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酷似成釉细胞瘤的原发性下颌骨结核性骨髓炎:一例报告及下颌骨结核性骨髓炎文献综述

Primary Mandibular Tuberculous Osteomyelitis Mimicking Ameloblastoma: A Case Report and Literature Review of Mandibular Tuberculous Osteomyelitis.

作者信息

Chalwade Chandrashekhar, Khosa Armaan, Ballary Kishor, Mago Raghav

机构信息

Department of Plastic Surgery, KEM Hospital, Parel, Mumbai, Maharashtra, India.

Plastic Surgery Clinic, Nayak Solitaire, Hosur, Hubli, Karnataka, India.

出版信息

Arch Plast Surg. 2024 Feb 29;51(2):187-195. doi: 10.1055/a-2217-8784. eCollection 2024 Mar.

Abstract

Primary tuberculous osteomyelitis involving the mandible represents less than 2% of skeletal locations. In this paper, we report a case of mandibular tuberculosis (TB) detected after histopathological analysis of the surgically resected specimen during surgical management of a suspected case of ameloblastoma. A 14-year-old male patient presented to us with history of right-sided chin swelling. The clinical examination revealed a swelling, involving right body and parasymphysis of mandible, measuring approximately 6 cm in length and 2 cm in width, extending from right lateral incisor till the first molar. Radiological scans revealed a large multiloculated osteolytic expansive lesion measuring 52 × 20 × 18 mm. Excision of the lesion was performed and reconstruction was done with iliac bone grafting. The histopathological findings revealed a granulomatous lesion, suggestive of tuberculous osteomyelitis. The patient was successfully treated with standard multidrug therapy. One year after completion of therapy, there were no signs of recurrence. Primary mandibular TB is an extremely rare entity. Its clinical presentation is not specific. Radiologically, TB has no characteristic appearance. The positive diagnosis is based on histology. Primary mandibular TB is rare and should be kept among differential diagnoses in susceptible population and in endemic areas.

摘要

累及下颌骨的原发性结核性骨髓炎在骨骼结核中所占比例不到2%。在本文中,我们报告了1例下颌骨结核病例,该病例是在对1例疑似成釉细胞瘤患者进行手术治疗时,对手术切除标本进行组织病理学分析后确诊的。一名14岁男性患者因右侧颏部肿胀前来就诊。临床检查发现下颌骨右侧体部及颏部有一肿物,长约6 cm,宽约2 cm,从右侧侧切牙延伸至第一磨牙。影像学检查显示一个巨大的多房性溶骨性膨胀性病变,大小为52×20×18 mm。对病变进行了切除,并采用髂骨移植进行重建。组织病理学检查结果显示为肉芽肿性病变,提示结核性骨髓炎。患者接受标准多药联合治疗后痊愈。治疗结束1年后,无复发迹象。原发性下颌骨结核是一种极为罕见的疾病。其临床表现不具特异性。在影像学上,结核也没有特征性表现。确诊依靠组织学检查。原发性下颌骨结核很罕见,在易感人群和流行地区应将其纳入鉴别诊断范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2a5/11001451/46bfa9c40d99/10-1055-a-2217-8784-i23mar0291cr-1.jpg

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