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淋巴结病的罕见病例:菊池-藤本病

A Rare Case of Lymphadenopathy: Kikuchi-Fujimoto Disease.

作者信息

Rezkalla Josh, Lynch Douglas W

机构信息

Univerisity of South Dakota Sanford School of Medicine.

Sanford Health Pathology Clinic, Sioux Falls, South Dakota.

出版信息

S D Med. 2017 Jul;70(7):311-313.

Abstract

A relatively unknown cause of cervical lymphadenopathy is Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis. This is a rare and benign condition that presents with painful cervical lymphadenopathy, fevers, night sweats, and weight loss. This disease is most prevalent in Asian women between the age of 20-35 years. The diagnosis of Kikuchi Disease is made histologically and is characterized by paracortical areas of necrosis and a notable complete absence of neutrophils. The painful lymphadenopathy can be simply treated with antipyretics, but due to its presenting symptoms of Kikuchi disease, it is often mistaken for malignant lymphoma. As such, accurate diagnosis is required to avoid unnecessary testing. The evaluation of lymphadenopathy without an obvious cause can be quite challenging. When patients present with relapsing remitting lymphadenopathy, Kikuchi disease may warrant consideration.

摘要

颈部淋巴结病的一个相对不为人知的病因是菊池-藤本病,也称为组织细胞坏死性淋巴结炎。这是一种罕见的良性疾病,表现为颈部淋巴结疼痛、发热、盗汗和体重减轻。这种疾病在20至35岁的亚洲女性中最为普遍。菊池病的诊断通过组织学进行,其特征是副皮质区坏死且明显完全没有中性粒细胞。疼痛性淋巴结病可用退烧药简单治疗,但由于菊池病的症状表现,它常被误诊为恶性淋巴瘤。因此,需要准确诊断以避免不必要的检查。对无明显病因的淋巴结病进行评估可能颇具挑战性。当患者出现复发缓解性淋巴结病时,可能需要考虑菊池病。

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