以眼眶周围蜂窝织炎为表现的鼻-脑毛霉病伴失明2例报告。

Clinical and experimental neurology Pub Date : 1994-01-01
T J O'Brien, P McKelvie
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引用次数: 0

摘要

本文报告两例老年非酮症糖尿病患者鼻-脑毛霉病,最初诊断为细菌性眶周蜂窝织炎并接受治疗。两例患者均表现为短暂的眶周疼痛和肿胀,随后迅速出现完全眼麻痹和失明。在正确诊断时,两例患者均已进展到下颅神经受累,CT表现为眼动脉和海绵窦血栓形成,其中1例患者有颈内动脉侵犯(MR血管造影显示)并导致脑梗死。一名患者静脉注射两性霉素B治疗,但在几天内死亡。第二例患者进行了积极的手术切除,存活了下来,但有明显的残余发病率。这些病例表明,任何出现眶蜂窝织炎的糖尿病患者都应排除毛霉病,特别是当有早期视力丧失时。手术和抗真菌药物的早期积极治疗通常是成功的,但如果诊断延迟,结果几乎是致命的。
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Rhinocerebral mucormycosis presenting as periorbital cellulitis with blindness: report of 2 cases.

Two cases of rhinocerebral mucormycosis in elderly, non-ketotic diabetics who were initially diagnosed and treated for bacterial periorbital cellulitis are reported. Both presented with a short history of periorbital pain and swelling followed rapidly by complete ophthalmoplegia and blindness. By the time of correct diagnosis, both cases were advanced with lower cranial nerve involvement, CT evidence of ophthalmic artery and cavernous sinus thrombosis and, in one, internal carotid artery invasion (demonstrated on MR angiography) with resultant cerebral infarction. One patient was treated with intravenous amphotericin B but died within a few days. The second patient had aggressive surgical resection and survived with significant residual morbidity. These cases illustrate that mucormycosis should be excluded in any diabetic patient presenting with orbital cellulitis, especially when there is early visual loss. Early aggressive treatment with surgery and antifungal agents is often successful whereas the outcome is almost universally fatal when the diagnosis is delayed.

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