A clinical case of morphea associated with Borrelia infection

DOI: https://doi.org/10.29296/25877305-2023-08-16
Issue: 
8
Year: 
2023

M. Abo Khadeejeh(1); I. Olenich(2); Z. Niewozinska(2); PhD; Professor I. Korsunskaya(3), MD
1-Peoples’ Friendship University of Russia, Moscow
2-Moscow Research and Practical Center of Dermatovenereology
and Cosmetology, Moscow Healthcare Department
3-Center for Theoretical Problems of Physicochemical Pharmacology,
Russian Academy of Sciences, Moscow

Scleroderma is an inflammatory disease that is evident as skin atrophy. The pathogenesis of scleroderma remains not completely understood. It is agreed that this disease arises from vascular changes, impaired fibroblast function, and immune dysfunction. The scientific literature also widely discusses an association between scleroderma and Borrelia infection. To date, there is no consensus regarding the mechanism of the influence of Lyme disease on the development of focal scleroderma. However, multiple cases of its occurrence after tick bites have been described. The authors want to draw the attention of specialists to this problem, by presenting their own case from practice. A thorough history collection and examination of patients with focal scleroderma are necessary in order to detect Borrelia infection and, conversely, there is a need for the close monitoring of patients with Lyme disease for the timely initiation of therapy for focal scleroderma.

Keywords: 
morphea
focal scleroderma
borreliosis
Lyme disease
methotrexate.



