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黑人黏液囊肿的临床病理、眼科、视觉特征及处理

Clinicopathologic, ophthalmic, visual profiles and management of mucoceles in blacks.

作者信息

Ajaiyeoba Ayotunde, Kokong Daniel, Onakoya Adekunle

机构信息

Department of Ophthalmology, University College Hospital, Ibadan, Nigeria.

出版信息

J Natl Med Assoc. 2006 Jan;98(1):63-6.

Abstract

The study aimed at finding out the clinicopathologic, ophthalmic and visual profiles, management and outcome of mucoceles of the paranasal sinuses in Nigerians. The study was a retrospective review of 20 cases of mucoceles who presented to the ENT clinic and referred to the eye clinic of the University College Hospital Ibadan, Nigeria. These included nine males and 11 females with a male:female ratio of approximately 1:1. Mucoceles commonly involved more than one sinus on the same side. The sinuses commonly involved were the frontoethmoidal sinuses, frontal sinus and maxillary sinuses. The preoperative visual acuity in 16 (80%) patients was 6/4-6/9, three (15%) had between 6/9-6/18, and one (5%) patient was CF ("count fingers") in the affected eyes. The majority (90%) of our patients presented with multiple ophthalmic features; however, proptosis was the most popular and ophthalmic presentation and occurred in 15 (75%) patients. Proptosis was nonaxial in all cases with inferior, lateral or inferolateral displacement. Degree of proptosis ranged from 1-20 mm. Other presentations were squint (leading to diplopia) observed in one (5%) patient and epiphora in another [one (5%)] patient. Poor vision appeared to be the main problem in one (5%) patient, while in another [one (5%)] patient, the affected eye was completely immobilized. One (5%) patient presented with orbital cellulitis. Common radiological findings included classical expansive appearance with loss of the normal scalloping appearance with dehiscence of the wall of the affected sinus as was observed in nine (45%) of our patients. All 20 patients had excision of mucoceles (frontoethmoidectomies). At surgery, 11 (55%) patients had a combination of dehiscence of medial and/or posterior walls, and/or floor of the orbit. Materials evacuated were mucopurulent in 15 (75%) cases, moldy in three (15%) and cheesy in two (10%). Nine (45%) patients had intact walls. Three (15%) patients developed orbital cellulitis as postoperative complication. Postoperatively, proptosis regressed spontaneously within one week of surgery in 17 (85%) patients. By six weeks, all the patients had a complete regression of proptosis and visual acuity returned to preoperative visual acuity level except the patient with preoperative visual acuity of CF. This patient later deteriorated and became NPL (no perception of light) in the affected eye. This was a peculiar case in that operative findings in this patient were suggestive of another coexisting pathology, which was later confirmed to be a non-Hodgkin's lymphoma of the orbit. After two months, only three (15%) reported back for follow-up. The study concluded that proptosis is a common feature of mucoceles of the paranasal sinuses and that visual affectation was rather uncommon. Also whilst mucopurulent materials formed the content of most mucoceles, surgical intervention caused proptosis to regress dramatically. However, due to the high default rate in our study, no categorical statement can be made about recurrence rate of these swellings.

摘要

该研究旨在查明尼日利亚人鼻窦黏液囊肿的临床病理、眼科及视觉特征、治疗方法及治疗结果。该研究是对20例鼻窦黏液囊肿病例的回顾性分析,这些病例均来自尼日利亚伊巴丹大学学院医院耳鼻喉科门诊,并转诊至眼科门诊。其中包括9名男性和11名女性,男女比例约为1:1。黏液囊肿通常累及同一侧的多个鼻窦。常见受累鼻窦为额筛窦、额窦和上颌窦。16例(80%)患者术前视力为6/4 - 6/9,3例(15%)患者视力在6/9 - 6/18之间,1例(5%)患者患眼视力为CF(“数指”)。大多数(90%)患者呈现多种眼科特征;然而,眼球突出是最常见的眼科表现,15例(75%)患者出现眼球突出。所有病例的眼球突出均为非轴性,表现为向下、向外或外下移位。眼球突出程度为1 - 20毫米。其他表现包括1例(5%)患者出现斜视(导致复视),另1例(5%)患者出现溢泪。视力下降似乎是1例(5%)患者的主要问题,而在另1例(5%)患者中,患眼完全固定不动。1例(5%)患者出现眶蜂窝织炎。常见的影像学表现包括典型的膨胀外观,受累鼻窦壁失去正常的扇贝样外观且有骨质缺损,9例(45%)患者出现此表现。所有20例患者均接受了黏液囊肿切除术(额筛窦切除术)。手术中,11例(55%)患者存在眶内侧壁和/或后壁及/或眶底骨质缺损。引流物为黏液脓性的有15例(75%),霉菌样的有3例(15%),干酪样的有2例(10%)。9例(45%)患者的鼻窦壁完整。3例(15%)患者术后出现眶蜂窝织炎并发症。术后,17例(85%)患者的眼球突出在术后1周内自发消退。到6周时,除术前视力为CF的患者外,所有患者的眼球突出均完全消退,视力恢复到术前水平。该患者后来病情恶化,患眼变为无光感(NPL)。这是一个特殊病例,该患者的手术所见提示存在另一种并存的病理情况,后来证实为眼眶非霍奇金淋巴瘤。两个月后,只有3例(15%)患者回来复诊。该研究得出结论,眼球突出是鼻窦黏液囊肿的常见特征,而视力受累相对少见。此外,虽然大多数黏液囊肿的内容物为黏液脓性,但手术干预可使眼球突出显著消退。然而,由于本研究中的高失访率,无法对这些肿物的复发率作出明确说明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b749/2594804/7acc81072c24/jnma00296-0075-a.jpg

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