Description
A 75-year-old man presented with a 2-month history of worsening chest and back pain. Physical examination revealed generalised bone tenderness with associated indirect pain; digital rectal examination indicated asymmetric prostatic induration. Laboratory examination revealed high serum alkaline phosphatase (1348 U/L (bone type, 73.2%)), high C reactive protein (4.5 mg/dL), high serum ferritin (2952 ng/mL) and high prostate-specific antigen (1346 ng/mL). A whole-body technetium-99m methyldiphosphonate (Tc-99m MDP) scan revealed increase in bone uptake with diminished soft tissue activity, faint kidney visualisation and bladder activity; a diagnosis of ‘super bone scan’ was made (figure 1). Prostate biopsy revealed adenocarcinoma. The diagnosis was bone metastases from prostate cancer. Antiandrogens and GnRH antagonists were administered. At the 3-month follow-up, the pain, alkaline phosphatase, serum ferritin and prostate-specific antigen had improved.
Super bone scan is a special condition of extremely high bone uptake relative to soft tissue with absent renal radioactivity visualisation (‘absent kidney sign’).1 About 40–60% of the injected Tc-99m MDP is excreted in the urine.2 Therefore, significant renal and bladder radioactivity are normal in most scans. A super bone scan may result from a widespread skeletal process in which there is increased deposition of the bone agent in sites of metabolically active bone. Super bone scans have been described in relation to several conditions such as metastatic disease (prostate/breast cancer), metabolic bone disease (Paget disease/hyperparathyroidism) and myeloproliferative disorders.2
Learning points.
Super bone scan is a special condition of extremely high bone uptake relative to soft tissue with absent or faint renal radioactivity visualisation.
In any normal bone scan, one expects to see the kidneys and bladder secondary to normal renal excretion of the tracer.
Super bone scan implicates diffuse metastatic disease, metabolic bone disease and myeloproliferative disorders.
Footnotes
Contributors: All authors were involved in the management of the patient. KS wrote the first draft. MI edited the manuscript.
Competing interests: None.
Patient consent: Obtained.
Provenance and peer review: Not commissioned; externally peer reviewed.
References
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