Allergy Asthma Respir Dis.  2019 Oct;7(4):212-217. 10.4168/aard.2019.7.4.212.

A pediatric case of eosinophilic granulomatosis with polyangiitis accompanied by heart failure mimicking an asthma attack

Affiliations
  • 1Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea. dongins0@snu.ac.kr

Abstract

Eosinophilic granulomatosis with polyangiitis (EGPA, also known as the Churg-Strauss syndrome) is a disorder characterized by asthma, peripheral eosinophilia and systemic vasculitis. It rarely occurs in children, so that physicians may frequently mistake it for a simple uncontrolled asthma. Since a subsequent cardiac involvement is critical for the prognosis, it is important to suspect EGPA in children with severe, uncontrolled asthma. The cardiac manifestations in EGPA are variable from asymptomatic electrocardiogram abnormalities to pericarditis with pericardial effusion, myocarditis with cardiomyopathy, heart failure, and sudden cardiac death. Although delayed treatment may lead to fatal cardiac complications in EGPA, adequate immune suppression can reverse cardiac impairment. We report a 14-year-old girl with persistent asthma refractory to steroids who was eventually diagnosed with an anti-neutrophil cytoplasmic antibody-negative EGPA.

Keyword

Eosinophilic granulomatosis with polyangiitis; Churg-Strauss syndrome; Child

MeSH Terms

Adolescent
Asthma*
Cardiomyopathies
Child
Churg-Strauss Syndrome
Cytoplasm
Death, Sudden, Cardiac
Electrocardiography
Eosinophilia
Eosinophils*
Female
Granulomatosis with Polyangiitis*
Heart Failure*
Heart*
Humans
Myocarditis
Pericardial Effusion
Pericarditis
Prognosis
Steroids
Systemic Vasculitis
Steroids

Figure

  • Fig. 1. Chest computed tomography reveals interlobular septal thickening and large amount of bilateral pleural effusion with passive atelectasis.

  • Fig. 2. A) Pretreatment echocardiography shows severe left ventricular dysfunction with ejection fraction of 19.1%. (B) Pretreatment cardiac magnetic resonance imaging reveals that late gadolinium enhancement at midinferior and inferolateral wall of left ventricle. (C) Duodenal biopsy shows mild eosinophilic infiltration (H&E, ×200). (D) Posttreatment echocardiography shows improved left ventricular ejection fraction of 45% without mitral regurgitation.

  • Fig. 3. Time changes in the blood eosinophilia, ejection fraction, B-type natriuretic peptide and degree of dyspnea during treatment. Green box indicates the blood eosinophil percent, solid line with square stands for the ejection fraction, and the dotted line with empty circle represents the B-type natriuretic peptide. Dyspnea scale is described using a modified Medical Research Council dyspnea scale.

  • Fig. 4. Chest radiographs before cyclophosphamide infusion (A), after the 1st cyclophosphamide infusion (B), and after the last infusion (C).


