Results 31 to 40 of about 5,601 (170)

Kikuchi-Fujimoto disease [PDF]

open access: yesBlood, 2017
![Figure][1] A 20-year-old man presented with a 3-week history of fevers, night sweats, weight loss, and increasing cervical adenopathy. A comprehensive infectious disease workup was negative.
Branko, Cuglievan, Roberto N, Miranda
  +5 more sources

Kikuchi‑Fujimoto disease [PDF]

open access: yesPolish Archives of Internal Medicine, 2009
A 14 year-old Bangladeshi girl presented with high fever, painful swellings in the neck, anorexia, weight loss and night sweating. On examination she had multiple enlarged and tender cervical lymph nodes. Other systems were normal. Laboratory investigations for sepsis and autoimmune diseases were negative. Initial fine needle aspiration and cytology of
Kołodziej‑Kłęk, Aneta   +3 more
  +9 more sources

Clinical Abdominal Kikuchi-Fujimoto Disease Resembling Macrophage Activation Syndrome Associated with Systemic Juvenile Idiopathic Arthritis: A Case Report [PDF]

open access: yes, 2022
A 13-year-old girl presented with fever for the past ten days without any other symptoms. Laboratory findings revealed leukopenia, low platelet count, and high lactate dehydrogenase and ferritin levels.
Fujita, Yuji   +4 more
core   +1 more source

Kikuchi-Fujimoto Disease: a Case Report

open access: yesActa Medica Iranica, 2015
Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is an idiopathic, self-limiting disorder and predominantly affects young women. We report a 35-year-old female who presented with soft to firm cervical lymphadenopathy and neck pain.
Mozaffar Aznab   +3 more
doaj   +1 more source

Kikuchi-Fujimoto disease: investigating comprehensive clinicopathological features and risk factors for recurrence. [PDF]

open access: yesHistopathology
Comprehensive clinicopathological analysis of 112 cases of Kikuchi‐Fujimoto disease (KFD) was conducted, and offered insights into recurrence risk factors and histopathological patterns. Recurrent KFD may fall between transient KFD and overt autoimmune disorders and lead to a better understanding of the aetiology of KFD.
Nishimura MF   +6 more
europepmc   +2 more sources

Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report

open access: yesBMC Infectious Diseases, 2021
Background We present a yet to be described association of SARS-CoV-2 infection with Kikuchi-Fujimoto disease. Case presentation A 32-year-old physician with history of SARS-CoV-2 infection presented to the emergency department with 2 weeks of fever ...
Samuel D. Racette   +7 more
doaj   +1 more source

Kikuchi-Fujimoto Disease: A Review [PDF]

open access: yesArchives of Pathology & Laboratory Medicine, 2018
Kikuchi-Fujimoto disease (KFD) is a rare entity characterized by subacute necrotizing lymphadenopathy and frequently associated with fever. Young adults of Asian ancestry are most commonly affected, but it has been reported worldwide. Despite many studies in the literature, the cause of KFD remains uncertain.
Anamarija M, Perry, Sarah M, Choi
openaire   +2 more sources

The Differential Diagnosis of Bilateral Pleural Effusion and Multiple Mediastinal Lymphadenopathies Includes Kikuchi-Fujimoto Disease

open access: yesJournal of Investigative Medicine High Impact Case Reports, 2020
Kikuchi-Fujimoto disease is an uncommon lymphohistiocytic disorder that frequently presents with acute or subacute clinical disease course. Cervical lymphadenopathy is the most common involved lymph node.
Chienhsiu Huang MD
doaj   +1 more source

Kikuchi Disease with enlargement of intramammary lymph node

open access: yesRadiology Case Reports, 2021
We describe a rare case of intramammary lymphadenopathy due to Kikuchi-Fujimoto disease. A 15-year old female presented to the Breast Clinic with complaints of a tender, palpable right breast lump.
Michael A Simon, MD   +4 more
doaj   +1 more source

Kikuchi-Fujimoto Disease

open access: yesArchives of Pathology & Laboratory Medicine, 2010
Abstract Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a self-limited condition, characterized by benign lymphadenopathy with associated fevers and systemic symptoms. It most commonly affects adults younger than 40 years of age and of Asian descent.
Charles Blake, Hutchinson, Endi, Wang
openaire   +4 more sources

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