Monoclonal gammopathy of undetermined significance increased the rate of infection in systemic lupus erythematosus

Author(s):  
Cui Lu ◽  
Chengde Yang ◽  
Junna Ye
Author(s):  
mahan shafie ◽  
Alireza hadizadeh ◽  
soheil khalaji ◽  
samaneh parsa

Our patient had previously been diagnosed with Ulcerative colitis. the clinical manifestations of the patient along with laboratory tests such as anti-dsDNA and proteinuria were also positive. Therefore, the clinical manifestation was consistent with SLE. in the following work up monoclonal gammopathy in serum electrophoresis was also detected.


Lupus ◽  
2007 ◽  
Vol 16 (6) ◽  
pp. 426-429 ◽  
Author(s):  
Y.M. Ali ◽  
M.B. Urowitz ◽  
D. Ibanez ◽  
D.D. Gladman

2019 ◽  
Vol 12 (3) ◽  
pp. 133-136 ◽  
Author(s):  
Carlos Quintero ◽  
Judith Corona ◽  
Mayra Ponce ◽  
Alejandro Avilés ◽  
Olga Gutierrez ◽  
...  

Author(s):  
Romelia Pinheiro Gonçalves ◽  
Fernando Barroso Duarte ◽  
Maritza Cavalcante Barbosa

Rheumatology ◽  
1988 ◽  
Vol 27 (5) ◽  
pp. 412-412 ◽  
Author(s):  
J FONT ◽  
L. CERVERA ◽  
L. PALLARES ◽  
A. LOPEZ-SOTO ◽  
L. INGELMO

2016 ◽  
Vol 1 (2) ◽  
Author(s):  
Arathi Ramamurthi ◽  
Lindsay Bicknell ◽  
Morgan McCarty

<p>Papular mucinosis is an uncommon, idiopathic disorder characterized by dermal mucin deposition and increased collagen in the skin and internal organs. Its clinical presentation is characterized by dome-shaped, flesh colored papules that are closely spaced or linearly arranged. Papular mucinosis has been individually associated with several entities that include discoid lupus erythematosus, systemic lupus erythematosus and monoclonal gammopathy of undetermined significance. We encountered a 60-year-old woman with papular mucinosis in the setting of three concurrent disorders: discoid lupus erythematous, systemic lupus erythematosus and IgG paraproteinemia. Furthermore, we have reported the first case in North America of papular mucinosis being successfully treated with intralesional hyaluronidase.</p>


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