Orbits

  • 文章类型: Journal Article
    在颅颌面外伤中经常注意到眼眶骨折。解剖结构的复杂性和与各种重要结构的接近性通常使这些骨折的手术管理复杂化。因此,作者试图以简化的方式回顾有关骨性眼眶及其软组织包膜的解剖结构的文献,并适当强调手术解剖学和手术角度对眼眶的探索。这篇叙述性文献综述的内容可能对年轻的颌面外科医生有用,并将有助于治疗眼眶骨折。
    Fractures of the orbit are frequently noted in craniomaxillofacial trauma. The complexity of the anatomy and the proximity to various vital structures often complicates the surgical management of these fractures. The authors have thus attempted to review the literature on anatomy of the bony orbit and its soft tissue envelope in a simplified manner with due emphasis on surgical anatomy and exploration of the orbit with a surgical perspective. The contents of this narrative literature review may be useful for young maxillofacial surgeons and will aid in the process of management of orbital fractures.
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    文章类型: English Abstract
    Esthetic and functional surgeries in the periocular region fall into the domain of oculoplastic, or plastic and reconstructive surgery and otorhinolaryngology. Oculoplasty is the largest surgical spectrum in ophthalmology including eyelids, orbits and the lacrimal system. Our purpose was to study the frequency of eyelid, lacrimal and orbital (oculoplastic) surgery at the CHU IOTA.
    METHODS: Retrospective medical chart review of all the patients who underwent oculoplastic surgery was conducted from October 2015 to September 2016.
    RESULTS: A total of 233 patients were included with 52% female and 48% male. Patients were 37 years old on average. In total, the surgery was performed on the eyelids in83 cases (35.6%), the orbits in 113 cases (48.5%) and the lachrymal system in 37 cases (15.9%).Eyelid surgery commonly resulted from eye trauma (43,3%), followed by malpositions (30,2%). Mutilating surgery accounted for 92% of the orbital surgery. External dacryocystorhinostomy was the main lacrimal surgery (42%) followed by canalicular lacerations 25%.
    CONCLUSIONS: Oculoplasticsurgeryoccupies an important place in the surgical activities of the ophthalmologic University hospital despite a larger volume for cataractsurgery. Our studydoesn\'t highlight the outcome of the surgery itself but the epidemiology to help decision makers in their eye health policy including the reduction of mutilating surgery and oculoplastic training.
    La chirurgie esthétique et fonctionnelle de la région périoculaire est du domaine de l\'oculoplastie, ainsi que de la chirurgie plastique et reconstructive et de l\'otorhinolaryngologie. L\'oculoplastie constitue le plus large éventail chirurgical en ophtalmologie regroupant la paupière, l\'orbite et le système lacrymal.
    OBJECTIVE: Etudier la fréquence des procédures chirurgicales orbito-palpébrales et lacrymales (oculoplasties) dans un centre de troisième référence.
    UNASSIGNED: Il s\'agissait d\'une étude rétrospective des dossiers de patients opérés pour pathologies oculoplastiques d\'octobre 2015 à septembre 2016.
    UNASSIGNED: Au total 233 patients ont été inclus dont 52% de sexe féminin et 48% de sexe masculin avec un âge moyen de 37 ans ; parmi lesquels 83 cas (35,6%) de chirurgie palpébrale, 113 cas (48,5%) de chirurgie orbitaire et 37 cas (15,9%) chirurgie lacrymale.La chirurgie palpébrale était dominée parréparationdesplaies traumatiques (43,3%), suivi des malpositions (30,2%). La chirurgie mutilante constituait 92% de la chirurgie orbitaire. La dacryocystorhinostomie par voie externe était la principale chirurgie lacrymale soit 42%, suivie des lacérations canaliculaires 25%.
    CONCLUSIONS: Notre étude ne met pas en exergue le résultat de la chirurgie elle-même, mais l\'épidémiologie du traitement chirurgical afin d\'aider les décideurs dans leur politique de santé oculaire notamment sur la réduction de la chirurgie mutilante et la formation oculoplastique.
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  • 文章类型: Journal Article
    背景:胎儿磁共振成像(MRI)可能显示超声检查隐匿性眼部异常。当被发现时,必须寻求后天原因和遗传关联。
    目的:我们的目的是评估有眼眶和/或眼球畸形的胎儿队列,以确定是否存在提示根本原因的成像模式。
    方法:我们搜索了连续9年在一家学术儿童医院进行的所有胎儿MRI报告,以了解眼眶和/或眼球异常。评估每个阳性检查和所有随访MRI的眼间距离,地球仪尺寸,形状和信号,大脑畸形.从病历中记录遗传和临床诊断。
    结果:3,085例胎儿中有76例(2.5%)被诊断为眼睛和/或眼球异常;50%的人进行了产后随访MR检查,都证实了胎儿的MRI检查结果.92%(70/76)患有并发脑畸形。67%(51/76)被诊断患有潜在的疾病,其中39%被基因证实。眼球异常最常见的诊断包括CHARGE(眼睛缺损,心脏异常,后鼻孔闭锁,发育迟缓和生殖器和耳朵异常)综合征,13三体综合征,营养不良症,全前脑和间脑-中脑交界处发育不良。与孤立的眼眶异常相比,基因诊断更可能是眼球异常(P=0.04)。67%的胎儿有眼部钙化,出血和/或晶状体异常具有潜在的母体危险因素(P=0.03).
