Lupus Erythematosus Panniculitis: Clinical and Histopathological Diagnostic Challenge

Author(s):  
Vashty Amanda Hosfiar ◽  
Agung M. Rheza ◽  
Sondang P. Sirait ◽  
Eyleny Meisyah Fitri ◽  
Rahadi Rihatmadja ◽  
...  
2018 ◽  
Vol 2 (1) ◽  
Author(s):  
Parigini Aníbal María ◽  
Diego María Clara de ◽  
Beguerie Julieta Ruiz ◽  
Paredes Victoria Duran ◽  
Anaya Javier

2021 ◽  
Vol 49 (5) ◽  
pp. 030006052110122
Author(s):  
Yimin Ma ◽  
Duanming Zhuang ◽  
Zhenguo Qiao

Celiac disease (CD) is a chronic immune-mediated intestinal disease that is characterized by production of autoantibodies directed against the small intestine. The main clinical manifestations of CD are typically defined as those related to indigestion and malabsorption. These manifestations include unexplained diarrhea or constipation, abdominal pain, bloating, weight loss, anemia, failure-to-thrive in children, and decreased bone density. Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by heterogeneous clinical manifestations, which may also involve the gastrointestinal tract. Comorbidity of CD and SLE is rare, and the overlapping symptoms and nonspecific clinical presentation may pose a diagnostic challenge to clinicians. We report here a case of SLE with CD, which mainly manifested as recurrent diarrhea, uncorrectable electrolyte disorders, and severe malnutrition. Through review, we hope to further improve our understanding and diagnostic level of this combination of diseases.


2021 ◽  
Vol 14 (1) ◽  
pp. e237243
Author(s):  
Diogo Hipolito-Fernandes ◽  
Maria Elisa Luís ◽  
Rita Flores ◽  
Rita Anjos

Subretinal fluid accumulation in a patient with systemic lupus erythematosus (SLE) may represent a diagnostic challenge. We present a case of a 43-year-old man with baseline diagnosis of SLE and hydroxychloroquine-associated maculopathy who reported progressive vision loss on the right eye, associated with corticosteroids use for an arthritic crisis. Ophthalmological examination did not reveal any acute finding. On optical coherence tomography, subretinal fluid in the perifoveal area was visible on the right eye, with corresponding enlargement of the visual field defect. An increased choroidal thickness was also visible. Fluorescein angiography revealed, on the right eye, two pinpoint areas of leakage and indocyanine green angiography signs of choroidal vascular hyperpermeability. Considering a diagnosis of a non-central central serous chorioretinopathy, corticosteroids use was interrupted, with resolution of the subretinal fluid. This case illustrates the relevance of a multimodal imaging approach to guide the diagnosis of patient with an SLE with subretinal fluid.


2016 ◽  
Vol 49 (1) ◽  
pp. 27-30
Author(s):  
Hsiao-Peng Huang ◽  
Yung-Chia Huang ◽  
Yuan-Sheng Tzeng ◽  
Chih-Hsin Wang ◽  
Tim-Mo Chen ◽  
...  

2021 ◽  
Author(s):  
Rubens Bonfiglioli ◽  
Vanessa Félix Nascimento Coelho ◽  
Andreza Lamonica ◽  
Thais de Campos Ferreira Pinto

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2020 ◽  
Vol 156 (5) ◽  
pp. 566
Author(s):  
Colleen K. Correll ◽  
Daniel D. Miller ◽  
Sheilagh M. Maguiness

2017 ◽  
Vol 31 (7) ◽  
pp. e318-e319 ◽  
Author(s):  
A.-L. Durand ◽  
J.-F. Goussot ◽  
D. Thiolat ◽  
A. Taieb ◽  
J. Marie ◽  
...  

2020 ◽  
Vol 13 (9) ◽  
pp. e232002
Author(s):  
Irene Alejandra Orbe Jaramillo ◽  
Carmen De Lucas Collantes ◽  
Amelia Martínez de Azagra ◽  
Elena Sebastián

Thrombotic thrombocytopaenic purpura (TTP) is a life-threatening thrombotic microangiopathy characterised by microangiopathic haemolytic anaemia, thrombocytopaenia and organ ischaemia. TTP is caused by a severe functional deficiency of ADAMTS13 activity. We describe a 10-year-old girl presenting anaemia and thrombocytopaenia with schistocytes. Urine protein to creatinine ratio was within nephrotic range. ADAMTS13 activity was 0%, and no anti-ADAMTS13 antibodies were found. A renal biopsy showed deposits of IgG, C3 and C1q in the capillary membrane, compatible with class V lupus nephritis. Therapeutic plasma exchange (TPE) was performed in conjunction with therapy consisting of steroids and mycophenolate mofetil. After 11 months of follow-up, the patient remains in remission with normal ADAMTS13 activity. Although acquired TTP is a rare finding in children, differential diagnosis of thrombotic microangiopathy should include ADAMTS13 and the assay should be performed early. TTP treatment is based on TPE, although the underlying disease must be ruled out to optimise treatment and prevent relapse.


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