References: 
  1. Jindal A.K., Handa S., Loganathan S.K. et al. Juvenile localized scleroderma: A single-centre experience from India. J Eur Acad Dermatol Venereol. 2023; 37 (3): 598–604. DOI: 10.1111/jdv.18765
  2. Jeon H., Kim C. Methotrexate for localized morphea with severe pain: A case report. Dermatol Online J. 2011; 17 (12): 12. DOI: 10.5070/D33c09t6cd
  3. Laxer R.M., Zulian F. Localized scleroderma. Curr Opin Rheumatol. 2006; 18 (6): 606–13. DOI: 10.1097/01.bor.0000245727.40630.c3
  4. Abbas L.F., Coias B.A., Jacobe B.A. et al. Hyaluronidase injections for treatment of symptomatic pansclerotic morphea-induced microstomia. JAAD Case Rep. 2019; 5 (10): 871–3. DOI: 10.1016/j.jdcr.2019.08.004
  5. Möhrenschlager M., Jung C., Ring J. et al. Effect of penicillin G on corium thickness in linear morphea of childhood: an analysis using ultrasound technique. Pediatric Dermatol. 1999; 16 (4): 314–6. DOI: 10.1046/j.1525-1470.1999.00082.x
  6. Zulian F., Vallongo C., Woo P. et al. Localized scleroderma in childhood is not just a skin disease. Arthritis Rheum. 2005; 52 (9): 2873–81. DOI: 10.1002/art.21264
  7. Aberer E., Kollegger H., Kristoferitsch W. et al. Neuroborreliosis in morphea and lichen sclerosus et atrophicus. J Am Acad Dermatol. 1988; 19 (5 Pt 1): 820–5. DOI: 10.1016/s0190-9622(88)70239-x
  8. Zulian F., Vallongo C., Patrizi A. et al. A long-term follow-up study of methotrexate in juvenile localized scleroderma (morphea). J Am Acad Dermatol. 2012; 67: 1151–6. DOI: 10.1016/j.jaad.2012.03.036
  9. Zulian F., Martini G., Vallongo C. et al. Methotrexate treatment in juvenile localized scleroderma: a randomized, double-blind, placebo-controlled trial. Arthritis Rheum. 2011; 63: 1998–2006. DOI: 10.1002/art.30264
  10. Schempp C., Bocklage H., Lange R. et al. Further evidence for Borrelia burgdorferi infection in morphea and lichen sclerosus et atrophicus confirmed by DNA amplification. J Invest Dermatol. 1993; 100 (5): 717–20. DOI: 10.1111/1523-1747.ep12472369
  11. Weide B., Walz T., Garbe C. Is morphoea caused by Borrelia burgdorferi? A review. Br J Dermatol. 2000; 142 (4): 636–44. DOI: 10.1046/j.1365-2133.2000.03407.x
  12. Aberer E., Neumann R., Stanek G. Is localised scleroderma a Borrelia infection? Lancet. 1985; 2 (8449): 278. DOI: 10.1016/s0140-6736(85)90329-0
  13. Aberer G., Stanek G. Histological evidence for spirochetal origin of morphea and lichen sclerosus et atrophicans. Am J Dermatopathol. 1987;9 (5): 374–9. DOI: 10.1097/00000372-198710000-00002
  14. Aberer E., Stanek G., Ertl M. et al. Evidence for spirochetal origin of circumscribed scleroderma (morphea). Acta Derm Venereol. 1987; 67 (3): 225–31.
  15. Weber K., Preac-Mursic V., Reimers C.D. Spirochetes isolated from two patients with morphea. Infection. 1988; 16 (1): 25–6. DOI: 10.1007/BF01646925
  16. Breier F.H., Aberer E., Stanek G. et al. Isolation of Borrelia afzelii from circumscribed scleroderma. Br J Dermatol. 1999; 140 (5): 925–30. DOI: 10.1046/j.1365-2133.1999.02828.x
  17. Aberer E., Klade H., Stanek G. et al. Borrelia burgdorferi and different types of morphea. Dermatologica. 1991; 182 (3): 145–54.
  18. Nakashima T., Maeda M., Hayashi T. et al. A case of generalized morphea with a high titer of anti-Borrelia burgdorferi antibodies. J Dermatol. 1999; 26 (12): 821–4. DOI: 10.1111/j.1346-8138.1999.tb02100.x
  19. Wojas-Pelc A., Wielowieyska-Szybińska D., Kiełtyka A. Presence of the antinuclear antibodies and antibodies to Borrelia burgdorferi among patients with morphea en plaque, deep linear scleroderma and atrophoderma Pasini-Pierini. Przegl Lek. 2002; 59 (11): 898–902.
  20. Ozkan S., Atabey N., Fetil E. et al. Evidence for Borrelia burgdorferi in morphea and lichen sclerosus. Int J Dermatol. 2000; 39 (4): 278–83. DOI: 10.1046/j.1365-4362.2000.00912.x
  21. Dillon W.I., Saed G.M., Fivenson D.P. Borrelia burgdorferi DNA is undetectable by polymerase chain reaction in skin lesions of morphea, scleroderma, or lichen sclerosus et atrophicus of patients from North America. J Am Acad Dermatol. 1995; 33 (4): 617–20. DOI: 10.1016/0190-9622(95)91281-9
  22. De Vito J.R., Merogi A.J., Vo T. et al. Role of Borrelia burgdorferi in the pathogenesis of morphea/scleroderma and lichen sclerosus et atrophicus: a PCR study of thirty-five cases. J Cutan Pathol. 1996; 23 (4): 350–8. DOI: 10.1111/j.1600-0560.1996.tb01309.x
  23. Fujiwara H., Fujiwara K., Hashimoto K. et al. Detection of Borrelia burgdorferi DNA (B garinii or B afzelii) in morphea and lichen sclerosus et atrophicus tissues of German and Japanese but not of US patients. Arch Dermatol. 1997; 133 (1): 41–4.
  24. Balmelli T., Piffaretti J.C. Association between different clinical manifestations of Lyme disease and different species of Borrelia burgdorferi sensu lato. Res Microbiol. 1995; 146 (4): 329–40. DOI: 10.1016/0923-2508(96)81056-4
  25. Schmidt B.L. PCR in laboratory diagnosis of human Borrelia burgdorferi infections. Clin Microbiol Rev. 1997; 10 (1): 185–201. DOI: 10.1128/CMR.10.1.185
  26. Arocha-Sandoval F., Amesty-Valbuena A., Urbina M. et al. Detection of Borrelia burgdorferi antibodies in a population sample of the state of Zulia. Invest Clin. 1994; 35 (2): 91–104.
  27. Palacios R., Torres A., Trujillo R. IgG antibody reactivity to Borrelia burgdorferi sensu stricto antigens in patients with morphea in Colombia. Int J Dermatol. 2003; 42 (11): 882–6. DOI: 10.1046/j.1365-4362.2003.01901.x
  28. Mejia-Terrazas G.E., López-Ruiz V.G., Infante-Cosio G. et al. Spinal cord stimulation in teenager with complex regional pain syndrome for Lymes disease. Case report and review of the literature. Acta Ortop Mex. 2015; 29 (4): 228–31.
  29. Palacios R., Osorio L.E., Giraldo L.E. et al. Positive IgG Western blot for Borrelia burgdorferi in Colombia. Mem Inst Oswaldo Cruz. 1999; 94 (4): 499–503. DOI: 10.1590/s0074-02761999000400013
  30. Burkot T.R., Schriefer M.E., Larsen S.A. Cross-reactivity to Borrelia burgdorferi proteins in serum samples from residents of a tropical country nonendemic for Lyme disease. J Infect Dis. 1997; 175 (2): 466–9. DOI: 10.1093/infdis/175.2.466
  31. Brown S.L., Hansen S.L., Langone J.J. Role of serology in the diagnosis of Lyme disease. JAMA. 1999; 282 (1): 62–6. DOI: 10.1001/jama.282.1.62
  32. Molins C.R., Delorey M.J., Replogle A. et al. Evaluation of bioMérieux's Dissociated Vidas Lyme IgM II and IgG II as a First-Tier Diagnostic Assay for Lyme Disease. J Clin Microbiol. 2017; 55 (6): 1698–706. DOI: 10.1128/JCM.02407-16