Results 21 to 30 of about 4,903,989 (176)

Kikuchi-Fujimoto disease [PDF]

open access: yesOrphanet Journal of Rare Diseases, 2006
Kikuchi-Fujimoto disease (KFD) is a benign and self-limited disorder, characterized by regional cervical lymphadenopathy with tenderness, usually accompanied with mild fever and night sweats.
Guilabert Antonio, Bosch Xavier
doaj   +2 more sources

Kikuchi-Fujimoto disease: Clinical and laboratory characteristics and outcome

open access: yesJournal of Global Infectious Diseases, 2014
Introduction: Kikuchi-Fujimoto disease is an uncommon disorder with worldwide distribution, characterized by fever and benign enlargement of the lymph nodes, primarily affecting young adults.
P S Rakesh   +7 more
doaj   +2 more sources

Kikuchi-Fujimoto disease involving retroperitoneal lymph nodes: An uncommon presentation

open access: yesHematology Reports, 2021
Kikuchi-Fujimoto disease is a self-limited disease of unknown etiology that is clinically defined by fevers accompanied by tender posterior cervical lymphadenopathy.
Jane Date Hon   +5 more
doaj   +2 more sources

Ulcerative Esophagitis With Marked Eosinophilic Infiltration and Fluorodeoxyglucose-Positron Emission Tomography Positivity Requiring Differentiation From Esophagogastric Junction Carcinoma. [PDF]

open access: yesDEN Open
ABSTRACT Esophagitis with marked eosinophilic infiltration, including eosinophilic esophagitis (EoE), can rarely present with ulceration or stricture. We report a rare case of positron emission tomography–positive esophagitis with marked eosinophilic infiltration accompanied by ulceration and stricture, requiring differentiation from esophagogastric ...
Kikuchi Y   +9 more
europepmc   +2 more sources

Immune-Checkpoint-Inhibitor-Related Bullous Pemphigoid During Avelumab Maintenance Therapy in a Patient With Metastatic Renal Pelvic Carcinoma: A Case Report. [PDF]

open access: yesIJU Case Rep
ABSTRACT Introduction Bullous pemphigoid is a rare cutaneous, immune‐related adverse event, and avelumab‐associated cases are extremely rare. Case Presentation A 76‐year‐old man receiving avelumab maintenance therapy for recurrent renal pelvic carcinoma developed pruritic erythema and tense blisters 20 days after the first dose.
Nara T   +9 more
europepmc   +2 more sources

Kikuchi-Fujimoto Disease Associated with Myasthenia Gravis: A Case Report [PDF]

open access: yesCase Reports in Medicine, 2010
Kikuchi-Fujimoto disease is a self-limited benign condition of unknown etiology characterized by cervical lymphadenopathy, fever, and leucopenia. An autoimmune hypothesis has been suggested and an association with systemic lupus erythematosus, Sjogren's ...
Olukayode Onasanya   +4 more
doaj   +2 more sources

A very rare localization of kikuchi-fujimoto disease: parotid gland

open access: yesB-ENT, 2020
Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis is a rare benign disorder characterized by necrotizing lymphadenitis, which was independently defined by Kikuchi and Fujimoto in 1972.
Mehmet Özgür Pınarbaşlı   +4 more
doaj   +3 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 Disease in Elderly: Report of a Rare Disease in an Unusual Age

open access: yesCase Reports in Clinical Practice, 2022
Kikuchi disease is a benign, self-limited, and rare condition presented mainly by lymphadenopathy and fever. Kikuchi disease is more common in women, especially women under 40.
Elnaz Sahebi   +3 more
doaj   +1 more source

A rare case of Kikuchi-Fujimoto disease (case report) [PDF]

open access: yesCaspian Journal of Pediatrics, 2018
Background: Kikuchi disease is a rare, benign, self-limited disease characterized primarily by fever and cervical lymphadenopathy. Diagnosis is based on excisional biopsy and pathologic study.
Ahmad Tamaddoni   +2 more
doaj   +1 more source

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