Results 71 to 80 of about 9,296 (170)
Dilemas de diagnóstico de linfadenite necrotizante (doença de Kikuchi-Fujimoto).
Kikuchi-Fujimoto disease, also called Histiocytic necrotizing lymphadentis, is a rare, benign and self-limited disease, with unknown etiology, that affects mainly young women, and is characterized by adenopathy (usually localized in the cervical region ...
Inês Antunes +8 more
doaj +1 more source
Familial Kikuchi-Fujimoto disease [PDF]
Kikuchi-Fujimoto disease (KFD) is a rare, self-limiting disease of unknown aetiology presenting with cervical lymphadenopathy, fever, vomiting, weight loss, night sweats and chills. Familial occurrence of KFD is reported very rarely in literature.
Krishnappa J +3 more
doaj +1 more source
Enigmatic Kikuchi-Fujimoto Disease A Comprehensive Review [PDF]
To determine the clinicopathologic significance of Kikuchi-Fujimoto disease (KFD) and review the literature on this condition, we conducted a MEDLINE search of English-language articles published between 1972 and December 2003. KFD has a worldwide distribution, and Asiatic people have a higher prevalence.
Xavier, Bosch +3 more
openaire +2 more sources
ABSTRACT Background Systemic inflammatory diseases (SIDs) have been reported in patients with sickle cell disease (SCD), but clinical data in children are scarce. Objectives To identify clinical and laboratory features at diagnosis of SID in children with SCD and to describe their evolution.
Caroline Vinit +19 more
wiley +1 more source
Kikuchi-Fujimoto disease: an unusual association with acute renal failure
Kikuchi-Fujimoto disease, also known as histiocytic necrotizing lymphadenitis of unknown etiopathogenesis, is a self-limited disease which frequently appears as feverish lymphadenomegaly, thus creating the need for differential diagnosis with lymphoma ...
Amanda Feliciano da Silva, MD +4 more
doaj +1 more source
Parinaud Oculoglandular Syndrome as a Prominent Presenting Feature of Kikuchi-Fujimoto Disease – A Case Report and Review of the Literature [PDF]
Kikuchi-Fujimoto disease (KFD) is an often under-diagnosed form of lymphadenitis that clinically mimics lymphoma. Ocular manifestations are rare in patients with KFD and are under-appreciated in the literature.
Bala, MD, PhD, Kamalesh K. +3 more
core +1 more source
Malaltia de Kikuchi-Fujimoto: presentació d'un cas pediàtric [PDF]
Introducció. La malaltia de Kikuchi-Fujimoto, o limfadenitis necrosant histiocítica, és una patologia benigna poc freqüent que es caracteritza per clínica de febre i limfadenopatia cervical.
Colomo Saperas, Lluís +5 more
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An enlarged ventricle is a representative feature of brain biotype 1 among the four brain biotypes classified by subcortical regional volume. ABSTRACT One of the challenges in diagnosing psychiatric disorders is that the results of biological and neuroscience research are not reflected in the diagnostic criteria.
Yuka Yasuda +41 more
wiley +1 more source
Kikuchi and Fujimoto's disease, also known as histiocytic necrotizing lymphadenopathy, is a rare and benign disorder of the lymph nodes of young adults.
Alice Reichert +4 more
doaj +1 more source
Doença de Kikuchi e Fujimoto [PDF]
A doença de Kikuchi e Fujimoto, também conhecida como Linfadenite Histiocítica Necrosante, é uma entidade clínico-patológica rara cuja etiologia permanece desconhecida; tem sido sugerida a possibilidade de uma etiologia auto-imune, mas também tem sido ...
Almeida, T +4 more
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