何杰金氏病临床表现不典型,伴共济失调-毛细血管扩张

M. Spasova, I. Ivanov, J. Grudeva-Popova, A. Stoyanova, H. Dimitrov, I. N. Moumdjiev
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引用次数: 0

摘要

作者报告了一位患有霍奇金病的4岁男性患者,他的临床表现、实验室数据和影像学检查都不典型,而且放射敏感性增加。这些是引起怀疑共济失调-毛细血管扩张的最初症状。淋巴瘤表现为右上后纵隔的实性肿瘤肿块,无外周淋巴结病变。甲胎蛋白明显增高,怀疑为生殖细胞瘤或神经母细胞瘤。部分切除肿瘤后,组织学显示何杰金氏病混合细胞。男孩接受DAL HD-95方案化疗,无异常毒性。上纵隔和中纵隔低剂量放疗后出现早期放射性食管炎,一年后出现大量心包积液。放射部位出现共济失调、球和皮肤毛细血管扩张。他反复肺部感染,在诊断为恶性淋巴瘤五年后死于严重肺炎并呼吸衰竭和肺动脉高压,没有霍奇金病复发的证据。
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Hodgkin's Disease with Atypical Clinical Presentation, Associated with Ataxia-Telangiectasia
The authors report a 4-year-old male with Hodgkin's disease with atypical clinical presentation, laboratory data and imaging studies as well as an increased radiosensitivity. These were the first symptoms which raised the suspicion of ataxia-telangiectasia. The lymphoma presented as a solid tumor mass in the right upper posterior mediastinum without peripheral lymphadenopathy. The alpha-fetoprotein was significantly increased and the diagnosis of a germ-cell tumor or neuroblastoma was suspected. After partial resection of the tumor the histology indicated Hodgkin's disease-mixed cellularity. The boy received chemotherapy according to DAL HD-95 protocol without any unusual toxicity. Low-dose radiation therapy of the upper and middle mediastinum was followed by early radiation-induced esophagitis and appearance of a large pericardial effusion one year later. Ataxia and bulbar and skin telangiectasias at the radiation site appeared in the next years. He suffered recurrent pulmonary infections and succumbed to severe pneumonia with respiratory failure and pulmonary hypertension five years after the diagnosis of malignant lymphoma without evidence of recurrence of Hodgkin's disease.
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