eMedicine Specialties > Neurology > Neurological Infections

Infectious Myositis: Differential Diagnoses & Workup

Author: Mohammed J Zafar, MD, FAAN, Associate Clinical Professor of Medicine, Kalamazoo Center for Medical Studies, Michigan State University; NeuroImager, Premier Medical Care, PC, Premier Radiology, Kalamazoo Neurologic Institute
Contributor Information and Disclosures

Updated: Aug 12, 2009

Differential Diagnoses

Acute Inflammatory Demyelinating Polyradiculoneuropathy
HIV-1 Associated Myopathies
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
HIV-1 Associated Neuromuscular Complications (Overview)
Dermatomyositis/Polymyositis
Metabolic Myopathies
Femoral Mononeuropathy
Paraneoplastic Autonomic Neuropathy

Other Problems to Be Considered

Cellulitis
Deep vein thrombosis
Hematoma
Osteomyelitis
Septic arthritis
Wasting syndrome
Idiopathic polymyositis

Workup

Laboratory Studies

  • Pyomyositis
    • Leukocytosis
    • Elevated erythrocyte sedimentation rate
    • Serum creatine kinase (CK) and aldolase usually normal
    • Blood culture results generally negative.
  • Trichinosis: Eosinophilia is suggestive of the diagnosis.
  • Serology
    • Viral titers
    • Toxoplasmal antibodies - Found more frequently in patients with polymyositis and dermatomyositis than in the general population
    • Lyme antibody titer - If enzyme-linked immunosorbent assay (ELISA) screening test result is positive, confirmed with a western blot test
  • Cysticercosis - Electrocardiogram
  • HTLV-1 infection - Serological tests to detect HTLV-1 antibodies in serum
  • Trypanosomiasis
    • Serological tests - ELISA (highly sensitive) or direct agglutination test.
    • Electrocardiogram
  • Influenza myositis
    • Elevated CK, mostly consisting of the MM (muscle) isoenzyme, as high as 500 times normal
    • Urine myoglobin - May be positive
    • Liver enzymes (aspartate aminotransferase [AST] and lactate dehydrogenase [LDH]) - May be elevated
    • Electrocardiogram
  • Coxsackievirus myositis
    • Rising coxsackievirus antibody titers
    • Isolation methods for group B coxsackievirus - Include inoculation of cell cultures

Imaging Studies

  • Pyomyositis
    • MRI is the imaging modality of choice for the diagnosis of pyomyositis. MRI is helpful in differentiating pyomyositis from osteomyelitis. It is especially useful in differentiating early muscle inflammation from abscess formation. MRI is also the best imaging modality for evaluation of pelvic infections.6
    • CT scanning may show hypertrophy of involved muscle groups and effacement of the fat planes. Contrast enhancement may indicate abscess formation. CT is also useful for distinguishing tumors and hematomas from abscess.
    • Ultrasound or MRI also may be used to localize involved muscle.
    • Gallium scan is useful for localization in the early stages of illness.
  • Tuberculous pyomyositis
    • MRI: Findings are consistent with an abscess (ie, low signal intensity on T1-weighted images and high signal intensity on T2-weighted images of affected muscles).
    • Following gadolinium infusion, peripheral rim enhancement is noted. This is indicated by subtle hyperintensity on T1-weighted images and hypointensity on T2-weighted images.
  • Cysticercosis with orbital involvement: Multiplanar imaging with MRI may be obtained to identify a cyst with a mural nodule. With gadolinium, a nodule shows intense enhancement.

Other Tests

Trichinosis: Skin test with trichinellar antigen is unreliable.

Procedures

  • HIV polymyositis: Electromyography (EMG) findings are similar to those of idiopathic polymyositis.
    • Short-duration motor unit potentials
    • Low-amplitude polyphasic motor unit potentials
    • Fibrillations
  • Trichinosis: EMG may reveal fibrillation potentials.
  • Lyme myositis: Changes of denervation may be seen in the involved muscles.
  • Pyomyositis: Needle aspiration is useful for the detection of purulent material and for microbiologic identification of the causative organism.

Histologic Findings

Trichinosis

Muscle biopsy is required to confirm diagnosis. Findings in the acute stage of larval invasion of the muscles include segmental necrosis and interstitial infiltrates composed mainly of eosinophils. The Trichinella species larvae sometimes can be seen in the muscle biopsy. However, encapsulated cysts (without larvae), granulomas, and focal calcification are more likely to be encountered.

Pyomyositis

Widespread necrosis of muscle fibers, perimysium, and blood vessels is noted. Pleomorphic inflammatory response consisting of both neutrophils and lymphocytes is noted.

Cysticercosis

The viable larvae produce little or no tissue reaction. However, rupture or death of a cysticercus (mature larva) evokes an acute inflammatory response with a pleomorphic exudate composed of neutrophils and eosinophils. Over time, fibrous tissue encapsulates the cysts. A chronic granulomatous response may surround the cysts.

Lyme myositis

Muscle biopsy shows atrophic fibers and an infiltrate consisting of lymphocytes, plasma cells, and macrophages. The spirochete of borreliosis can be detected in muscle fibers by the modified Dieterle silver stain method (see Media file 4).

Histopathology: Borrelia burgdorferi spirochetes ...

Histopathology: Borrelia burgdorferi spirochetes in Lyme disease, with Dieterle silver stain. Courtesy of Centers for Disease Control and Prevention and Dr Edwin P. Ewing, Jr.

