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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Main Authors: Veeraraghavan Meyyur Aravamudan, Phang Kee Fong, Yang Shiyao Sam, Pavel Singh, Siok-Bian Ng, Gollamudi Satya Pavan Kumar
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2017/1251950
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spelling doaj-6e563362d39b41a7ab32e497dbaa82b02020-11-24T22:01:22ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352017-01-01201710.1155/2017/12519501251950A Rare Case of Primary Bilateral Adrenal LymphomaVeeraraghavan Meyyur Aravamudan0Phang Kee Fong1Yang Shiyao Sam2Pavel Singh3Siok-Bian Ng4Gollamudi Satya Pavan Kumar5Department of Advanced Internal Medicine, National University Hospital, 5 Lower Kent Ridge Road, 119074, SingaporeDepartment of Advanced Internal Medicine, National University Hospital, 5 Lower Kent Ridge Road, 119074, SingaporeDepartment of Advanced Internal Medicine, National University Hospital, 5 Lower Kent Ridge Road, 119074, SingaporeDepartment of Radiology, National University Hospital, 5 Lower Kent Ridge Road, 119074, SingaporeDepartment of Pathology, National University of Singapore, National University Hospital, 5 Lower Kent Ridge Road, 119074, SingaporeDepartment of Advanced Internal Medicine, National University Hospital, 5 Lower Kent Ridge Road, 119074, SingaporeLymphoma 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.http://dx.doi.org/10.1155/2017/1251950
collection DOAJ
language English
format Article
sources DOAJ
author Veeraraghavan Meyyur Aravamudan
Phang Kee Fong
Yang Shiyao Sam
Pavel Singh
Siok-Bian Ng
Gollamudi Satya Pavan Kumar
spellingShingle Veeraraghavan Meyyur Aravamudan
Phang Kee Fong
Yang Shiyao Sam
Pavel Singh
Siok-Bian Ng
Gollamudi Satya Pavan Kumar
A Rare Case of Primary Bilateral Adrenal Lymphoma
Case Reports in Medicine
author_facet Veeraraghavan Meyyur Aravamudan
Phang Kee Fong
Yang Shiyao Sam
Pavel Singh
Siok-Bian Ng
Gollamudi Satya Pavan Kumar
author_sort Veeraraghavan Meyyur Aravamudan
title A Rare Case of Primary Bilateral Adrenal Lymphoma
title_short 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_sort rare case of primary bilateral adrenal lymphoma
publisher Hindawi Limited
series Case Reports in Medicine
issn 1687-9627
1687-9635
publishDate 2017-01-01
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.
url http://dx.doi.org/10.1155/2017/1251950
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