Preview

Current Pediatrics

Advanced search

Severe Antiphospholipid Syndrome in a Child with Chicken Pox: Clinical Case

https://doi.org/10.15690/vsp.v23i4.2769

Abstract

Background. Antiphospholipid syndrome develops at autoimmune diseases, pregnancy, or genetic predisposition, and it is characterized by high risk of thrombosis in arterial, venous, and capillary vessels. This syndrome in children is rare, and necrotic skin lesions occur in the most extreme cases. Clinical case description. A child, 1 year old, with chicken pox has developed hemorrhagic rash on his back, swelling of the left shoulder and forearm on the 4th day of the disease. Medical treatment included acyclovir, ceftriaxone, sodium heparin. Aggravation of hemorrhagic rash over the body, spread of edema from the left shoulder to upper arm and neck, formation of flaccid bubble and necrosis locus (75 cm) on the outer upper third of the left shoulder were noted on the 5th-6th day. Increase in the levels of antibodies to 2-glycoprotein I (IgG — 48.9 U/ml, IgM — > 100 U/ml) and cardiolipin (IgM — 73.0 U/ml) was revealed. The diagnosis “antiphospholipid syndrome” was established. All necrotized tissues were removed on the 11th day, and the wound defect (86 cm) was subsequently covered by mesh skin grafts. The levels of antibodies (IgG + IgM) to 2-glycoprotein I remained high, 45.2 U/mL, 12 weeks after the onset of the disease. Thus, it has confirmed the development of antiphospholipid syndrome. The child continued treatment with warfarin (3.75 mg/day) with INR control. Conclusion. Hemorrhagic skin lesions in children with infectious diseases requires laboratory diagnostics of antiphospholipid syndrome, early prescription of anticoagulant and antiplatelet therapy, and surgical support.

About the Authors

Elena M. Kamaltynova
Regional Children’s Hospital ; Siberian State Medical University
Russian Federation

Tomsk


Disclosure of interest:

Not declared. 



Roman V. Bocharov
Regional Children’s Hospital ; Siberian State Medical University ; Emergency Hospital No.2
Russian Federation

Tomsk 


Disclosure of interest:

Not declared. 



Vladimir G. Pogorelko
Siberian State Medical University ; Emergency Hospital No.2
Russian Federation

Tomsk


Disclosure of interest:

Not declared. 



Tatyana V. Zgerskay
G.E. Sibirtsev Children’s Infectious Diseases Hospital
Russian Federation

Tomsk


Disclosure of interest:

Not declared. 



References

1. Soybilgic A, Avcin T. Pediatric APS: State of the Art. Curr Rheumatol Rep. 2020;22(3):9. doi: https://doi.org/10.1007/s11926-020-0887-9

2. Kornyushina EA. Current approaches to treatment of antiphospholipid syndrome during pregnancy: a case report. Journal of Obstetrics and Women’s Diseases. 2018;67(6):100–105. (In Russ). doi: https://doi.org/10.17816/JOWD676100-105

3. Reshetnyak TM, Cheldieva FA, Nurbayeva KS, et al. Antiphospholipid syndrome: diagnosis, mechanism of development, issues of therapy. Tromboz, gemostaz I reologiya. 2020;(4):4–21. (In Russ). doi: https://doi.org/10.25555/THR.2020.4.0940

4. Sayar Z, Moll R, Isenberg D, Cohen H. Thrombotic antiphospholipid syndrome: A practical guide to diagnosis and management. Thromb Res. 2021;198:213–221. doi: https://doi.org/10.1016/j.thromres.2020.10.010

5. Aguiar CL, Soybilgic A, Avcin T, Myones BL. Pediatric antiphospholipid syndrome. Curr Rheumatol Rep. 2015;17(4):27. doi: https://doi.org/10.1007/s11926-015-0504-5

6. Avcin T, Cimaz R, Rozman B. The Ped-APS Registry: the antiphospholipid syndrome in childhood. Lupus. 2009;18(10): 894–899. doi: https://doi/prg/10.1177/0961203309106917

7. Madison JA, Gockman K, Hoy C, et al. Pediatric antiphospholipid syndrome: clinical features and therapeutic interventions in a single center retrospective case series. Pediatr Rheumatol Online J. 2022;20(1):17. doi: https://doi.org/10.1186/s12969-022-00677-8

8. Wincup C, Ioannou Y. The Differences Between Childhood and Adult Onset Antiphospholipid Syndrome. Front Pediatr. 2018;6:362. doi: https://doi.org/10.3389/fped.2018.00362

