伪装成t细胞淋巴瘤的菊池病

IF 0.1 Q4 PATHOLOGY AJSP: reviews & reports Pub Date : 2022-01-01 DOI:10.1097/PCR.0000000000000496
Barina Aqil, Amandeep Kaur
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引用次数: 0

摘要

Kikuchi-Fujimoto病,也被称为组织细胞坏死性淋巴结炎,在亚洲最为普遍,并在世界其他地区得到越来越多的认识。通常多发于女性,表现为发热和局部颈淋巴肿大。它通常会在几周到6个月的时间内自行消退。其最初的临床特征通常与淋巴瘤相似,临床医生和病理学家都可能误诊。菊池病与系统性红斑狼疮有关。我们报告一例菊池病,发生在一个25岁的女性患者,伪装成一个t细胞淋巴瘤。
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Kikuchi Disease Masquerading as a T-Cell Lymphoma
Abstract Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis, is most prevalent in Asia and has been increasingly recognized in other parts of the world. It usually occurs more frequently in females and presents as fever and localized cervical lymphadenopathy. It resolves spontaneously, usually over a period of several weeks up to 6 months. Its initial clinical features are commonly similar to that of a lymphoma, and it can be misdiagnosed both by clinicians and pathologists. Kikuchi disease has been associated with systemic lupus erythematosus. We report a case of Kikuchi disease that occurred in a 25-year-old female patient that masqueraded as a T-cell lymphoma.
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