Results 111 to 120 of about 4,903,989 (176)
Haploinsufficiency A20 misdiagnosed as PFAPA (periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis) syndrome with Kikuchi disease. [PDF]
Jo KJ, Park SE, Cheon CK, Oh SH, Kim SH.
europepmc +1 more source
Proliferative Sparganosis Due to Spirometra mansoni in a Dog: A Detailed Diagnostic Picture
Innumerable small oval cystic structures were identified in the peritoneal cavity of a young dog presenting with abdominal distension and weight gain. A combination of diagnostics confirmed these structures as Spirometra mansoni plerocercoids and established a diagnosis of proliferative sparganosis.
Stephanie Middlemast +3 more
wiley +1 more source
Clinical and histological appearance of Kikuchi Disease-Like Inflammatory Pattern (KLIP)
Brufau-Cochs, Magí
core +1 more source
Kikuchi disease in a child. [PDF]
Kikuchi disease, also called histocytic necrotizing lymphadenitis or focal histiocytic lymphadenitis, is a rare, idiopathic and generally self limited cause of lymphadenitis. It was first described in 1972 in Japan. The most common clinical manifestation
Hassan, K +3 more
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Kikuchi-Fujimoto disease in 21-year-old man
Kikuchi-Fujimoto disease also known as histiocytic necrotizing lymphadenitis is a benign disorder characterized histologically by necrotic foci surrounded by histiocytic aggregates, and with the absence of neutrophils.
Saeid Aminiafshar +2 more
doaj
Baffled with fever and lymphadenopathy: neither infection nor malignancy, think Kikuchi disease. [PDF]
Hussain A, Gondal M, Yousuf H, Iqbal M.
europepmc +1 more source
Aims Clozapine‐induced agranulocytosis (CIA) is traditionally considered an idiosyncratic, dose‐independent reaction. However, emerging evidence suggests that clozapine‐related inflammatory events may exhibit dose‐dependent characteristics, leading us to hypothesize that CIA risk may similarly relate to early cumulative exposure.
Yuki Kikuchi +5 more
wiley +1 more source
Kikuchi-Fujimoto Disease: a Case Report
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.
Naser Kamalian +3 more
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Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report
Kikuchi–Fujimoto Disease (KFD) is a rare, typically self-limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small-vessel vasculitis.
Yusuf Kagzi +4 more
doaj +1 more source
A case of Kikuchi disease through skin
History and Objectives: Since several reports of this rare disease has been published and it has limited and benign characteristics and after one or two months it reverts into normality and frequently is mistaken on the basis of pathologic and clinical ...
Sharifi, H.
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