Last Updated on October 29, 2023
Pyomyositis is characterized by suppuration within skeletal muscles, manifesting as single or multiple abscesses. It is also known as tropical pyomyositis as it affects tropical people more commonly. Pyomyositis is common in tropical regions but is rare in temperate climates but showing rise and association with HIV infection or other immunosuppressive conditions, including diabetes mellitus, cancer, connective tissue diseases, and cirrhosis.
The term pyomyositis or tropical pyomyositis should be restricted to primary muscle abscess arising de novo and not for intermuscular abscess, abscess extending into muscles from adjoining tissues or abscess secondary to septicemia.
Staphylococcus aureus is the most common organism. Commonly involved muscles are the quadriceps, glutei, pectoralis major, serratus anterior, biceps, iliopsoas, gastrocnemius, abdominal and spinal muscles.
Other terms for this are myositis tropicans and tropical skeletal muscle abscess, and tropical myositis.
The classical presentation is with muscle abscess, the hallmark of the disease is not an abscess but finding myositis on a biopsy specimen of involved muscle. Therefore, some authors prefer the term myositis instead of pyomyositis.
The disease is seen in all age groups, although young males are the most susceptible group. Maximum incidence is seen at 10–40 years of age with a male-to-female ratio of 1.5:1.
Causes of Pyomyositis
- Staphylococcus aureus
- Most common
- Group A streptococcus accounts for another 1%–5% of cases
- Uncommon Organisms
- Streptococcus (groups B, C, G)
- Pneumococcus
- Neisseria
- Haemophilus
- Aeromonas
- Serratia
- Yersinia
- Pseudomonas
- Klebsiella
- Escherichia.
- Rare Organisms
- Salmonella
- Citrobacter
- Fusobacterium
- Anaerobes
- Mycobacterium
Pathogenesis of Pyomyositis
Skeletal muscle tissue is resistant to bacterial infections under normal circumstances. Sequestration of iron by myoglobin, an essential nutritional requirement of proliferating bacteria is considered responsible for this property.
Sequestration of iron thus results in slower growth of bacteria and helps to prevent infection.
Experimental studies have failed to produce abscesses even in cases of direct inoculation.
But the damaged muscle is susceptible to hematogenous invasion by bacteria with subsequent abscess formation.
Following occurrences are considered to be causing the damage which might make muscles susceptible.
- Blunt trauma or vigorous
- Nutritional deficiencies
- Viral and parasitic infections
It has also been suggested that an abnormality of the immune system may be the underlying cause in many cases.
Intravenous drug abuse impairs cellular and humoral immunity and is a risk factor.
Tropical pyomyositis is also increasingly documented in persons infected with HIV.
Mechanisms include muscle damage caused by HIV infection per se, zidovudine therapy, infections caused by parasites and mycobacteria, and impaired host defenses including dysfunction of helper T-cells and granulocytes.
Other immunosuppressive conditions, including diabetes mellitus, cancer, connective tissue diseases, and cirrhosis also increase the risk.
Stages of Pyomyositis
Invasive stage
- Duration of symptoms <10 days
- Pain in affected muscle
- Low-grade fever
- Wooden or hard stiffness on palpation of muscle
- Mild leucocytosis
- Needle aspiration negative for pus
- The invasive stage may resolve itself, mimicking fibromyalgia or may progress to the next stage of suppuration.
Suppurative Stage
- Duration of symptoms 10–21 days
- Edema
- Marked tenderness of affected muscle
- Pyrexia
- Leucocytosis
- Needle aspiration yields pus
Late or Septic
- Duration of symptoms >21 days
- Fluctuant swelling in the muscle
- High-grade fever
- Severely ill
- Septicemia
- Leucocytosis
- Needle aspiration yields pus
Clinical Presentation
In the invasive stage, the presenting symptoms are fever and painful firm swelling. There could be erythema over the swelling. But erythema is absent in deep-seated infections.
The swelling is tender and woody inconsistency.
In the suppurative stage [1-3 weeks], an abscess forms in the muscle. There would be high-grade fever and other systemic symptoms. This is the usual stage when the patient seeks the consultation.
Most cases are present at this time. The classical signs of abscess, fluctuation, and erythema, may be lacking because the overlying muscle is tense. Needle aspiration at this stage yields pus. Regional lymph nodes are not involved.
If the abscess remains untreated [>3 weeks], the spread of infection occurs which may lead to bacteremia, followed by septicemia, septic shock, acute renal failure, and metastatic abscesses.
Rarely, the patients may present with toxic shock syndrome or pyrexia of unknown origin. The patients may present with pressure effects of the abscess. Depending on the site it could be the acute abdomen, compression of the spinal cord or compartment syndrome.
