Arquivos de Asma, Alergia e Imunologia
https://www.aaai-asbai.org.br/article/doi/10.5935/2526-5393.20170028
Arquivos de Asma, Alergia e Imunologia
Comunicação Clínica e Experimental

Doença sistêmica relacionada à IgG4 com linfopenia: relato de caso e breve revisão de literatura

IgG4-related systemic disease associated with lymphopenia: case report and brief literature review

Leonardo Oliveira Mendonça; Julia Biegelmeyer; João Paulo de Assis; Larissa Costa Amorim; Mauricio Levy-Neto; Jorge Kalil; Milton de Arruda Martins; Fabio Morato Castro; Myrthes Toledo de Barros

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Resumo

A doença sistêmica relacionada à IgG4 é uma doença emergente, recentemente descrita, caracterizada clinicamente por aumento parcial ou total de um órgão, e, por isso, com amplo espectro de manifestações clínicas. Esta é uma doença sistêmica fibroinflamatória, patologicamente provocada pela infiltração de plasmoblastos IgG4 positivos que levam à inflamação eosinofílica do tecido e, consequentemente, fibrose estoriforme. Quando o diagnóstico é precoce, a melhora clínica e resposta sustentada com corticosteroides sistêmicos é impressionante. O diagnóstico é baseado em critérios patológicos, mas, recentemente, alguns trabalhos têm descrito que plasmoblastos no soro podem servir como um fator independente para auxiliar no diagnóstico da doença. Este artigo descreve uma apresentação atípica da doença relacionada à IgG4, em um paciente linfopênico com medição inconclusiva de plasmoblastos no soro.

Palavras-chave

Imunoglobulina G, eosinófilos, hipergamaglobulinemia, imunoglobulinas, serosite, IgG4, doença sistêmica relacionada à IgG4.

Abstract

IgG4-related systemic disease is a recently described, emerging condition, clinically characterized by partial or total enlargement of an organ, with a broad spectrum of clinical manifestations. It is a systemic fibroinflammatory condition caused by the infiltration of IgG4-positive plasmablasts that lead to eosinophilic inflammation of tissues and consequently storiform fibrosis. When diagnosis is early, clinical improvement and maintained response achieved with systemic corticosteroids is impressive. Diagnosis is based on pathological criteria, but recent papers have described that serum plasmablasts may serve as an independent factor to aid in diagnosis. This paper describes an atypical presentation of IgG4-related disease in a lymphopenic patient with inconclusive serum plasmablast measurement.

Keywords

Immunoglobulin G, eosinophils, hypergammaglobulinemia, immunoglobulins, serositis, IgG4, IgG-4 related systemic disease.

Referências

1. Engelhart S, Glynn RJ, Schur PH. Disease associations with isolated elevation of each of the four IgG subclasses. Semin Arthritis Rheum. 2017; no prelo.

2. Stone JH, Zen Y, Deshpande V. IgG4-related disease. N Engl J Med. 2012;366:539-51.

3. Nirula A, Glaser SM, Kalled SL, Taylor FR. What is IgG4? A review of the biology of a unique immunoglobulin subtype. Curr Opin Rheumatol. 2011;23:119-24.

4. Rispens T, Ooievaar-De Heer P, Vermeulen E, Schuurman J, Van der Neutkolfschoten M, Aalberse RC. Human IgG4 binds to IgG4 and conformationally altered IgG1 via Fc-Fc interactions. J Immunol. 2009;182:4275-81.

5. Wallace ZS, Deshpande V, Mattoo H, Mahajan VS, Kulikova M, Pillai S, Stone JH. IgG4-Related Disease: Clinical and Laboratory Features in One Hundred Twenty-Five Patients. Arthritis Rheumatol. 2015;67:2466-75.

6. Anchez-Castanon M, las Heras-Castano G, Lopez-Hoyos M. Autoimmune pancreatitis: an underdiagnosed autoimmune disease with clinical, imaging and serological features. Autoimmun Rev. 2010;9:237-40.

7. Kubo K, Yamamoto K. IgG4-related disease. Int J Rheum Dis. 2016;19:747-62.

8. Wallace ZS, Mattoo H, Carruthers M, Vinay MS, Emanuel DT, Lee H, et al. Plasmablasts as a biomarker for IgG4-related disease, independent of serum IgG4 concentrations. Ann Rheum Dis. 2015;74:190-5.

