Indian Journal of Nephrology About us |  Subscription |  e-Alerts  | Feedback | Login   
  Print this page Email this page   Small font sizeDefault font sizeIncrease font size
 Home | Current Issue | Archives| Ahead of print | Search |Instructions |  Editorial Board  

Users Online:465

Official publication of the Indian Society of Nephrology
  Search
 
  
 ~  Similar in PUBMED
 ~  Search Pubmed for
 ~  Search in Google Scholar for
 ~Related articles
 ~  Article in PDF (690 KB)
 ~  Citation Manager
 ~  Access Statistics
 ~  Reader Comments
 ~  Email Alert *
 ~  Add to My List *
* Registration required (free)  

 
   Abstract
  Introduction
  Case Report
  Discussion
   References
   Article Figures

 Article Access Statistics
    Viewed568    
    Printed4    
    Emailed0    
    PDF Downloaded22    
    Comments [Add]    

Recommend this journal

 


 
  Table of Contents  
CASE REPORT
Year : 2017  |  Volume : 27  |  Issue : 1  |  Page : 81-83
 

Thrombotic microangiopathy: An unusual cause of renal failure in rheumatoid arthritis


Department of Nephrology, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu, India

Date of Web Publication2-Jan-2017

Correspondence Address:
J Dhanapriya
Department of Nephrology, Madras Medical College and Rajiv Gandhi Government General Hospital, Chennai, Tamil Nadu
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-4065.179207

Rights and Permissions

  Abstract 


Rheumatoid arthritis (RA) is one of the commonest rheumatological diseases. Renal involvement is not common but can occur as a result of chronic inflammation as part of disease process or drug toxicity. Thrombotic microangiopathy (TMA) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ failure of variable severity. Only a few cases of TMA in patients with RA were reported to date. We describe a 45-year-old female patient with RA who presented with oliguria and edema. Renal biopsy showed TMA with patchy cortical necrosis. She improved with hemodialysis and plasmapheresis.


Keywords: Hemodialysis, plasmapheresis, renal biopsy, rheumatoid arthritis


How to cite this article:
Sakthirajan R, Dhanapriya J, Dineshkumar T, Gopalakrishnan N, Murugan S, Balasubramaniyan T. Thrombotic microangiopathy: An unusual cause of renal failure in rheumatoid arthritis. Indian J Nephrol 2017;27:81-3

How to cite this URL:
Sakthirajan R, Dhanapriya J, Dineshkumar T, Gopalakrishnan N, Murugan S, Balasubramaniyan T. Thrombotic microangiopathy: An unusual cause of renal failure in rheumatoid arthritis. Indian J Nephrol [serial online] 2017 [cited 2017 Apr 29];27:81-3. Available from: http://www.indianjnephrol.org/text.asp?2017/27/1/81/179207





  Introduction Top


Renal disease in rheumatoid arthritis (RA) is usually asymptomatic and is detected only on biochemical investigations.[1] Manifestations include glomerulonephritis, amyloidosis, tubulointerstitial nephritis, and drug toxicity.[2] Thrombotic microangiopathy (TMA) results in thrombocytopenia, microangiopathic hemolytic anemia (MAHA), and thrombotic occlusion of the microvasculature.[3] Primary TMA includes hemolytic-uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP). Secondary TMA is associated with neoplasia, autoimmune diseases (antiphospholipid antibody syndrome, systemic lupus erythematosus (SLE), and others), infections, and drugs.[4] We report here a female patient with RA who developed TMA and improved subsequently with plasmapheresis.


