Primary Unilateral Adrenal Anaplastic Large Cell Lymphoma: Remission by Chemotherapy.

JCEM case reports Pub Date : 2024-12-06 eCollection Date: 2024-12-01 DOI:10.1210/jcemcr/luae229
Daisuke Goto, Yumie Takeshita, Kosuke Nagai, Hisanori Goto, Yujiro Nakano, Toshinari Takamura
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Abstract

Primary malignant lymphomas originating in the adrenal gland, particularly of T-cell origin, are extremely rare. Here we present the primary unilateral adrenal anaplastic large cell lymphoma case. A 64-year-old Japanese male initially presented with fatigue and appetite loss. Computed tomography imaging revealed a unilateral adrenal mass with multiorgan invasion, posing challenges in differentiation from adrenal carcinoma. A biopsy from the metastatic site in the right lateral vastus muscle was obtained, and immunohistochemistry revealed that tumor cells were positive for CD30 and CD56 and negative for CD3, CD15, CD20, CD43, perforin, granzyme B, epithelial membrane antigen, and anaplastic lymphoma kinase. Ultimately, the patient was diagnosed with primary unilateral adrenal anaplastic large cell lymphoma. Although he achieved complete response to chemotherapy, he died 4 months after complete response due to cholecystitis and lymphoma recurrence.

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原发性单侧肾上腺间变性大细胞淋巴瘤:化疗缓解。
原发性恶性淋巴瘤起源于肾上腺,尤其是起源于t细胞,是非常罕见的。我们报告一例原发性单侧肾上腺间变性大细胞淋巴瘤。一名64岁的日本男性最初表现为疲劳和食欲不振。计算机断层成像显示单侧肾上腺肿块伴多器官侵犯,对肾上腺癌的鉴别提出了挑战。对右外侧股肌转移部位进行活检,免疫组化显示肿瘤细胞CD30和CD56呈阳性,CD3、CD15、CD20、CD43、穿孔素、颗粒酶B、上皮膜抗原和间变性淋巴瘤激酶呈阴性。最终,患者被诊断为原发性单侧肾上腺间变性大细胞淋巴瘤。虽然他对化疗取得了完全缓解,但在完全缓解后4个月,他因胆囊炎和淋巴瘤复发而死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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