Skip to main content
Top
Published in: Clinical Rheumatology 7/2019

01-07-2019 | Polymyositis | Case Based Review

Juvenile polymyositis associated with ureteral necrosis: a diagnostic and therapeutic dilemma—case report and review of the literature

Authors: Ruby Haviv, Tania Zehavi, Avishalom Pomeranz, Ilan Leibovitch, Amos Neheman, Yosef Uziel

Published in: Clinical Rheumatology | Issue 7/2019

Login to get access

Abstract

We describe an 11-year-old girl, diagnosed with juvenile polymyositis (JPM), who developed right ureteral obstruction secondary to necrosis. We emphasize the dilemmas regarding optimal timing for surgical intervention and medical treatment. Vascular involvement, which could be a part of juvenile dermatomyositis, may also be a feature of JPM. We discuss the association between vasculopathy and ureteral necrosis and review the literature regarding similar conditions. Whether the ureteral necrosis is a specific feature of vasculopathy, or a result of visceral calcinosis, needs to be further explored.
Literature
1.
go back to reference Stübgen JP (2017) Juvenile dermatomyositis/polymyositis and lymphoma. J Neurol Sci 377:19–24CrossRef Stübgen JP (2017) Juvenile dermatomyositis/polymyositis and lymphoma. J Neurol Sci 377:19–24CrossRef
2.
go back to reference Enders FB, Bader-Meunier B, van Royen-Kerkhof A et al (2017) Consensus-based recommendations for the management of juvenile dermatomyositis. Ann Rheum Dis 76:329–340CrossRef Enders FB, Bader-Meunier B, van Royen-Kerkhof A et al (2017) Consensus-based recommendations for the management of juvenile dermatomyositis. Ann Rheum Dis 76:329–340CrossRef
3.
go back to reference Grossiord A, Lacert P et al (1978) A case of bilateral ureteral necrosis in dermatomyositis in a child. Annals de Medicine Interne 129(1):1–3 Grossiord A, Lacert P et al (1978) A case of bilateral ureteral necrosis in dermatomyositis in a child. Annals de Medicine Interne 129(1):1–3
4.
go back to reference Bléry M, Lacert P, Touboul A (1978) Lithiasis and bilateral necrosis of the ureters occurring during dermatomyositis. A definite entity or a coincidence? J Radiol Electrol Med Nucl 59(4):279–282PubMed Bléry M, Lacert P, Touboul A (1978) Lithiasis and bilateral necrosis of the ureters occurring during dermatomyositis. A definite entity or a coincidence? J Radiol Electrol Med Nucl 59(4):279–282PubMed
5.
go back to reference Le Guillou M, Richard F, Küss R et al (1980) Bilateral ureteral necrosis in a child with dermatomyositis. Eur Urol 6(3):190–191CrossRef Le Guillou M, Richard F, Küss R et al (1980) Bilateral ureteral necrosis in a child with dermatomyositis. Eur Urol 6(3):190–191CrossRef
6.
go back to reference Borrelli M, Prado MJ, Arap S et al (1988) Ureteral necrosis in dermatomyositis. J Urol 139(6):1275–1277CrossRef Borrelli M, Prado MJ, Arap S et al (1988) Ureteral necrosis in dermatomyositis. J Urol 139(6):1275–1277CrossRef
7.
go back to reference Duarte JD, Denes FT, Salum AM (2006) Ureteral calcinosis in juvenile dermatomyositis: successful precocious surgical management. International Brazilian J Urol 32(5):574–577CrossRef Duarte JD, Denes FT, Salum AM (2006) Ureteral calcinosis in juvenile dermatomyositis: successful precocious surgical management. International Brazilian J Urol 32(5):574–577CrossRef
8.
go back to reference Huang KH, Hsieh SC, Chen J et al (2007) Dermatomyositis associated with bilateral ureteral spontaneous rupture. J Formosan Med Association 106(3):251–254CrossRef Huang KH, Hsieh SC, Chen J et al (2007) Dermatomyositis associated with bilateral ureteral spontaneous rupture. J Formosan Med Association 106(3):251–254CrossRef
