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A Rare Case of Primary Bilateral Adrenal Lymphoma

Lymphoma may involve the adrenal glands, but primary lymphoma is rare. Only a few cases have been reported in medical literature. Primary adrenal lymphoma is extremely rare, accounting for <1% of non-Hodgkin lymphomas. We here present a case of a middle-aged female who presented with persistent f...

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Autores principales: Meyyur Aravamudan, Veeraraghavan, Kee Fong, Phang, Sam, Yang Shiyao, Singh, Pavel, Ng, Siok-Bian, Kumar, Gollamudi Satya Pavan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516737/
https://www.ncbi.nlm.nih.gov/pubmed/28757874
http://dx.doi.org/10.1155/2017/1251950
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author Meyyur Aravamudan, Veeraraghavan
Kee Fong, Phang
Sam, Yang Shiyao
Singh, Pavel
Ng, Siok-Bian
Kumar, Gollamudi Satya Pavan
author_facet Meyyur Aravamudan, Veeraraghavan
Kee Fong, Phang
Sam, Yang Shiyao
Singh, Pavel
Ng, Siok-Bian
Kumar, Gollamudi Satya Pavan
author_sort Meyyur Aravamudan, Veeraraghavan
collection PubMed
description Lymphoma may involve the adrenal glands, but primary lymphoma is rare. Only a few cases have been reported in medical literature. Primary adrenal lymphoma is extremely rare, accounting for <1% of non-Hodgkin lymphomas. We here present a case of a middle-aged female who presented with persistent fever for three weeks. She also reported significant weight loss of more than 10 kgs over the duration of three months. Computed tomography of the thorax and abdomen and pelvis demonstrated bilateral adrenal masses. She underwent short Synacthen test which showed evidence of adrenal insufficiency. She underwent CT-guided adrenal gland biopsy. Histology of adrenal gland biopsy showed features consistent with diffuse large B-cell lymphoma. She was started on R-CHOP chemotherapy and had a good clinical response and remained in complete remission for five months after chemotherapy.
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spelling pubmed-55167372017-07-30 A Rare Case of Primary Bilateral Adrenal Lymphoma Meyyur Aravamudan, Veeraraghavan Kee Fong, Phang Sam, Yang Shiyao Singh, Pavel Ng, Siok-Bian Kumar, Gollamudi Satya Pavan Case Rep Med Case Report Lymphoma may involve the adrenal glands, but primary lymphoma is rare. Only a few cases have been reported in medical literature. Primary adrenal lymphoma is extremely rare, accounting for <1% of non-Hodgkin lymphomas. We here present a case of a middle-aged female who presented with persistent fever for three weeks. She also reported significant weight loss of more than 10 kgs over the duration of three months. Computed tomography of the thorax and abdomen and pelvis demonstrated bilateral adrenal masses. She underwent short Synacthen test which showed evidence of adrenal insufficiency. She underwent CT-guided adrenal gland biopsy. Histology of adrenal gland biopsy showed features consistent with diffuse large B-cell lymphoma. She was started on R-CHOP chemotherapy and had a good clinical response and remained in complete remission for five months after chemotherapy. Hindawi 2017 2017-07-05 /pmc/articles/PMC5516737/ /pubmed/28757874 http://dx.doi.org/10.1155/2017/1251950 Text en Copyright © 2017 Veeraraghavan Meyyur Aravamudan et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Meyyur Aravamudan, Veeraraghavan
Kee Fong, Phang
Sam, Yang Shiyao
Singh, Pavel
Ng, Siok-Bian
Kumar, Gollamudi Satya Pavan
A Rare Case of Primary Bilateral Adrenal Lymphoma
title A Rare Case of Primary Bilateral Adrenal Lymphoma
title_full A Rare Case of Primary Bilateral Adrenal Lymphoma
title_fullStr A Rare Case of Primary Bilateral Adrenal Lymphoma
title_full_unstemmed A Rare Case of Primary Bilateral Adrenal Lymphoma
title_short A Rare Case of Primary Bilateral Adrenal Lymphoma
title_sort rare case of primary bilateral adrenal lymphoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516737/
https://www.ncbi.nlm.nih.gov/pubmed/28757874
http://dx.doi.org/10.1155/2017/1251950
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