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Recurrent Pott's puffy tumor, a rare clinical entity

机译:复发性Pott肿块肿瘤,罕见的临床实体

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Sir, Pott's puffy tumor, a feature of osteomyelitis of the frontal bone, is a rare entity in post-antibiotic era. It has been reported in older children and very rarely in adults. A 29-year-old man met with a road traffic accident,causing open wound over forehead, 5 years back. He was operated by bicoronal flap approach, with obliteration of frontal sinus with fat. Five years after surgery, he had boggy forehead swelling, with intense pain. Local examination showed erythema and tense edema of the right upper lid, as well as forehead swelling measuring 8x6 cm [Figure 1]. There was thinning of skin, suggestive of pus under pressure with impending rupture of abscess. On palpation, warm, tender, fluctuating and doughy pitting edema in the region of frontal sinus was found, with breach in continuity in anterior wall of frontal sinus. Rest of the general examination revealed no abnormality. Twenty-five milliliters of thick, yellow-colored pus was aspirated. Pus culture grew Staphylococcus aureus, sensitive to levofloxacin. He was relieved on medical therapy and refused surgical intervention. After symptom-free period of 2 months, there was recurrence of swelling of forehead. Contrast computerized tomography (CE-CT) [Figures 2] showed soft tissue swelling and edema around the superior aspect of the right orbit with slight proptosis. There was breach in the continuity in anterior wall of frontal sinus with foamy foreign body-like material (later identified as fat). Posterior bony wall of frontal sinus was intact and thickened, suggesting chronic osteomyelitis. Frontal recess was clear; no discharge was seen on nasal endoscopy. Evacuation of pus, debridement of necrotic tissue, granulation and resection of osteomyelitic bone was done by osteoplastic flap technique. Using a 4-mm, 30-degree endoscope, frontal recess and frontal ostia were widened; sialastic drain was put for drainage of sinus through the nose. Reconstruction/ obliteration was deferred due to underlying oste...
机译:主席先生,波特骨肿的肿瘤是额骨骨髓炎的特征,在后抗生素时代是罕见的。据报道,在大一点的儿童中,很少有成年人。一名29岁的男子在5年前遇到一次道路交通事故,其额头上有开放性伤口。他经双冠状动脉瓣入路手术,伴有脂肪消除了额窦。手术五年后,他的前额肿胀,剧烈疼痛。局部检查显示右上眼睑红斑和紧张性水肿,以及额头肿胀为8x6 cm [图1]。皮肤变薄,提示在压力下脓液,脓肿即将破裂。触诊时发现额窦区域有温暖,柔软,起伏和发霉的点蚀性水肿,额窦前壁连续性破裂。其余的一般检查未发现异常。抽出二十五毫升厚的黄色脓液。脓液培养出金黄色葡萄球菌,对左氧氟沙星敏感。他因药物治疗而放心,并拒绝手术干预。 2个月的无症状期后,额头肿胀复发。对比计算机断层扫描(CE-CT)[图2]显示右眼眶上方软组织肿胀和水肿,并伴有轻微眼球突出。额窦前壁的连续性被泡沫状异物样物质破坏(后来鉴定为脂肪)。额窦后骨壁完整并增厚,提示慢性骨髓炎。额叶凹陷清晰;鼻内窥镜检查未见分泌物。排脓,坏死组织清创,肉芽形成和髓母骨切除是通过骨塑瓣技术完成的。使用4毫米,30度内窥镜加宽额凹和额孔。唾液排泄用于鼻窦鼻窦的引流。由于潜在的渗透,重建/闭塞被推迟。

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