Associated with Anticardiolipin Antibodies in a Young Woman with Systemic Lupus Erythematosus

Total Page:16

File Type:pdf, Size:1020Kb

Associated with Anticardiolipin Antibodies in a Young Woman with Systemic Lupus Erythematosus Ann Rheum Dis: first published as 10.1136/ard.48.10.853 on 1 October 1989. Downloaded from Annals of the Rheumatic Diseases 1989; 48: 853-855 Cerebrovascular accident and myocardial infarction associated with anticardiolipin antibodies in a young woman with systemic lupus erythematosus YORAM MAARAVI,' EYAL RAZ,1 DAN GILON,' AND ALAN RUBINOW2 From the 'Department ofMedicine, Mount Scopus, and the 2Rheumatology Unit, Department ofMedicine A, Hadassah University Hospital, Jerusalem, Israel SUMMARY A 26 year old woman with systemic lupus erythematosus, including malar rash, photosensitivity, and arthritis, developed a cerebrovascular accident and acute myocardial infarction. High titres to antinuclear factor, anti-DNA antibodies, positive Venereal Disease Research Laboratory (VDRL) test, and anticardiolipin antibodies were found in her serum. A possible association between the presence of anticardiolipin antibodies and the two major thrombotic events is discussed. Recent studies suggest that anticardiolipin anti- normal. The erythrocyte sedimentation rate was 97 bodies may be responsible for a variety of laboratory mm/h. Haemogram and coagulation tests were copyright. and clinical phenomena in up to 61% of patients normal. Urinary sediment, serum electrolytes, with systemic lupus erythematosus (SLE). These albumin, liver and kidney function tests, serum include lupus anticoagulant, biological false positive cholesterol, triglycerides, and high density lipopro- test for syphilis, thrombocytopenia, recurrent tein cholesterol were normal. Creatine kinase was abortions, intrauterine fetal death, and thrombo- initially 182 U/l (normal <100 U/l) and reached a embolism. 1-5 peak of 376 U/l on the second day, while aspartate We describe here a young woman with SLE, not aminotransferase was initially 30 U/l (normal receiving corticosteroid treatment, who developed a <40 U/1) and increased to 60 U/l. The electro- cerebrovascular accident and acute myocardial in- cardiogram on admission showed a non-Q wave http://ard.bmj.com/ farction in the presence of a high titre of anticardio- infarction of the inferior wall. Echocardiography lipin antibodies. disclosed neither valvular abnormalities nor vegetations. Antinuclear antibody titre was 3 on a Case report 1-4 scale. Venereal Disease Research Laboratory (VDRL) titre was 1/16. Anticardiolipin antibody A 26 year old woman was admitted in February 1986 concentration (measured by radioimmunoassay because of crushing anterior chest pain of a few using 125I protein A as a detecting developer) was on October 1, 2021 by guest. Protected hours' duration. From the age of 12 she was known 6090 cpm (normal <2000). Anti-DNA antibodies to have had a butterfly malar rash, photosensitivity, were 22 ig/ml (normal <1.5). Serum C3 was and recurrent bouts of arthritis. Five years before 530 mg/l and C4 was 340 mg/l (normal 600-1100 admission she developed a left hemispheric cerebro- and 250-500 respectively). A skin biopsy showed no vascular accident due to thrombotic obstruction of evidence of vasculitis. the left internal carotid artery, which was confirmed On admission to the intensive care unit she by carotid arteriography. She denied risk factors for responded remarkably to sublingual nitrates and ischaemic heart disease, taking oral contraceptives, calcium channel blockers. Treatment with nitrates or receiving corticosteroid treatment. On admission and aspirin was started during the following hours. she appeared acutely ill and her vital signs were The laboratory investigation indicated that she had SLE, and treatment with prednisone (60 mg/day) Accepted for publication 20 February 1989. Correspondence to Dr Yoram Maaravi, Department of Medicine, was started. In the remainder of her hospital course Hadassah University Hospital, Mount Scopus, PO Box 24035, we noticed severe emotional lability, which was Jerusalem 91240, Israel. attributed to her basic disease and to the steroid 853 Ann Rheum Dis: first published as 