  Case Report Top


A 45-year-old woman presented with oliguria and edema for 2 days. She was known to have RA and was taking oral steroids and diclofenac tablets on and off as self-medication. There was no history of diarrhea, fever, native medication, or any other drug intake. On examination, she had edema legs, pulse rate of 80/min, and blood pressure of 130/80 mm/Hg. Urinalysis showed 3 + protein, 5–6 red cells/hpf; urine protein creatinine ratio 2.8. Hemoglobin was 9.2 g/dl; total count 5600/cu.mm; platelet count 80,000/cu.mm; peripheral smear numerous schistocytes; blood urea 200 mg/dl; serum creatinine 12 mg/dl; prothrombin time 12.3 s; INR 0.9; activated partial thromboplastin time 38.5 s; serum lactate dehydrogenase (LDH) 931 IU/L; total bilirubin1.2 mg/dl; indirect bilirubin 0.8 mg/dl; and direct Coomb's test negative. She received supportive treatment and was started on hemodialysis. Rheumatoid factor and anti-cyclic citrullinated peptide antibodies were positive; antinuclear antibody (ANA) and anti dsDNA antibody were negative. Serum C3 and C4 levels were normal. Anti– Sjogren's syndrome related antigen A (SSA), anti-Sjogren's syndrome related antigen B (SSB), anti-SM, anti-U1RNP anti-JO antibodies and serum antineutrophil cytoplasmic antibodies were negative. Antiphospholipid, anticardiolipin, and lupus anticoagulant antibodies were also negative.

Renal biopsy revealed patchy cortical necrosis, fibrin thrombi, and fragmented red blood cells (RBCs) [Figure 1] occluding capillary loops in 4/7 glomeruli. Interstitial hemorrhage and edema were observed. Tubular epithelial cells showed signs of acute injury. Subintimal swelling was noted in arterioles. Immunofluorescence was negative for all stains. She received totally 6 sessions of plasmapheresis (two plasma volume exchanges each time) after which her platelet count and LDH levels were normalized. She was started on 1 mg/kg/day prednisolone tapered over next 6 months. Her renal failure improved and was discharged with serum creatinine of 2.2 mg/dl. She was started on methotrexate and at 2 years after presentation, her creatinine was 1.5 mg/dl without further recurrence of TMA.
Figure 1: Renal biopsy showing fibrin thrombi and fragmented red blood cells in glomerulus (H and E)

Click here to view



  Discussion Top


RA is a chronic systemic disease characterized by persistent inflammatory synovitis, involving peripheral joints in a symmetric distribution. RA affects about 1% of the population.[5] TMA was defined as pathological lesions characterized by endothelial injury and platelet-rich thrombi formation in microvasculature, leading to MAHA, thrombocytopenia, and end-organ ischemic damages.[6] Amorosi and Ultmann defined the classic pentad of thrombocytopenia, MAHA, acute renal impairment, neurologic abnormalities, and fever.[7] However, the dyad of otherwise unexplained thrombocytopenia and MAHA are sufficient to diagnose of TMA.[8]

Although TMA occurs in association with connective tissue disorders (CTDs), TMA in RA is rarely reported. To our knowledge, only two case reports and a case study [9],[10],[11] with RA and TMA have been described so far. Nomura et al.[9] published a case report of a 35-year-old female patient with RA presenting with TMA and antiphospholipid syndrome. She had thrombocytopenia, positivity for lupus anticoagulant and ANA. She was treated successfully with monthly cyclophosphamide pulse therapy. Kfoury Baz et al. reported another female patient presenting with TTP at 18 months after onset of RA. She was tested negative for ANA and antiphospholipid antibodies and was treated with plasma exchanges and glucocorticoids.[10]

The pathogenetic mechanisms behind the development of TMA in RA are linked to severe deficiency of ADAMTS13 (a disintegrin and metalloprotease with thrombospondin-1-like domains) due to autoantibodies that alter its function.[9],[10] ADAMTS13 is a plasma enzyme involved in cleavage of unusually large (UL) von Willebrand factor (vWF) multimers into smaller and less adhesive vWF forms. Failure to degrade these UL-vWF multimers leads to excessive platelet aggregation and microvascular occlusion.

In a study of 127 patients with CTD and TMA including 10 patients with RA, severe deficiency of ADAMTS13 activity was seen and was closely associated with the presence of anti-ADAMTS13 IgG antibodies.[11] Therapeutic plasma exchange resulted in high remission rate in patients with SLE than in patients with RA.

