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成釉细胞瘤手术切除后偶然发现的下颌骨结核:一例报告

Mandibular tuberculosis fortuitously discovered after surgical resection of an ameloblastoma: A case report.

作者信息

Elzouiti Zainab, Elayoubi Fahd, Tsen Adil Eabdenbi

机构信息

Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Oujda, Morocco.

Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Oujda, Morocco.

出版信息

Int J Surg Case Rep. 2021 Oct;87:106399. doi: 10.1016/j.ijscr.2021.106399. Epub 2021 Sep 16.

Abstract

INTRODUCTION

Mandibular localization of tuberculosis is rare and represents less than 2% of skeletal locations. Its clinical and radiological features are not specific. In this paper, we report a case of fortuitous discovery of mandibular tuberculosis after a histopathological analysis of the surgical resected specimen during surgical management of an ameloblastoma.

PRESENTATION OF CASE

A 50-year-old female patient was admitted to our department with a 2 years history of left cheek swelling, the clinical examination revealed a left cheek swelling, extending from the mandibular angle to below of temporomandibular joint, measuring approximately 5 cm in diameter. The swelling was firm to hard in consistency, and cervical lymphadenopathy of submandibular region was noticed. Computed tomography (CT) scan revealed a large multiloculated osteolytic expansive lesion measuring 56 ∗ 48 ∗ 53 mm. An interrupting hemimandibulectomy, was performed from the left parasymphys opposite to 33 tooth, extending to the left temporomandibular joint. The histopathological findings confirmed the diagnosis of ameloblastoma, with negative free margin. A mandibular and lymph node tuberculosis were associated with giant cells and caseating necrosis. The patient was successfully treated with a standard anti-tuberculosis therapy.

DISCUSSION

Ameloblastoma is a benign odontogenic tumor, 80% of these tumors are found in the mandible. Primary mandibular tuberculosis is an extremely rare entity. Its clinical presentation is not specific. Radiologically, tuberculosis has no characteristic appearance. However, it is possible to evoke it in case of a lytic image of the mandible. The positive diagnosis is based on histology. The treatment is medical, but surgery is necessary for some cases.

CONCLUSION

The association between ameloblastoma and mandibular tuberculosis represents an extremely rare entity. Mandibular tuberculosis is rare and should be considered as a possible diagnosis in pandemic areas.

摘要

引言

下颌骨结核的定位罕见,占骨骼部位结核的比例不到2%。其临床和放射学特征不具有特异性。在本文中,我们报告了1例在成釉细胞瘤手术治疗过程中,对手术切除标本进行组织病理学分析后偶然发现下颌骨结核的病例。

病例介绍

一名50岁女性患者因左侧脸颊肿胀2年入住我科。临床检查发现左侧脸颊肿胀,从下颌角延伸至颞下颌关节下方,直径约5厘米。肿胀质地硬,下颌下区有颈部淋巴结肿大。计算机断层扫描(CT)显示一个大的多房性溶骨性膨胀性病变,大小为56×48×53毫米。从与33号牙相对的左下颌骨旁正中至左颞下颌关节进行了间断性半侧下颌骨切除术。组织病理学检查结果证实为成釉细胞瘤,切缘阴性。下颌骨和淋巴结结核伴有巨细胞和干酪样坏死。患者接受标准抗结核治疗后成功治愈。

讨论

成釉细胞瘤是一种良性牙源性肿瘤,其中80%发生在下颌骨。原发性下颌骨结核是一种极其罕见的疾病。其临床表现不具有特异性。在放射学上,结核没有特征性表现。然而,在下颌骨出现溶骨性影像时有可能怀疑该病。阳性诊断基于组织学检查。治疗以药物为主,但在某些情况下手术是必要的。

结论

成釉细胞瘤与下颌骨结核的关联是一种极其罕见的情况。下颌骨结核罕见,在流行地区应考虑将其作为一种可能的诊断。

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