sphenoid sinus mucocele

  • 文章类型: Case Reports
    粘膜瘤是局部侵入性但良性扩张性囊性病变,可出现在鼻旁窦内。孤立性蝶窦黏液囊肿(SSM)相当罕见,占所有鼻旁窦黏液囊肿的不到1%。由于蝶窦的关键位置和靠近重要结构,SSM可引起多种症状和并发症。我们报告了一例53岁的男子,他突然出现视力丧失,并被发现患有孤立的SSM。外科引流和SSM管理后,患者出院后视力完全恢复。
    Mucoceles are locally invasive but benign expansive cystic lesions that can arise within paranasal sinuses. Isolated sphenoid sinus Mucoceles (SSM) are quite rare, comprising less than 1% of all paranasal sinus mucoceles. Due to the critical position and proximity of the sphenoid sinus to vital structures, SSMs can cause a multitude of symptoms and complications. We report a case of a 53-year-old man who presented with sudden vision loss and was found to have an isolated SSM. Following surgical drainage and management of the SSM, the patient had full recovery of visual acuity upon discharge.
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  • 文章类型: Case Reports
    未经证实:报告一例罕见的Woakes\'综合征,表现为双侧视力丧失。
    未经证实:一名28岁男性,左眼有1年视力丧失史,右眼突然视力丧失后,他被转诊到神经眼科诊所。对视力丧失的临床发现和假定的病理生理基础进行了详细的审查。
    未经证实:神经影像学显示双侧巨大鼻息肉,蝶窦黏液囊肿形成,蝶窦内的视神经裂开.脉冲皮质类固醇治疗后右眼视力恢复;然而,即使在鼻息肉切除术和黏液囊肿引流后,左眼的视力仍然严重受损。
    未经授权:对于原因不明的视力丧失患者,应寻找鼻窦疾病,因为及时干预可以挽救这些患者的视力。
    UNASSIGNED: To report a rare case of Woakes\' syndrome presented with bilateral vision loss.
    UNASSIGNED: A 28-year-old male with a 1-year history of vision loss in the left eye was referred to the neuro-ophthalmology clinic after sudden vision loss in his right eye. A detailed review of clinical findings and the presumed pathophysiological basis of vision loss was performed.
    UNASSIGNED: Neuroimaging revealed bilateral massive nasal polyps, sphenoid sinus mucocele formation, and optic nerve dehiscence inside the sphenoid sinus. The vision in the right eye was restored after pulse corticosteroid therapy; however, the left eye remained severely visually compromised even after nasal polypectomy and mucocele drainage.
    UNASSIGNED: Sinonasal disorders should be sought for patients with unexplained vision loss, as prompt intervention could be vision-saving in these patients.
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  • 文章类型: Case Reports
    蝶窦黏液囊肿(SSMs)很少引起急性双侧视力丧失。我们,特此,报告一例罕见的SSM病例,患者为一名20岁女性,患者出现突然发作的双侧视力减退。右眼(RE)的最佳矫正视力为20/400,左眼(LE)的手部运动为20/400。两只眼睛都有迟钝的瞳孔反应。双眼眼底正常。初始治疗开始于双侧球后神经炎的临时诊断,但影像学显示有一个巨大的SSM压迫双侧视神经.患者接受了紧急手术减压。RE的视力提高到20/20,LE提高到20/400。在所有非典型视神经炎的病例中,都需要高度怀疑压缩性病变的临床指标。
    Sphenoid sinus mucoceles (SSMs) can rarely cause acute bilateral vision loss. We, hereby, report such a rare case of SSM in a 20-year-old female who presented with sudden onset bilateral diminution of vision. The best-corrected visual acuity was 20/400 in the right eye (RE) and hand movements in the left eye (LE). Both eyes had sluggish pupillary reactions. Both eyes had normal fundus. Initial treatment was started with a provisional diagnosis of bilateral retrobulbar neuritis, but imaging revealed a large SSM compressing bilateral optic nerves. The patient underwent urgent surgical decompression. Vision in RE improved to 20/20 and LE to 20/400. A high index of clinical suspicion for compressive lesions is needed in all cases of atypical optic neuritis.