10.1136/ard.48.10.853 on 1 October 1989. Downloaded from 854 Maaravi, Raz, Gilon, Rubinow treatment. During the ensuing 30 months her tion and anticardiolipin antibodies inpatients with corticosteroid treatment was tapered slowly and, SLE is rare. Recently, Asherson et all and others25 presently (January 1989), she is receiving 10 mg described myocardial infarction associated with prednisone daily and aspirin, and functions normally. anticardiolipin antibodies in young patients suffer- ing from SLE, 'lupus-like' disease, and the 'primary' antiphospholipid syndrome. These data suggest that Discussion anticardiolipin antibodies may have had a patho- genetic role in the ischaemic events in our patient as The patient described here meets five of.the revised well as in others. criteria for SLE6: malar rash, photosensitivity, arthritis, positive antinuclear antibody test, and We gratefully acknowledge the help of Mrs Shirley Roth in the an immunological disorder (positive VDRL). Her preparation of this manuscript. clinical course is remarkable in that despite relatively mild disease that did not require intensive treatment she developed two life threatening thrombotic References events in the brain and heart. 1 Harris E N, Gharavi A E, Boey M L, et al. Anticardiolipin Cardiac involvement in SLE is well recognised antibodies detection by radioimmunoassay and association with thrombosis in SLE. Lancet 1983; ii: 1211-4. and most frequently manifests as pericarditis, myo- 2 Harris E N, Loizou S, Englert H, et al. Anticardiolipin carditis, and endocarditis.7 8 Myocardial infarction antibodies and lupus anticoagulant. Lancet 1984; iii: 1099. during the course of SLE is rare and only a few cases 3 Harris E N, Gharavi A E, Loizou S, et al. Cross-reactivity of have been reported.>18 The pathogenesis of antiphospholipid antibodies. J Clin Lab Immunol 1985; 16: 1-6. 4 Harris E N, Asherson R A, Gharavi A E, Morgan S H, Derue myocardial infarction in SLE is usually related to G J, Hughes G R V. Thrombocytopenia in SLE and related coronary atherosclerosis, possibly accelerated by autoimmune disorders: association with anticardiolipin anti- corticosteroid administration.11 Furthermore, bodies. Br J Haematol 1985; 59: 227-30. in coronary arteritis is a rare process, which may 5 Derue G J, Englert H J, Harris E N, et al. Fetal loss SLE: association with anticardiolipin antibodies. J Obstet Gynecolcopyright. culminate in myocardial infarction in patients with Neotal Nurs 1985; 5: 207-9. SLE.10 Our patient's youth, the lack of risk factors 6 Tan E M, Cohen A S, Fries J S, et al. The 1982 revised criteria for coronary heart disease, and the previous for the classification of SLE. Arthritis Rheum 1982; 25: 1271-7. 7 Libman E, Sacks B. A hitherto undescribed form of valvular thrombotic event in the presence of anticardiolipin and mural endocarditis. Arch Intern Med 1924; 33: 701-32. antibodies support the contention that the myo- 8 Dubois E L, Tuffanelli D L. Clinical manifestations of SLE: cardial infarction was due to coronary artery throm- computer analysis of 520 cases. JAMA 1964; 190: 104-11. bosis. 9 Homcy C J, Liberthson R R, Fallon J T, Gross S, Miller L M. report of six Anticardiolipin antibodies are detected in a spec- Ischemic heart disease in SLE in the young patient: cases. Am J Cardiol 1982; 49: 478-84. trum of autoimmune disorders, and high serum 10 Badui E, Garcia-Rubi D, Robles E, et al. Cardiovascularhttp://ard.bmj.com/ concentrations have been measured in up to 61% of manifestations of SLE. Prospective study of 100 patients. patients with SLE.1 Harris et al provided data Angiology 1985; 36: 431-41. anticardio- 11 Bulkley B H, Roberts W C. The heart in SLE and the changes suggesting that lupus anticoagulant and induced in it by corticosteroid therapy: a study of 36 necropsy lipin antibodies are identical and show closely patients. Am J Med 1975; 58: 243-64. related specificity. Their presence is associated with 12 Tsakraklides V G, Blieden L C, Edwards J E. Coronary recurrent fetal loss, thrombocytopenia, and recur- atherosclerosis and myocardial infarction associated with sys- temic lupus erythematosus. Am Heart J 1974; 87: 637-41. rent thromboembolic events, which is attributed to Kawai C. Acute 13 Takatsu Y, Hattori R, Sakaguohi K, Yui Y, on October 1, 2021 by guest. Protected their inhibition of the prothrombinase complex.45 myocardial infarction associated with systemic lupus erythema- Among the thromboembolic events, cerebral in- tosus documented by coronary arteriograms. Chest 1985; 88: farction was frequent. 