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Massive calcium pyrophosphate deposition (CPPD) affecting the temporomandibular joint – A case report and review of the literature 影响颞下颌关节的大量焦磷酸钙沉积(CPPD)--病例报告和文献综述
Q3 Dentistry Pub Date : 2024-04-29 DOI: 10.1016/j.omsc.2024.100358
Yousuf Qundos, Payam Farzad, Caroline Robertsson

Calcium pyrophosphate deposition (CPPD) is a condition where calcium pyrophosphate crystals cause arthritis. Its occurrence in the temporomandibular joint (TMJ) is sparingly reported in the literature. Non-surgical treatment modalities consist of non-steroidal anti-inflammatory drugs, colchicine, and intra-articular cortisone injection. In the TMJ, previous reports have described resection of affected joint with reconstruction. We present a case of an extensive CPPD lesion affecting the left TMJ requiring surgical resection and reconstruction with a custom made TMJ prosthesis alongside with a review of the existing literature.

焦磷酸钙沉积症(CPPD)是焦磷酸钙结晶导致关节炎的一种病症。文献中很少有关于其在颞下颌关节(TMJ)中发生的报道。非手术治疗方法包括非甾体抗炎药、秋水仙碱和关节内注射可的松。对于颞下颌关节,以往的报告描述了切除受影响的关节并进行重建的方法。我们介绍了一例左侧颞下颌关节广泛CPPD病变的病例,该病例需要进行手术切除,并使用定制的颞下颌关节假体进行重建,同时还对现有文献进行了回顾。
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引用次数: 0
Simple bone cyst of the mandible 下颌骨单纯骨囊肿
Q3 Dentistry Pub Date : 2024-04-27 DOI: 10.1016/j.omsc.2024.100357
Paolo Boffano , Anna Maria Agnone , Muhammad Ruslin

Simple bone cysts (SBCs) are nonneoplastic intraosseous cavities without an epithelial lining, surrounded by bony walls and either empty or containing liquid and/or connective tissue: they were first described in 1929 as a distinct entity of disease. The characteristic that distinguishes SBCs from true cysts is the absence of epithelial lining, that allow us to regard SBCs as pseudocysts.

In the literature, SBCs have been referred to as solitary bone cysts, idiopathic bone cysts, unicameral cysts, traumatic bone cysts, hemorrhagic bone cysts, primary bone cysts, and extravasation cysts.

The pathogenesis of SBC remains uncertains. Radiographically, SBCs usually present as isolated unilocular radiolucencies with well-defined borders. When SBC extends to the interdental bone, the characteristic radiographic “scalloping effect” can be observed. The differential diagnosis includes apical periodontitis, odontogenic keratocyst, central giant cell granuloma, ameloblastoma, odontogenic myxoma, and central and neurogenic neoplasms.

Surgery (curettage) is the gold standard treatment as it allows both diagnosis and treatment by generation of a blood clot in the vacant cavity of SBCs: bone usually regenerates progressively within 6–12 months. Recurrence rate is almost negligible.

The aim of the present article is to present and discuss the diagnosis and management of a case of SBC.

单纯性骨囊肿(SBCs)是一种非肿瘤性骨内空腔,无上皮衬里,周围为骨壁,空腔或内含液体和/或结缔组织:1929 年首次被描述为一种独特的疾病实体。在文献中,SBC 被称为单发性骨囊肿、特发性骨囊肿、单腔囊肿、外伤性骨囊肿、出血性骨囊肿、原发性骨囊肿和外渗囊肿。从影像学上看,SBC 通常表现为孤立的单眼放射状肿物,边界清晰。当 SBC 扩展到牙间骨时,可观察到放射学上特有的 "扇形效应"。鉴别诊断包括根尖牙周炎、牙源性角化囊肿、中央巨细胞肉芽肿、髓母细胞瘤、牙源性肌瘤以及中枢性和神经性肿瘤。手术(刮除术)是金标准治疗方法,因为它可以在 SBC 的空腔中产生血凝块,从而进行诊断和治疗:骨通常会在 6-12 个月内逐渐再生。本文旨在介绍和讨论一例 SBC 的诊断和治疗。
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引用次数: 0
Classic Kaposi's sarcoma of the oral cavity occurring in an immunocompetent Polynesian man 一名免疫功能正常的波利尼西亚男子口腔中发生的典型卡波西肉瘤
Q3 Dentistry Pub Date : 2024-04-18 DOI: 10.1016/j.omsc.2024.100355
Leon Kong , Abdul-Kader Ebrahim , Duncan Lamont