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  • 文章类型: Case Reports
    蝶窦黏液囊肿(SSM)是眶尖综合征(OAS)的罕见原因。当在常规鼻窦成像中不明显可见粘液囊肿超出鼻窦时,SSM的神经系统并发症的诊断可能会延迟。
    我们介绍了一例76岁的男性患者,其瞳孔保留眼肌麻痹与单侧左SSM引起的下垂相关,其中颈内动脉多普勒超声显示远端亚闭塞波模式。
    在磁共振成像(MRI)中发现了鼻窦占据,并在计算机断层扫描(CT)扫描和MR血管造影中进行了进一步评估。CT或MR血管造影均未显示相邻结构受压的明确证据。颈内动脉多普勒超声显示高阻波形和降低的波速有助于诊断。术中确认结构受压,蝶窦引流后无症状出院。
    在第一份报告中,患者的颈动脉多普勒超声检查结果为神经表现为蝶窦黏液囊肿,颈内动脉的高阻力波形可能有助于区分单纯性鼻窦炎和侵袭性黏液囊肿.
    UNASSIGNED: Sphenoid sinuses mucocele (SSM) is an uncommon cause of orbital apex syndrome (OAS). Diagnosis of neurological complications in SSM might be delayed when the expansion of mucocele beyond the sinuses is not evident in conventional sinuses imaging.
    UNASSIGNED: We present a case of a 76-years old man with spared-pupil ophthalmoplegia associated with ptosis caused by a unilateral left SSM in which internal carotid artery Doppler ultrasound showed distal sub-occlusion waves pattern.
    UNASSIGNED: Sinus occupation was noted in the magnetic resonance imaging (MRI) and was further evaluated in computed tomography (CT) scan and MR angiography. Nor CT or MR angiography showed clear evidence of neighboring structures compression. Doppler ultrasound of internal carotid showed high-resistance waveforms and decreased wave velocities helping diagnosis. Structures compression was confirmed intra-operatively and the patient was discharged asymptomatic after sphenoid sinus drainage.
    UNASSIGNED: In this first report of carotid Doppler ultrasound findings in a patient with a neurological presentation of a sphenoid sinus mucocele, a high-resistance waveform of the internal carotid may help differentiate uncomplicated sinusitis from invasive mucocele.
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  • 文章类型: Case Reports
    粘液囊肿是窦腔的囊性和扩张性病变。在蝶窦中并不常见,其管理非常具有挑战性,尤其是在喀麦隆等中低收入国家。一名43岁的女性因慢性头痛和视力障碍而被神经科医生转介给我们。疼痛对镇痛药无反应。体格检查不明显,头部CT扫描显示蝶窦腔有囊肿样病变。提出了外科内镜治疗,并用基本的内镜器械实现,包括用粘液囊肿的引流打开空腔。在蝶窦的前壁上开了一个大开口,以确保持续引流并防止复发。蝶窦黏液囊肿是一种罕见的疾病,它的诊断可能很困难。确认需要特定的成像和治疗目前已经确立,但可以使用基本工具进行管理。
    A mucocele is a cystic and expansive lesion of the sinus cavities. It is uncommon in the sphenoid sinus and its management is quite challenging especially in low to middle income countries like Cameroon. A 43-years-old female was referred to us by a neurologist for chronic headache and visual disturbances. The pain was unresponsive to analgesics. Physical examination was non-remarkable and a head CT scan realized showed a cyst-like lesion in the sphenoid sinus cavity. Surgical endoscopic treatment was proposed and realized with basic endoscopic instruments, consisting of opening the cavity with drainage of the mucocele. A large opening was made on the anterior wall of the sphenoid sinus, in order to ensure continuous drainage and prevent a recurrence. Sphenoid sinus mucocele is a rare condition, and its diagnosis can be difficult. Confirmation requires specific imaging and treatment is presently well established, but it can be managed with basic tools.
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  • 文章类型: Journal Article
    Neurological manifestations associated with sphenoid sinus mucocele (SSM) are easily misdiagnosed due to nonspecific symptoms. The objective is to analyze and report the clinical features of SSM presenting with neurological manifestations, to allow an earlier diagnosis and more timely intervention for this disease.
