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Superficial low‐grade fibromyxoid sarcoma
BACKGROUND: Low‐grade fibromyxoid sarcoma (LGFMS) typically involves deep soft tissue (beneath the fascia) of the proximal extremities and trunk. Long‐term follow‐up has shown a high rate of local recurrence, metastasis, and death. To the best of our knowledge, there is only one previous large serie...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091772/ https://www.ncbi.nlm.nih.gov/pubmed/36074249 http://dx.doi.org/10.1111/cup.14325 |
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author | Ronen, Shira Ko, Jennifer S. Rubin, Brian P. Kilpatrick, Scott E. Wang, Wei‐Lien Lazar, Alexander J. Goldblum, John R. Billings, Steven D. |
author_facet | Ronen, Shira Ko, Jennifer S. Rubin, Brian P. Kilpatrick, Scott E. Wang, Wei‐Lien Lazar, Alexander J. Goldblum, John R. Billings, Steven D. |
author_sort | Ronen, Shira |
collection | PubMed |
description | BACKGROUND: Low‐grade fibromyxoid sarcoma (LGFMS) typically involves deep soft tissue (beneath the fascia) of the proximal extremities and trunk. Long‐term follow‐up has shown a high rate of local recurrence, metastasis, and death. To the best of our knowledge, there is only one previous large series focusing on superficial LGFMS suggesting superficial tumors are disproportionately more common in children and may have a better prognosis. Our study's primary goals are to confirm these findings and increase general awareness that LGFMS may arise in superficial soft tissue. METHODS: We retrieved our cases of superficial LGFMS diagnosed between 2008 and 2020. Available slides were reviewed, and clinical data and follow‐up information were obtained. RESULTS: The patients included nine males and 14 females with a median age of 29 years; eight (35%) were children (<18 years) and five (22%) were young adults (18–30 years). The majority involved the lower extremities (65%). The tumors were primarily centered in the subcutis (91%) and dermis (9%). Microscopically, they had typical features of LGFMS with alternating fibrous and myxoid zones composed of bland, slightly hyperchromatic spindled cells. All were positive for MUC4 by immunohistochemistry and/or FUS rearrangement by FISH. Follow‐up on 14 cases ranged from 11 to 148 months (median 61 months) with no evidence of recurrences or distant metastases. CONCLUSIONS: Compared to conventional deep‐seated counterparts, superficial LGFMS is more likely to occur in the extremities of children and young adults and may have a better clinical outcome. Further studies with longer follow‐up will likely help support these findings. |
format | Online Article Text |
id | pubmed-10091772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Blackwell Publishing Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100917722023-04-13 Superficial low‐grade fibromyxoid sarcoma Ronen, Shira Ko, Jennifer S. Rubin, Brian P. Kilpatrick, Scott E. Wang, Wei‐Lien Lazar, Alexander J. Goldblum, John R. Billings, Steven D. J Cutan Pathol Original Articles BACKGROUND: Low‐grade fibromyxoid sarcoma (LGFMS) typically involves deep soft tissue (beneath the fascia) of the proximal extremities and trunk. Long‐term follow‐up has shown a high rate of local recurrence, metastasis, and death. To the best of our knowledge, there is only one previous large series focusing on superficial LGFMS suggesting superficial tumors are disproportionately more common in children and may have a better prognosis. Our study's primary goals are to confirm these findings and increase general awareness that LGFMS may arise in superficial soft tissue. METHODS: We retrieved our cases of superficial LGFMS diagnosed between 2008 and 2020. Available slides were reviewed, and clinical data and follow‐up information were obtained. RESULTS: The patients included nine males and 14 females with a median age of 29 years; eight (35%) were children (<18 years) and five (22%) were young adults (18–30 years). The majority involved the lower extremities (65%). The tumors were primarily centered in the subcutis (91%) and dermis (9%). Microscopically, they had typical features of LGFMS with alternating fibrous and myxoid zones composed of bland, slightly hyperchromatic spindled cells. All were positive for MUC4 by immunohistochemistry and/or FUS rearrangement by FISH. Follow‐up on 14 cases ranged from 11 to 148 months (median 61 months) with no evidence of recurrences or distant metastases. CONCLUSIONS: Compared to conventional deep‐seated counterparts, superficial LGFMS is more likely to occur in the extremities of children and young adults and may have a better clinical outcome. Further studies with longer follow‐up will likely help support these findings. Blackwell Publishing Ltd. 2022-11-02 2023-02 /pmc/articles/PMC10091772/ /pubmed/36074249 http://dx.doi.org/10.1111/cup.14325 Text en © 2022 The Authors. Journal of Cutaneous Pathology published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Ronen, Shira Ko, Jennifer S. Rubin, Brian P. Kilpatrick, Scott E. Wang, Wei‐Lien Lazar, Alexander J. Goldblum, John R. Billings, Steven D. Superficial low‐grade fibromyxoid sarcoma |
title | Superficial low‐grade fibromyxoid sarcoma |
title_full | Superficial low‐grade fibromyxoid sarcoma |
title_fullStr | Superficial low‐grade fibromyxoid sarcoma |
title_full_unstemmed | Superficial low‐grade fibromyxoid sarcoma |
title_short | Superficial low‐grade fibromyxoid sarcoma |
title_sort | superficial low‐grade fibromyxoid sarcoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091772/ https://www.ncbi.nlm.nih.gov/pubmed/36074249 http://dx.doi.org/10.1111/cup.14325 |
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