Bone Marrow Failure in Prostate Cancer: A Rare Case Initially Disguised as Thrombotic Thrombocytopenic Purpura
Sunil R Dommaraju, Michael Shodiya, Kathryn Henick

TL;DR
A rare case of prostate cancer metastasizing to the bone marrow was initially mistaken for a blood disorder called thrombotic thrombocytopenic purpura.
Contribution
This case report highlights the diagnostic challenge of bone marrow metastasis from prostate cancer masquerading as thrombotic thrombocytopenic purpura.
Findings
Bone marrow metastasis from prostate cancer can present with symptoms resembling thrombotic thrombocytopenic purpura.
Only six percent of metastatic castrate-sensitive prostate cancer cases have biopsy-proven bone marrow metastasis.
BM involvement in prostate cancer complicates prognosis and requires further research into targeted therapies.
Abstract
Prostate cancer is the second most common cause of cancer-related death and the leading cause of new cancer cases in men in the United States. Bone trabeculae are the most common site of metastasis for prostate cancer, but bone marrow (BM) involvement is rare. Around six percent of patients with new metastatic castrate-sensitive prostate cancer (mCSPC) have biopsy-proven BM metastasis. We present a case of mCSPC with BM metastasis initially disguised as thrombotic thrombocytopenic purpura (TTP). Initial presentation revealed anemia and thrombocytopenia with a peripheral blood smear indicating thrombotic microangiopathy. Empiric treatment for TTP was initiated, but the patient showed no improvement. A BM biopsy performed on hospital day 5 for further work-up of the refractory cytopenias eventually identified metastatic prostate adenocarcinoma. The patient started androgen deprivation…
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Taxonomy
TopicsHemoglobinopathies and Related Disorders · Erythropoietin and Anemia Treatment · Acute Myeloid Leukemia Research
