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Common fibro-osseous lesions of the paranasal sinuses.

机译:鼻旁窦的常见纤维骨病变。

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Osteomas are the most common fibro-osseous lesions in the paranasal sinuses. They are infrequent, with an incidence of 0.43%, and are seen in upto 3% of sinus CT series. Histologically, they are made of dense lamellar bone without haversian canals, or otherwise mature bone. Thus, they appear radiographically as- well-circumscribed dense masses attached to the originating bone by either a broad- or narrow-based pedicle. The three theories of pathogenesis are developmental, traumatic, and infectious. They may arise from residual cartilaginous rests or as a reaction to an inciting event.Most frequently, osteomas are asymptomatic and are discovered incidentally. When they do cause symptoms, headache is most frequent, followed by sinusitis, pain, and facial or cranial deformation. Complications arise when an osteoma has grown large enough to impinge on surrounding structures. Obstructive sinusitis, mucocele formation, and intrusion on the intra-cranial and orbital spaces with resultant maladies have all been reported in association with paranasal sinus osteomas. Treatment is by surgical excision, frequently possible via endoscopic techniques, although some of the more lateral frontal sinus lesions are more easily removed via an osteoplastic or combined approach. It is often necessary to perform a Draf II or III, or an endoscopic modified Lothrop procedure, to gain adequate endoscopic exposure. A surgeon should expect and be prepared to manage periorbital and dural injuries, as they are occasionally unavoidable when removing these lesions via either endoscopic or external approaches.Fibrous dysplasia and ossifying fibroma are other fibro-osseous lesions found in the paranasal sinuses. Fibrous dysplasia affects children and characteristically "burns out" during puberty. It is deforming but not destructive and appears as a ground glass density on plain film radiograph or CT. In the polyostotic form, it is associated with McCune-Albright syndrome. A conservative treatment strategy is recommended, reserving surgical intervention for symptomatic lesions. Ossifying fibroma is more serious. Appearing asa well-circumscribed lesion with an eggshell-thin wall and a hypodense cen-ter, OF can be locally destructive and should be aggressively and completely excised.
机译:骨瘤是鼻旁窦中最常见的纤维骨病变。它们很少见,发生率为0.43%,在窦性CT系列中最多见3%。从组织学上讲,它们是由密集的片状骨制成,没有哈弗里斯运河或其他成熟的骨头。因此,它们在放射学上表现为由宽阔或狭窄的椎弓根附着在起源骨上的放射学上良好界定的致密肿块。发病机理的三种理论是发育性,创伤性和感染性。它们可能源于残留的软骨休息或作为对煽动性事件的反应。大多数情况下,骨瘤无症状且偶然发现。当它们确实引起症状时,头痛最常见,其次是鼻窦炎,疼痛以及面部或颅骨变形。当骨瘤长到足以撞击周围的结构时,就会出现并发症。据报道,阻塞性鼻窦炎,黏液囊肿形成,侵入颅内和眶间隙并伴有疾病,都与鼻旁窦骨瘤有关。尽管通常通过内窥镜技术可能通过外科切除术进行治疗,但是通过骨增生或联合方法更容易去除一些额外侧窦病变。通常需要执行Draf II或III或内窥镜改良的Lothrop手术,以获得足够的内窥镜曝光量。外科医生应期望并做好处理眶周和硬脑膜损伤的准备,因为通过内镜或外部方法清除这些病变有时是不可避免的。纤维异常增生和骨化性纤维瘤是在鼻旁窦中发现的其他纤维性骨病变。纤维异常增生会影响儿童,并在青春期出现典型的“倦怠”现象。它正在变形,但没有破坏性,在平片X射线照片或CT上显示为毛玻璃密度。在多骨形式中,它与McCune-Albright综合征相关。建议采取保守的治疗策略,保留对症状性病变的手术干预。骨化性纤维瘤更为严重。 OF表现为边界清楚的病灶,壁薄如蛋壳,中心呈低密度,可能是局部破坏性的,应积极彻底切除。

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