In younger children, the complaint may be of refusal to use the affected limb. For example, there could be an inability or refusal to walk.
Diagnosis of Pyomyositis
Aspiration of pus from the muscle or muscle biopsy with culture and tissue staining in cases of absent abscesses is the gold standard for diagnosis (pus may be sterile in 15%–30% of cases).
Muscle biopsy also helps to exclude osteosarcoma, polymyositis, trypanosomiasis, toxoplasmosis, cysticercosis, and trichinosis.
Lab Studies
Blood Investigations
Routine lab tests reveal anemia, leucocytosis, raised erythrocyte sedimentation rate, and C-reactive protein.
Blood cultures have low positivity.
Serum levels of muscle enzymes—that is, aldolase, creatine phosphokinase, aminotransferase, and lactic dehydrogenase—are normal or slightly raised.
Tests for immunodeficient states
- HIV
- Diabetes
- Rheumatological disorders
- Malignancies should be carried out, along with immunoglobulin levels.
Histopathology
- Edematous separation of fibers
- Patchy myocytolysis
- Lymphocytes and plasma cells.
- Suppuration with bacteria and polymorphonuclear leucocytes.
Needle Aspiration
The swelling should be aspirated with a large-bore needle (not smaller than 18 gauge) to
confirm the presence of pus. The aspirated pus is usually yellowish in color but may be brownish or blood-stained.
Microbiological Examination
The aspirated [ and/or drained pus] should be subjected to gram staining, aerobic and anaerobic culture, and drug sensitivity.
A biopsy of the abscess wall and/or muscle is taken at the time of open drainage should also be cultured.
Imaging
Electromyography
Short duration, low amplitude polyphasic potentials
Ultrasonography
First imaging investigation usually
Characteristic features are
- Muscle swelling;
- Hypoechoic areas in the muscle belly
- Heterogenous hypoechoic areas
- Hyperechoic areas.
X-ray
X-rays of the affected part esp the limb should always be done to rule out acute osteomyelitis.
Otherwise, x-rays would be normal. However, it should be remembered that x-ray changes in osteomyelitis may take about 10 days to appear and in the early period, the x-ray may be normal in spite of osteomyelitis.
The chest x-ray may be done if there are chest symptoms present due to complications like pneumonia etc.
MRI
MRI is the modality of choice for accurate assessment of muscle involvement.
Muscle edema [high T2 signal], fluid collection with peripheral contrast enhancement and diffuse muscle enlargement are seen. MRI is especially useful in deeply seated muscles.
MRI with gadolinium enhancement can increase the confidence of identifying or excluding the presence of abscess but this may give high-dose irradiation to the child.
CT
Enlargement and decreased attenuation of the affected muscle with effacement and stranding of surrounding fat planes.
If an abscess is present it will appear as an intramuscular fluid collection with peripheral rim-enhancement.
Differential Diagnoses
- Pyrexia of unknown origin
- Muscle contusion
- Septic arthritis
- Osteomyelitis
- Cellulitis
- Muscle hematoma
- Deep vein thrombosis
- Muscle rupture or muscle strain
- Osteosarcoma of muscle
- Trichinosis
- Leptospirosis
- Cysticercosis
- Toxoplasmosis
Treatment of Pyomyositis
Pyomyositis demands aggressive management. This includes immediate administration of broad-spectrum antibiotics.
Diffuse myositis without abscess may respond to an antimicrobial agent alone but abscess may develop eventually requiring drainage. Following this, the abscess cavity must be prevented from premature closure by packing and daily dressing.
First-generation cephalosporin along with aminoglycosides are commonly used empirical antibiotics and once a culture sensitivity report is available, the antibiotics are changed accordingly.
For HIV infection and immunosuppressed patients, clindamycin may be added.
The treatment should be continued till the wound is clean, the leucocyte count becomes normal, and the patient is afebrile for 7–10 days.
The affected part, especially limbs are splinted for rest.
Patients may be anemic, particularly those presenting late. Any severe anemia may require correction by blood transfusion. Patients who are malnourished will require some form of nutritional support and rehabilitation.
REFERENCES
- Gibson RK, Rosenthal SJ, Lukert BP. Pyomyositis: increasing recognition in temperate climates. Am J Med1984;77:768–72.
- Malhotra P, Singh S, Sud A, et al. Tropical pyomysitis—experience of a tertiary care hospital in North West India. J Assoc Physicians India2000;48:1057–60.
- Bonafede P, Butler J, Kimbrough R, et al. Temperate zone pyomyositis. West J Brook I. Pyomyositis in children, caused by anaerobic bacteria. J Pediatr Surg1996;31:394–6.