19 20 Eight out of nine patients 147-9. of 14 Shalev Y, Green L, Pollack A, Bentwich Z. Myocardial with cerebral infarction had hi2gh concentrations infarction with central retinal artery occlusion in a patient with anticardiolipin antibodies.1 19 20 In addition, Petri antinuclear antibody-negative systemic lupus erythematosus. et al found that 50% of patients with SLE and Arthritis Rheum 1985; 28: 1185-7. cerebral infarction had raised anticardiolipin anti- 15 Vermylen J, Blockmans D, Spitz B, Deckmyn H. Thrombosis and immune disorders. Clin Haematol 1986; 15: 393-412. body concentrations.21 16 Asherson R A, Harris E N, Gharavi A, Hughes G R V. Furthermore, anticardiolipin antibodies may be a Myocardial infarction in systemic lupus erythematosus and useful marker in monitoring disease activity in 'lupus like' disease. Arthritis Rheum 1986; 29: 1292-3. infarction patients with SLE.22 23 It is noteworthy that recur- 17 Asherson R A, Mackay I R, Harris E N. Myocardial man vein women with in a young with systemic lupus erythematosus, deep rent fetal loss in anticardiolipin thrombosis and antibodies to phospholipid. Br HeartJ 1986; 56: antibodies/lupus anticoagulant can be reduced signi- 190-3. ficantly by the use of steroids and aspirin.24 18 Asherson R A, Kamashta M A, Baguley E, Oakley C H, The association between acute myocardial infarc- Rowell N R, Hughes G R V. Myocardial infarction and Ann Rheum Dis: first published as 10.1136/ard.48.10.853 on 1 October 1989. Downloaded from Major thrombotic events in a young woman with SLE 855 antiphospholipid antibodies in SLE, 'lupus-like' disease and the 22 Raz E, Michaeli J, Rosenmann E, Rubinow A, Popovtzer 'primary' antiphospholipid syndrome.
Recommended publications
  • Domino Effect in a Patient with Epstein-Barr Virus Infection and Autoimmunity: a Case Report Case Report Appointments Scheduled
    International Journal of Case Report Clinical Rheumatology Domino effect in a patient with Epstein- Barr Virus infection and autoimmunity: A case report The link between autoimmune diseases and viral infections has been characterized, but specific Margarite Matossian, Carrie mechanisms behind this association remain a current area of investigation. Whether viral infections Crook, Alec Goldberg, Anna trigger or unmask autoimmunity, or if the pathologies occur concurrently, is not yet completely Stathopoulos, Justin Tien, understood. Specifically, Epstein - Barr virus (EBV) is implicated in several autoimmune disorders, Sheela Sheth, Osaid Saqqa & including Systemic Lupus Erythematosus (SLE). It is hypothesized that common immunologic Christopher Dale Shamburger* pathways are activated in the two pathologic states. This case report is an example of this confusing Department of Medicine, Tulane University presentation, and the importance of recognizing the association between autoimmunity and viral Health Sciences Center, New Orleans LA infections. This patient presented with symptoms concerning for SLE and hepatic autoimmunity 70115, USA with serology suggesting a recent infection with EBV. Given this complicated presentation, it is *Author for correspondence: difficult to determine which disease state presented first in patients with evidence of both SLE and EBV infection and whether this information is clinically relevant for ongoing treatment and [email protected] monitoring. Here, we provide an in-depth discussion of current genomic and immunological research that supports the associations amongst these disease pathologies. Introduction by an intricate psychiatric history. Then Autoimmune diseases have increased in we discuss the contribution of infection to frequency in industrialized countries over autoimmune disease states and important recent years [1]. The etiology of autoimmune distinctions between autoimmune diseases diseases, a self-reactive adaptive immune and autoinflammatory responses.
