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Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report

RATIONALE: Follicular dendritic cell sarcoma (FDCS) is an intermediate-grade malignancy originating from follicular dendritic cells. Nodal FDCS is the most common type, meaning that the extranodal type may not be recognized and could be easily misdiagnosed. Reported extranodal sites include the head...

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Autores principales: Cho, Yong Jin, Han, Song Iy, Lim, Sung-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428715/
https://www.ncbi.nlm.nih.gov/pubmed/34516525
http://dx.doi.org/10.1097/MD.0000000000027209
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author Cho, Yong Jin
Han, Song Iy
Lim, Sung-Chul
author_facet Cho, Yong Jin
Han, Song Iy
Lim, Sung-Chul
author_sort Cho, Yong Jin
collection PubMed
description RATIONALE: Follicular dendritic cell sarcoma (FDCS) is an intermediate-grade malignancy originating from follicular dendritic cells. Nodal FDCS is the most common type, meaning that the extranodal type may not be recognized and could be easily misdiagnosed. Reported extranodal sites include the head and neck, retroperitoneum, spleen, liver, and gastrointestinal tract. FDCS in the soft tissue is extremely rare. PATIENT CONCERNS: A 75-year-old male presented with complaints of a localized swelling and intra-muscular soft tissue mass in the left upper thigh. DIAGNOSIS: The present tumor consisted of fascicular or vague storiform-arranged spindle cells with less pleomorphism and many lymphoid aggregates. Tumor cells were positive for CD21, CD35, CD68, vimentin, and EGFR. Intra-muscular FDCS was confirmed by immunohistochemical studies. INTERVENTIONS: The patient received a wide marginal excision, followed by adjuvant radiotherapy. OUTCOMES: Symptomatic improvements were achieved and no subsequent relapses were observed. LESSONS: If the tumor arises in the extranodal sites, especially in the soft tissue, it is difficult to include FDCS in the differential diagnosis. When the immunoprofile is not consistent with that of common spindle cell tumors, immunostaining for follicular dendritic cell markers such as CD21, CD23, and CD35, as well as further immunohistochemistry for D2-40, CD68, EGFR, Epstein-Barr virus, and BRAF can be helpful for the diagnosis and subtyping of FDCS. To the best of our knowledge, the present case is the first case of intramuscular FDCS.
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spelling pubmed-84287152021-09-13 Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report Cho, Yong Jin Han, Song Iy Lim, Sung-Chul Medicine (Baltimore) 5700 RATIONALE: Follicular dendritic cell sarcoma (FDCS) is an intermediate-grade malignancy originating from follicular dendritic cells. Nodal FDCS is the most common type, meaning that the extranodal type may not be recognized and could be easily misdiagnosed. Reported extranodal sites include the head and neck, retroperitoneum, spleen, liver, and gastrointestinal tract. FDCS in the soft tissue is extremely rare. PATIENT CONCERNS: A 75-year-old male presented with complaints of a localized swelling and intra-muscular soft tissue mass in the left upper thigh. DIAGNOSIS: The present tumor consisted of fascicular or vague storiform-arranged spindle cells with less pleomorphism and many lymphoid aggregates. Tumor cells were positive for CD21, CD35, CD68, vimentin, and EGFR. Intra-muscular FDCS was confirmed by immunohistochemical studies. INTERVENTIONS: The patient received a wide marginal excision, followed by adjuvant radiotherapy. OUTCOMES: Symptomatic improvements were achieved and no subsequent relapses were observed. LESSONS: If the tumor arises in the extranodal sites, especially in the soft tissue, it is difficult to include FDCS in the differential diagnosis. When the immunoprofile is not consistent with that of common spindle cell tumors, immunostaining for follicular dendritic cell markers such as CD21, CD23, and CD35, as well as further immunohistochemistry for D2-40, CD68, EGFR, Epstein-Barr virus, and BRAF can be helpful for the diagnosis and subtyping of FDCS. To the best of our knowledge, the present case is the first case of intramuscular FDCS. Lippincott Williams & Wilkins 2021-09-10 /pmc/articles/PMC8428715/ /pubmed/34516525 http://dx.doi.org/10.1097/MD.0000000000027209 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 5700
Cho, Yong Jin
Han, Song Iy
Lim, Sung-Chul
Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report
title Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report
title_full Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report
title_fullStr Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report
title_full_unstemmed Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report
title_short Intra-muscular follicular dendritic cell sarcoma in the thigh: A case report
title_sort intra-muscular follicular dendritic cell sarcoma in the thigh: a case report
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428715/
https://www.ncbi.nlm.nih.gov/pubmed/34516525
http://dx.doi.org/10.1097/MD.0000000000027209
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