    结论:畸形眼珠与脑畸形和遗传异常有关。眼部钙化,出血和/或晶状体异常可能与母体危险因素有关.当检测到眼球大小或形状异常时,应考虑遗传检查。
    Fetal magnetic resonance imaging (MRI) may reveal sonographically occult ocular abnormalities. When discovered, acquired causes and genetic associations must be sought.
    We aim to evaluate a fetal cohort with orbit and/or globe malformations to determine whether there are imaging patterns that suggest the underlying cause.
    We searched all fetal MRI reports performed at an academic children\'s hospital over 9 consecutive years for orbit and/or globe abnormalities. Each positive exam and all follow-up MRIs were evaluated for interocular distance, globe size, shape and signal, and brain malformations. Genetic and clinical diagnoses were recorded from the medical record.
    Seventy-six of 3,085 fetuses (2.5%) were diagnosed with ocular and/or globe abnormalities; 50% had postnatal follow-up MR exams, all confirming the fetal MRI findings. Ninety-two percent (70/76) had concurrent brain malformations. Sixty-seven percent (51/76) were diagnosed with an underlying disorder and 39% of these were genetically proven. The most common diagnoses with ocular globe abnormalities included CHARGE (coloboma of the eye, heart anomaly, choanal atresia, retardation and genital and ear anomalies) syndrome, trisomy 13 syndrome, dystroglycanopathy, holoprosencephaly and diencephalic-mesencephalic junction dysplasia. Genetic diagnoses were more likely with ocular globe abnormalities than isolated orbital abnormalities (P=0.04). Sixty-seven percent of fetuses with ocular calcifications, hemorrhage and/or lens abnormalities had potential maternal risk factors (P=0.03).
    Malformed ocular globes are associated with brain malformations and genetic abnormalities. Ocular calcifications, hemorrhage and/or lens abnormalities may be associated with maternal risk factors. Genetic work-up should be considered when an ocular globe size or shape abnormality is detected.
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  • 文章类型: Journal Article
    Treatment strategies and recommended surveillance imaging differ for head and neck cancers depending on subsite and neoplasm type, and pose confusion for referring physicians and interpreting radiologists. The superior soft tissue resolution offered by magnetic resonance imaging is most useful in the surveillance of cancers with high propensities for intraorbital, intracranial, or perineural disease spread, which most commonly include those arising from the sinonasal cavities, nasopharynx, orbits, salivary glands, and the skin. This article discusses recommended surveillance protocoling and reviews treatment approaches, common posttreatment changes, and pearls for identifying disease recurrence in a subsite-based approach.
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  • 文章类型: Journal Article
    OBJECTIVE: T2/FLAIR hyperintensity of the optic nerve/optic nerve head has been described as a sensitive finding in idiopathic intracranial hypertension using post-contrast 3D-T2/FLAIR imaging. The purpose of this study is to assess whether hyperintensity on non-enhanced 2D-T2/FLAIR imaging occurs more likely in diseased patients than controls and to evaluate the relationship between FLAIR signal and visual parameters MATERIALS AND METHODS: A retrospective case-control study was performed of patients with idiopathic intracranial hypertension and controls who underwent orbital MRI. Three neuroradiologists reviewed the FLAIR images, subjectively evaluating for hyperintense signal within the optic nerves/optic nerve heads using a 5-point Likert Scale. Quantitative assessment of optic nerve signal using regions of interests was performed. Clinical parameters were extracted. The diagnostic performance was evaluated, and Spearman correlation calculated to assess the relationship between FLAIR signal and visual outcomes.
    RESULTS: The sensitivity of abnormal FLAIR signal within the optic nerves and optic nerve heads in patients with idiopathic intracranial hypertension ranged from 25-54% and 4-29%, respectively, with specificities ranging from 67-92% and 83-100%. Quantitative assessment revealed a significant difference in CNR between cases and controls in the left posterior optic nerve (p=.002). A positive linear relationship existed between abnormal optic nerve head signal and papilledema grade (OD: p=.02, OS: p=.008) but not with other visual parameters.
    CONCLUSIONS: T2/FLAIR hyperintensity in the optic nerve/optic nerve head may support the diagnosis of idiopathic intracranial hypertension but its absence should not dissuade it. If present, abnormal signal in the optic nerve head correlates with papilledema.
