Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report
Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right...
Ausführliche Beschreibung
Autor*in: |
Hughes, Liam P. [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2022 |
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Anmerkung: |
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 |
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Übergeordnetes Werk: |
Enthalten in: SN comprehensive clinical medicine - [Cham] : Springer International Publishing, 2019, 4(2022), 1 vom: 21. Juni |
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Übergeordnetes Werk: |
volume:4 ; year:2022 ; number:1 ; day:21 ; month:06 |
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DOI / URN: |
10.1007/s42399-022-01210-4 |
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Katalog-ID: |
SPR047367415 |
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520 | |a Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. | ||
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700 | 1 | |a Harrop, James S. |4 aut | |
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10.1007/s42399-022-01210-4 doi (DE-627)SPR047367415 (SPR)s42399-022-01210-4-e DE-627 ger DE-627 rakwb eng Hughes, Liam P. verfasserin (orcid)0000-0001-7900-5151 aut Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. Myxoma (dpeaa)DE-He213 Paraspinal tumor (dpeaa)DE-He213 Spine surgery (dpeaa)DE-He213 Lumbar spine (dpeaa)DE-He213 Prodoehl, John Paul aut Elia, Christopher J. aut Sabourin, Victor aut Curtis, Mark T. aut Harrop, James S. aut Enthalten in SN comprehensive clinical medicine [Cham] : Springer International Publishing, 2019 4(2022), 1 vom: 21. Juni (DE-627)1037103696 (DE-600)2947252-0 2523-8973 nnns volume:4 year:2022 number:1 day:21 month:06 https://dx.doi.org/10.1007/s42399-022-01210-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 4 2022 1 21 06 |
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10.1007/s42399-022-01210-4 doi (DE-627)SPR047367415 (SPR)s42399-022-01210-4-e DE-627 ger DE-627 rakwb eng Hughes, Liam P. verfasserin (orcid)0000-0001-7900-5151 aut Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. Myxoma (dpeaa)DE-He213 Paraspinal tumor (dpeaa)DE-He213 Spine surgery (dpeaa)DE-He213 Lumbar spine (dpeaa)DE-He213 Prodoehl, John Paul aut Elia, Christopher J. aut Sabourin, Victor aut Curtis, Mark T. aut Harrop, James S. aut Enthalten in SN comprehensive clinical medicine [Cham] : Springer International Publishing, 2019 4(2022), 1 vom: 21. Juni (DE-627)1037103696 (DE-600)2947252-0 2523-8973 nnns volume:4 year:2022 number:1 day:21 month:06 https://dx.doi.org/10.1007/s42399-022-01210-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 4 2022 1 21 06 |
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10.1007/s42399-022-01210-4 doi (DE-627)SPR047367415 (SPR)s42399-022-01210-4-e DE-627 ger DE-627 rakwb eng Hughes, Liam P. verfasserin (orcid)0000-0001-7900-5151 aut Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. Myxoma (dpeaa)DE-He213 Paraspinal tumor (dpeaa)DE-He213 Spine surgery (dpeaa)DE-He213 Lumbar spine (dpeaa)DE-He213 Prodoehl, John Paul aut Elia, Christopher J. aut Sabourin, Victor aut Curtis, Mark T. aut Harrop, James S. aut Enthalten in SN comprehensive clinical medicine [Cham] : Springer International Publishing, 2019 4(2022), 1 vom: 21. Juni (DE-627)1037103696 (DE-600)2947252-0 2523-8973 nnns volume:4 year:2022 number:1 day:21 month:06 https://dx.doi.org/10.1007/s42399-022-01210-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 4 2022 1 21 06 |
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10.1007/s42399-022-01210-4 doi (DE-627)SPR047367415 (SPR)s42399-022-01210-4-e DE-627 ger DE-627 rakwb eng Hughes, Liam P. verfasserin (orcid)0000-0001-7900-5151 aut Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. Myxoma (dpeaa)DE-He213 Paraspinal tumor (dpeaa)DE-He213 Spine surgery (dpeaa)DE-He213 Lumbar spine (dpeaa)DE-He213 Prodoehl, John Paul aut Elia, Christopher J. aut Sabourin, Victor aut Curtis, Mark T. aut Harrop, James S. aut Enthalten in SN comprehensive clinical medicine [Cham] : Springer International Publishing, 2019 4(2022), 1 vom: 21. Juni (DE-627)1037103696 (DE-600)2947252-0 2523-8973 nnns volume:4 year:2022 number:1 day:21 month:06 https://dx.doi.org/10.1007/s42399-022-01210-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 4 2022 1 21 06 |
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Hughes, Liam P. @@aut@@ Prodoehl, John Paul @@aut@@ Elia, Christopher J. @@aut@@ Sabourin, Victor @@aut@@ Curtis, Mark T. @@aut@@ Harrop, James S. @@aut@@ |
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Hughes, Liam P. misc Myxoma misc Paraspinal tumor misc Spine surgery misc Lumbar spine Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report |
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Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report Myxoma (dpeaa)DE-He213 Paraspinal tumor (dpeaa)DE-He213 Spine surgery (dpeaa)DE-He213 Lumbar spine (dpeaa)DE-He213 |
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intramuscular myxoma of the lumbar paraspinal musculature: case report |
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Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report |
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Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 |
abstractGer |
Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 |
abstract_unstemmed |
Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. In this case, the patient is a 57-year-old female who presented with an incidental finding of a right paraspinal mass at the L4 level on routine magnetic resonance imaging (MRI). Using intraoperative navigation, an incision was made along the paraspinal muscles, and the tumor was removed with margins. The patient stayed for overnight observation and was then discharged the following morning with no complications and proper pain management. At 1-year follow-up, she was clinically doing well with no radiographic evidence of recurrence. This report demonstrates the 9th documented case of an IMM in the lumbosacral paraspinal musculature. IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection. © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022 |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR047367415</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519200635.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">220622s2022 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s42399-022-01210-4</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR047367415</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s42399-022-01210-4-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Hughes, Liam P.</subfield><subfield code="e">verfasserin</subfield><subfield code="0">(orcid)0000-0001-7900-5151</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Intramuscular Myxoma of the Lumbar Paraspinal Musculature: Case Report</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2022</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Paraspinal intramuscular myxomas (IMMs) are exceedingly uncommon and may cause neurological symptoms due to mass effect on the spinal cord, although most present as large, painless masses. 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IMMs are distinct from other myxoid tumors in that they have no recurrence rate if the tumor is resected in its entirety with appropriate margins; therefore, it is essential to consider this pathology prior to surgical planning to ensure maximal resection.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Myxoma</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Paraspinal tumor</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Spine surgery</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Lumbar spine</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Prodoehl, John Paul</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Elia, Christopher J.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sabourin, Victor</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Curtis, Mark T.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Harrop, James S.</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">SN comprehensive clinical medicine</subfield><subfield code="d">[Cham] : Springer International Publishing, 2019</subfield><subfield code="g">4(2022), 1 vom: 21. 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