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首页> 外文期刊>Upsala journal of medical sciences. >Eosinophilic granuloma arising from the pelvis in children: A report of three cases.
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Eosinophilic granuloma arising from the pelvis in children: A report of three cases.

机译:儿童骨盆引起的嗜酸性肉芽肿:三例报告。

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Eosinophilic granuloma (EG) is a benign tumor-like condition which is characterized by a clonal proliferation of Langerhans-type histiocytes and defined as a local form of Langerhans cell histiocytosis (LCH). The radiographic appearances of EG are quite different depending on the phase of the disease and the site of involvement. A status of EG in the bone is divided into acute and chronic phases. Radiologically acute phase of EG is difficult to differentiate from a malignant bone tumor such as Ewing's sarcoma or acute osteomyelitis. Chronic phase of EG may mimic a chronic osteomyelitis or a benign bone tumor. We report 3 children's cases of EG in the pelvis which showed quite different radiological features and clinical courses. A 6-year-old boy (Case 1) had an osteolytic lesion with slightly defined margins in the right acetabulum. A 4-year-old boy (Case 2) had a radiologically similar-looking lesion in the left acetabulum. These lesions resembled radiologically chronic osteomyelitis (Brodie's abscess) or a benign bone tumor and healed spontaneously after biopsy. A 2-year-old boy (Case 3) had an osteolytic lesion with ill-defined margin in the ilium. It was difficult to differentiate from a malignant tumor such as Ewing's sarcoma, or acute osteomyelitis. The lesion became enlarged after needle biopsy. In spite of an additional curettage, the osteolytic lesion remained in the left pelvis in 1 year. Treatment for EG is controversial. Curettage of the affected site and bone grafting is usually accomplished. However, some EG heal spontaneously. It is of great importance to understand the natural course of EG and this knowledge will give us the opportunity to avoid unnecessary treatment. EG with poor osteolytic margins may progress further after biopsy. EG with well-defined margins may heal spontaneously after biopsy only.
机译:嗜酸性肉芽肿(EG)是一种良性肿瘤样疾病,其特征在于朗格汉斯型组织细胞的克隆增殖,并且被定义为朗格汉斯细胞组织细胞增生症(LCH)的局部形式。 EG的影像学表现根据疾病的阶段和受累部位而有很大不同。骨中的EG状态分为急性期和慢性期。 EG的放射学急性期很难与恶性骨肿瘤(如尤因氏肉瘤或急性骨髓炎)区分开。 EG的慢性期可模仿慢性骨髓炎或良性骨肿瘤。我们报告了3名儿童的骨盆EG病例,这些病例表现出完全不同的放射学特征和临床过程。一名6岁男孩(病例1)患有溶骨性病变,右髋臼边缘微微界定。一个4岁男孩(案例2)在左髋臼中有一个看起来与放射学相似的病变。这些病变类似于放射学上慢性的骨髓炎(布罗迪氏脓肿)或良性骨肿瘤,并在活检后自愈。一个2岁男孩(病例3)患有骨溶解性病变,with骨边缘未明确定义。很难与恶性肿瘤如尤因氏肉瘤或急性骨髓炎区分开。穿刺活检后病变扩大。尽管有额外的刮除术,但溶骨性病变仍保留在左骨盆中一年。 EG的治疗是有争议的。通常完成刮除患处并植骨。但是,某些EG会自愈。了解EG的自然过程非常重要,这一知识将为我们提供避免不必要治疗的机会。溶骨切缘差的EG活检后可能会进一步发展。边缘明确的EG仅在活检后才能自愈。

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