Results 91 to 100 of about 3,532 (210)
Immunity, Inflammation and Disease, Volume 13, Issue 1, January 2025.The diagnosis of Kikuchi‐Fujimoto disease remains challenging and often requires invasive biopsy. Serum alkaline phosphatase levels were < 50% of the age‐ and sex‐specific median values in patients with Kikuchi‐Fujimoto's disease. Decreased serum alkaline phosphatase levels, mainly when assessed as a percentage of age‐ and sex‐specific reference ...
Shintaro Fujiwara +2 more
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Clinical features of low serum alkaline phosphatase levels in children: A retrospective study
Pediatrics International, Volume 67, Issue 1, January/December 2025.Abstract Background Serum alkaline phosphatase (ALP), a biomarker of bone and liver metabolism, is often elevated in children; however, the lower reference limit is rarely considered. Hypophosphatasia (HPP) is characterized by low ALP levels and impaired mineralization of bone and teeth.
Mami Kurihara +4 more
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Brainstem Encephalitis as an Atypical Neurologic Complication Following Kikuchi–Fujimoto Disease
Case Reports in Neurological Medicine, Volume 2025, Issue 1, 2025.We report an uncommon and peculiar case of a patient who developed brainstem encephalitis between three and four months after recovering from an episode of Kikuchi–Fujimoto disease (KFD). She presented acutely with oscillopsia and persistent irrepressible hiccups, for which brainstem stroke was initially suspected.
Youjiang Tan +2 more
wiley +1 more source
KIKUCHI-FUJIMOTO DISEASE: CASE REPORT
Eurasian Journal of Medicine, 2019 Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis, is a unique form of self-limiting lymphadenitis and typically affects the head and neck regions. It usually occurs in young adults and has a female predilection.
Fazlı Erdoğan +2 more
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A Young Woman with Fever and Cervical Lymphadenopathy
European Journal of Case Reports in Internal Medicine, 2015 Kikuchi-Fujimoto's disease is a self-limiting and rare disorder of unknown aetiology. The typical presentation includes fever, cervical lymphadenopathy and night sweats.
Aída Gil-Díaz +4 more
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Clinical Analysis of 44 Children with Subacute Necrotizing Lymphadenitis
Infection and Drug Resistance, 2022 Yue Zheng, Yue Du, Wan-Hong Zhu, Cheng-Guang Zhao Department of Pediatrics, Shengjing Hospital of China Medical University, Shenyang, 111004, People’s Republic of ChinaCorrespondence: Cheng-Guang Zhao, Department of Pediatrics, Shengjing Hospital of ...
Zheng Y, Du Y, Zhu WH, Zhao CG
doaj
Subacute Necrotizing Lymphadenitis : Immunohistochemicla Study of 118 cases [PDF]
, 1989 의학과/석사[영문] [한글] 아급성 괴사성 림프절염은 주로 젊은 여자의 경부림프절을 침범하는 림프절염으로서 19 72년 Fujimoto등과 Kikuchi에 의하여 처음 보고된 이래, 많은 학자들이 그 임상적 및 조 직학적 특징에 관하여 보고 하고 있으나 그 발생기전은 아직 잘 밝혀져 있지 않다.
김경호
core
Histiocytic necrotizing lymphadenitis: Report of a case.
Nishi Nihon Hifuka, 1989 40才女子。繰り返す原因不明の38℃代の発熱, 圧痛を伴う全身の表在リンパ節腫脹, 自覚症のない浸潤性小紅斑を主訴に来院。皮膚病理組織像は真皮浅膚の血管周囲性単核細胞浸潤であり, 非特異的な反応性皮疹と思われた。頸部リンパ節病理組織像は, いわゆるstarly skyの像を呈し, 組織球性壊死性リンパ節炎と診断した。発熱, 皮疹, リンパ節腫脹は自然経過で寛解し, 軽快後3年以上を経た現在も再燃をみていない。
Norio TAKAHASHI +3 more
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Kikuchi-Fujimoto disease: a case report and the evaluation of diagnostic procedures
BMC Oral Health, 2019 Background Kikuchi-Fujimoto disease, known as histiocytic necrotizing lymphadenitis, is a benign, self-limiting and systemic disorder involving lymph nodes with unknown aetiology.
Shenjie Xu, Weilian Sun, Jiamei Liu
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Kikuchi histiocytic necrotizing lymphadenitis: clinicopathological and immunohistochemical study
Eastern Mediterranean Health Journal, 2001 Clinical, morphological and immunohistochemical features of 10 cases having the lymphnodal histological pattern of Kikuchi disease were examined. Two of these were diagnosed as systemic lupus erythematosus [SLE]. Morphologically, Kikuchi disease and SLE were nearly indistinguishable.
T A, Helal, W, Talaat, M F, Danial
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