Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?

Non-Hodgkin lymphomas of the hypothalamus and pituitary are rare. They usually remain clinically silent until onset of compressive features affecting surrounding structures. When symptomatic, patients most commonly present with diabetes insipidus, headaches, ophthalmoplegia and/or bilateral hemianop...

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Main Authors: Uzma Khan, Anton Borg, Radu Beltechi, Hiten Mehta, Timothy Robbins, Harpal Randeva, Pratibha Machenahalli
Format: Article
Language:English
Published: SMC MEDIA SRL 2021-12-01
Series:European Journal of Case Reports in Internal Medicine
Subjects:
Online Access:https://www.ejcrim.com/index.php/EJCRIM/article/view/2980
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author Uzma Khan
Anton Borg
Radu Beltechi
Hiten Mehta
Timothy Robbins
Harpal Randeva
Pratibha Machenahalli
author_facet Uzma Khan
Anton Borg
Radu Beltechi
Hiten Mehta
Timothy Robbins
Harpal Randeva
Pratibha Machenahalli
author_sort Uzma Khan
collection DOAJ
description Non-Hodgkin lymphomas of the hypothalamus and pituitary are rare. They usually remain clinically silent until onset of compressive features affecting surrounding structures. When symptomatic, patients most commonly present with diabetes insipidus, headaches, ophthalmoplegia and/or bilateral hemianopia.  We report a case of a 67-year-old Caucasian female with a history of B-cell lymphoma in complete remission. She presented with left oculomotor nerve palsy and was subsequently found to have a sellar/suprasellar mass lesion on MRI. Alongside hypocortisolism and hypogonadotropic hypogonadism, she developed transient diabetes insipidus during her illness. Her clinical course was characterized by rapid intracranial progression of the sellar mass. MR spectroscopy suggested a diagnosis of lymphoma. Diagnostic biopsy confirmed high-grade diffuse large B-cell CNS lymphoma; this changed the definitive management from surgical excision to chemotherapy. Despite treatment, she succumbed to her illness within 7 months of initial presentation. This case highlights the aggressive nature of CNS lymphomas and the need for a high index of suspicion in an unusual presentation of sellar/suprasellar mass lesions.
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spelling doaj.art-2423d1d7fb33452f9eac20c8aa0207862022-12-21T19:48:51ZengSMC MEDIA SRLEuropean Journal of Case Reports in Internal Medicine2284-25942021-12-0110.12890/2021_0029802515Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?Uzma Khan0https://orcid.org/0000-0002-5559-9300Anton Borg1Radu Beltechi2Hiten Mehta3Timothy Robbins4Harpal Randeva5Pratibha Machenahalli6Department of Endocrinology & Diabetes, University Hospitals Coventry & Warwickshire NHS Trust, UKDepartment of Haematology, South Warwickshire NHS Foundation Trust, UK Department of Neurosurgery, University Hospitals Coventry & Warwickshire NHS Trust, UKDepartment of Clinical Radiology, University Hospitals Coventry & Warwickshire NHS Trust, UKDepartment of Endocrinology & Diabetes, University Hospitals Coventry & Warwickshire NHS Trust, UKDepartment of Endocrinology & Diabetes, University Hospitals Coventry & Warwickshire NHS Trust, UKDepartment of Endocrinology & Diabetes, University Hospitals Coventry & Warwickshire NHS Trust, UKNon-Hodgkin lymphomas of the hypothalamus and pituitary are rare. They usually remain clinically silent until onset of compressive features affecting surrounding structures. When symptomatic, patients most commonly present with diabetes insipidus, headaches, ophthalmoplegia and/or bilateral hemianopia.  We report a case of a 67-year-old Caucasian female with a history of B-cell lymphoma in complete remission. She presented with left oculomotor nerve palsy and was subsequently found to have a sellar/suprasellar mass lesion on MRI. Alongside hypocortisolism and hypogonadotropic hypogonadism, she developed transient diabetes insipidus during her illness. Her clinical course was characterized by rapid intracranial progression of the sellar mass. MR spectroscopy suggested a diagnosis of lymphoma. Diagnostic biopsy confirmed high-grade diffuse large B-cell CNS lymphoma; this changed the definitive management from surgical excision to chemotherapy. Despite treatment, she succumbed to her illness within 7 months of initial presentation. This case highlights the aggressive nature of CNS lymphomas and the need for a high index of suspicion in an unusual presentation of sellar/suprasellar mass lesions.https://www.ejcrim.com/index.php/EJCRIM/article/view/2980non-hodgkin lymphomacns lymphomapituitary macroadenomasellar mass
spellingShingle Uzma Khan
Anton Borg
Radu Beltechi
Hiten Mehta
Timothy Robbins
Harpal Randeva
Pratibha Machenahalli
Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?
European Journal of Case Reports in Internal Medicine
non-hodgkin lymphoma
cns lymphoma
pituitary macroadenoma
sellar mass
title Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?
title_full Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?
title_fullStr Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?
title_full_unstemmed Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?
title_short Non-Hodgkin Lymphoma Causing Hypopituitarism Can Imaging Help Diagnosis and Management?
title_sort non hodgkin lymphoma causing hypopituitarism can imaging help diagnosis and management
topic non-hodgkin lymphoma
cns lymphoma
pituitary macroadenoma
sellar mass
url https://www.ejcrim.com/index.php/EJCRIM/article/view/2980
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