    [Show full text]
  • Pediatric Motor Inflammatory Neuropathy: the Role Of
    brain sciences Case Report Pediatric Motor Inflammatory Neuropathy: The Role of Antiphospholipid Antibodies Claudia Brogna 1,2,*, Marco Luigetti 3 , Giulia Norcia 1, Roberta Scalise 1, Gloria Ferrantini 1, Beatrice Berti 1, Domenico M. Romeo 4, Raffaele Manna 5, Eugenio Mercuri 1 and Marika Pane 1 1 Pediatric Neurology and Nemo Clinical Centre, Fondazione Policlinico Universitario A. Gemelli IRCSS, Università Cattolica del Sacro Cuore, 00168 Roma, Italy; [email protected] (G.N.); [email protected] (R.S.); [email protected] (G.F.); [email protected] (B.B.); [email protected] (E.M.); [email protected] (M.P.) 2 Pediatric Neuropsichiatric Unit, ASL, 83100 Avellino, Italy 3 Institute of Neurology, Fondazione Policlinico Universitario A. Gemelli IRCSS, Università Cattolica del sacro Cuore, 00168 Roma, Italy; [email protected] 4 Pediatric Neurology, Fondazione Policlinico Universitario A. Gemelli IRCSS, Università Cattolica del Sacro Cuore, 00168 Roma, Italy; [email protected] 5 Periodic Fevers Research Centre and rare disease. Department of Internal Medicine, Fondazione Policlinico Universitario A. Gemelli IRCSS, Università Cattolica del Sacro Cuore, 00168 Roma, Italy; raff[email protected] * Correspondence: [email protected] Received: 4 February 2020; Accepted: 5 March 2020; Published: 7 March 2020 Abstract: We report the clinical case of a nine-year-old girl who presented with progressive motor neuropathy, revealed via the detection of a higher delay in F-wave recording using digitalized nerve conduction/electromyography. Since the lupus anticoagulant (LAC) positivity, detected using diluted Russell viper venom time (dRVVT), switched to persistent serological anticardiolipin immunoglobulin G (IgG) positivity, a possible non-thrombotic antiphospholipid antibody (aPL)-related clinical manifestation was suspected, and intravenous immunoglobulin treatment (IVIG) was started.
    [Show full text]
  • RDL/Labcorp Cross Reference Guide
    RDL/LabCorp Cross Reference Guide Profiles RDL Order Code RDL Test/Panel Name LabCorp Test No. LabCorp Test Name 1228 ANA 12 Plus Profile 520180 ANA 12 Plus Profile (RDL) 1230 ANA 12 Plus Profile, Do All 520175 ANA 12 Plus Profile, Do all (RDL) 1201 ANA 12 Profile 520188 ANA Profile 12 (RDL) 1206 ANA Profile 12, Do All 520299 ANA 12 Profile , Do All (RDL) 1100 ANA Profile I 520185 ANA Profile 11 (RDL) 1020 ANA Profile II 520185 ANA Profile 11 (RDL) 994 ANCA Panel 520149 ANCA Profile (RDL) 3003 Antiphospholipid Ab Panel I 500711 Lupus Anticoagulant/Cardiolipin Antibody (Esoterix) 3004 Antiphospholipid Ab Panel II 504400 Antiphospholipid Syndrome (APS), Comprehensive (Esoterix) 644 Anti-Saccharomyces 164657 Saccharomyces cerevisiae Profile 1292 Anti-Synthetase Panel 520193 Anti-Synthetase Profile (RDL) 996 Arthritis Panel 520205 Arthritis Profile (RDL) Autoimmune Liver Disease Panel, 558 520197 Autoimmune Liver Disease Profile (RDL) Comprehensive 1044 Celiac Disease Ab Panel 165142 Celiac Antibodies tTG IgA, EMA IgA, Total IgA with Reflex to tTG IgG 705 Hepatitis Panel II 322744 Hepatitis Panel, Acute ILDdxComplete (Interstitial Lung Disease 3008 520210 ILDdx Profile (RDL) Complete) Inflammatory Bowel Disease (IBD) Profile with Anti-Pancreatic Antibodies 1265 Inflammatory Bowel Disease Panel 520190 (RDL) 354 Interstitial Lung Disease Panel II 520202 Interstitial Lung Disease Profile (RDL) 1065 Lupus Activity Panel 520195 Lupus Activity Profile (RDL) 3002 Lupus Anticoagulant Panel 500070 Lupus Anticoagulant Profile (Esoterix) 342 Lupus Renal
    [Show full text]
  • 32 Mechanism of Thrombosis in Antiphospholipid Syndrome: Binding to Platelets Joan-Carles Reverter and Dolors Tàssies