Kaposi's sarcoma (KS) is an uncommon angioproliferative tumour. In its classic form, it rarely affects the head and neck. The etiologic agent in KS is Human Herpesvirus type-8 (HHV-8) infection. Populations in which KS occurs in the setting of immunocompetence tend to have high rates of seropositivity for HHV-8, including Mediterranean and Jewish people. Descriptions of KS in immunocompetent Polynesian individuals are almost non-existent. A reason for this may be the relative inaccessibility, both geographically and culturally, of indigenous peoples living in the Oceanic area. High rates of HHV-8 seropositivity have recently been reported in indigenous Melanesian populations of Vanuatu, New Caledonia and Papua New Guinea, a region neighbouring Polynesia. This paper is the first to describe classic KS isolated to the oral cavity in an immunocompetent patient of Polynesian ancestry and highlights the need for further research to clarify the risk of KS emerging in this region.

卡波西肉瘤(KS)是一种不常见的血管增生性肿瘤。典型的卡波西肉瘤很少发生在头颈部。KS 的病原体是人类疱疹病毒 8 型(HHV-8)感染。在免疫功能正常的人群中,KS 的 HHV-8 血清阳性率往往很高,其中包括地中海人和犹太人。关于免疫功能正常的波利尼西亚人感染 KS 的描述几乎不存在。其中一个原因可能是生活在大洋洲地区的原住民在地理和文化上都相对偏远。最近有报道称,在邻近波利尼西亚的瓦努阿图、新喀里多尼亚和巴布亚新几内亚的美拉尼西亚土著居民中,HHV-8 血清阳性率很高。本文首次描述了波利尼西亚血统的免疫功能正常患者口腔中分离出的典型 KS,并强调了进一步研究的必要性,以明确该地区出现 KS 的风险。
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引用次数: 0
Zygomatic implant on a severely resorbed maxillary arch in a HIV positive patient. Considerations in medical work up and treatment planning: A case report 在 HIV 阳性患者严重吸收的上颌牙弓上植入颧骨种植体。医疗工作和治疗计划中的考虑因素:病例报告
Q3 Dentistry Pub Date : 2024-03-22 DOI: 10.1016/j.omsc.2024.100350
Dana C. Jackson Sr. , Priti P. Lotlikar

Background

The indications for using zygomatic implantsinvolve cases with severe resorption of the maxillary arch resulting in inadequate bone volume. The case report aims to review the HIV virus and current protocols, perioperative management and the surgical approach of zygomatic implant placement in combination with traditional implants in an HIV-positive patient.

Case report

A 59-year-old HIV positive male patient presents with atrophic maxillary and mandibular arches. Surgical placement of two zygomatic implants, two endosseous implants in the maxillary arch, and six endosseous implants in the mandibular arch. A reduction of a large palatal tori was also performed. The patient exhibited no complications after the surgical procedure. The hybrid prostheses were inserted post surgically without any issues.

Conclusion

Zygomatic implants can be an optimal treatment option for prosthetic rehabilitation in patients with atrophic maxilla for better functionality and aesthetics. This case demonstrates the perioperative work up and placement of zygomatic implants in a medically stable HIV-positive patient with no adverse effects five months post-operation. Various surgical approaches may be utilized with excellent patient acceptance and predictable outcomes.

背景使用颧骨种植体的适应症包括上颌牙弓严重吸收导致骨量不足的病例。本病例报告旨在回顾一名 HIV 阳性患者的 HIV 病毒和当前方案、围手术期管理以及颧骨种植体植入结合传统种植体的手术方法。手术植入了两颗颧骨种植体,在上颌牙弓植入了两颗骨内种植体,在下颌牙弓植入了六颗骨内种植体。此外,还进行了一个大腭环的缩小手术。手术后患者没有出现任何并发症。结论颧骨种植体可以作为上颌骨萎缩患者修复的最佳治疗方案,以获得更好的功能性和美观性。本病例展示了一名病情稳定的艾滋病病毒阳性患者的围手术期工作和颧骨种植体植入情况,术后五个月无不良反应。可以采用多种手术方法,患者接受度高,效果可预测。
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引用次数: 0
The impact of case reporting on our specialty 编者的话"病例报告对我们专业的影响
Q3 Dentistry Pub Date : 2024-03-14 DOI: 10.1016/j.omsc.2024.100354
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引用次数: 0
Twiddler's syndrome and INSPIRE hypoglossal nerve stimulator malfunction 捻发音综合征和 INSPIRE 舌下神经刺激器故障
Q3 Dentistry Pub Date : 2024-03-07 DOI: 10.1016/j.omsc.2024.100353
Jennifer W. Bergstrom , Allen Cheng , Baber Khatib , Ashish Patel