Our patient, who had RA for 5 years, presented with features suggestive of TMA. Renal biopsy showed platelet-fibrin thrombi and fragmented RBCs in glomeruli and patchy cortical necrosis. The possibility of SLE, mixed connective tissue disorder, antiphospholipid syndrome, and drug-induced TMA was ruled out. However, atypical HUS, which may have been unmasked by the inflammatory process in this patient, could not be ruled out. Testing for ADAMTS13 deficiency, antibodies against ADAMTS13, factor H and anti-factor H autoantibodies was not done due to logistic reasons. She was treated with high-dose steroids and plasmapheresis following which her renal function improved. She was started on methotrexate due to high disease activity and currently on follow-up. To conclude, the possibility of renal TMA should be considered in RA patients who present with renal failure as timely diagnosis and treatment with plasmapheresis improve the long-term renal outcome.

Acknowledgment

We would like to thank Dr. Anila Abraham Kurien, Nephropathologist, Center for Renal and Urological Pathology Pvt Ltd, Chennai, for her help in renal biopsy evaluation.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
Boers M. Renal disorders in rheumatoid arthritis. Semin Arthritis Rheum 1990;20:57-68.  Back to cited text no. 1
    
2.
Helin HJ, Korpela MM, Mustonen JT, Pasternack AI. Renal biopsy findings and clinicopathologic correlations in rheumatoid arthritis. Arthritis Rheum 1995;38:242-7.  Back to cited text no. 2
    
3.
Barbour T, Johnson S, Cohney S, Hughes P. Thrombotic microangiopathy and associated renal disorders. Nephrol Dial Transplant 2012;27:2673-85.  Back to cited text no. 3
    
4.
Portolés J, de Tomás E, Espinosa A, Gallego E, Nieva GS, Blanco J. Thrombotic thrombocytopenic purpura and acute renal failure in adult Still's disease. Nephrol Dial Transplant 1997;12:1471-3.  Back to cited text no. 4
    
5.
Lee DM, Weinblatt ME. Rheumatoid arthritis. Lancet 2001;358:903-11.  Back to cited text no. 5
    
6.
George JN, Kremer Hovinga JA, Terrell DR, Vesely SK, Lämmle B. The oklahoma thrombotic thrombocytopenic purpura-hemolytic uremic syndrome registry: The Swiss connection. Eur J Haematol 2008;80:277-86.  Back to cited text no. 6
    
7.
Amorosi EL, Ultmann JE. Thrombotic thrombocytopenic purpura: Report of 16 cases and review of literature. Medicine 1966;45:139-59.  Back to cited text no. 7
    
8.
George JN. Clinical practice. Thrombotic thrombocytopenic purpura. N Engl J Med 2006;354:1927-35.  Back to cited text no. 8
    
9.
Nomura M, Okada J, Tateno S, Kobayashi Y, Kondo H. Renal thrombotic microangiopathy in a patient with rheumatoid arthritis and antiphospholipid syndrome: Successful treatment with cyclophosphamide pulse therapy and anticoagulant. Intern Med 1994;33:484-7.  Back to cited text no. 9
    
10.
Kfoury Baz EM, Mahfouz RA, Masri AF. Thrombotic thrombocytopenic purpura in a patient with rheumatoid arthritis treated by plasmapheresis. Ther Apher 1999;3:314-6.  Back to cited text no. 10
    
11.
Matsuyama T, Kuwana M, Matsumoto M, Isonishi A, Inokuma S, Fujimura Y. Heterogeneous pathogenic processes of thrombotic microangiopathies in patients with connective tissue diseases. Thromb Haemost 2009;102:371-8.  Back to cited text no. 11
    


    Figures

  [Figure 1]



 

Top
Print this article  Email this article
 

    

Indian Journal of Nephrology
Published by Wolters Kluwer - Medknow
Online since 20th Sept '07