    This was a retrospective cross-sectional study including 19 patients. The detailed clinical information of 19 patients with the initial symptom of neurological manifestations caused by SSM presenting at the Second Affiliated Hospital of Wenzhou Medical University between January 2000 and May 2018 were retrospectively analyzed. Collected data including symptoms, signs, neuroimaging, and pathologic diagnoses.
    There were eleven males and 8 females, and their ages ranged from 23 to 71 years. Headache was the most frequent symptom, in 12 of the 19 patients presenting as the initial symptom. The visual disturbance included visual loss (4/19), diplopia (3/19), and another patient had both visual loss and diplopia. Neurophysical examination found that 4 patients presented with oculomotor nerve palsy, 4 patients had optic nerve or abducens nerve palsy, and 1 patient had optic neuropathy, oculomotor nerve palsy and abducens nerve palsy simultaneously. All patients underwent endoscopic surgery and had postoperative clinical symptom improvement.
    Headache is the most common symptom of SSM and should be on the differential diagnosis of patients presenting with headache, even if in isolation. The results suggest that CT and MRI are the best tools in diagnosis of SSM and endoscopic sphenoidotomy is a safe and effective method in the treatment of SSM.
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  • 文章类型: Case Reports
    Sphenoid sinus mucoceles (SSMs) are rare, benign lesions that can expand, often presenting with ocular symptoms-decreased vision, diplopia, visual field defects, proptosis, and external ophthalmoplegia. Reported cases are few, visual compromise varies, and factors affecting visual prognosis are poorly characterized. We investigate whether prompt surgical intervention (within 2 weeks of visual symptom onset) affects best-corrected visual acuity (BCVA) regained in patients with vision loss secondary to compressive SSM. We present a retrospective review of three cases and published literature to date. Our primary outcome was BCVA regained after surgical intervention; secondary outcomes included change in visual field defect and ophthalmological symptoms other than vision loss. Our three cases of SSM varied in onset, ranging from several hours to several months with patients aged from 13 to 80 years. All patients had severe vision loss to light perception (LP) or worse. Rapid neuro-imaging and urgent surgical intervention improved vision to count fingers at best. Of the two patients who underwent prompt decompression, one improved from no LP to LP and the other did not recover any vision. The patient who had visual loss for 3 months before intervention improved from LP to 20/400. Findings from our literature search, which yielded 12 cases of urgent intervention, supported the variability in visual prognosis despite prompt surgical intervention. SSMs are rare, pathologically benign lesions which can expand to cause ocular involvement. Prompt diagnosis and surgical decompression are recommended, but visual recovery may be limited even with urgent intervention.
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    文章类型: Case Reports
    We report a case of first-episode sphenoid mucocele successfully treated via transnasal endoscopic drainage and marsupialization of the mucocele. A 55 year-old female presented with persistent right-side facial numbness (in the areas of the first and second branches of the trigeminal nerve) and right-side ptosis. Computed tomography (CT) imaging and Magnetic resonance imaging (MRI) revealed opacification and expansion of the right-side sphenoid sinus lesion. The lesion was diagnosed as right-side sphenoid mucocele affecting the functions of the trigeminal (first and second branches), and oculomotor nerves. Transnasal endoscopic drainage and marsupialization of the mucocele result in rapid regression of these symptoms.
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  • 文章类型: Case Reports
    A sphenoid mucocele often presents late due to its deep seated anatomical site. And it has varied presentation due to its loose relationship to the cavernous sinus and the base of the skull. We describe a case of large sphenoid sinus mucocele. A middle aged old man suddenly developed third cranial nerve palsy. Brain imaging study revealed an isolated sphenoid sinus mucocele, compressing right cavernous sinus. Endoscopic marsupialization of the mucocele via transnasal approach led to complete resolution of the third cranial nerve palsy. Involvement of the third cranial nerve in isolated mucocele is rare but important neurosurgical implications which must be excluded. In addition, proper and timely treatment must be performed to avoid permanent neurologic deficit.
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