scholarly journals Kikuchi-Fujimoto Disease Associated with Myasthenia Gravis: A Case Report

2010 ◽  
Vol 2010 ◽  
pp. 1-3
Author(s):  
Olukayode Onasanya ◽  
David Nochlin ◽  
Victor Casas ◽  
Leema Reddy Peddareddygari ◽  
Raji P. Grewal

Kikuchi-Fujimoto disease is a self-limited benign condition of unknown etiology characterized by cervical lymphadenopathy, fever, and leucopenia. An autoimmune hypothesis has been suggested and an association with systemic lupus erythematosus, Sjogren's disease, and antiphospholipid syndrome has been noted. We report a 27-year-old male who presented for evaluation of weakness and he was diagnosed with seropositive generalized myasthenia gravis and underwent a thymectomy. He was stable until five months post-thymectomy, when he developed a high fever associated with nontender cervical lymphadenopathy, chills, and night sweats. Histopathology of a cervical lymph gland biopsy was compatible with Kikuchi-Fujimoto lymphadenitis. He improved spontaneously and was asymptomatic at the followup six months later. Our case expands the association of Kikuchi-Fujimoto disease with autoimmune disorders to include myasthenia gravis.

2018 ◽  
Vol 25 ◽  
pp. 81-83
Author(s):  
MMR Khan ◽  
MK Rahman ◽  
PM Basak ◽  
K Khanam ◽  
BK Pal ◽  
...  

Kikuchi’s disease is a rare, benign, self-limiting disorder, characterized clinically by fever and regional lymphadenopathy. Histopathologic features of lymph nodes in Kikuchi’s disease are characteristic and permit differentiation of this benign condition from lymphomas, systemic lupus erythematosus and infectious lymphadenopathies. We report a female patient presenting with fever and tender cervical lymphadenopathy. An excisional biopsy of the lymph node reveale lymphadenitis, consistent with Kikuchi’s disease.TAJ 2012; 25: 81-83


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.


2004 ◽  
Vol 19 (1) ◽  
pp. 134 ◽  
Author(s):  
Mi-Jeong Park ◽  
Yun-A Kim ◽  
Shin-Seok Lee ◽  
Byeong-Chae Kim ◽  
Myeong-Kyu Kim ◽  
...  

Lupus ◽  
2000 ◽  
Vol 9 (2) ◽  
pp. 156-157 ◽  
Author(s):  
R E Barbosa ◽  
S Córdova ◽  
J C Cajigas

1983 ◽  
Vol 72 (7) ◽  
pp. 941-946
Author(s):  
Tadayoshi YOSHIDA ◽  
Makoto HASEGAWA ◽  
Atsuko YAGI ◽  
Masako FURUYA ◽  
Hirashi ASATO ◽  
...  

1988 ◽  
Vol 77 (12) ◽  
pp. 1894-1895 ◽  
Author(s):  
Ikuo KINOSHITA ◽  
Kunihiko NAGASATO ◽  
Kohji SHIBAYAMA ◽  
Hidenori MATSUO ◽  
Masakatsu MOTOMURA ◽  
...  

Author(s):  
Richard B. Rosenbaum

The neurological manifestations of systemic lupus erythematosus are protean: headache, affective disorders, cognitive dysfunction, seizures, strokes, psychosis, acute confusional states, myelopathies, chorea, mimics of demyelinating disease, meningitis, polyneuropathy, mononeuropathy or mononeuritis multiplex, cranial neuropathies, autonomic dysfunction, Guillain-Barre syndrome, or myasthenia gravis make an incomplete list. Each neurological manifestation needs to be analyzed separately to understand pathogenesis, possible relation to primary lupus-related inflammation and vasculopathy, and optimal treatment.


The Lancet ◽  
1963 ◽  
Vol 282 (7309) ◽  
pp. 662-665 ◽  
Author(s):  
Donato Alarcón-Segovia ◽  
RichardF. Galbraith ◽  
JorgeE. Maldonado ◽  
FrankM. Howard

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