Results 61 to 70 of about 1,477 (190)

Serum Alkaline Phosphatase Levels in Pediatric Kikuchi‐Fujimoto Disease: A Retrospective Observational Analysis

open access: yesImmunity, 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
wiley   +1 more source

Clinical features of low serum alkaline phosphatase levels in children: A retrospective study

open access: yesPediatrics 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
wiley   +1 more source

Brainstem Encephalitis as an Atypical Neurologic Complication Following Kikuchi–Fujimoto Disease

open access: yesCase 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

open access: yesEurasian 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
doaj  

Clinical Analysis of 44 Children with Subacute Necrotizing Lymphadenitis

open access: yesInfection 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  

A Young Woman with Fever and Cervical Lymphadenopathy

open access: yesEuropean 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
doaj   +1 more source

Kikuchi‐Fujimoto disease following SARS‐CoV‐2 infection: A rare disease with increased incidence during the COVID‐19 pandemic?

open access: yesRespirology Case Reports, Volume 12, Issue 6, June 2024.
A 24‐year‐old man developed fever and painful neck swelling 1 month after recovering from COVID‐19. He was diagnosed with post COVID‐19 Kikuchi‐Fujimoto disease. Abstract Kikuchi‐Fujimoto Disease (KFD), also known as Kikuchi disease or Kikuchi histiocytic necrotizing lymphadenitis, is a rare and self‐limiting condition characterized by cervical ...
Cheuk Cheung Derek Leung   +7 more
wiley   +1 more source

Histiocytic necrotizing lymphadenitis (Kikuchi lymphadenitis) in an HIV-positive patient

open access: yes, 2002
A linfadenite necrosante histiocítica, ou linfadenite de Kikuchi (LK), é uma forma rara de linfadenite, geralmente de curso clínico auto-limitado. Raros casos de LK associados à infecção pelo vírus da imunodeficiência humana (HIV) foram relatados, sendo ...
VASSALLO, José   +2 more
core  

Kikuchi-Fujimoto disease: a case report and the evaluation of diagnostic procedures

open access: yesBMC 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
doaj   +1 more source

Histiocytic necrotizing lymphadenitis: Report of a case.

open access: yesNishi 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
openaire   +2 more sources

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