嗜酸性肉芽肿伴异时性放线菌病1例并文献复习

Soundararajan K, S. Prabhu, Pallavi Sabarad, R. Abdulla
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引用次数: 0

摘要

嗜酸性肉芽肿(EG)是一种病因不明的组织细胞增多症。病变表现为单个或多个骨破坏区域,伴轻度至重度疼痛,或在某些情况下无症状。本文报告一例EG伴放线菌病,患者为11岁男性,左颊前庭22 ~ 24岁。组织病理学表现为结缔组织中密集的细胞浸润,由丰富的嗜酸性粒细胞和非典型细胞混合组成。4个月后,同一患者报告在腭区复发。组织病理学切片显示放线菌菌落,伴EG特征。异时性放线菌病合并EG在文献中非常罕见。本文报告了一例新的EG伴放线菌病,并回顾了以往报道的放线菌病伴其他病变的病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Eosinophilic granuloma with metachronous actinomycosis – A case report with literature review
Eosinophilic granuloma (EG) is a type of histiocytosis X with uncertain etiology. The lesion manifests as single or multiple areas of bone destruction with mild-to-severe pain or may be asymptomatic in some cases. In this article, a case of EG with actinomycosis is reported which occurred in an 11-year-old male in the left buccal vestibule extending from 22 to 24. Histopathologically, it showed dense, cellular infiltrate in the connective tissue composed of abundant eosinophils intermixed with atypical cells. After 4 months, the same patient reported with a recurrence in the palatal region. Histopathologically, the section showed some colonies of actinomycosis along with the features of EG. EG with metachronous actinomycosis is very rare in the literature. This article reports a new case of EG with actinomycosis and reviews previously reported cases of actinomycosis associated with other lesions.
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