    32 Mechanism of Thrombosis in Antiphospholipid Syndrome: Binding to Platelets Joan-Carles Reverter and Dolors Tàssies Introduction Antiphospholipid antibodies (aPL) are related to thrombosis in the antiphospho- lipid syndrome (APS) [1, 2] and numerous pathophysiological mechanisms have been suggested involving cellular effects, plasma coagulation regulatory proteins, and fibrinolysis [3, 4]: aPL may act as blocking agents directly inhibiting antigen enzymatic or co-factor function of hemostasis; may bind fluid-phase antigens of hemostasis involved proteins and then decrease plasma antigen levels by clearance of immune complexes; may form immune complexes with their antigens that may be deposited in blood vessels causing inflammation and tissue injury; may cause dysregulation of antigen–phospholipid binding due to cross-linking of membrane bound antigens; and may trigger cell mediated events by cross-linking of antigen bound to cell surfaces or cell surface receptors [3, 4]. Moreover, several characteris- tics of the aPL, such as the concentration, class/subclass, affinity or charge, and several characteristics of the antigens, as the concentration, size, location or charge, may influence which of the theoretical autoantibody actions will occur in vivo [3]. Among the cellular mechanisms supposed to be involved, platelets have been considered as one of the most promising potential target for circulating aPL that may cause antibody mediated thrombosis as a part of the clinical spectrum of the autoimmune disorder of the APS. In the present chapter we will focus on the inter- actions that involve aPL binding to platelet membrane or platelet membrane bound antigens. Platelets as Target for aPL Platelets play a central role in primary hemostasis involving platelet adhesion to the injured blood vessel wall, followed by platelet activation, granule release, shape change, and rearrangement of the outer membrane phospholipids and proteins, transforming them into a highly efficient procoagulant surface [5].
    [Show full text]
  • Significant Factors Associated with Lupus Nephritis P Alba, L Bento, M J Cuadrado, Y Karim, M F Tungekar, I Abbs, M a Khamashta, D D’Cruz,Grvhughes
    556 EXTENDED REPORT Ann Rheum Dis: first published as 10.1136/ard.62.6.556 on 1 June 2003. Downloaded from Anti-dsDNA, anti-Sm antibodies, and the lupus anticoagulant: significant factors associated with lupus nephritis P Alba, L Bento, M J Cuadrado, Y Karim, M F Tungekar, I Abbs, M A Khamashta, D D’Cruz,GRVHughes ............................................................................................................................. Ann Rheum Dis 2003;62:556–560 Background: Lupus nephritis (LN) is a common manifestation in patients with systemic lupus erythema- tosus (SLE). Autoantibodies and ethnicity have been associated with LN, but the results are controver- sial. Objective: To study the immunological and demographic factors associated with the development of LN. Patients and methods: A retrospective case-control study of 127 patients with biopsy-proven LN, and 206 randomly selected patients with SLE without nephritis as controls was designed. All patients had attended our lupus unit during the past 12 years. Standard methods were used for laboratory testing. Results: Patients with LN were significantly younger than the controls at the time of SLE diagnosis See end of article for (mean (SD) 25.6 (8.8) years v 33.7 (12.5) years; p<0.0001). The proportion of patients of black eth- authors’ affiliations nic origin was significantly higher in the group with nephritis (p=0.02). There were no differences in ....................... sex distribution or duration of follow up. A higher proportion of anti-dsDNA, anti-RNP, anti-Sm, and Correspondence to: lupus anticoagulant (LA) was seen in the group with nephritis (p=0.002; p=0.005; p=0.0001; Dr M J Cuadrado, Lupus p=0.01, respectively).