9. Deshpande V, Zen Y, Chan JKC, Yi EE, Sato Y, Yoshino T, et al. Consensus statement on the pathology of IgG4-related disease. Mod Pathol. 2012;25:1181-92.

10. Thompson A, Whyte A. Imaging of IgG4-related disease of the head and neck. Clin Radiol. 2017;no prelo.

11. Narayan AK, Baer A, Fradin J. Sonographic findings of IgG4-related disease of the salivary glands: case report and review of the literature. J Clin Ultrasound. 2017;no prelo.

12. Khosroshahi A, Stone JH. A clinical overview of IgG4-related systemic disease. Curr Opin Rheumatol. 2011;23:57-66.

13. Takahashi H, Yamamoto M, Suzuki C, Naishiro Y, Shinomura Y, Imai K. The birthday of a new syndrome: IgG4-related diseases constitute a clinical entity. Autoimmun Rev. 2010;9:591-4.

14. Okazaki K, Uchida K, Koyabu M, Miyoshi H, Takaoka M. Recent advances in the concept and diagnosis of autoimmune pancreatitis and IgG4-related disease. J Gastroenterol. 2011;46:277-88. Referências

15. Sah RP, Chari ST, Pannala R, Sugar A, Claim JE, Ley MJ, et al. Differences in clinical profile and relapse rate of type 1 versus type

2 autoimmune pancreatitis. Gastroenterology. 2010;139:140-8.

16. Cheuk W, Chan JK. IgG4-related sclerosing disease: a critical appraisal of an evolving clinicopathologic entity. Adv Anat Pathol. 2010;17:303-32

17. Soliotis F, Mavragani CP, Plastiras SC, Rontogianni D, Skopouli FN, Moutsopoulos HM. IgG4-related disease: a rheumatologist’s perspective. Clin Exp Rheumatol. 2014;32:724-7.

18. Ishida A, Furuya N, Nishisaka T, Nishisaka T, Mineshita M, Miyazawa T. IgG4-related Pleural Disease Presenting as a Massive Bilateral Effusion. J Bronchology Interv Pulmunol. 2014;21:237-41.

19. Erlij D, Ramos D, Montana J, Kusnir P, Correa G, Neira O. IgG4- related disease, the new "great mimicker": Report of one case. Rev Med Chil. 2014;142:646-50.

20. Ishida M, Hodohara K, Furuya A, Fujishiro A, Okuno H, Yoshii M, et al. Concomitant occurrence of IgG4-related pleuritis and periaortitis: a case report with review of the literature. Int J Clin Exp Pathol. 2014;7:808-14.

21. Choi JH, Sim JK, Oh JY, Lee EJ, Hur GY, Lee SH, et al. A Case of IgG4-Related Disease Presenting as Massive Pleural Effusion and Thrombophlebitis. Tuberc Respir Dis (Seoul). 2014;76:179-83.

22. Rossi G, Marchioni A, Guicciardi N, Cadioli A, Cavazza A. Recurrent pleural and pericardium effusions in a white woman with IgG4-related syndrome. Am J Surg Pathol. 2009;33:802-3.

23. Della Torre E, Mattoo H, Mahajan VS, Carruthers M, Pillai S, Stone JH. Prevalence of Atopy, eosinophilia, and IgE elevation in IgG4- related disease. Allergy. 2014;69:269-72.

24. Hamano H, Kawa S, Horiuchi A, Unno H, Furuya N, Akamatsu T, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med. 2001;344:732-8.

25. Harano Y, Honda K, Akiyama Y, Kotajima L, Arioka H. A case of IgG4-Related Hypophysitis presented with Hypopituitarism and Diabetes Insipidus. Clin Med Insights Case Rep. 2015;8:23-6.

26. Mattoo H, Mahajan VS, Della-Torre E, Sekigami Y, Carruthers M, Wallace ZS, et al. De novo oligoclonal expansions of circulating plasmablasts in active and relapsing IgG4-related disease. J Allergy Clin Immunol. 2014;134:679-87.

27. Zen Y, Nakanuma Y. IgG4-related disease: a cross-sectional study of 114 cases. Am J Surg Pathol. 2010;34:1812-9.

28. Khosroshahi A, Wallace ZS, Crowe JL, Akamizu T, Azumi A, Carruthers MN, et al. International Consensus Guidance Statement on the Management and Treatment of IgG4-Related Disease. Arthritis Rheumatol. 2015;67:1688-99.


Submetido em:
10/04/2017

Aceito em:
24/04/2017

6a5104cfa953957128658e24 aaai Articles
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