Sherwani Rana K, Akhtar Kafil, Qadri Shagufta, Ray Prasenjit Sen
Department of Pathology, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, UttarPradesh, India.
BMJ Case Rep. 2014 Apr 3;2014:bcr2013200274. doi: 10.1136/bcr-2013-200274.
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.
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。