    [Show full text]
  • Hepatic Manifestations of the Antiphospholipid Syndrome
    EDITORIAL Hepatic Manifestations of the Antiphospholipid Syndrome Key words: autoimmune hepatitis, Sjogren's syndrome, Budd- autoimmune hepatitis (7). Examinations prior to liver biopsy Chiari syndrome, nodular regenerative hyperpla- revealed a greatly prolonged APTT,and the patient was found sia to be positive for IgG anticardiolipin antibody and lupus anti- coagulant. However, this patient showedno signs of thrombo- sis or any other symptomssuggestive ofAPS. In this issue, Katayama et al (8) report a case of Sjogren's Antiphospholipid syndrome (APS) is characterized by the syndrome complicated with autoimmune hepatitis and APS. presence of antiphospholipid antibodies (anticardiolipin anti- bodies and/or lupus anticoagulant) in association with symp- See also p 73. toms including venous/arterial thromboses, recurrent fetal loss and thrombocytopenia. Thromboticepisodes mayoccur at any In previously reported cases of autoimmune hepatitis asso- part of the circulation system, hence, any organ may be in- ciated with the presence of antiphospholipid antibodies, anti- volved. As for hepatic involvement, the most well knownmani- nuclear antibody was present, but the presence of anti-SS-A festation ofAPSis Budd-Chiari syndrome, which is caused antibody or sicca symptomshave not been documented. There- mostly by obstruction of hepatic veins or inferior vena cava. fore, this case may possibly be the first documented case of Pelletier et al (1) have reported that of their 22 non-tumourous autoimmune hepatitis with APSand Sjogren's syndrome. Their Budd-Chiari patients, 4 had antiphospholipid antibodies with- patient had autoimmune hepatitis, and Sjogren's syndrome out other causes of hepatic vein thrombosis. Amongthese 4 confirmed by Schirmer's test and sialography. The patient patients, 2 seemed to have primary APS, i.e., no signs of other showed positive for (32-GPI dependent anticardiolipin antibody autoimmunediseases such as SLE.
    [Show full text]
  • Evaluation of Clinical and Laboratory Findings of 147 Patients with Systemic Lupus Erythematosus: the Relationship Between Anti-CCP and Arthritis
    J Surg Med. 2019;3(3):227-230. Research article DOI: 10.28982/josam.503850 Araştırma makalesi Evaluation of clinical and laboratory findings of 147 patients with systemic lupus erythematosus: The relationship between anti-CCP and arthritis Sistemik lupus eritematozuslu 147 hastanın klinik ve laboratuvar bulgularının değerlendirilmesi: Anti CCP ile artrit arasındaki ilişkinin incelenmesi Ali Ekin 1, Ayşe Ergüney Çefle 2 1 Department of Internal Medicine, Bingol Abstract State Hospital, Bingol, Turkey Aim: Anti-cyclic citrullinated peptide antibodies (Anti-CCP) is considered as a novel marker in the assessment of 2 Department of Internal Medicine, Division of Rheumatology, Faculty of Medicine, Kocaeli rheumatoid disorders. Some studies have emphasized the importance of anti-CCP in indicating erosive arthropathy in University, Kocaeli, Turkey Systemic Lupus Erythematosus (SLE), like Rheumatoid Arthritis (RA). These studies have reported that the chance of erosive arthritis development is significantly increased in anti-CCP-positive patients. This study aimed to investigate ORCID ID of the author(s) the relationship between anti-CCP and arthritis along with other clinical and laboratory parameters in patients with AE: 0000-0003-3692-1293 SLE. AEÇ: 0000-0002-3273-7969 Methods: A total of 147 SLE patients who had been admitted to Kocaeli University Medical Faculty, Department of Internal Medicine, Division of Rheumatology between January 2001 and October 2015 were included in this retrospective study. SLE diagnosis was verified according to American College of Rheumatology (ACR) and/or The Systemic Lupus Erythematosus International Collaborating Clinics (SLICC) criteria. Patients whose diagnosis was not definite and not having anti-CCP were excluded. Results: Female/male ratio was found as 5.6, and the mean age was calculated as 43.9±11.85 years.
