医学
平滑肌肉瘤
原发性肿瘤
病理
平滑肌肿瘤
放射科
癌症
转移
内科学
作者
L. Kropp,Gene P. Siegal,Garrett M. Frampton,Michael G. Rodriguez,Svetlana B. McKee,Robert M. Conry
出处
期刊:Rare Tumors
[SAGE Publishing]
日期:2016-11-01
卷期号:8 (4): 155-158
被引量:4
摘要
We report the first case of primary intraosseous smooth muscle tumor of uncertain malignant potential (STUMP) which is analogous to borderline malignant uterine smooth muscle tumors so designated. The tumor presented in the femur of an otherwise healthy 30-year-old woman. Over a 3-year period, the patient underwent 11 biopsies or resections and 2 cytologic procedures. Multiple pathologists reviewed the histologic material including musculoskeletal pathologists but could not reach a definitive diagnosis. However, metastases eventually developed and were rapidly progressive and responsive to gemcitabine and docetaxel. Molecular characterization and ultrastructural analysis was consistent with smooth muscle origin, and amplification of unmutated chromosome 12p and 12q segments appears to be the major genomic driver of this tumor. Primary intraosseous STUMP is thought to be genetically related to leiomyosarcoma of bone, but likely representing an earlier stage of carcinogenesis. Wide excision and aggressive follow-up is warranted for this potentially life-threatening neoplasm.
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