Histopathology: Borrelia burgdorferi spirochetes ...

Histopathology: Borrelia burgdorferi spirochetes in Lyme disease, with Dieterle silver stain. Courtesy of Centers for Disease Control and Prevention and Dr Edwin P. Ewing, Jr.


Trypanosomiasis

Sections of infected tissues may reveal clusters of amastigotes in muscle cells surrounded by acute or chronic inflammation.

Influenza myositis

Muscle fiber necrosis without inflammatory change is observed. Influenza viral particles have been identified in muscle fibers under electron microscopy. Muscle fiber regeneration is seen in some, with an inflammatory response consisting of mononuclear and polymorphonuclear leukocytes.

More on Infectious Myositis

Overview: Infectious Myositis
Differential Diagnoses & Workup: Infectious Myositis
Treatment & Medication: Infectious Myositis
Follow-up: Infectious Myositis
Multimedia: Infectious Myositis
References

References

  1. O'Neill DS, Baquis G, Moral L. Infectious myositis. A tropical disease steals out of its zone. Postgrad Med. Aug 1996;100(2):193-4, 199-200. [Medline].

  2. Crum NF. Bacterial pyomyositis in the United States. Am J Med. Sep 15 2004;117(6):420-8. [Medline].

  3. Reimers CD, de Koning J, Neubert U, et al. Borrelia burgdorferi myositis: report of eight patients. J Neurol. May 1993;240(5):278-83. [Medline].

  4. Costa RM, Dumitrascu OM, Gordon LK. Orbital myositis: diagnosis and management. Curr Allergy Asthma Rep. Jul 2009;9(4):316-23. [Medline].

  5. Wong SL, Anthony EY, Shetty AK. Pyomyositis due to Streptococcus pneumoniae. Am J Emerg Med. Jun 2009;27(5):633.e1-3. [Medline].

  6. Trusen A, Beissert M, Schultz G, et al. Ultrasound and MRI features of pyomyositis in children. Eur Radiol. May 2003;13(5):1050-5. [Medline].

  7. Simpson DM, Citak KA, Godfrey E, et al. Myopathies associated with human immunodeficiency virus and zidovudine: can their effects be distinguished?. Neurology. May 1993;43(5):971-6. [Medline].

  8. Belman AL, Preston T, Milazzo M. Human immunodeficiency virus and acquired immunodeficiency syndrome. In: Goetz, Pappert, eds. Textbook of Clinical Neurology;1999:898-900. [Medline].

  9. Hays AP, Gamboa ET. Acute viral myositis. In: Engel, Franzini-Armstrong, eds. Myology: Basic and Clinical. 2nd ed. 1994:1399-409.

  10. Heffner RH Jr, Schochet SS Jr. Skeletal muscle. In: Anderson's Pathology. Vol 2. 10th ed. 1996:2666-7.

  11. Kim JY, Park YH, Choi KH, et al. MRI of tuberculous pyomyositis. J Comput Assist Tomogr. May-Jun 1999;23(3):454-7. [Medline].

  12. Patel SR, Olenginski TP, Perruquet JL, Harrington TM. Pyomyositis: clinical features and predisposing conditions. J Rheumatol. Sep 1997;24(9):1734-8. [Medline].

  13. Tulio AM et al. Strickland TG. American trypanosomiasis. 7th ed. Hunter's Tropical Medicine; 1991:628-37.

Further Reading

Keywords

infectious myopathy, infectious polymyositis, pyomyositis, HIV infection

Contributor Information and Disclosures

Author

Mohammed J Zafar, MD, FAAN, Associate Clinical Professor of Medicine, Kalamazoo Center for Medical Studies, Michigan State University; NeuroImager, Premier Medical Care, PC, Premier Radiology, Kalamazoo Neurologic Institute
Mohammed J Zafar, MD, FAAN is a member of the following medical societies: American Academy of Neurology, American Medical Association, American Society of Neuroimaging, and Michigan State Medical Society
Disclosure: Nothing to disclose.

Medical Editor

Roberta J Seidman, MD, Associate Professor of Clinical Pathology, Stony Brook University; Director of Neuropathology, Department of Pathology, Stony Brook University Medical Center
Roberta J Seidman, MD is a member of the following medical societies: American Academy of Neurology, American Association of Neuropathologists, New York Association of Neuropathologists (The Neuroplex), and Suffolk County Society of Pathologists
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Florian P Thomas, MD, MA, PhD, Drmed, Director, Spinal Cord Injury Unit, St Louis Veterans Affairs Medical Center; Director, National MS Society Multiple Sclerosis Center; Professor, Department of Neurology and Psychiatry, Associate Professor, Institute for Molecular Virology, and Department of Molecular Microbiology and Immunology, St Louis University
Florian P Thomas, MD, MA, PhD, Drmed is a member of the following medical societies: American Academy of Neurology, American Paraplegia Society, and National Multiple Sclerosis Society
Disclosure: Nothing to disclose.

CME Editor

Matthew J Baker, MD, Consulting Staff, Collier Neurologic Specialists, Naples Community Hospital
Matthew J Baker, MD is a member of the following medical societies: American Academy of Neurology
Disclosure: Nothing to disclose.

Chief Editor

Nicholas Y Lorenzo, MD, Chief Editor, eMedicine Neurology; Consulting Staff, Neurology Specialists and Consultants
Nicholas Y Lorenzo, MD is a member of the following medical societies: Alpha Omega Alpha and American Academy of Neurology
Disclosure: Nothing to disclose.

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