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Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization

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 p...

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Autores principales: Kropp, Lauren, Siegal, Gene P., Frampton, Garrett M., Rodriguez, Michael G., McKee, Svetlana, Conry, Robert M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136771/
https://www.ncbi.nlm.nih.gov/pubmed/27994831
http://dx.doi.org/10.4081/rt.2016.6507
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author Kropp, Lauren
Siegal, Gene P.
Frampton, Garrett M.
Rodriguez, Michael G.
McKee, Svetlana
Conry, Robert M.
author_facet Kropp, Lauren
Siegal, Gene P.
Frampton, Garrett M.
Rodriguez, Michael G.
McKee, Svetlana
Conry, Robert M.
author_sort Kropp, Lauren
collection PubMed
description 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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spelling pubmed-51367712016-12-19 Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization Kropp, Lauren Siegal, Gene P. Frampton, Garrett M. Rodriguez, Michael G. McKee, Svetlana Conry, Robert M. Rare Tumors Case Report 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. PAGEPress Publications, Pavia, Italy 2016-11-17 /pmc/articles/PMC5136771/ /pubmed/27994831 http://dx.doi.org/10.4081/rt.2016.6507 Text en ©Copyright L. Kropp et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kropp, Lauren
Siegal, Gene P.
Frampton, Garrett M.
Rodriguez, Michael G.
McKee, Svetlana
Conry, Robert M.
Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization
title Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization
title_full Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization
title_fullStr Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization
title_full_unstemmed Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization
title_short Primary Intraosseous Smooth Muscle Tumor of Uncertain Malignant Potential: Original Report and Molecular Characterization
title_sort primary intraosseous smooth muscle tumor of uncertain malignant potential: original report and molecular characterization
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136771/
https://www.ncbi.nlm.nih.gov/pubmed/27994831
http://dx.doi.org/10.4081/rt.2016.6507
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