Eosinophilic granuloma: an unusual finding in adults

B. F. B. B. Abreu, M. Duarte, M. Grande, N. M. Lima Neto, Edimeire F. Ottoni
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Abstract

A 45-year-old man presents with occipital headache for about one month, resistant to analgesic therapy, and palpable nodule at the pain site. At initial evaluation, the nodule was 1.5 cm in diameter without apparent skin alteration. Ultrasonography revealed a well-defined osteolytic lesion and doubtful communication with the dura mater. The study was complemented with computed tomography and contrast-enhanced magnetic resonance, both identifying lytic lesion with soft tissue component and contrast enhancement, without diffusion restriction, guiding the diagnostic hypothesis of eosinophilic granuloma. Surgical treatment with mass excision and anatomopathological evaluation was made, which confirmed the radiological diagnostic hypothesis. After three months of follow-up, the patient remained symptom-free and radiographic control showed no signs of relapse.
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嗜酸性肉芽肿:成人罕见的发现
男性,45岁,枕部头痛约1个月,镇痛治疗无效,疼痛部位可触及结节。初步评估时,结节直径为1.5 cm,无明显的皮肤改变。超声检查显示明显的溶骨病变,与硬脑膜的连接可疑。本研究辅以计算机断层扫描和磁共振造影增强,均可识别有软组织成分的溶解性病变和增强的对比,无扩散限制,指导嗜酸性肉芽肿的诊断假设。手术切除肿块并进行解剖病理评估,证实了影像学诊断假设。随访3个月后,患者仍无症状,影像学检查显示无复发迹象。
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来源期刊
Jornal Brasileiro de Patologia e Medicina Laboratorial
Jornal Brasileiro de Patologia e Medicina Laboratorial Health Professions-Medical Laboratory Technology
CiteScore
1.30
自引率
0.00%
发文量
0
审稿时长
20 weeks
期刊介绍: The Jornal Brasileiro de Patologia e Medicina Laboratorial (Brazilian Journal of Pathology and Laboratory Medicine), a continuation of Jornal Brasileiro de Patologia (Brazilian Journal of Pathology), and published quarterly (March, June, September and December) is directed towards the publication of scientific articles that contribute to the development of the area of Laboratory Medicine (Clinical Pathology, Pathology, Cytopathology). It accepts the following categories of articles: original articles, review articles, case reports, short communications, updating articles, letters to editors and reviews.
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