burden due to underreporting in rural areas with poor healthcare access. A 17-year-old female of the Azande tribe, Bantu ethnicity, presented with a four-year history of a massive, painless right mandibular swelling causing significant facial asymmetry. Examination revealed a large mass (13.8 x 11.5 x 11 cm). A CT scan indicated a unilocular cystic lesion. Histopathology confirmed ameloblastoma with follicular and plexiform patterns. The patient underwent a right total hemi-mandibulectomy, and the excised tumor (19 x 16×10 cm) was classified as an intraluminal unicystic ameloblastoma. This case emphasizes the presentation of a giant unicystic ameloblastoma in a young individual from sub-Saharan Africa, a demographic often underreported. The delayed presentation and substantial tumor size underscore diagnostic and management challenges in resource-limited settings. This report highlights the need for enhanced awareness and improved healthcare access for timely intervention in these populations. Vigilant long-term follow-up is essential due to the tumor's recurrence potential.

摘要

成釉细胞瘤是一种具有局部侵袭性的良性牙源性肿瘤,约占颌骨肿瘤的1%。虽然通常影响30至60岁的成年人,但该病例突出了其在一名17岁患者中的发生情况。全球发病率各不相同,与尼日利亚和南非相比,非非洲人群的发病率较低(每年约为百万分之0.5),在这些地区黑人人群易感性增加。包括乌干达在内的撒哈拉以南非洲地区的流行病学数据有限,由于医疗服务难以到达的农村地区报告不足,可能低估了负担。一名17岁的阿赞德部落女性,班图族裔,有四年右侧下颌骨巨大无痛性肿胀病史,导致明显面部不对称。检查发现一个大肿块(13.8×11.5×11厘米)。CT扫描显示为单房囊性病变。组织病理学证实为具有滤泡状和丛状结构的成釉细胞瘤。患者接受了右侧全下颌骨半切除术,切除的肿瘤(19×16×10厘米)被分类为腔内单囊性成釉细胞瘤。该病例强调了在撒哈拉以南非洲的一名年轻个体中出现巨大单囊性成釉细胞瘤,这一人群的病例报告往往不足。就诊延迟和肿瘤体积巨大凸显了资源有限环境下的诊断和管理挑战。本报告强调需要提高认识并改善医疗服务可及性,以便对这些人群进行及时干预。由于肿瘤有复发的可能性,进行长期密切随访至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1398/12352428/bb5af8a072e4/IMCRJ-18-1003-g0001.jpg

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