Pyomyositis
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Yamuna Kondapally, M.B.B.S[2]
Synonyms and keywords: Tropical pyomyositis; Myositis tropicans; Bungpagga; Lambo lambo; Tropical skeletal muscle abscess; Myositis purulenta tropica
Overview
Pyomyositis, also known as tropical pyomyositis or myositis tropicans is a bacterial infection of the skeletal muscles which results in a pus-filled abscess. Pyomyositis is more common in tropical areas but can also occur in the temperate zones. Pyomyositis is most often caused by the bacterium Staphylococcus aureus.[1] The infection can affect any skeletal muscle, but most often infects the large muscle groups such as the quadriceps or gluteal muscles. In tropical regions, the infection often follows minor trauma, while in temperate zones the infection typically occurs in people with immune deficiencies. The abscess within the muscle is drained surgically and antibiotics are administered to fully clear the infection.
Historical Perspective
- Traquair credited Virchow for the earliest mention of pyomyositis, however it was first described by Scriba in 1885 as a disease endemic to tropics. Hence the term tropical myositis.[2]
Classification
Pyomyositis may be classified according to international classification of diseases-10(ICD-10) into
- M60.0 Infectious myositis, Tropical pyomyositis (optionally, B95-B97 to indicate the infectious agent; B95.6 for Staphylococcus aureus)[2][3]
Pathophysiology
Pathogenesis
Gross
Microscopic histopathological analysis
Images
Causes
Common causes of pyomyositis include: Bacteria Most common cause
- Staphylococcus aureus(95% of cases)
Less common bacteria
- Group A Streptococci
- Streptococcal pneumoniae
- Escherichia coli
- Pseudomonas mallei
- Pseudomonas pseudomallie
Differentiating Pyomyositis from Other Diseases
Epidemiology and Demographics
Age
Pyomyositis is mainly a disease of children(2-5 yrs) but infection may occur in any age group.
Tropical countries
Pyomyositis is more common in the tropics, Where it accounts for 4% of all hospital admissions.
Temperate countries
In temperate countries like United states, pyomyositis was a rare condition(accounting for 1 in 3000 pediatric admissions), but has become more common since the appearance of the USA300 strain of MRSA.
Risk Factors
Screening
Natural History, Complications, and Prognosis
Natural History
Complications
Prognosis
Diagnosis
Diagnostic Criteria
History and Symptoms
Physical Examination
Laboratory Findings
Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
- Pyomyositis[4]
- Preferred regimen (3): Cefazolin 2 g IV q8h (if MSSA)
- Alternate regimen: Vancomycin 1 g IV q12h (if MRSA)
Surgery
Prevention
References
- ↑ Chauhan, S.; Jain, S.; Varma, S.; Chauhan, SS. (2004). "Tropical pyomyositis (myositis tropicans): current perspective". Postgrad Med J. 80 (943): 267–70. PMID 15138315. Unknown parameter
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ignored (help) - ↑ 2.0 2.1 , S., et al. "Tropical pyomyositis (myositis tropicans): current perspective." Postgraduate medical journal 80.943 (2004): 267-270.
- ↑ Wikipedia(2016).https://de.wikipedia.org/wiki/Pyomyositis Accessed on August 15,2016
- ↑ Gilbert, David (2015). The Sanford guide to antimicrobial therapy. Sperryville, Va: Antimicrobial Therapy. ISBN 978-1930808843.