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源自上颌骨的颅内成釉细胞瘤:一种多学科手术方法

Intracranial Ameloblastoma Arising from the Maxilla: An Interdisciplinary Surgical Approach.

作者信息

Quick-Weller Johanna, Koch Felix, Dinc Nazife, Lescher Stephanie, Baumgarten Peter, Harter Patrick, Scheerer Friedrich, Sader Robert, Seifert Volker, Marquardt Gerhard, Freiman Thomas

机构信息

Department of Neurosurgery, Goethe-University Frankfurt, Frankfurt, Germany.

Department of Oral, Cranio-Maxillofacial, and Facial Plastic Surgery, Goethe-University Frankfurt, Frankfurt, Germany.

出版信息

J Neurol Surg A Cent Eur Neurosurg. 2017 Nov;78(6):582-587. doi: 10.1055/s-0036-1594236. Epub 2016 Dec 30.

DOI:10.1055/s-0036-1594236
PMID:28038480
Abstract

Ameloblastomas are a rare tumor entity accounting for only 10% of all odontogenic tumors. They mostly originate from the mandible. Only a few cases are known to grow aggressively and to invade the orbit, nasal cavity, or even the brain.  We present the case of a 57-year-old patient who was admitted with a huge tumor involving the nasal cavity, the left maxilla, and the anterior fossa. Histologic diagnosis was made by biopsy. A combined two-stage neurosurgical maxillofacial approach was planned. First the intracranial tumor mass was removed using bifrontal trepanation. A duraplasty was sewn in to cover the brain. In the second procedure, a combined bifrontal and midfacial approach was used by craniofacial plastic surgeons and neurosurgeons. A perisinusoidal tumor mass and retropharyngeal tumor mass was removed up to the skull base. The left orbit was completely exenterated, and a fibular bone-muscle graft was used for palatal, orbital, and facial reconstruction. The facial vein and artery were carefully prepared to feed the bone-muscle graft by end-to-end anastomoses.  Ameloblastomas are very rare slow-growing tumors that show a tendency to recur. They are responsible for only 1% of all oral tumors. Their growth can be enormous, and they can extend into sinusoidal cavities, the orbit, and the brain. Complex and extensive palliative surgery can ease the concerns of these patients and prolong their survival.

摘要

成釉细胞瘤是一种罕见的肿瘤类型,仅占所有牙源性肿瘤的10%。它们大多起源于下颌骨。已知只有少数病例会侵袭性生长并侵犯眼眶、鼻腔甚至脑部。 我们报告一例57岁患者,因巨大肿瘤累及鼻腔、左上颌骨和前颅窝入院。通过活检进行组织学诊断。计划采用联合两阶段神经外科颌面手术方法。首先,采用双额开颅术切除颅内肿瘤肿块。缝合硬脑膜成形术以覆盖脑部。在第二步手术中,颅面整形外科医生和神经外科医生采用联合双额和中面部手术方法。切除鼻窦周围肿瘤肿块和咽后肿瘤肿块直至颅底。完全切除左眼眶,并使用腓骨骨肌瓣进行腭部、眼眶和面部重建。仔细准备面静脉和动脉,通过端端吻合为骨肌瓣供血。 成釉细胞瘤是非常罕见的生长缓慢的肿瘤,有复发倾向。它们仅占所有口腔肿瘤的1%。其生长范围可能很大,可延伸至鼻窦腔、眼眶和脑部。复杂而广泛的姑息性手术可缓解这些患者的担忧并延长其生存期。

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Intracranial Ameloblastoma Arising from the Maxilla: An Interdisciplinary Surgical Approach.源自上颌骨的颅内成釉细胞瘤:一种多学科手术方法
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The treatment of ameloblastoma based on pathologic and anatomic principles.基于病理和解剖学原则的成釉细胞瘤治疗。
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引用本文的文献

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Maxillary Ameloblastoma with Local Recurrence, Orbital Invasion, and Systemic Metastases: A Case Report and Review of the Literature.伴局部复发、眼眶侵犯及全身转移的上颌成釉细胞瘤:1例报告并文献复习
Case Rep Ophthalmol. 2024 Mar 19;15(1):238-245. doi: 10.1159/000537707. eCollection 2024 Jan-Dec.
2
Ameloblastoma and Intracranial Involvement: The Current Challenge of the Radical Surgical Treatment. Comprehensive Review of the Literature and Institution experience.成釉细胞瘤与颅内累及:根治性手术治疗的当前挑战。文献综述与机构经验总结
J Maxillofac Oral Surg. 2022 Mar;21(1):34-43. doi: 10.1007/s12663-021-01643-9. Epub 2021 Sep 24.
3
Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review.
纯内镜经蝶窦治疗伴颅内侵犯的颅底成釉细胞瘤:病例报告及文献复习
Surg Neurol Int. 2020 Aug 1;11:228. doi: 10.25259/SNI_45_2020. eCollection 2020.