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Eosinophilia as a first sign of Hodgkin′s lymphoma: A case report

机译:嗜酸性粒细胞增多是霍奇金淋巴瘤的首发征象:一例病例报告

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Introduction. It is well known that eosinophilia appears in a malignant disease. Frequency of all Hodgkin`s lymphoma patients is estimated to about 15%. Prognostic importance of this phenomenon is not completely investigated. Therefore we decided to present a female patient with eosinophilia, six months before lymphoma appearance. Case report. We presented a 51- years old female, from Serbia, who had eosinophilia (1,530–2,040 eosinophils per μL of blood), six months before Hodgkin's lymphoma appearance. Eosinophilic granuloma was confirmed by tumor’s biopsy and histopathologic examination, from the right femoral region. As eosinophilia was increasing, lymph nodes became enlarged (120 × 65 mm diameter), in the right parailiac region. All infectious and allergic examinations did not reveal eosinophilia's cause. Histopathologic revision was made with added immunohistochemical stains 17 months after tumor's biopsy. The diagnosis was changed from eosinophilic granuloma to mixed cellularity Hodgkin's lymphoma. After conducted Ann Arbor staging classification, II B clinical stage was established. The treatment was done by chemotherapy according to adriamycin, bleomycin, vinblastine, dacarbarine (ABVD) protocol, with 6 courses. Complete remission of the disease was achieved after 4 courses. Eosinophils number dropped to 640 per μl blood. Conclusion. Eosinophilia without revealed cause can precede Hodgkin's lymphoma. We suggest careful search for enlarged lymph nodes, anywhere in the patients’ body who suffer from eosinophilia. Timely and accurate histopathologic diagnostic is a right way to resolve such conditions.
机译:介绍。众所周知,嗜酸性粒细胞增多症是一种恶性疾病。估计所有霍奇金淋巴瘤患者的发生率约为15%。这种现象的预后重要性尚未完全调查。因此,我们决定在淋巴瘤出现前六个月为一名女性嗜酸性粒细胞增多症患者提供治疗。案例报告。我们介绍了一位来自塞尔维亚的51岁女性,她在霍奇金淋巴瘤出现前六个月患有嗜酸性粒细胞增多症(每微升血液中有1,530–2,040嗜酸性粒细胞)。肿瘤的活检和组织病理学检查证实了嗜酸性肉芽肿来自右股骨区域。随着嗜酸性粒细胞增多,右侧副神经旁的淋巴结变大(直径120×65 mm)。所有感染性和过敏性检查均未显示嗜酸性粒细胞增多的原因。肿瘤活检后17个月,通过添加免疫组织化学染色剂进行组织病理学修订。诊断从嗜酸性肉芽肿改为混合细胞性霍奇金淋巴瘤。在进行Ann Arbor分期分类后,建立了II B临床阶段。根据阿霉素,博来霉素,长春碱,达卡巴林(ABVD)方案通过化学疗法进行治疗,共分6个疗程。 4个疗程后,该病完全缓解。嗜酸性粒细胞数量降至每微升血液640。结论。没有明确原因的嗜酸性粒细胞增多可先于霍奇金淋巴瘤。我们建议您仔细检查患有嗜酸性粒细胞增多症的患者体内任何地方的淋巴结是否肿大。及时而准确的组织病理学诊断是解决此类疾病的正确方法。

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