Histiocytic necrotizing lymphadenitis in the context of systemic lupus erythematosus (SLE): Is histiocytic necrotizing lymphadenitis in SLE associated with skin lesions?

Lupus ◽  
2011 ◽  
Vol 20 (8) ◽  
pp. 809-819 ◽  
Author(s):  
SK Kim ◽  
MS Kang ◽  
BY Yoon ◽  
DY Kim ◽  
SK Cho ◽  
...  
2019 ◽  
Vol 57 (1) ◽  
pp. 72-77
Author(s):  
Taro Horino ◽  
Osamu Ichii ◽  
Yoshio Terada

Abstract Kikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare, benign, self-limiting disease characterized by cervical lymphadenopathy and fever. Since KFD was first reported in 1972, the validity of this clinical entity has been controversial and its aetiology remains unknown. Herein, we report a case of a patient with KFD, which was believed to be associated with systemic lupus erythematosus.


Lupus ◽  
1993 ◽  
Vol 2 (3) ◽  
pp. 207-208 ◽  
Author(s):  
M. Satoh ◽  
Minoru Satoh ◽  
Hidetomo Nakamoto ◽  
Kenji Okubo ◽  
Ajay K. Ajmani

2018 ◽  
Vol 2018 ◽  
pp. 1-5 ◽  
Author(s):  
Mihaela Găman ◽  
Ana-Maria Vlădăreanu ◽  
Camelia Dobrea ◽  
Minodora Onisâi ◽  
Cristina Marinescu ◽  
...  

Kikuchi–Fujimoto disease (KFD) or histiocytic necrotizing lymphadenitis is a rare disease that is frequently underdiagnosed due to clinical features that are similar to those of non-Hodgkin lymphomas, systemic lupus erythematosus (SLE), or infectious reactive lymphadenopathy. An excisional biopsy is required. We report a young Caucasian female diagnosed with KFD with skin lesions, complicating with SLE. The clinical course, laboratory, and CT findings are described, as are histopathologic features, for a better recognition of this rare disorder in clinical practice.


Lupus ◽  
2013 ◽  
Vol 23 (2) ◽  
pp. 183-187 ◽  
Author(s):  
Z Meng ◽  
Z-R Shi ◽  
G-Z Tan ◽  
J Yin ◽  
J Wu ◽  
...  

1993 ◽  
Vol 16 (1) ◽  
pp. 69-74
Author(s):  
Kazuyo Kurosawa ◽  
Terufumi Fukui ◽  
Shin Aizawa ◽  
Sadao Kashiwazaki ◽  
Keisuke Toyama

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