Neuropediatrics 2000; 31(2): 108
DOI: 10.1055/s-2000-7484
Letter to the Editor

Georg Thieme Verlag Stuttgart · New York

Sydenham Chorea or Primary Antiphospholipid Syndrome?

U. Kiechl-Kohlendorfer1 , H. Ellemunter1 , S. Kiechl 2
  • 1 Department of Pediatrics, University of Innsbruck, Austria
  • 2 Department of Neurology, University of Innsbruck, Austria
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Sir,

We appreciate the comment of Al-Matar et al. On emphasising Sydenham chorea as an important differential diagnosis to chorea in primary antiphospholipid syndrome (PAPS), they raised an important issue. Both conditions have been proposed as sharing similar pathogenetic mechanisms involving antineuronal antibodies [[5], [8]]. Actually, it may be difficult to differentiate these diseases without an extensive laboratory work-up and long-term monitoring of given patients. According to the modified Jones criteria [[2]] Sydenham chorea is the exclusion diagnosis suitable even in the absence of specific confirmatory findings, and PAPS ranks among the various other diagnoses to be ruled out.

As to our patients [[6]], several lines of evidence are in conflict with the diagnosis of Sydenham chorea: 1. Two patients had typical features of PAPS distinct from chorea, even if these abnormalities were only mildly expressed: One exhibited thrombocytopenia while the other experienced steadily deteriorating valvulitis and, recently, an episode of spontaneous cerebral venous sinus thrombosis; 2. Although aCL antibodies may temporarily occur at high titers in rheumatic fever [[4]] long-term persistence, as required for the diagnosis of PAPS, has not yet been reported. In the series of patients from Chile cited by Al-Matar and co-workers levels of aCL antibodies of patients with Sydenham chorea normalised within 132 days after disease onset [[4]]. Other investigators altogether failed to find high aCL antibody levels in patients with rheumatic fever [[1], [3], [7]]. Furthermore, presence of lupus anticoagulant is an unusual finding in rheumatic fever. Our patients all showed consistently elevated aCL antibody titers for ≥ six months and one was positive for the lupus anticoagulant [[6]].

In all, according to the current diagnostic criteria the illness of our patients must be classified as PAPS. We agree, however, with Al-Matar et al that whenever uncertainties remain about the correct diagnostic attribution (e.g. at the first visit), antibiotic prophylaxis should not be denied.

References

  • 1 Asherson R A, Hughes G RV, Gledhill R, Quinn N P. Absence of antibodies to cardiolipin in patients with Huntington's chorea, Sydenham's chorea and acute rheumatic fever.  J Neurol Neurosurg Psychiatry. 1988;  51 1458
  • 2 Dajani A S, Ayoub E, Bierman F Z, Bisno A L, Denny F W, Durack D T. et al . Guidelines for the diagnosis of rheumatic fever: Jones Criteria, updated 1992, American Heart Association.  Circulation. 1993;  87 302-307
  • 3 Diniz R E, Goldenberg J, Andrade L E, Leser P G, Silva N P, Roizenblatt S. et al . Antiphospholipid antibodies in rheumatic fever chorea.  J Rheumatol. 1994;  21 1367-1368
  • 4 Figueroa F, Berrios X, Gutierrez M, Carrion F, Goycolea J P, Riedel I. et al . Anticardiolipin antibodies in acute rheumatic fever.  J Rheumatol. 1992;  19 1175-1180
  • 5 Furie R, Ishikawa T, Dhawan V, Eidelberg D. Alternating hemichorea in primary antiphospholipid syndrome: evidence for contralateral striatal hypermetabolism.  Neurology. 1994;  44 2197-2199
  • 6 Kiechl-Kohlendorfer U, Ellemunter H, Kiechl S. Chorea as the presenting clinical feature of primary antiphospholipid syndrome in childhood.  Neuropediatrics. 1999;  30 66-98
  • 7 Narin N, Kutukculer N, Narin F, Keser G, Doganavsargil E. Anticardiolipin antibodies in acute rheumatic fever and chronic rheumatic heart disease: is there a significant association?.  Clin Exp Rheumatol. 1996;  14 567-569
  • 8 Weindl A, Kuwert T, Leenders K L, Poremba M, Grafin von Einsiedel H, Antonini A. et al . Increased striatal glucose consumption in Sydenham's chorea.  Mov Disord. 1993;  8 437-444

U. Kiechl-Kohlendorfer1
H. Ellemunter1
S. Kiechl2

1 Department of Pediatrics 2 Department of Neurology, University of Innsbruck

Anichstrasse 35

6020 Innsbruck

Austria

    >