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  • 文章类型: Journal Article
    背景:涉及颅神经(CNs)的神经淋巴瘤病很少见。我们寻求更好地了解眼眶和眶后颅神经神经淋巴瘤病的主要疾病部位和传播模式。
    方法:淋巴瘤患者和CNII神经淋巴瘤病的MRI证据,III,IV,对V1或V2进行回顾性分析。在MRI上记录人口统计学和原发性疾病部位以及神经淋巴瘤病的部位。Wilcoxon秩和检验用于比较神经淋巴瘤病与淋巴瘤类型和生存率的部位数量。
    结果:该研究包括18名患者。最常见的淋巴瘤类型是弥漫性大B细胞(DLBCL)(n=9)和边缘区(n=3)。在9名患者中,淋巴瘤表现为肿块(n=7)或直接累及眼眶的浸润性疾病(n=2);在6中,颌面部肿块直接扩散到CNs;在3中,远处的淋巴瘤扩散到眼眶CNs。总的来说,注意到81个神经淋巴瘤病部位。最常见的部位是上颌神经(V2),包括眶下裂或圆孔(17例;19条神经),翼腭窝(16例;19神经),海绵窦(9例;12神经)。DLBCL的神经淋巴瘤病部位数量明显低于其他淋巴瘤类型(p=0.007)。神经淋巴瘤病的部位数量不影响生存率(p=0.26)。病理诊断和MRI记录全部神经淋巴瘤病之间的平均间隔为病理诊断后39天。
    结论:根据我们的研究结果,眼眶中的神经淋巴瘤病似乎经常与眼眶和/或颌面部肿块相关,通常涉及CNV2,翼腭窝,还有海绵窦.与其他淋巴瘤相比,DLBCL可能与神经淋巴瘤病的较少部位相关。在淋巴瘤患者中,对于神经淋巴瘤病的早期发现,必须进行系统的搜索。
    BACKGROUND: Neurolymphomatosis involving the cranial nerves (CNs) is rare. We sought a better understanding of the primary disease sites and patterns of spread in neurolymphomatosis of the orbit and retro-orbital cranial nerves.
    METHODS: Patients with lymphoma and MRI evidence of neurolymphomatosis of CN II, III, IV, V1, or V2 were retrospectively reviewed. Demographics and primary disease site and sites of neurolymphomatosis on MRI were recorded. Wilcoxon rank sum test was used to compare number of sites of neurolymphomatosis with lymphoma type and survival.
    RESULTS: The study included 18 patients. The most frequent types of lymphoma were diffuse large B-cell (DLBCL) (n = 9) and marginal zone (n = 3). In 9 patients, lymphoma presented as a mass (n = 7) or infiltrative disease (n = 2) directly involving the orbit; in 6, a maxillofacial mass spread directly to CNs; and in 3, lymphoma at remote sites spread to orbital CNs. Overall, 81 sites of neurolymphomatosis were noted. The most common sites were the maxillary nerve (V2) including at the infraorbital fissure or foramen rotundum (17 patients; 19 nerves), pterygopalatine fossa (16 patients; 19 nerves), and cavernous sinus (9 patients; 12 nerves). Number of sites of neurolymphomatosis was significantly lower for DLBCL than for other lymphoma types (p = 0.007). Number of sites of neurolymphomatosis did not affect survival (p = 0.26). The mean interval between the pathologic diagnosis and MRI documentation of the full extent of neurolymphomatosis was 39 days after pathologic diagnosis.
    CONCLUSIONS: Based on our study results, neurolymphomatosis in the orbit appears to be frequently associated with an orbital and/or maxillofacial mass and commonly involves CN V2, the pterygopalatine fossa, and the cavernous sinus. DLBCL may be associated with fewer sites of neurolymphomatosis than other lymphomas. In patients with lymphoma, a systematic search for neurolymphomatosis is imperative for early detection.
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  • 文章类型: Journal Article
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  • 文章类型: Case Reports
    Cachexia is a significant contributor to cancer mortality as it is responsible for up to 30% of cancer deaths. Magnetic resonance imaging offers a noninvasive approach to detect features of cachexia. T1-weighted images of cachectic patients have a \"pseudo fat-saturated\" appearance secondary to disappearance of subcutaneous and fascial fat throughout the body, as well as fat in the bone marrow. Orbital fat remains preserved until late disease. We present 2 cases with these classic imaging findings of cancer cachexia in the subcutaneous tissues of the head, neck, and spine. This imaging phenomenon is often misinterpreted by radiologists and may lead to delayed diagnosis or unnecessary repeat imaging.
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  • 文章类型: Case Reports
    We present an interesting case of biopsy-proven multiorgan metastatic invasive lobular carcinoma to the orbits and kidney, initially presenting in a 76-year-old woman with diplopia. Invasive lobular carcinoma is a less common subtype of breast cancer and is often difficult to detect on imaging with an unusual metastatic pattern when compared to invasive ductal carcinoma. Metastatic invasive lobular carcinoma most frequently involves the orbits, ovaries, gastrointestinal tract, retroperitoneum and bone. Disease involving these organ systems detected on imaging should raise concern for metastatic disease when appropriate.
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  • 文章类型: Case Reports
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