Primary adrenal lymphoma as a cause of adrenal insufficiency, a report of two cases

Author:

Grønning Kaja1,Sharma Archana1,Mastroianni Maria Adele2,Karlsson Bo Daniel3,Husebye Eystein S45,Løvås Kristian45,Nermoen Ingrid16

Affiliation:

1. 1Department of Endocrinology, Akershus University Hospital, Lorenskog, Norway

2. 2Department of Haematology, Akershus University Hospital, Lorenskog, Norway

3. 3Department of Radiology, Akershus University Hospital, Lorenskog, Norway

4. 4Department of Clinical Science and K.G. Jebsen Center of Autoimmune Disorders, University of Bergen, Bergen, Norway

5. 5Department of Medicine, Haukeland University Hospital, Bergen, Norway

6. 6Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway

Abstract

Summary Primary adrenal lymphoma (PAL) is a rare cause of adrenal insufficiency. More than 90% is of B-cell origin. The condition is bilateral in up to 75% of cases, with adrenal insufficiency in two of three patients. We report two cases of adrenal insufficiency presenting at the age of 70 and 79 years, respectively. Both patients had negative 21-hydroxylase antibodies with bilateral adrenal lesions on CT. Biopsy showed B-cell lymphoma. One of the patients experienced intermittent disease regression on replacement dosage of glucocorticoids. Learning points: Primary adrenal lymphoma (PAL) is a rare cause of adrenal insufficiency. Bilateral adrenal masses of unknown origin or in individuals with suspected extra-adrenal malignancy should be biopsied quickly when pheochromocytoma is excluded biochemically. Steroid treatment before biopsy may affect diagnosis. Adrenal insufficiency with negative 21-hydroxylase antibodies should be evaluated radiologically.

Publisher

Bioscientifica

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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