Summary:
Chronic osteomyelitis from Staphylococcus aureus
Radiography of the left femur revealed lucency with fuzzy sclerotic
margin of Brodie's abscess and bony remodeling (Figure 1). MR
imaging showed an ovoid well-circumscribed area of low T1 signal
intensity with peripheral ring enhancement and surroundin
Diagnosis
Chronic osteomyelitis from
Staphylococcus aureus
Findings
Radiography of the left femur revealed lucency with fuzzy sclerotic
margin of Brodie's abscess and bony remodeling (Figure 1). MR
imaging showed an ovoid well-circumscribed area of low T1 signal
intensity with peripheral ring enhancement and surrounding bone
marrow edema (Figures 2 through 3). The short tau inversion
recovery (STIR) images showed high signal intensity within the
marrow, which is characteristic of osteomyelitis (Figure 4).
Incision and trephination were performed; pathologic examination
after orthopedic intramedullary placement is shown in Figure 5. A
tobramycinimpregnated cemented implant was subsequently placed
(Figure 6), and the patient was treated with 6 weeks of intravenous
antibiotics. The cemented implant was removed after 8 weeks.
Discussion
Osteomyelitis presents in 3 stages with ill-defined transitions:
Acute, subacute, and chronic.
1 Transition from acute to
subacute or chronic indicates that therapeutic measures have been
inadequate or inappropriate or that the organisms are especially
resistant to accepted modes of therapy. Four routes of infection
predominate: Hematogenous spread, contiguous spread (usually
cutaneous, sinus, or dental in origin), direct implantation
(usually from trauma), or postoperative infection.
1
Hematogenous spread is usually caused by
Staphylococcus
aureus. Delay in the treatment of osteomyelitis significantly
decreases the cure rate and increases the rate of complications and
morbidity.
2 The differential diagnostic considerations
for osteolytic foci in the epiphysis include giant-cell tumor,
clear-cell chondrosarcoma, osteonecrosis, fibrous dysplasia,
intraosseus ganglion, and subchondral cyst.
1
The radiographic findings may be normal for the first 10 to 21
days after the onset of infection because 30% to 50% of bone
density must be lost before a lucency can be
appreciated.2 Detection of chronic osteomyelitis is also
difficult because a sequestrum is visible in only 9% of cases.
Progressive changes on serial radiographs have a sensitivity of 14%
and specificity of 70%.2
Radiographs are typically obtained first, but the detection of
marrow abnormality on MRI is a more sensitive indicator of
osteomyelitis than are the lytic changes seen on plain
radiography.3 Osteomyelitis is visible as a low signal
intensity on T1-weighted images and high signal intensity on
T2weighted, STIR, or fat-saturated images.2 The STIR
pulse sequence is considered highly sensitive for abnormalities
with a negative predictive value approaching 100% for acute
osteomyelitis. The STIR images have a lower spatial resolution and
cannot clearly illustrate the differentiation of abscess from
soft-tissue edema.2
Acute and chronic osteomyelitis can be differentiated in several
ways. MR imaging findings that suggest the presence of active
chronic osteomyelitis include sequestra, cloacae, abscesses, and
subperiosteal fluid collection. MRI findings favoring acute
infection include a wide zone of transition and poor definition
between normal and diseased marrow. Findings favoring chronic
infection include a relatively sharp interface between normal and
diseased marrow.2
Brodie's abscess is a form of subacute to chronic osteomyelitis,
classically defined as a sharply delineated focus of infection
lined by granulation tissue and frequently surrounded by eburnated
bone.4This case revealed a rounded, well-circumscribed
area of low T1 signal intensity with gadolinium administration
characteristic of chronic osteomyelitis.2 It has also
been reported that the more profound the T2 signal intensity in the
bone marrow, the more likely the abnormality is
osteomyelitis.2
CONCLUSION
The authors have presented a case of chronic osteomyelitis with
characteristic radiographic, MR, and pathologic features. MR
imaging can be very helpful in the workup of patients suspected of
having this diagnosis.
- Resnick D. Diagnosis of Bone and Joint Disorders.Vol 3. 4th ed.
Philadelphia, PA: W.B. Saunders; 2002:2378-2379, 2418-2419.
- Tehranzadeh J, Wong E, Wang F, Sadighpour M. Imaging of
osteomyelitis in the mature skeleton. Radiol Clin North
Am.2001;39:223-250.
- Jurriaans E, Singh NP, Finlay K, Friedman L. Imaging chronic
recurrent multifocal osteomyelitis. Radiol Clin North
Am.2001;39:305-327.
- Resnick D. Bone and Joint Imaging.2nd ed. Philadelphia, PA:
W.B. Saunders; 1996:650.
Products used
- Omniscan (GE Healthcare, Princeton, NJ)
- 1.5T MR scanner (Philips Medical Systems, Bothell, WA)
- Plain film equipment (GE Healthcare, Waukesha, WI)