Reference

References

1. Churg J, Strauss L. Allergic granulomatosis, allergic angiitis, and periar-teritis nodosa. Am J Pathol. 1951; 27:277–301.
2. Sinico RA, Bottero P. Churg-Strauss angiitis. Best Pract Res Clin Rheumatol. 2009; 23:355–66.
Article
3. Yano T, Ishimura S, Furukawa T, Koyama M, Tanaka M, Shimoshige S, et al. Cardiac tamponade leading to the diagnosis of eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome): a case report and review of the literature. Heart Vessels. 2015; 30:841–4.
Article
4. Seeliger B, Sznajd J, Robson JC, Judge A, Craven A, Grayson PC, et al. Are the 1990 American College of Rheumatology vasculitis classification criteria still valid? Rheumatology (Oxford). 2017; 56:1154–61.
Article
5. Comarmond C, Pagnoux C, Khellaf M, Cordier JF, Hamidou M, Viallard JF, et al. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): clinical characteristics and longterm followup of the 383 patients enrolled in the French Vasculitis Study Group cohort. Arthritis Rheum. 2013; 65:270–81.
Article
6. Mahr A, Moosig F, Neumann T, Szczeklik W, Taillé C, Vaglio A, et al. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): evolutions in classification, etiopathogenesis, assessment and management. Curr Opin Rheumatol. 2014; 26:16–23.
7. Gendelman S, Zeft A, Spalding SJ. Childhood-onset eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss syndrome): a contemporary singlecenter cohort. J Rheumatol. 2013; 40:929–35.
Article
8. Eleftheriou D, Gale H, Pilkington C, Fenton M, Sebire NJ, Brogan PA. Eosinophilic granulomatosis with polyangiitis in childhood: retrospective experience from a tertiary referral centre in the UK. Rheumatology (Oxford). 2016; 55:1263–72.
Article
9. Guillevin L, Cohen P, Gayraud M, Lhote F, Jarrousse B, Casassus P. Churg-Strauss syndrome. Clinical study and longterm follow-up of 96 patients. Medicine (Baltimore). 1999; 78:26–37.
Article
10. Jung SH, Kim KH, Nam SM, Park HC, Chu HK, Whang IS, et al. A case of Churg-Strauss syndrome with manifestations of esophageal ulcer, acute acalculous cholecystitis and ischemic colitis. Korean J Intern Med. 1993; 45:369–75.
11. Lee WJ, Hwang JW, Kim E, Yune S, Ha JM, Yoon N, et al. Churg-Strauss syndrome presenting as acute acalculous cholecystitis. Allergy Asthma Respir Dis. 2013; 1:388–90.
Article
12. Choi JY, Kim JE, Choi IY, Lee JH, Kim JH, Shin C, et al. Churg-Strauss syndrome that presented with mediastinal lymphadenopathy and calcu-lous cholecystitis. Korean J Intern Med. 2016; 31:179–83.
Article
13. Greco A, Rizzo MI, De Virgilio A, Gallo A, Fusconi M, Ruoppolo G, et al. Churg-Strauss syndrome. Autoimmun Rev. 2015; 14:341–8.
Article
14. Guillevin L, Lhote F, Gayraud M, Cohen P, Jarrousse B, Lortholary O, et al. Prognostic factors in polyarteritis nodosa and Churg-Strauss syndrome. A prospective study in 342 patients. Medicine (Baltimore). 1996; 75:17–28.
Article
15. Hazebroek MR, Kemna MJ, Schalla S, Sanders-van Wijk S, Gerretsen SC, Dennert R, et al. Prevalence and prognostic relevance of cardiac involvement in ANCA-associated vasculitis: eosinophilic granulomatosis with polyangiitis and granulomatosis with polyangiitis. Int J Cardiol. 2015; 199:170–9.
Article
16. Park S, Kim T, Kim HJ, Shin B, Park SY, Kwon HS, et al. Heart transplantation in a patient with eosinophilic granulomatosis with polyangiitis known as Churg-Strauss syndrome. Allergy Asthma Respir Dis. 2015; 3:159–63.
Article
17. Jeong HC, Kim KH, Cho JY, Song JE, Yoon HJ, Seon HJ, et al. Cardiac involvement of churg-strauss syndrome as a reversible cause of dilated cardiomyopathy. J Cardiovasc Ultrasound. 2015; 23:40–3.
Article
18. Szczeklik W, Sokołowska BM, Zuk J, Mastalerz L, Szczeklik A, Musiał J. The course of asthma in Churg-Strauss syndrome. J Asthma. 2011; 48:183–7.
Article
19. Kim S, Marigowda G, Oren E, Israel E, Wechsler ME. Mepolizumab as a steroid-sparing treatment option in patients with Churg-Strauss syndrome. J Allergy Clin Immunol. 2010; 125:1336–43.
Article
20. Wechsler ME, Akuthota P, Jayne D, Khoury P, Klion A, Langford CA, et al. Mepolizumab or placebo for eosinophilic granulomatosis with polyangiitis. N Engl J Med. 2017; 376:1921–32.
Article
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