Empty Nose Syndrome with Unilateral Ethmoidal Mucopyocoele – An Extremely Rare Presentation

Sama Rizvi, Rishita Kalra, V. K. Pathak, P. Nayak
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Abstract

Empty nose syndrome (ENS) is a poorly understood and rare iatrogenic disorder resulting from the destruction of normal nasal tissue. ENS is a recognized complication after turbinate excision. These patients suffer from endonasal crusting and dryness and a paradoxical sensation of nasal obstruction. These complications of ENS predispose these patients to recurrent sino-nasal infections. Here we have reported the case of a 20-year-old female with right-sided nasal obstruction and headache. On diagnostic nasal endoscopy (DNE), the right nasal cavity was devoid of all anatomical landmarks. A hidden ethmoidal mucopyocoele was identified on radiological evaluation . This was drained surgically. Patient’s symptoms improved drastically postoperatively. Despite the fact that occurrence of rhino-sinusitis is common in patients of ENS, a mucocoele or mucopyocoele has never been reported previously. To the best of our knowledge, this is the first ever reported case of ENS with ethmoidal mucopyocoele in a young, immuno-competent patient.
伴有单侧筛窦黏液囊肿的空鼻综合征-一种极为罕见的表现
空鼻综合征(ENS)是一种罕见的医源性疾病,由于正常鼻腔组织的破坏而引起。ENS是鼻甲切除后公认的并发症。这些患者患有鼻内结痂和干燥以及鼻阻塞的矛盾感觉。ENS的这些并发症使这些患者易发生复发性鼻黏膜感染。我们在此报告一位20岁女性右侧鼻塞及头痛的病例。在诊断性鼻内窥镜检查(DNE)中,右鼻腔没有任何解剖标志。影像学检查发现一隐蔽性筛窦粘液囊肿。这是通过手术排出的。患者术后症状明显好转。尽管鼻鼻窦炎在ENS患者中很常见,但以前从未报道过粘液囊肿或粘液囊肿。据我们所知,这是首次报道的ENS合并筛窦黏液囊肿的年轻、免疫能力强的患者。
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