    [Show full text]
  • Northwestern Medicine
    How to put in your own Photo: Go to ‘View-Slide Master’ Go to ‘Insert-Picture’ Browse to the image you would like to place. Image should be 1024x768, 1200x900, or other 4:3 aspect ratio Select image and click OK Scale to full screen size if To live with lupus, necessary. Click image, go to ‘Format- we need to know Send to Back’ about lupus. Zineb Aouhab, MD Assistant Professor of Medicine Loyola University Medical Center 1 Division of Rheumatology Where did the word “lupus” come from? • The word ‘lupus’ is derived from the Latin word for “wolf”. • Named in the 13th century by the physician “Rogerius”. • He described the rash as erosive facial lesions as a consequence of a wolf's bite. • The facial rash is also called “Butterfly rash” because it resembles a butterfly shape. 2 What is lupus? • Lupus is an autoimmune disease. • It causes chronic inflammation in the body. • It can affect any organ of the body such as the kidneys, gastrointestinal tract, lungs, heart, and joints. 3 What happens in the body? • In normal people, the immune system forms antibodies to fight against infections. • In people with lupus, the immune system become overactive (like a bad allergic reaction) and produces a different types of antibodies. • These antibodies attack the person’s own organs causing organ damage. 4 Factors to consider in lupus • Lupus usually appears between the age of 15-45. • Lupus is much more common in females compared to males. Ratio 9:1 • Lupus is characterized by episodes of flares (when people feel very ill) and periods of remission (when people feel well and back to baseline).
    [Show full text]
  • 24 Lupus Anticoagulants: Mechanistic and Diagnostic Considerations Jef M
    24 Lupus Anticoagulants: Mechanistic and Diagnostic Considerations Jef M. M. C. Arnout and Jos Vermylen Introduction Antiphospholipid syndrome (APS) is defined as the association of antiphospholipid antibodies (aPL) with arterial or venous thrombosis, recurrent foetal loss, thrombo- cytopenia, or neurological disorders [1–3]. The gradual development of the notion APS started in the 1950ss with the recognition of two laboratory curiosities in a subset of patients with systemic lupus erythematosus (SLE). In these patients, rheumatologists frequently found a chronic biological false positive test for syphilis, whereas hematologists described a non-specific coagulation inhibitor manifested by prolongation of the whole blood clotting time and the prothrombin time, without reduction of any specific clotting factor then measurable [1–3]. The non-specific coagulation inhibitor which appeared not to be associated with a bleeding tendency was named the “lupus anticoagulant” by Feinstein and Rapaport [4] and was regarded as a laboratory curiosity until Bowie et al [5] drew the attention to the high prevalence of thrombotic complications in SLE patients with this “anticoagu- lant.” The LA was later also found to be associated with obstetric complications and thrombocytopenia [6]. Only in the 1980s did it became clear that antibodies interacting with anionic phospholipids are responsible for the in vitro LA effect and the chronic biological false positive syphilis serology [7]. This led to the development of better-defined LA tests and the so-called anticardiolipin test in which antibodies binding to solid phase cardiolipin (aCL) are measured [8, 9]. With these improved assays, the majority of SLE patients with a LA also had elevated aCL levels and a statistically significant relation between these 2 types of aPL was observed.
    [Show full text]
  • A Rare Case of Overlapping Syndrome of ANCA-Associated Glomerulonephritis and Copyright: Systemic Lupus Erythematosus © 2018 Jessica F, Et Al
    www.symbiosisonline.org Symbiosis www.symbiosisonlinepublishing.com Case Report Journal of Rheumatology and Arthritic Diseases Open Access A Rare Case of Overlapping Syndrome of ANCA- Associated Glomerulonephritis and Systemic Lupus Erythematosus Jessica Frey1* and Hajra Shah2 1Neurology Resident, Department of Neurology, West Virginia University, 1 Medical Center Drive, Morgantown WV 26505 USA 2Assistant Professor of Medicine, Department of Rheumatology, West Virginia University, 1 Medical Center Drive, Morgantown WV 26505 USA Received: June 15, 2018; Accepted: July 15, 2018; Published: July 23, 2018 *Corresponding author: Jessica Frey, MD, 99 Lakeside Drive, Morgantown WV 26508, USA. Tel: 412-523-8284; Fax: 304-598-6442; E-mail: [email protected] Abstract mechanisms, prognosis, and management of these two conditions, especially in context of one another. Introduction: Two very interesting rheumatologic diagnoses include Systemic Lupus Erythematosus (SLE) and Anti-Neutrophil Case Report Cytoplasmic Antibody (ANCA)-negative Vasculitis. It is rare to see these two conditions diagnosed in the same patient. This case analyzes We present the case of a 69 year old female with two the complex interactions between these two disease states. simultaneous new diagnoses of SLE and ANCA-negative Vasculitis. Case: This is the case of a 69 year old female who presented with shortness of breath, hematuria, and renal failure. Lab work was pulmonaryHer past medical hypertension. history Herwas presentingsignificant forsymptoms hypothyroidism, included gastro esophageal reflux disease, and recently diagnosed antibody, normal complement levels and a negative Vasculitis panel. one week of increasing shortness of breath, pleuritic chest pain, Renalsignificant biopsy for was elevated consistent ANA (1:1280),with ANCA-associated positive double-stranded Vasculitis (AAV).
