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Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review

We report a case of interdigitating dendritic cell sarcoma (IDCS) originating from the adrenal gland. A 57-year-old middle-aged woman with no previous history of malignancy came to our hospital after color Doppler ultrasound revealed a right adrenal mass. An abdominal computed tomography scan also s...

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Autores principales: Hao, Peng, Cao, Liang, Li, Yangming, Lin, Dong, Hu, Tinghui, Wu, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593323/
https://www.ncbi.nlm.nih.gov/pubmed/34772309
http://dx.doi.org/10.1177/03000605211055410
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author Hao, Peng
Cao, Liang
Li, Yangming
Lin, Dong
Hu, Tinghui
Wu, Tao
author_facet Hao, Peng
Cao, Liang
Li, Yangming
Lin, Dong
Hu, Tinghui
Wu, Tao
author_sort Hao, Peng
collection PubMed
description We report a case of interdigitating dendritic cell sarcoma (IDCS) originating from the adrenal gland. A 57-year-old middle-aged woman with no previous history of malignancy came to our hospital after color Doppler ultrasound revealed a right adrenal mass. An abdominal computed tomography scan also showed an adrenal mass. Postoperative pathology confirmed the diagnosis of IDCS. After complete surgical removal of the adrenal tumor, the patient has been disease-free for 1 year. IDCS may have a good prognosis after surgical resection. To our knowledge, this is only the second reported case of IDCS in the adrenal region.
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spelling pubmed-85933232021-11-17 Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review Hao, Peng Cao, Liang Li, Yangming Lin, Dong Hu, Tinghui Wu, Tao J Int Med Res Case Report We report a case of interdigitating dendritic cell sarcoma (IDCS) originating from the adrenal gland. A 57-year-old middle-aged woman with no previous history of malignancy came to our hospital after color Doppler ultrasound revealed a right adrenal mass. An abdominal computed tomography scan also showed an adrenal mass. Postoperative pathology confirmed the diagnosis of IDCS. After complete surgical removal of the adrenal tumor, the patient has been disease-free for 1 year. IDCS may have a good prognosis after surgical resection. To our knowledge, this is only the second reported case of IDCS in the adrenal region. SAGE Publications 2021-11-12 /pmc/articles/PMC8593323/ /pubmed/34772309 http://dx.doi.org/10.1177/03000605211055410 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Hao, Peng
Cao, Liang
Li, Yangming
Lin, Dong
Hu, Tinghui
Wu, Tao
Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
title Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
title_full Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
title_fullStr Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
title_full_unstemmed Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
title_short Interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
title_sort interdigitating dendritic cell sarcoma located in the adrenal gland: a case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8593323/
https://www.ncbi.nlm.nih.gov/pubmed/34772309
http://dx.doi.org/10.1177/03000605211055410
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