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儿童呈现长期发热和无菌性脑膜炎的菊池-藤本病:一例报告

Kikuchi-Fujimoto disease presenting with prolonged fever and aseptic meningitis in a child: a case report.

作者信息

Li Panying, Yang Jing, Mao Li, Huang Li, Ni Qian

机构信息

The Second Clinical Medical College, Lanzhou University, Lanzhou, China.

Pediatric Nephrology Department, The Second Hospital of Lanzhou University, Lanzhou, China.

出版信息

Front Pediatr. 2025 May 8;13:1572816. doi: 10.3389/fped.2025.1572816. eCollection 2025.

Abstract

Kikuchi-Fujimoto Disease (KFD) is a rare, self-limiting lymphadenitis that predominantly affects young women of Asian descent and is less frequently encountered in children. The disease is characterized by focal and indurated cervical lymphadenopathy with fever and other infrequent systemic manifestations, including neurologic symptoms that are rare. This report details the diagnosis and treatment of a 14-year-old male with an atypical case of KFD. He exhibited a fever that persisted for over 1 month together with dizziness, nausea, arthralgia, night sweats, weight loss, and splenomegaly. On day 16 following fever onset, he presented with symptoms of aseptic meningitis, with symptoms of cervical lymph node swelling and pain only manifesting on day 25 after fever onset. Positron emission tomography (18F-FDG PET/CT) revealed the enlargement of lymph nodes in several regions of the body. After considering a diagnosis of lymphoma, KFD was ultimately diagnosed via cervical lymph node biopsy. His condition improved following oral prednisone administration. This case report highlights the complex disease course of KFD and the difficulties associated with diagnosing it at an early stage. KFD is rarely considered in the differential diagnosis for children with prolonged unexplained fever, especially with delayed lymphadenopathy, leading to potential misdiagnosis and unnecessary investigations.

摘要

菊池-藤本病(KFD)是一种罕见的自限性淋巴结炎,主要影响亚洲血统的年轻女性,儿童中较少见。该病的特征是局灶性和硬结性颈部淋巴结病,伴有发热和其他不常见的全身表现,包括罕见的神经系统症状。本报告详细介绍了一名14岁男性非典型KFD病例的诊断和治疗。他持续发热超过1个月,伴有头晕、恶心、关节痛、盗汗、体重减轻和脾肿大。发热开始后第16天,他出现无菌性脑膜炎症状,颈部淋巴结肿大和疼痛症状直到发热开始后第25天才出现。正电子发射断层扫描(18F-FDG PET/CT)显示身体多个部位的淋巴结肿大。在考虑淋巴瘤诊断后,最终通过颈部淋巴结活检确诊为KFD。口服泼尼松后他的病情有所改善。本病例报告强调了KFD复杂的病程以及早期诊断的困难。对于长期不明原因发热的儿童,尤其是伴有延迟性淋巴结病的儿童,在鉴别诊断中很少考虑KFD,这可能导致误诊和不必要的检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b63/12094979/ee80e48ccf04/fped-13-1572816-g001.jpg

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