Abstract
In this report, we present a case of liver uptake seen on a bone scan that was due to diffuse metastatic disease from breast carcinoma. We discuss possible etiologies for the uptake and offer an algorithm to narrow the differential diagnosis.
Hepatic uptake of 99mTc-methylene diphosphonate is an unexpected finding and should trigger a set of questions by the interpreting physician, as the distinction between technical and pathologic causes is critical to direct further evaluation of the patient.
CASE REPORT
A 54-y-old woman had a past medical history of right breast cancer and had undergone mastectomy with breast reconstruction and chemotherapy 2 y before presentation. She developed a fever and was admitted to the hospital for further evaluation. Laboratory studies were remarkable for elevated levels of alkaline phosphatase (413 U/L), aspartate aminotransferase (300 U/L), and alanine aminotransferase (272 U/L).
As part of the work-up, a 99mTc-methylene diphosphonate bone scan was obtained to evaluate for osseous metastasis. Three hours after intravenous administration of 814 MBq (22 mCi) of 99mTc-methylene diphosphonate, anterior and posterior whole-body and spot views were obtained. Whole-body images showed abnormal ill-defined radiotracer uptake in the right upper quadrant of the abdomen, suggesting liver uptake (Figs. 1 and 2). A subtle photopenic defect was present over the right upper anterior thorax, corresponding to the patient’s known breast implant.
Given the patient’s history of breast cancer and the abnormal results from the liver function studies, concern about metastatic disease to the liver was raised. She underwent further evaluation with contrast-enhanced CT of the chest, abdomen, and pelvis, which confirmed hepatomegaly with extensive metastases (Fig. 3). The patient began to experience mental status changes secondary to hepatic encephalopathy and, less than 2 wk after the bone scan, died.
DISCUSSION
In view of the abnormal liver uptake on the bone scan, the need for a regimented interpretation algorithm in this patient was strongly suggested, especially since a detailed history was not available. We recommend the following approach when one is faced with such a case. First, determine whether the patient has undergone a recent nuclear medicine study that would interfere with the bone scan. Examples include a 99mTc-sulfur colloid or 99mTc-labeled white blood cell scan within the last day or an 111In-labeled white blood cell or 67Ga scan within the last week. Additional uptake within the spleen would point toward recent 99mTc-sulfur colloid or 111In-labeled white blood cell injection, whereas activity in the colon would support 67Ga administration. The next step is to determine whether the dose of 99mTc-methylene diphosphonate was degraded by excess alumina chemical impurity, resulting in colloid formation with subsequent liver uptake. The maximum permissible amount of aluminum ion is 10 μg/mL of 99mTc eluate. Diffuse liver uptake with reduced bone uptake supports this conclusion (1). Uptake may also be present in the spleen and bone marrow (2). Finally, one should consider whether the patient has primary or metastatic liver disease. Heterogeneous uptake in the liver is more suggestive of primary and metastatic disease, and the liver may also be enlarged.
CONCLUSION
When faced with unexpected hepatic uptake on a bone scan, the interpreting physician must first exclude technical factors before recommending a work-up for liver disorders. In particular, the presence of alumina and recent administration of various radiopharmaceuticals can mimic liver disease. The interpreting physician should consider all available clues, particularly when a sufficient history is not available. These clues include a high index of suspicion for signs of metastatic disease, a search for additional uptake in the spleen and gastrointestinal tract to suggest prior administration of various radiopharmaceuticals, and scrutiny of the distribution of liver uptake.
DISCLOSURE
No potential conflict of interest relevant to this article was reported.
Footnotes
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Published online Dec. 23, 2014.
REFERENCES
- Received for publication July 30, 2014.
- Accepted for publication October 15, 2014.