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当罕见病遇上现实:三级医疗中心的一例菊池-藤本病病例

When Rare Meets Reality: A Case of Kikuchi-Fujimoto Disease in Tertiary Care Center.

作者信息

Sharma Indrika, Shinde Raju K, Rewale Venkatesh M, Nagtode Tushar, Keerti Akshunna

机构信息

General Surgery, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

Internal Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.

出版信息

Cureus. 2024 Aug 13;16(8):e66747. doi: 10.7759/cureus.66747. eCollection 2024 Aug.

Abstract

Kikuchi-Fujimoto disease is a very rare disease, basically involving young adults and ubiquitously distributed. It is characterized by fever and benign lymph node swelling. The distinguishing features of this disease are cervical lymphadenopathy, constitutional symptoms resembling tuberculosis, and its penchant to affect young people of Oriental or Asian descent, especially women. We describe an instance of a 42-year-old female who arrived with multiple neck swellings. On physical examination, there was palpable right-sided cervical lymphadenopathy, while laboratory investigations were essentially within normal limits except for raised erythrocyte sedimentation rate and anemia. After cefepime and nonsteroidal anti-inflammatory medications were administered, symptoms subsided, and lymphadenopathy receded in the patient. This case supports the importance of histological evaluation to reach an exact diagnosis and guide treatment and the need to consider Kikuchi-Fujimoto disease in the differential diagnosis of lymphadenopathy.

摘要

菊池-藤本病是一种非常罕见的疾病,主要累及年轻人,分布广泛。其特征为发热和良性淋巴结肿大。本病的显著特点是颈部淋巴结病、类似结核病的全身症状,以及倾向于影响东方或亚洲血统的年轻人,尤其是女性。我们描述了一例42岁女性,她因多处颈部肿胀前来就诊。体格检查发现右侧颈部可触及淋巴结肿大,而实验室检查除红细胞沉降率升高和贫血外基本正常。给予头孢吡肟和非甾体类抗炎药后,症状缓解,患者的淋巴结肿大消退。该病例支持组织学评估对于准确诊断和指导治疗的重要性,以及在淋巴结病的鉴别诊断中考虑菊池-藤本病的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2976/11392504/16c5c9cc9c26/cureus-0016-00000066747-i01.jpg

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