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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...

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Autores principales: Ronen, Shira, Ko, Jennifer S., Rubin, Brian P., Kilpatrick, Scott E., Wang, Wei‐Lien, Lazar, Alexander J., Goldblum, John R., Billings, Steven D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd. 2022
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.
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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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