9.
go back to reference Gerami P, Sontheimer RD et al (2007) A systematic review of juvenile-onset clinically amyopathic dermatomyositis. Brit J Dermatol 157(4):637–644CrossRef Gerami P, Sontheimer RD et al (2007) A systematic review of juvenile-onset clinically amyopathic dermatomyositis. Brit J Dermatol 157(4):637–644CrossRef
10.
go back to reference Shah M, Rider LG et al; with the Childhood Myositis Heterogeneity Collaborative Study Group (2013) The clinical phenotypes of the juvenile idiopathic inflammatory myopathies. Medicine (Baltimore) 92(1):25–41CrossRef Shah M, Rider LG et al; with the Childhood Myositis Heterogeneity Collaborative Study Group (2013) The clinical phenotypes of the juvenile idiopathic inflammatory myopathies. Medicine (Baltimore) 92(1):25–41CrossRef
11.
go back to reference Rider LG, Nistala K (2016) The juvenile idiopathic inflammatory myopathies: pathogenesis, clinical and autoantibody phenotypes, and outcomes. J Int Med 280:24–38CrossRef Rider LG, Nistala K (2016) The juvenile idiopathic inflammatory myopathies: pathogenesis, clinical and autoantibody phenotypes, and outcomes. J Int Med 280:24–38CrossRef
12.
go back to reference Rider LG, Lindsley CB, Miller FW (2016) Juvenile dermatomyositis. In: Petty RE, Laxer RM, Lindsley CB, Wedderburn LR (eds) Textbook of pediatric rheumatology, 7th edn. Elsevier, Philadelphia, pp 351–383CrossRef Rider LG, Lindsley CB, Miller FW (2016) Juvenile dermatomyositis. In: Petty RE, Laxer RM, Lindsley CB, Wedderburn LR (eds) Textbook of pediatric rheumatology, 7th edn. Elsevier, Philadelphia, pp 351–383CrossRef
13.
go back to reference Ruperto N, Pistorio A et al; Oliveira S, for the Paediatric Rheumatology International Trials Organisation (PRINTO) (2016) Prednisone versus prednisone plus ciclosporin versus prednisone plus methotrexate in new-onset juvenile dermatomyositis: a randomised trial. Lancet 387(10019):671–678CrossRef Ruperto N, Pistorio A et al; Oliveira S, for the Paediatric Rheumatology International Trials Organisation (PRINTO) (2016) Prednisone versus prednisone plus ciclosporin versus prednisone plus methotrexate in new-onset juvenile dermatomyositis: a randomised trial. Lancet 387(10019):671–678CrossRef
14.
go back to reference Rider LG, Miller FW (2011) Phenotypes as clues to deciphering the clinical presentations, pathogenesis, and treatment of the idiopathic inflammatory myopathies. JAMA 305(2):183–190CrossRef Rider LG, Miller FW (2011) Phenotypes as clues to deciphering the clinical presentations, pathogenesis, and treatment of the idiopathic inflammatory myopathies. JAMA 305(2):183–190CrossRef
15.
go back to reference Moghadam-Kia S, Aggarwal R, Oddis CV (2017) Biologics for idiopathic inflammatory myopathies. Curr Opinion Rheumatol 29(6):645–651 Moghadam-Kia S, Aggarwal R, Oddis CV (2017) Biologics for idiopathic inflammatory myopathies. Curr Opinion Rheumatol 29(6):645–651
Metadata
Title
Juvenile polymyositis associated with ureteral necrosis: a diagnostic and therapeutic dilemma—case report and review of the literature
Authors
Ruby Haviv
Tania Zehavi
Avishalom Pomeranz
Ilan Leibovitch
Amos Neheman
Yosef Uziel
Publication date
01-07-2019
Publisher
Springer London
Published in
Clinical Rheumatology / Issue 7/2019
Print ISSN: 0770-3198
Electronic ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-019-04576-4

Other articles of this Issue 7/2019

Clinical Rheumatology 7/2019 Go to the issue