Abstract

Lymphoma may occasionally involve the adrenal glands, but primary adrenal lymphoma (PAL) is very rare and only few cases have been reported. We present a case of a 60-year-old, otherwise healthy, woman, with bilateral PAL presenting with adrenal insufficiency. The patient responded initially upon administration of large doses of intravenously hydrocortisone with total remission of symptoms. An abdominal computerized tomography scan demonstrated bilateral adrenal lesions but did not demonstrate any other pathology. Since metastatic malignant disease was suspected a positron-emission-tomography scan was performed only showing significant uptake in the adrenal glands. Endocrine evaluation did not reveal abnormal function of any hormonal system and the patient was scheduled for bilateral adrenalectomy. However the clinical condition deteriorated rapidly and the patient was readmitted to hospital before surgery was performed. A new computerized tomography scan showed rapid progression of disease with further enlargement of the adrenal masses and both pulmonary and hepatic metastasis. Needle biopsy was performed but the patient refused further treatment and died before a diagnosis was obtained. The immuneohistochemical diagnosis was large B-cell lymphoma. This case should remind clinicians that PAL may be a cause of bilateral adrenal incidentaloma especially if the patient presents with adrenal insufficiency.

Highlights

  • Primary adrenal lymphoma (PAL) is rare whereas secondary involvement of the adrenal glands in nodal non-Hodgkin lymphoma occurs more often and is present in approximately 25% of cases [1].Primary extranodal lymphoma occurs in 1/3 of patients but primary involvement of the endocrine system is not frequent (3%) and most often involves the thyroid gland [2].The rare cases of PAL may present with bilateral involvement and is more often histologically of diffuse large B-cell type

  • Adrenal insufficiency may be the primary symptom of presentation, especially with bilateral involvement as in bPAL [4]

  • A high degree of suspicion is important in order to obtain a diagnosis quickly and initiate treatment since prognosis is poor

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Summary

Introduction

Primary adrenal lymphoma (PAL) is rare whereas secondary involvement of the adrenal glands in nodal non-Hodgkin lymphoma occurs more often and is present in approximately 25% of cases [1]. Primary extranodal lymphoma occurs in 1/3 of patients but primary involvement of the endocrine system is not frequent (3%) and most often involves the thyroid gland [2]. The rare cases of PAL may present with bilateral (bPAL) involvement and is more often histologically of diffuse large B-cell type. Immunodysfunction, as observed with human immunodeficiency virus infection or autoimmunity, may predispose to the disease but is not obligate [3]. Adrenal insufficiency may be the primary symptom of presentation, especially with bilateral involvement as in bPAL [4]. A high degree of suspicion is important in order to obtain a diagnosis quickly and initiate treatment since prognosis is poor

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