Volume 11 Supplement 2

Proceedings of 20th Pediatric Rheumatology European Society (PReS) Congress

Open Access

PReS-FINAL-2255: Primary pyomiositis in children: a challenging diagnosis

  • V Moressa1,
  • S Pastore1,
  • M Pavan1,
  • C Bracaglia2 and
  • L Lepore1
Pediatric Rheumatology201311(Suppl 2):P245

https://doi.org/10.1186/1546-0096-11-S2-P245

Published: 5 December 2013

Introduction

Primary Pyomiositis (PM) is an uncommon and potentially serious bacterial infection of striated muscle. It is typically a tropical disease but its frequency has been increasing in the Western Countries.

Staphylococcus Aureus is the most frequently isolated organism from blood samples of patients affected by this condition. The rarity in temperate climates of this potentially fatal disease and its non-specific signs can represent a diagnostic challenge, leading to a dangerous diagnostic delay.

Objectives

The aim of our study is to identify a common diagnostic profile in order to provide an early diagnosis.

Methods

A retrospective review was conducted to analyze the experience of two pediatric Italian hospitals (Clinica Pediatrica, IRCCS Burlo Garofolo, Trieste and Ospedale Pediatrico Bambino Gesù, Roma) from 2005 to 2013.

Results

Over the 8-year period, 12 cases were identified (8 boys and 4 girls). None of them presented immunocompromising conditions.

Mean age at diagnosis was 10,8 years (range 3 months-15 years); the most commonly involved muscle was the gluteal one (8/12 cases); in 4/12 cases other muscles were involved (iliopsoas, obturator and abdominal oblique muscle).

All of the patients presented with pain, fever and limp with limitation in movements.

Physical examination revealed in all cases limitation on flexion and abduction of the hip and pain at pressure of the involved muscles.

One patient, a 3 months-old baby, presented with fever, irritability, lack of appetite and pain at the attempt to move the affected muscles.

A history of local trauma was present in two cases. Laborator findings showed rise in acute phase reactants in all cases, whereas creatinine kinase was normal in all our patients. Xray and Ultrasound examinations were performed in all cases and were always negative. On the contrary MRI was diagnostic in all cases, showing swelling of the involved muscles.

In all cases antibiotic therapy was conducted intravenously for two weeks, therefore orally for a total of four-six weeks. One patient required surgical drain.

Conclusion

PM is a rare deep, subacute bacterial infection of the skeletal muscle.

Once considered a tropical countries' prerogative, now it is appearing more frequently in temperate climate areas.

Its rarity and the lack of specific symptoms can lead to a diagnostic delay and fatal complications. Septic arthritis represents the main differential diagnosis, therefore MRI, the gold standard for this disease, should be performed as soon as possible in any child with fever, pain and limp without a precise articular involvement and a recognized infectious focus.

Disclosure of interest

None declared.

Authors’ Affiliations

(1)
IRCCS Burlo Garofolo
(2)
Bambino Gesù Paediatric Hospital

Copyright

© Moressa et al.; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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