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下颌骨嗜酸性肉芽肿:诊断难题

Eosinophilic granuloma of the mandible: a diagnostic dilemma.

作者信息

Sherwani Rana K, Akhtar Kafil, Qadri Shagufta, Ray Prasenjit Sen

机构信息

Department of Pathology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, UttarPradesh, India.

出版信息

BMJ Case Rep. 2014 Apr 3;2014:bcr2013200274. doi: 10.1136/bcr-2013-200274.

Abstract

Eosinophilic granuloma (EG) is a rare histiocytic disorder resulting from clonal proliferation of Langerhans cells. It accounts for less than 1% of all osseous neoplasms and has a predilection for involving the axial skeleton. Although suspicion of the disease may arise from clinical features and radiographic demonstration of destructive bone lesions, it is still difficult to make a correct diagnosis without proper pathological evaluation. This is more evident when common differentials mimicking EG, both clinically and radiologically, need to be ruled out. This report describes a case of unifocal EG of the mandible occurring in a 4-year-old boy whose initial presentation led to confusion between osteomyelitis, primary bone tumour and lymphoma. A final diagnosis of EG was established after histopathological examination of the biopsy specimen.

摘要

嗜酸性肉芽肿(EG)是一种由朗格汉斯细胞克隆性增殖引起的罕见组织细胞疾病。它占所有骨肿瘤的比例不到1%,且好发于中轴骨骼。尽管根据临床特征和骨质破坏病变的影像学表现可能会怀疑该病,但若无恰当的病理评估,仍难以做出正确诊断。当需要排除临床和影像学上酷似EG的常见鉴别诊断时,这一点更为明显。本报告描述了一例发生在一名4岁男孩下颌骨的单灶性EG病例,其最初表现导致在骨髓炎、原发性骨肿瘤和淋巴瘤之间产生混淆。对活检标本进行组织病理学检查后确诊为EG。

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