Dong Ping, Wang Li, Shen Guohua, Li Lin
Department of Nuclear Medicine.
Department of Pancreatic Surgery, West China Hospital, Sichuan University, Chengdu, P.R. China.
Medicine (Baltimore). 2019 Mar;98(11):e14818. doi: 10.1097/MD.0000000000014818.
Primary adrenal non-Hodgkin lymphomas are predominant diffuse large B cell lymphoma with frequently bilateral adrenal involvement, but the occurrence of nasal type extranodal NK/T cell lymphoma is relatively rare.
A 40-year-old woman complaining of left back pain for 2-month was admitted to our department.
Based on the feature of enhanced computed tomography (CT) images which showed huge bilateral well-defined adrenal masses with heterogeneous enhancement, she was tentatively diagnosed as having primary adrenal malignancy. Postoperative pathology revealed the diagnosis of primary adrenal Epstein-Barr virus-associated nasal type extranodal NK/T-cell lymphoma.
Then, she underwent F-fluoro-2-deoxy-D-glucose (F-FDG) positron emission tomography (PET)/CT examination for staging, which showed homogeneously increased FDG uptake in the right adrenal gland and left thigh subcutaneous lesion, as well as heterogeneous increased FDG uptake in the left adrenal gland region with no abnormal uptake in the nasal cavity. Subsequently, the patient has performed 7 cycles of gemcitabine, L-asparaginase, ifosfamide, dexamethasone, etoposide (GLIDE) regimen and autologous stem cell transplantation.
Fortunately, the subsequent 2 follow-up FDG PET/CT scans within 1 year revealed complete resolution with no abnormal FDG uptake in the initially involved sites after 7 cycles of GLIDE chemotherapy and autologous stem cell transplantation.
The enhanced CT and FDG PET/CT features of primary adrenal extranasal NK/T cell lymphoma are huge bilateral well-defined adrenal masses with heterogeneous enhancement, high FDG uptake, especially with subcutaneous involvement. And the awareness of this entity may help clinicians to differentiate it from other primary adrenal tumors and make reasonable therapeutic strategies. Besides, FDG PET/CT scan is very useful for the treatment follow-up of the primary adrenal extranasal NK/T cell lymphoma.
原发性肾上腺非霍奇金淋巴瘤主要为弥漫性大B细胞淋巴瘤,常双侧肾上腺受累,但鼻型结外NK/T细胞淋巴瘤的发生相对少见。
一名40岁女性因左背痛2个月入院。
根据增强计算机断层扫描(CT)图像特征,显示双侧肾上腺有巨大边界清晰的肿块,强化不均匀,初步诊断为原发性肾上腺恶性肿瘤。术后病理显示为原发性肾上腺爱泼斯坦-巴尔病毒相关鼻型结外NK/T细胞淋巴瘤。
随后,她接受了F-氟-2-脱氧-D-葡萄糖(F-FDG)正电子发射断层扫描(PET)/CT检查以进行分期,结果显示右肾上腺和左大腿皮下病变处FDG摄取均匀增加,左肾上腺区域FDG摄取不均匀增加,鼻腔无异常摄取。随后,患者进行了7个周期的吉西他滨、L-天冬酰胺酶、异环磷酰胺、地塞米松、依托泊苷(GLIDE)方案及自体干细胞移植。
幸运的是,随后1年内的2次随访FDG PET/CT扫描显示,在接受7个周期的GLIDE化疗和自体干细胞移植后,最初受累部位的FDG摄取完全消失,无异常。
原发性肾上腺鼻外NK/T细胞淋巴瘤的增强CT和FDG PET/CT特征为双侧肾上腺有巨大边界清晰的肿块,强化不均匀,FDG摄取高,尤其是伴有皮下受累。认识到这种疾病有助于临床医生将其与其他原发性肾上腺肿瘤区分开来,并制定合理的治疗策略。此外,FDG PET/CT扫描对原发性肾上腺鼻外NK/T细胞淋巴瘤的治疗随访非常有用。