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Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report
BACKGROUND: Follicular dendritic cell sarcoma (FDCS) is a rare malignancy. In addition to the classical histopathologic features, it has also some special morphological variants that can present a challenge in the diagnosis of this disease. CASE PRESENTATION: A 45-year-old male who presented with a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694554/ https://www.ncbi.nlm.nih.gov/pubmed/31412904 http://dx.doi.org/10.1186/s13000-019-0869-2 |
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author | Wu, You-Li Wu, Feng Mbako, Robinson Ateh Zhang, Yu Duan, Guang-Jie Yan, Xiao-Chu |
author_facet | Wu, You-Li Wu, Feng Mbako, Robinson Ateh Zhang, Yu Duan, Guang-Jie Yan, Xiao-Chu |
author_sort | Wu, You-Li |
collection | PubMed |
description | BACKGROUND: Follicular dendritic cell sarcoma (FDCS) is a rare malignancy. In addition to the classical histopathologic features, it has also some special morphological variants that can present a challenge in the diagnosis of this disease. CASE PRESENTATION: A 45-year-old male who presented with a left supraclavicular mass was given a final diagnosis of FDCS after lymph node biopsy. The specimen obtained during radical resection revealed five different morphologies, including the classical histological appearance and atypical areas resembling desmoplastic infiltrative carcinoma, anaplastic large cell lymphoma (ALCL), hemangiopericytoma and classical Hodgkin’s lymphoma (CHL). Immunohistochemistry was notable for positive CD21 and CD23 expression across all morphologies. Given the atypical appearance and location, the specimen was initially misdiagnosed as a metastatic carcinoma based on histology alone at an outside institution. The patient eventually underwent surgical resection followed by adjuvant chemotherapy and radiation. Despite treatment, the disease progressed, and the patient passed away 36 months after surgery. CONCLUSIONS: This unusual case of FDCS contains four types of atypical histomorphologies within a single tumor specimen, including those resembling ALCL and hemangiopericytoma which are described here for the first time. Our report further expands the histopathologic spectrum of FDCS and may help assist in the diagnosis of other such challenging cases. |
format | Online Article Text |
id | pubmed-6694554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66945542019-08-19 Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report Wu, You-Li Wu, Feng Mbako, Robinson Ateh Zhang, Yu Duan, Guang-Jie Yan, Xiao-Chu Diagn Pathol Case Report BACKGROUND: Follicular dendritic cell sarcoma (FDCS) is a rare malignancy. In addition to the classical histopathologic features, it has also some special morphological variants that can present a challenge in the diagnosis of this disease. CASE PRESENTATION: A 45-year-old male who presented with a left supraclavicular mass was given a final diagnosis of FDCS after lymph node biopsy. The specimen obtained during radical resection revealed five different morphologies, including the classical histological appearance and atypical areas resembling desmoplastic infiltrative carcinoma, anaplastic large cell lymphoma (ALCL), hemangiopericytoma and classical Hodgkin’s lymphoma (CHL). Immunohistochemistry was notable for positive CD21 and CD23 expression across all morphologies. Given the atypical appearance and location, the specimen was initially misdiagnosed as a metastatic carcinoma based on histology alone at an outside institution. The patient eventually underwent surgical resection followed by adjuvant chemotherapy and radiation. Despite treatment, the disease progressed, and the patient passed away 36 months after surgery. CONCLUSIONS: This unusual case of FDCS contains four types of atypical histomorphologies within a single tumor specimen, including those resembling ALCL and hemangiopericytoma which are described here for the first time. Our report further expands the histopathologic spectrum of FDCS and may help assist in the diagnosis of other such challenging cases. BioMed Central 2019-08-14 /pmc/articles/PMC6694554/ /pubmed/31412904 http://dx.doi.org/10.1186/s13000-019-0869-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Wu, You-Li Wu, Feng Mbako, Robinson Ateh Zhang, Yu Duan, Guang-Jie Yan, Xiao-Chu Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
title | Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
title_full | Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
title_fullStr | Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
title_full_unstemmed | Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
title_short | Nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
title_sort | nodal follicular dendritic cell sarcoma with four atypical histomorphologic features: an unusual case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694554/ https://www.ncbi.nlm.nih.gov/pubmed/31412904 http://dx.doi.org/10.1186/s13000-019-0869-2 |
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