Obstructive sleep apnea (OSA) is characterized by recurrent upper airway collapse during sleep. Since FDA approval in 2014, INSPIRE hypoglossal nerve stimulators have been used for the treatment of moderate to severe OSA in patients who are unable to use CPAP. In this case report we discuss malfunction of a hypoglossal nerve stimulator due to rotational manipulation of the implanted device that is patient generated. This phenomenon is called Twiddler's Syndrome and has been demonstrated with other implantable medical devices. We review risk factors associated with Twiddler's syndrome, and strategies for mitigating risk of occurrence.

阻塞性睡眠呼吸暂停(OSA)的特点是睡眠时上气道反复塌陷。自 2014 年获得 FDA 批准以来,INSPIRE 舌下神经刺激器已被用于治疗无法使用 CPAP 的中重度 OSA 患者。在本病例报告中,我们讨论了舌下神经刺激器因患者产生的对植入装置的旋转操作而发生故障的问题。这种现象被称为 Twiddler's 综合征,其他植入式医疗设备也曾出现过这种情况。我们回顾了与 Twiddler's 综合征相关的风险因素以及降低发生风险的策略。
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引用次数: 0
Epithelial-myoepithelial carcinoma of soft palate case report and literature review 软腭上皮-肌上皮癌病例报告和文献综述
Q3 Dentistry Pub Date : 2024-03-02 DOI: 10.1016/j.omsc.2024.100351
Ciro Emiliano Boschetti , Romolo Fragola , Rita Vitagliano , Giuseppe Colella , Mario Santagata , Marco Montella , Gianpaolo Tartaro

The epithelial-myoepithelial carcinoma (EMC) is a rare neoplasm of the salivary glands with an incidence <1% of all cancers affecting them. It commonly affects the parotid gland and less frequently the submandibular gland and minor salivary glands. EMC is a rare low-grade tumor characterized biphasic tubular structure composed by an internal layer of luminal ductal cells surrounded by clear cells of myoepithelial origin. The patient had good prognostic factors determined in previous studies, and achieved complete treatment-response. Further accumulation of cases and long-term follow-up data are needed to elucidate the pathophysiology and prognosis of epithelial-myoepithelial carcinoma.

上皮-肌上皮癌(EMC)是一种罕见的唾液腺肿瘤,发病率占所有唾液腺癌症的 1%。它通常影响腮腺,较少影响颌下腺和小唾液腺。EMC 是一种罕见的低级别肿瘤,具有双相管状结构,内层为管腔导管细胞,周围为透明的肌上皮细胞。该患者在既往研究中具有良好的预后因素,并获得了完全的治疗反应。需要进一步积累病例和长期随访数据,以阐明上皮-肌上皮癌的病理生理学和预后。
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引用次数: 0
Pathologic fracture of mandibular ramus in a patient with familial dysautonomia: A case report 一名家族性自律神经失调症患者的下颌骨横突病理性骨折:病例报告
Q3 Dentistry Pub Date : 2024-03-02 DOI: 10.1016/j.omsc.2024.100352
Patrick J. Nolan , David Koslovsky , Drew Roberts

Familial dysautonomia is a rare disease that impairs the development of sensory nerves, afferent autonomic nerves, and afferent baroreflex pathways. This ultimately results in decreased pain receptors, decreased thermal sensation, blood pressure instability, dysphagia, optic neuropathy, and gait ataxia. The authors are documenting a case of a familial dysautonomia patient who suffered a pathological fracture of the left mandible approximately 4 months after undergoing routine third molar surgery. Due to the patient's inability to perceive pain and lack proprioception, this fracture went undiagnosed until facial swelling was visible. Familial dysautonomia patients require special consideration regarding anesthesia, surgery, and postoperative follow up.

