Belimumab in refractory systemic lupus erythematosus pleural effusion

2022 ◽  
Vol 158 (1) ◽  
pp. 42-43
Author(s):  
Vicenç Torrente-Segarra ◽  
Maria Bonet
Lupus ◽  
2021 ◽  
pp. 096120332110103
Author(s):  
Alfonso Ragnar Torres Jimenez ◽  
Nayma Ruiz Vela ◽  
Adriana Ivonne Cespedes Cruz ◽  
Alejandra Velazquez Cruz ◽  
Alma Karina Bernardino Gonzalez

Shrinking Lung Syndrome (SLS) is a rare and little known complication associated with Systemic Lupus Erythematosus (SLE), characterized by progressive and unexplainable dyspnea, pleuritic pain, small pulmonary volumes and elevation of the diaphragm on chest X-rays as well as restrictive pattern on pulmonary function tests. Objective To describe clinical, radiological and treatment characteristics in pediatric patients with SLS. Material and methods This is a descriptive and retrospective study in patients under 16 years old with the diagnosis of SLE complicated by SLS at the General Hospital. National Medical Center La Raza. Clinical, radiological and treatment variables were analyzed. Results are shown in frequencies and percentages. Results Data from 11 patients, 9 females and 2 males were collected. Mean age at diagnosis of SLS was 12.2 years. Age at diagnosis of SLE was 11.1 years. SLEDAI 17.3. Renal desease 72%, hematological 91%, lymphopenia 63%, mucocutaneous 72%, neurological 9%, arthritis 54%, serositis 91%, fever 81%, secondary antiphospholipid syndrome, low C3 72%, low C4 81%, positive ANA 91%, positive anti-DNA 91%. Regarding clinical manifestations of SLE: cough 81%, dyspnea 91%, hipoxemia 81%, pleuritic pain 71%, average oxygen saturation 83%. Chest X-rays findings: right hemidiaphragm affection 18%, left 63%, bilateral 18%. Elevated hemidiaphragm 91%, atelectasis 18%, pleural effusion 91%, over one third of the cardiac silhouette under the diphragm 36%, bulging diaphragm 45%, 5th. anterior rib that crosses over the diaphragm 91%. M-mode ultrasound: diaphragmatic hypomotility 100%, pleural effusion 63%. Pulmonary function tests: restrictive pattern in 45% of the cases. Treatment was with supplementary oxygen 100%, intubation 18%, antibiotics 100%, steroids 100%, intravenous immunoglobulin 54%, plasmapheresis 18%, cyclophosphamide 54% and rituximab 18%. The clinical course was favorable in 81%. Conclusions SLS should be suspected in patients with SLE and active disease who present hipoxemia, pleuritic pain, cough, dyspnea, pleural effusion and signs of restriction on chest X-rays. Therefore, a diaphragmatic M-mode ultrasound should be performed in order to establish the diagnosis.


Reumatismo ◽  
2019 ◽  
Vol 71 (2) ◽  
pp. 108-112 ◽  
Author(s):  
G. Tansir ◽  
P. Kumar ◽  
A. Pius ◽  
S.K. Sunny ◽  
M. Soneja

Systemic lupus erythematosus (SLE) is a chronic inflammatory multisystem autoimmune disease. Ascites when associated with pleural effusion and raised CA-125 levels in SLE patient, is known as pseudo-pseudo Meigs’ syndrome (PPMS). This is the case of a 22-year-old lady who presented with complaints of abdominal distension for one month and had a history of spontaneous abortion in the past. Abdominal imaging did not reveal any tumor and after extensive workup a diagnosis of PPMS was made. She was successfully treated with steroids, hydroxychloroquine and cyclophosphamide.


Medicine ◽  
2018 ◽  
Vol 97 (42) ◽  
pp. e12871
Author(s):  
Alexia D’Andréa ◽  
Damien L. Peillet ◽  
Christine Serratrice ◽  
Pierre-Augute Petignat ◽  
Virginie Prendki ◽  
...  

1989 ◽  
Vol 31 (1) ◽  
pp. 78-84 ◽  
Author(s):  
Shinobu Waga ◽  
Kiyotaka Nukii ◽  
Kazuhiko Sugimoto ◽  
Hiroshi Tanaka ◽  
Hidetsugu Furukawa ◽  
...  

2021 ◽  
Vol 3 (1) ◽  
pp. 73-82
Author(s):  
Limdawati Kwee

The systemic lupus erythematosus (SLE) is an autoimmune disease characterized by theformation of autoantibodies that attack various organ systems. Patients with SLE who presentwith pleural effusion are so rare that they are often not diagnosed early. Whereas with earlydiagnosis and proper management, the rate of recurrence and complications can decrease, thequality of life for people with SLE will also be better. This research is descriptive qualitativeresearch with a case study approach. This case report discusses a young woman who presentedwith respiratory failure resulting from a massive pleural effusion. The patient is known to have ahistory of chronic hematological disorders in the form of thrombocytopenia. During treatment,the patient developed psychiatric disorders in the form of delirium and hallucinations. The patientwas then diagnosed as SLE based on the 2018 EULAR / ACR criteria with the degree of disease activity classified as severe. The patient responded well to steroid induction therapy,azathioprine, and hydroxychloroquine. It was concluded that the diagnosis of SLE should beconsidered in cases of pleural effusion with a history of chronic thrombocytopenia and psychiatricdisorders. Early and appropriate management of severe SLE will provide a good prognosis. Keywords: systemic lupus erythematosus; respiratory failure; pleural effusion; neuropsychiatricSLE


2019 ◽  
pp. 28-31
Author(s):  
Rosana Quintana ◽  
M. Emilia Sattler ◽  
Marisol Ferrer

A 59-year-old male patient with a diagnosis of systemic lupus erythematosus and pulmonary consolidation associated with mediastinal polyadenopathies and pleural effusion, with chronic and torpid evolution. Differential dignoses and clinical implications are discussed.


2009 ◽  
Vol 5 (6) ◽  
pp. 289-290
Author(s):  
Mireya Elizabeth González Leija ◽  
Mauricio Orrantia Vertiz ◽  
Miguel Á. Vázquez Zaragoza

Respiration ◽  
1992 ◽  
Vol 59 (3) ◽  
pp. 173-175 ◽  
Author(s):  
Demosthenes Bouros ◽  
Panagiotis Panagou ◽  
Lambros Papandreou ◽  
Ioannis Kottakis ◽  
Constantinos Tegos

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