Results 61 to 70 of about 9,296 (170)
Kikuchi-Fujimoto disease: a case report and the evaluation of diagnostic procedures
BMC 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
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Hodgkin lymphoma misdiagnosed as Kikuchi-Fujimoto disease – how important it is to confirm an unusual diagnosis [PDF]
, 2020 Kikuchi-Fujimoto disease (KFD) is an extremely rare, self-limiting disorder of unknown etiology, with most cases occurring in Asia. The treatment of KFD is mainly supportive with NSAIDs or steroids in isolated cases.
Piotr Krych, Wiktoria Grcuk
core +2 more sources
Medical Journal of Indonesia, 2005 Kikuchi-Fujintoto disease (KFD) was first reported by 2 Japanese pathologists, Kikuchi and Fujimoto, independently in 1972. KFD is an idiopathic, self-limited necrotizing lymphadenitis. The most common clinical manifestation is cervical lymphadenopathy accompanied by fever, myalgia, leukopenia, and skin rash.
openaire +2 more sources
Kikuchi‐Fujimoto disease: A rare case report from Nepal
Clinical Case Reports, 2021 Clinicians and pathologists must be aware of the occurrence of Kikuchi‐Fujimoto Disease, as one of the differential diagnoses of cervical lymphadenopathy.
Rahul Rauniyar +6 more
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Role of growth factors in the pathogenesis of tissue fibrosis in systemic sclerosis. [PDF]
, 2010 The most severe clinical and pathologic manifestations of systemic sclerosis (SSc) are the result of a fibrotic process characterized by the excessive and often progressive deposition of collagen and other connective tissue macromolecules in skin and ...
Castro, Susan V. +2 more
core +2 more sources
Heterozygous germline TET2 loss‐of‐function variants associated with an ALPS‐like phenotype
British Journal of Haematology, Volume 206, Issue 5, Page 1330-1334, May 2025.Summary Germline homozygous loss‐of‐function mutations in TET2 result in significant childhood immunodeficiency that resembles autoimmune lymphoproliferative syndrome and predisposes one to lymphoma. The implications of heterozygous variants are less well understood.
Sean Harrop +13 more
wiley +1 more source
DEN Open, Volume 5, Issue 1, April 2025.Abstract Objectives This study aimed to determine the impact of the coronavirus disease 2019 (COVID‐19) pandemic on the treatment of acute cholangitis caused by choledocholithiasis. Methods The Japanese government declared a state of emergency in April 2020 due to the COVID‐19 pandemic.
Jun‐ichi Hanatani +27 more
wiley +1 more source
Necrotizing Histiocytic Lymphadenitis: Report of two cases (Kikuchi-Fujimoto disease)
مجله دانشگاه علوم پزشکی گرگان, 2004 Kikuchi-Fujimoto disease is a necrotizing Lymphadenitis with benign self-limit process in young women with fever, cervical lymphadenopathy and increased ESR with leukopenia. In this report we introduce 2 females with Kikuchi-Fujimoto disease.
M.Sharbatdaran (MD) +2 more
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