家族性自律神经失调症是一种罕见疾病,会损害感觉神经、传入性自律神经和传入性气压反射通路的发育。最终导致痛觉减退、热觉减退、血压不稳、吞咽困难、视神经病变和步态共济失调。作者记录了一例家族性自主神经功能障碍患者的病例,该患者在接受常规第三磨牙手术约 4 个月后,左下颌骨发生病理性骨折。由于患者无法感知疼痛且缺乏本体感觉,该骨折一直未得到诊断,直到面部肿胀才显现出来。家族性自主神经功能障碍患者在麻醉、手术和术后随访方面需要特别注意。
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引用次数: 0
How do I expose the inferior alveolar nerve for microneurosurgical repair? 如何暴露下牙槽神经进行显微神经外科修复?
Q3 Dentistry Pub Date : 2024-02-17 DOI: 10.1016/j.omsc.2024.100349
Michael Miloro

This technical note describes an innovation that addresses a clinical problem in iatrogenic inferior alveolar nerve (IAN) repair. The options for IAN exposure (Miloro, 1995) are less than ideal since they offer limited access and visibility and/or the exposure itself has a risk of inducing iatrogenic IAN injury. This technical note offers the option to perform IAN exposure via a unilateral sagittal split osteotomy (SSO). There are inherent risks of mild transient IAN paresthesia, malocclusion, bad splits, and the additional cost of rigid fixation hardware (Peleg et al., 2021). The significance of this technique is that it permits wide access for IAN reconstruction in cases where the IAN injury is in the posterior mandible (eg. due to mandibular third molar removal) where another option for access is limited. This technique will improve patient care by facilitating IAN exposure and repair. There should be no challenges or delays to implementing this innovation for surgeons who perform orthognathic surgery and nerve repair.

本技术说明介绍了一项创新技术,该技术解决了先天性下牙槽神经(IAN)修复的临床问题。暴露下牙槽神经(IAN)的方法(Miloro,1995 年)并不理想,因为它们提供的通道和可视性有限,并且/或者暴露本身有诱发下牙槽神经先天性损伤的风险。本技术说明提供了通过单侧矢状面劈开截骨术(SSO)进行 IAN 暴露的选择。该方法存在轻度一过性 IAN 麻痹、咬合不正、劈裂不良以及刚性固定硬件额外费用等固有风险(Peleg 等人,2021 年)。该技术的重要意义在于,当 IAN 损伤位于下颌后部(例如,由于下颌第三磨牙切除术),而其他入路选择有限时,该技术可为 IAN 重建提供宽阔的入路。这项技术将有助于 IAN 的暴露和修复,从而改善对患者的护理。对于进行正颌外科手术和神经修复的外科医生来说,实施这项创新技术应该不会遇到任何挑战或延误。
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引用次数: 0
Abducens nerve palsy following Le Fort 1 maxillary osteotomy Le Fort 1 上颌骨截骨术后出现视神经麻痹
Q3 Dentistry Pub Date : 2024-02-14 DOI: 10.1016/j.omsc.2024.100347
Frederik Piccart , Jan Vanhove , Constantinus Politis

This case report presents a rare but significant complication of abducens nerve palsy following Maxillary Le Fort I osteotomy. The patient, who underwent the procedure for trans palatal distraction indication, experienced left-sided abducens nerve palsy, characterized by the inability to abduct the ipsilateral eye. Undesired fracture patterns can extend to neighbouring structures. The report discusses the management strategies employed and the outcome of this specific complication. By sharing this case, it aims to increase awareness of the potential risks associated with Maxillary Le Fort I osteotomy and provide insights for optimizing surgical outcomes and improving patient safety.

本病例报告介绍了上颌乐堡 I 型截骨术后出现的一种罕见但严重的外展神经麻痹并发症。该患者是因经腭牵引适应症而接受手术的,术后出现左侧外展神经麻痹,表现为同侧眼球无法外展。意想不到的骨折模式可能会延伸到邻近的结构。本报告讨论了这一特殊并发症的处理策略和结果。通过分享这一病例,旨在提高人们对上颌乐堡I型截骨术潜在风险的认识,并为优化手术效果和提高患者安全提供见解。
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引用次数: 0
期刊
Oral and Maxillofacial Surgery Cases
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