9. Hosseini NS, Babael S, Ramini H, et al. Cutaneous microvascular occlusion syndrome as the first manifestation of catastrophic lupusassociated antiphospholipid antibody syndrome: a case report. J Med Case Rep. 2023;17(1):375. doi: https://doi.org/10.1186/s13256-023-04068-9

10. Abdel-Wahab N, Lopez-Olivo MA, Pinto-Patarroyo GP, SuarezAlmazor ME. Systematic review of case reports of antiphospholipid syndrome following infection. Lupus. 2016;25(14):1520–1531. doi: https://doi.org/10.1177/0961203316640912

11. Reshetnyak TM. Antiphospholipid syndrome: diagnosis and clinical manifestations (a lecture). Rheumatology Science and Practice. 2014;52(1):56–71. (In Russ). doi: https://doi.org/10.14412/1995-4484-2014-56-71

12. Reshetnyak TM, Shcherbakova MYu, Zhdanova LV, Nasonov EL. Antiphospholipid syndrome, antiphospholipid antibodies and genetic thrombophilia in children with somatic pathology. Rheumatology Science and Practice. 2008;46(4):48–57. (In Russ). doi: https://doi.org/10.14412/1995-4484-2008-536

13. Tectonidou MG, Andreoli L, Limper M, et al. General recommendations for the treatment of antiphospholipid syndrome in adults. Ann Rheumdis. 2019;78(10):1296–1304. doi: https://doi.org/10.1136/annrheumdis-2019-215213

14. Madison JA, Zuo Y, Knight JS. Pediatric antiphospholipid syndrome. Eur J Rheumatol. 2020;7(Suppl 1):S3–S12. doi: https://doi.org/10.5152/eurjrheum.2019.19160

15. Demir S, Keskin A, Sağ E, et al. The challenges in diagnosing pediatric primary antiphospholipid syndrome. Lupus. 2022;31(10): 1269–1275. doi: https://doi.org/10.1177/09612033221108853

16. Khalimova FT. Immuno-genetic markers of hereditary predisposition to antiphospholipid reaction. Vestnik Akademii meditsinskikh nauk Tadzhikistana. 2017;(4):82–85. (In Russ).

17. Bitsadze V, Yakubova F, Khizroeva J, et all. Catastrophic Antiphospholipid Syndrome. Int J Mol Sci. 2024;25(1):668. doi: https://doi.org/10.3390/ijms25010668

18. Shcherbakova MYu, Reshetnyak TM, Zhdanova LV. Antiphospholipid syndrome in children with somatic pathology. Pediatria. Journal n.a. G.N. Speransky. 2008;87(4): 119–124. (In Russ).

19. Rosina S, Chighizola CB, Ravelli A, Cimaz R. Pediatric Antiphospholipid Syndrome: from Pathogenesis to Clinical Management. Curr Rheumatol Rep. 2021;23(2):10. doi: https://doi.org/10.1007/s11926-020-00976-7

20. Theron A, Dautremay O, Boissier E, et al. Idiopathic purpura fulminans associated with anti-protein S antibodies in children: a multicenter case series and systematic review. Blood Adv. 2022;6(2):495–502. doi: https://doi.org/10.1182/bloodadvances.2021005126

21. Chen L, Yin J, Liu X, et al. Thromboembolic complications of Mycoplasma pneumoniae pneumonia in children. Clin Respir J. 2023;17(3):187–196. doi: https://doi.org/10.1111/crj.13584

22. Theron A, Ayadi S, Boissier E, et al. Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies. Front Pediatr. 2023;11:1197795. doi: https://doi.org/10.3389/fped.2023.1197795

23. Campanelli A, Kaya G, Ozsahin AH, et al. Purpura fulminans in a child as a complication of chickenpox infection. Dermatology. 2004;208(3):262–264. doi: https://doi.org/10.1159/000077315

24. Negrini S, Pappalardo F, Murdaca G, et al. The antiphospholipid syndrome: from pathophysiology to treatment. Clin Exp Med. 2017;17(3):257–267. doi: https://doi.org/10.1007/s10238-016-0430-5

25. Amoura Z, Bader-Meunier B, Bal Dit Soller C, et al. French National Diagnostic and Care Protocol for antiphospholipid syndrome in adults and children. Rev Med Interne. 2023;44(9):495–520. doi: https://doi.org/10.1016/J.REVMED.2023.08.004


Review

For citations:


Kamaltynova E.M., Bocharov R.V., Pogorelko V.G., Zgerskay T.V. Severe Antiphospholipid Syndrome in a Child with Chicken Pox: Clinical Case. Current Pediatrics. 2024;23(4):234-240. (In Russ.) https://doi.org/10.15690/vsp.v23i4.2769

Views: 315


ISSN 1682-5527 (Print)
ISSN 1682-5535 (Online)