Affiliation:
1. Department of Internal Medicine and Cancer Research Center, Korea
2. Department of Pathology, Seoul National University College of Medicine, Seoul, Korea
Abstract
Background Metastasis of unknown origin in bone marrow is infrequent, although, when it occurs, adenocarcinoma is the most common histologic type. Involvement of bone marrow by a spindle cell tumor and presentation with hypercalcemia are very rare. Method This report describes a 21-year-old man with diffuse bone marrow involvement from a spindle cell tumor. Results The patient presented with low back pain, anemia, thrombocytopenia, azotemia, and hypercalcemia. Bone marrow biopsy revealed a spindle cell tumor that was positive for vimentin staining but whose primary site could not be identified. A bone marrow scan revealed absence of uptake, which suggested systemic disease. We treated this case as a type of sarcoma by giving combined chemotherapy consisting of vincristine, actinomycin-D and cyclophosphamide. The patient showed a clinical response for seven months, but the disease progressed despite chemotherapy and he died one year after diagnosis. Conclusions We have documented a rare case of spindle cell tumor involving bone marrow without evidence of the tumor's primary site.
Subject
Cancer Research,Oncology,General Medicine
Cited by
1 articles.
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