Results 41 to 50 of about 1,477 (190)

“Reactions in Leprosy: Updated Insights Into Pathophysiology, Clinical Spectrum, and Therapeutic Approaches—A Narrative Review”

Health Science Reports, Volume 9, Issue 5, May 2026.
ABSTRACT Background and Aims Reaction in leprosy is an immune‐mediated acute inflammatory episodes that occur in the natural course of Hansen's disease. Reaction can occur before, during, or after starting multidrug therapy and is a major cause of nerve damage, morbidity, and disability in affected individuals.
Bhaskar Gupta, Manesha Singh, Mohamad Goldust, Kinnor Das, Surajit Gorai, Prajwal Pudasaini, Seema Sitaula, Achyut Pokhrel, Esna Thapa, Sunil Jaiswal   +9 more
wiley   +1 more source

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.
europepmc   +2 more sources

Negative Correlation Between Serum Ferritin and CD4+ Lymphocytes: A Retrospective Study on Kikuchi‐Fujimoto Disease

Immunity, Inflammation and Disease, Volume 14, Issue 2, February 2026.
This retrospective cohort study indicates that patients with Kikuchi–Fujimoto disease demonstrated immunosuppression characterized by decreased counts of circulating CD3+ and CD4+ lymphocytes. Moreover, serum ferritin levels were inversely correlated with CD4+ lymphocyte counts, suggesting a potential role of ferritin in immune dysregulation in Kikuchi–
Peng Zhong, Xiwen Sang, Yu Yang, Zhenzhou Wang   +3 more
wiley   +1 more source

Axillary histiocytic necrotizing lymphadenitis (Kikuchi disease)

Journal of Hospital General Medicine
A 31-year-old Japanese woman with no significant medical history presented with a 10-day history of fever and left axillary pain. She denied recent trauma, contact with cats, or vaccinations.
Takayuki Ando, Hirohisa Fujikawa, Yoshifumi Uwamino, Junji Haruta   +3 more
doaj   +1 more source

Tuberculosis Masquerading as Behcet's Disease‐Pseudo Bechet's Syndrome: A Case‐Based Review of Literature

Respirology Case Reports, Volume 14, Issue 1, January 2026.
We report a case of recurrent oral/scrotal ulcers with systemic symptoms in a 33‐year‐old man masked pulmonary tuberculosis: imaging showed cavitary consolidations with effusion, and thoracoscopic pleural biopsy demonstrated acid‐fast bacilli. Anti‐tubercular therapy led to complete resolution, underscoring TB as a key Behçet's mimic to exclude before ...
Rinoosha Rachel, Naveen Polavarapu, Jithin Mathew, Virender Pratibh Prasad, Venkata Nagarjuna Maturu   +4 more
wiley   +1 more source

Investigation of Prognostic Factors in Patients With Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy

European Journal of Neurology, Volume 33, Issue 1, January 2026.
This graphical abstract shows GFAP‐IgG detection using tissue‐based and cell‐based assays (top). It illustrates the selection of patients for comparing favorable and unfavorable prognosis groups (bottom left). Finally, it presents multiple regression analysis results identifying predictors of poor prognosis 6 months after admission (bottom right ...
Akio Kimura, Akira Takekoshi, Yoichi Maekawa, Keiko Tanaka, Yoshihisa Yamano, Kuniaki Saito, Masao Takemura, Takayoshi Shimohata   +7 more
wiley   +1 more source

Histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease) after laparoscopic Roux-en-Y gastric bypass for morbid obesity: a case report

, 2012
Introduction Kikuchi-Fujimoto disease, or histiocytic necrotizing lymphadenitis, is a rare, benign, autoimmune condition characterized by lymphadenopathy, fever and neutropenia. It is a self-limited condition of unknown etiology.
Vazquez-Camuñas M, Gallego-Perales, Jose Luis, Garcia-Arnes Juan, Ricardo Gomez-Huelgas, M Rosa Bernal-Lopez, Jose Luis Gallego-Perales, Garcia-Arnes, Juan, Bernal-Lopez M, Vazquez-Camuñas, M. Luz, Bernal-Lopez, M. Rosa, M Luz Vazquez-Camuñas, Juan Garcia-Arnes, Gomez-Huelgas Ricardo, Gómez-Huelgas, Ricardo, Gallego-Perales Jose   +14 more
core   +1 more source

Rare Association between Kikuchi's Disease and Systemic Lupus Erythematosus [PDF]

Iranian Journal of Medical Sciences, 2009
Histiocytic necrotizing lymphadenitis or Kikuchi's disease is arare, benign condition of unknown etiology, which is usuallycharacterized by cervical lymphadenopathy and fever.
Mohammadhassan Jokar, Zahra Mirfeizi, Kambiz Javidi   +2 more
doaj  

Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report

Case Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.
Kikuchi–Fujimoto Disease (KFD) is a rare, typically self‐limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small‐vessel vasculitis. Central nervous system (CNS) involvement in KFD is exceedingly rare and has been described in isolated cases, including encephalitis, aseptic meningitis, and ...
Yusuf Kagzi, Suban Amatya, Ashutosh Gupta, Kanika Sharma, Shitiz Sriwastava, Semonti Nandi   +5 more
wiley   +1 more source

Histiocytic necrotizing lymphadenitis. Report of three cases [PDF]

, 2008
Histiocytic necrotizing lymphadenitis (HNL), also known as Kikuchi's disease is a rare condition of unknown etiology Patients present with cervical lymph node enlargement fever and malaise. The diagnosis is made by excision biopsy.
Gac Espinoza, Patricio, Amat Vidal, José, Rossi F., Ricardo, Carreño Toro, Laura, Cabané Toledo, Patricio, Franco S., Carmen, Huidobro G., Felipe, Covarrubias C., Patricio   +7 more
core