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罕见病变、不寻常部位、非典型表现:一例嗜酸性粒细胞增多性血管淋巴样增生症

Rare lesion, unusual location, uncommon presentation: a case of angiolymphoid hyperplasia with eosinophilia.

作者信息

Ciaramicolo N, Custódio M, de Sousa S C O M, Naclério-Homem M G

机构信息

Oral and Maxillofacial Surgery.

Department of Oral and Maxillofacial Pathology, School of Dentistry, University of São Paulo, São Paulo, Brazil.

出版信息

Br J Oral Maxillofac Surg. 2019 Jun;57(5):479-480. doi: 10.1016/j.bjoms.2019.01.023. Epub 2019 May 1.

Abstract

Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare vascular proliferation of unknown pathogenesis that may be related to trauma. Although it affects mainly the head and neck, the zygomatic area is rarely involved. We report a case that affected the zygomatic region of a 46-year-old black man. The lesion had been present for about a year and the patient reported that it appeared after a facial injury during a soccer match. Clinical and tomographic investigations suggested a benign tumour, and the lesion was excised through an intraoral approach. Histopathological examination showed the unexpected diagnosis of ALHE. This tumour was interesting because of its rarity, and also because of its unusual site within the head and neck region. The diagnosis of ALHE is hardly ever considered in the differential diagnosis of zygomatic nodules.

摘要

伴有嗜酸性粒细胞增多的血管淋巴样增生症(ALHE)是一种发病机制不明的罕见血管增生性疾病,可能与创伤有关。虽然它主要累及头颈部,但很少累及颧骨区域。我们报告一例发生在一名46岁黑人男性颧骨区域的病例。该病变已存在约一年,患者报告称其在一场足球比赛中面部受伤后出现。临床和断层扫描检查提示为良性肿瘤,通过口内入路切除了病变。组织病理学检查显示意外诊断为ALHE。这种肿瘤因其罕见性以及在头颈部区域内不寻常的部位而令人关注。在颧骨结节的鉴别诊断中,几乎从未考虑过ALHE的诊断。

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