    [Show full text]
  • Autoantibodies Diagnostic Tools for Autoimmune Disorders
    Autoantibodies Diagnostic tools for autoimmune disorders What are autoantibodies? Despite these limitations, autoantibodies are a valuable tool for the diagnosis (when considered with other clinical Autoantibodies bind non-foreign structures within us and have and laboratory information) and monitoring of many been found in most well-defined autoimmune disorders. They autoimmune disorders. also occur in other disorders with an inflammatory component and even in some malignant disorders as paraneoplastic phenomena. How is tissue injury caused in With a few important exceptions, autoantibodies have no direct autoimmune disorders? Are role in pathogenesis and their main value is as a ‘marker’ adding autoantibodies always pathological? weight to a clinical diagnoses. Much tissue damage in autoimmune diseases is probably Circulating forms of autoantibodies may be detected by mediated by T cells and their effector mechanisms, rather than assays on serum. Tissue-bound antibodies may also be by B cells and their products, autoantibodies. Systemic lupus detected by direct immunofluorescence studies of non-fixed erythematosus and other connective tissue disorders are biopsy specimens. characterised by polyclonal self-reactive B cell expansions. Normal immune system functions include the recognition of, and Do autoantibodies ever occur naturally, discrimination between, self and non-self targets and unleashing without clinical associations? of effector mechanisms, such as complement proteins, cytotoxic T cells, cytokines and other phagocytic cells onto non-self Low-level autoantibodies occur naturally and more commonly in targets. persons who are older, female, have chronic diseases and often a family history of autoimmune abnormalities. These natural Autoantibody production is a consequence of ongoing autoantibodies occur in low concentrations and have weak recognition of self targets by both T and B cells.
    [Show full text]
  • Colonic Ulcers in Propylthiouracil Induced Vasculitis with Secondary
    338 ADVERSE DRUG REACTION Postgrad Med J: first published as 10.1136/pgmj.2004.026104 on 5 May 2005. Downloaded from Colonic ulcers in propylthiouracil induced vasculitis with secondary antiphospholipid syndrome P D Gaburri, J M F Chebli, Aˆ Attalla, C M N Pereira, H L Bonfante, E V Martins Junior, A K Gaburri ............................................................................................................................... Postgrad Med J 2005;81:338–340. doi: 10.1136/pgmj.2004.026104 migratory polyarthritis, and fever during the past 15 months. A 48 year old white woman was admitted to the hospital She was taking propylthiouracil 100 mg a day over a period because of several bouts of migratory polyarthritis, weight of three years for hyperthyroidism. The symptoms had loss, fever, and abdominal pain over a period of 15 months. worsened in the past two months and an intense deteriora- She had been taking propylthiouracil 100 mg daily for three tion of general physical state occurred. She needed frequent years for hyperthyroidism treatment. A test for antineutrophil use of opioids orally in the past two weeks to relieve cytoplasmic autoantibodies (ANCA) was positive with a abdominal pain. There was no blood or mucus in the stools. perinuclear pattern of staining. Antiphospholipid antibodies On admission she was pale—haemoglobin concentration were also detected. Colonoscopy showed several ulcers on 9.4 g%—and her temperature was 38˚C. Blood pressure was intestinal mucosa and the biopsy specimen showed intense 120/80 mm Hg and a painful hepatomegaly was noticed. The microscopic vasculitis. The patient is well after methylpredni- spleen was felt 7 cm below the left costal margin and an solone pulse therapy and eight months of oral azathioprine.
    [Show full text]