木村病:一种罕见且难以诊断的疾病。

Head and neck pathology Pub Date : 2022-03-01 Epub Date: 2021-07-19 DOI:10.1007/s12105-021-01359-9
Clayton Bishop, Alyeesha Wilhelm, Duncan Watley, Felix Olobatuyi, Orly Coblens, Rohan Joshi
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引用次数: 2

摘要

木村病是一种罕见的累及头颈部的炎症性疾病。由于其罕见和各种发现,明确的诊断可能难以确定。通过组织病理学特征,包括滤泡增生、反应性生发中心、大量嗜酸性粒细胞增多、嗜酸性微脓肿、保留的淋巴结结构、war薄- finkeldy多核细胞和包膜纤维化,将木村病与其他疾病(包括血管淋巴样增生)区分出来。在这里,我们描述的临床表现,病理和诊断的一个39岁的病例在得克萨斯州的一个学术中心治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Kimura Disease: A Rare and Difficult to Diagnose Entity.

Kimura Disease: A Rare and Difficult to Diagnose Entity.

Kimura Disease: A Rare and Difficult to Diagnose Entity.

Kimura disease (KD) is a rare inflammatory disorder which involves the head and neck. Due to its rarity and various findings, definitive diagnosis can be difficult to ascertain. Kimura disease is distinguished from other conditions, including angiolymphoid hyperplasia, by histopathological features including follicular hyperplasia, reactive germinal centers, abundant eosinophilia, eosinophilic microabscesses, preserved nodal architecture, Warthin-Finkeldy polykaryocytes, and capsular fibrosis. Herein, we describe the clinical presentation, pathology, and diagnosis of a single case of a 39-year-old treated at an academic center in Texas.

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