2002
DOI: 10.1046/j.1440-1673.2001.00989.x
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Soft tissue uptake on 99mTc methylene diphosphonate bone scan imaging: Pictorial review

Abstract: 99mTechnetium methylene diphosphonate (MDP) bone isotope may accumulate in many extra-osseous sites due to a variety of both benign and malignant conditions. This finding on a bone scan can be crucial to the diagnosis and may not be apparent in other imaging or the clinical evaluation of the patient. We present a pictorial review sampling some of the many causes of extra-osseous 99mTc MDP accumulation.

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Cited by 42 publications
(26 citation statements)
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“…Previous reports showed that sometimes tracer uptake during bone scintigraphy precedes detection of ectopic calcification by other modalities, such as CT or plain radiography. 11 In our case the increased HMDP uptake preceded the detection of ectopic calcification by CT in the affected muscles.…”
Section: Discussionsupporting
confidence: 58%
“…Previous reports showed that sometimes tracer uptake during bone scintigraphy precedes detection of ectopic calcification by other modalities, such as CT or plain radiography. 11 In our case the increased HMDP uptake preceded the detection of ectopic calcification by CT in the affected muscles.…”
Section: Discussionsupporting
confidence: 58%
“…It is imperative that the interpreting physician has an understanding of the wide range of causes of uptake in extraosseous structures, because many of these findings are artifactual or related to quality-control issues and could be misinterpreted as disease [6]. The detection, proper analysis, and reporting of these extraosseous findings are important because they may alert the referring physician to previously undetected disease processes [6,7].…”
Section: Extraosseous Radiotracer Distribution On Bone Scintigraphy Pmentioning
confidence: 99%
“…The range of underlying entities can generally be categorized into several basic classes according to mechanism: vascular entities (altered regional blood flow, blood volume, capillary permeability, and com- partmental sequestration), neoplasms, extraosseous calcifications (dystrophic or tissue injury), and metabolic entities (metabolic bone disease or malignant calcification) [3][4][5][6][7]. It should be noted that these mechanisms are often multifactorial [6].…”
Section: Extraosseous Radioactivity In Soft-tissue Structures Comparmentioning
confidence: 99%
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“…[1234] Multiple factors can affect extra-osseous MDP uptake: (1) Technical factors, (2) primary malign and metastatic lesions, (3) soft tissue, (4) amyloidosis, (5) infraction, (6) hypercalcemia, (7) inflammation, (8) chemotherapy and (9) radiotherapy. [5678] MDP accumulates, especially within calcified hepatic metastasis. However, in the present case, liver metastasis not showed calcification in CT examination.…”
Section: Discussionmentioning
confidence: 99%