Karimi Fariba
Endocrinology and Metabolism Research Center, Shiraz University, Shiraz, Iran.
Int J Endocrinol Metab. 2017 Oct 26;15(4):e12014. doi: 10.5812/ijem.12014. eCollection 2017 Oct.
Primary adrenal lymphoma is rare, with a few cases reported in the literature. Most often it manifests as bilateral adrenal lesions and adrenal insufficiency is a common complication.
A 53-year-old male was referred with abdominal discomfort and darkening of the skin since 1 month prior to admission. His workups detected large bilateral adrenal masses. The patient was admitted due to hypotension, and was diagnosed with adrenal insufficiency. Laboratory studies showed high erythrocyte sedimentation rate (ESR), lactate dehydrogenase (LDH), and adrenocorticotropin levels. There was no other organ involvement and computed tomography (CT)-guided percutaneous biopsy of the adrenal gland revealed B-cell type of non-Hodgkin lymphoma. Replacement therapy with glucocorticoid and mineralocorticoid was initiated with remission of symptoms. After 3 months of chemotherapy his condition improved, but the patient worsened thereafter and died 2 months later.
However, this case reminded the importance of considering primary adrenal lymphoma in the differential diagnosis of bilateral adrenal masses, especially if the patient presents with adrenal insufficiency.
原发性肾上腺淋巴瘤较为罕见,文献中仅有少数病例报道。其通常表现为双侧肾上腺病变,肾上腺功能不全是常见并发症。
一名53岁男性因入院前1个月出现腹部不适和皮肤变黑前来就诊。检查发现双侧肾上腺有巨大肿块。患者因低血压入院,被诊断为肾上腺功能不全。实验室检查显示红细胞沉降率(ESR)、乳酸脱氢酶(LDH)和促肾上腺皮质激素水平升高。无其他器官受累,肾上腺CT引导下经皮活检显示为B细胞型非霍奇金淋巴瘤。开始使用糖皮质激素和盐皮质激素替代治疗,症状缓解。化疗3个月后病情改善,但此后患者病情恶化,2个月后死亡。
然而,该病例提醒我们在双侧肾上腺肿块的鉴别诊断中,尤其是患者出现肾上腺功能不全时,考虑原发性肾上腺淋巴瘤的重要性。