上颌成釉细胞瘤:外科医生的一个谜

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Nigerian Postgraduate Medical Journal Pub Date : 2009-04-01 DOI:10.4314/NMJ.V50I2.53265
S. Ajike, O. Omisakin, E. Adebayo, N. Chom, M. Samaila
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引用次数: 3

摘要

背景:成釉细胞瘤是一种良性但局部侵袭性的牙源性肿瘤。在世界范围内,上颌成釉细胞瘤是罕见的,但其发现较晚,使适当的治疗困难。大多数发生在下颌骨,约5-20%发生在上颌骨。目的:分析尼日利亚扎里亚Ahmadu Bello大学教学医院口腔颌面科和尼日利亚卡杜纳Alba诊所和医疗中心收治的21例上颌成釉细胞瘤病例。研究设计:回顾性研究1993年1月至2008年8月上颌成釉细胞瘤病例。对患者的性别、年龄、肿瘤部位、临床表现、放射学特征、生物学和组织病理学分型、手术治疗和复发情况进行分析。结果:本组共发现350例成釉细胞瘤,其中上颌成釉细胞瘤21例(6%)。21例患者中男性13例,女性8例,男女比例为1.6:1,年龄范围为17 ~ 55岁(平均38.14岁),以4、5岁为高峰(61.9%)。肿瘤持续时间为3个月至14年。单侧肿胀18例,双侧肿胀3例。上颌成釉细胞瘤临床表现为奇形怪状肿大,累及上颌窦19例,伴有牙齿活动/脱落。影像学上,有20个多房性和1个单房性透光病变。最常见的组织病理类型为滤泡型(11.52.4%)。共有21名患者接受了22项手术;21例上颌切除,1例去核。18例患者随访3个月~ 10年,其中3例(16.7%)复发。结论:a型成釉细胞在上颌骨少见。虽然上颌成釉细胞瘤在组织学上与下颌骨的成釉细胞瘤难以区分,但它是非常致命的。在这项研究中取得的一个很好的结果是由于根治性治疗多房品种。术后康复仍然是一个挑战。建议定期终身随访。
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Maxillary ameloblastoma: An enigma for the surgeon
Background:Ameloblastoma is a benign but locally aggressive odontogenic tumour. Worldwide, maxillary ameloblastoma is rare but its late detection renders adequate treatment difficult. Majority occur in the mandible with about 5-20% occurring in the maxillary bone. Objective: The purpose of this study was to analyze 21 cases of maxillary ameloblastoma seen and managed at the Oral and Maxillofacial Unit of Ahmadu Bello University Teaching Hospital, Zaria, Nigeria and Alba Clinic and Medical Centre, Kaduna, Nigeria. Study Design:A retrospective study of cases of maxillary ameloblastoma from all cases of ameloblastoma seen from January 1993 to August 2008. Data with respect to patient's sex, age, tumour location, clinical presentation, radiologic features, biological and histopathologic type, surgical treatment and recurrences were analyzed. Results:Out of 350 cases of ameloblastoma seen within the period, 21(6%) Patients were with maxillary am eloblastoma. Of the 21 cases, there were 13 males and 8 females, a male female ratio of 1.6 to 1, with an age range of 17-55 years (mean = 38.14), peaking at the 4 th and 5 th decades of life (61.9%). Tumour duration was from 3 months to 14 years. There were 18 unilateral and 3 bilateral swellings. Clinically, maxillary ameloblastoma presented with grotesque swellings, with antral involvement in 19 cases, teeth mobility/exfoliation. Radiologically, there were 20 multilocular and 1 unilocular radiolucent lesions. The most common histopathologic type was follicular (11, 52.4%).there were 22 procedures done on 21 patients; 21 maxillectomies and 1 enucleation. Follow up period of 18 patients was between 3 months and 10 years from which 3(16.7%) recurrences were observed. Conclusion:Ameloblastum a is uncommon in the maxilla. While maxillary ameloblastoma is indistinguishable histologically from its mandibular counterpart, it is very lethal. An excellent result achieved in this study was due to the radical mode of treatment of the multilocular variety. Rehabilitation postoperatively remains a challenge. Periodic life-long follow-up is recommended.
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来源期刊
Nigerian Postgraduate Medical Journal
Nigerian Postgraduate Medical Journal MEDICINE, GENERAL & INTERNAL-
CiteScore
1.90
自引率
0.00%
发文量
52
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