Results 41 to 50 of about 3,532 (210)

Report of a rare case of histiocytic necrotizing lymphadenitis with bilateral pleural effusion diagnosed via cervical lymph node biopsy. [PDF]

Sao Paulo Med J, 2018
CONTEXT: Histiocytic necrotizing lymphadenitis (HNL) is a rare disorder that is often benign and self-limiting. There have been reports of co-occurrence of HNL with other diseases, including systemic lupus erythematosus, hemophagocytic syndrome and ...
Liu X, Huang S, Jiang G.
europepmc   +4 more sources

Necrotizing histiocytic lymphadenitis due to three cases applying with painful cervical lymphadenopathy

Asian Journal of Medical Sciences, 2021
Necrotizing Histiocytic Lymphadenitis (NHL)is an idiopathic reason of lymphadenopathy which rather affects the young population. In this article, 3 cases which have applied to our Internal Medicine Policlinic with painful lymphadenopathy within four ...
Bulent Yardimci
doaj   +1 more source

Localised Kikuchi-Fujimoto Disease With Mediastinal Lymphadenopathy: A Case Initially Mimicking Malignant Lymphoma on Endobronchial Ultrasound-Guided Transbronchial Needle Aspiration Cytology. [PDF]

Respirol Case Rep
We report a rare case of isolated mediastinal Kikuchi–Fujimoto disease (KFD) in a 37‐year‐old woman, which was initially misinterpreted as malignant lymphoma based on EBUS‐TBNA cytology. Definitive diagnosis was achieved through video‐assisted thoracoscopic surgery, revealing characteristic massive necrosis and histiocytic infiltration.
Nishiyama K, Hasegawa T, Ishimine T, Nagae R, Shimabukuro T, Nishiyama M, Fukuzato N, Murayama Y, Tamaki K, Kakazu O, Ohta M.   +10 more
europepmc   +2 more sources

Serum Cytokine Profiling Differentiates Underlying Diseases in Cytokine Storm Syndrome. [PDF]

Arthritis Rheumatol
Serum cytokine profiling was performed using Luminex (48 cytokines) and ELISA (5 cytokines). Assessment of key cytokines (IFN‐α, IL‐18, IL‐6, CXCL9) delineated five dominant inflammatory patterns: I, IFN‐α–dominant CSS; II, IL‐18–dominant CSS; III, IL‐6–dominant CSS; IV, IFN‐γ–dominant CSS; and V, IL‐6 & IFN‐γ intermediate CSS.
Kaneko S, Hatano M, Shimbo A, Miyaoka F, Irabu H, Akutsu Y, Hayashi Y, Mizuta M, Nakagishi Y, Akamine K, Iwata N, Furuno K, Tanaka T, Ueno K, Fujita S, Yokoyama K, Minato T, Izawa K, Yasumi T, Matsubayashi T, Hosoya T, Nishikawa H, Fujimura J, Asano R, Sugita Y, Watanabe K, Kobayashi A, Endo T, Eguchi K, Nishikomori R, Yasuoka R, Asano T, Kanno M, Hamada K, Fujita Y, Hayashi D, Watanabe S, Shiba T, Yasuda S, Mori M, Kanegane H, Takagi M, Shimizu M.   +42 more
europepmc   +2 more sources

Clinicopathological Features, Treatment Response, and Outcome of Rosai-Dorfman Disease in Two Children. [PDF]

Clin Case Rep
ABSTRACT Rosai‐Dorfman disease is a rare non‐Langerhans cell histiocytic disorder. It is common in male children and young adults of African descent. It is classified into sporadic and familial types. The most common clinical presentation is massive bilateral cervical lymphadenopathy associated with constitutional symptoms. Histiocytic emperipolesis is
Evele G, Francine K, Bardin R.
europepmc   +2 more sources

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

B-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, Şükrü Turan, Mustafa Açıkalın, Ercan Kaya, Melek Kezban Gürbüz   +4 more
doaj   +3 more sources

Kikuchi-Fujimoto Disease in a Crohn’s Patient

Case Reports in Gastroenterology, 2022
Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare, benign, focal, self-limiting disease. We report a unique case of KFD in a patient with coexisting Crohn’s disease.
Danial H. Shaikh, Haider Ghazanfar, Tegveer Sandhu, Ali Naqqi Ul Hussain, Harish Patel   +4 more
doaj   +1 more source

SLE Developing in a Follow-Up Patient of Kikuchi’s Disease: A Rare Disorder [PDF]

Journal of Clinical and Diagnostic Research, 2013
Kikuchi’s disease or the Kikuchi-Fujimoto Disease (KFD) is a very rare, self-limiting, benign form of histiocytic necrotizing lymphadenitis, which is mostly seen in young females.
Anupam Patra, Sujit Kumar Bhattacharya
doaj   +1 more source

Case Report: Kikuchi-Fujimoto Disease: A case of supraclavicular lymphadenopathy [version 2; peer review: 2 approved]

F1000Research, 2021
Kikuchi-Fujimoto Disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare cause of cervical lymphadenopathy. Patients usually present with localized lymphadenopathy, fever and fatigue.
Shiza Sarfraz, Hamza Rafique, Hassam Ali, Syed Zawahir Hassan   +3 more
doaj   +1 more source

Hemophagocytic lymphohistiocytosis with recurrent Kikuchi-Fujimoto disease [PDF]

Yeungnam University Journal of Medicine, 2021
Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a self-limiting lymphadenitis. It is a benign disease mainly characterized by high fever, lymph node swelling, and leukopenia. Hemophagocytic lymphohistiocytosis (HLH)
Sang Min Lee, Young Tae Lim, Kyung Mi Jang, Mi Jin Gu, Jong Ho Lee, Jae Min Lee   +5 more
doaj   +1 more source