T1-weighted MRI imaging features of pathologically proven non-pedal osteomyelitis.

Abstract:

RATIONALE AND OBJECTIVES:The objective of our study was to determine if the T1-weighted magnetic resonance imaging (MRI) features associated with diabetic pedal osteomyelitis are present in histopathologically proven cases of non-pedal osteomyelitis. MATERIALS AND METHODS:Seventy-five patients with a histopathologically proven diagnosis of non-pedal osteomyelitis and a preoperative MRI were identified between 2000 and 2007. The MRIs were retrospectively reviewed for signal characterization of T1-weighted images, including the signal intensity compared with skeletal muscle, distribution of abnormal signal intensity, and pattern of abnormal signal intensity. A subsequent chart review was performed to identify potential clinical factors that were more associated with atypical T1 features of osteomyelitis. Fisher's exact test was performed to determine if there was a statistically significant difference in the T1-weighted imaging features of the hematogenous and nonhematogenous mechanisms of infection. RESULTS:Seventy of 75 cases demonstrated T1-weighted imaging features typical of pedal osteomyelitis with a confluent region of decreased signal intensity, hypointense, or isointense relative to skeletal muscle in a geographic pattern with medullary distribution. Of the 5 cases that did not demonstrate the typical T1 features associated with pedal osteomyelitis, 4 were considered to have a hematologic mechanism of infection given the absence of surgery, skin ulceration, or a penetrating injury. CONCLUSION:The majority of cases of non-pedal osteomyelitis in our study demonstrate the typical T1-weighted imaging features previously documented to correlate with the diagnosis of pedal osteomyelitis. The cases in our series that did not demonstrate the typical T1-weighted features were predominantly secondary to a hematologic mechanism of infection.

journal_name

Acad Radiol

journal_title

Academic radiology

authors

Howe BM,Wenger DE,Mandrekar J,Collins MS

doi

10.1016/j.acra.2012.07.015

subject

Has Abstract

pub_date

2013-01-01 00:00:00

pages

108-14

issue

1

eissn

1076-6332

issn

1878-4046

pii

S1076-6332(12)00419-9

journal_volume

20

pub_type

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