Metastatic bilateral adrenal sarcomatoid carcinoma: Evaluation by 18F-FDG PET/CT.

Swati Rachh, Patel Nilam
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引用次数: 3

Abstract

Sarcomatoid carcinoma of the adrenal gland is an uncommon presentation of malignant adrenal tumors and bilateral presentation is extremely rare. It is an extremely rare occurrence, unusual symptoms, and both epithelioid and sarcomatoid components in histology are a challenge to diagnose sarcomatoid carcinoma of adrenal origin. The majority of patients are diagnosed at a later stage while having metastatic disease and succumb due to disease within a few months of diagnosis due to the aggressive nature of the disease. Probably due to the advanced disease at the time of diagnosis; patients diagnosed having adrenal sarcomatoid tumor have a very poor prognosis. In nonmetastatic disease, adjuvant chemotherapy is suggested after the removal of the tumor. It is essential to diagnose these tumors earliest to treat with effective treatment modalities. The present study describes the rare case of sarcomatoid carcinoma involving the bilateral adrenal gland with metastasis to bones, lymph nodes, and pleura evaluated by 18F-FDG PET/CT.

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转移性双侧肾上腺肉瘤样癌:18F-FDG PET/CT评价。
肾上腺肉瘤样癌是一种少见的恶性肾上腺肿瘤,双侧表现极为罕见。这是一种非常罕见的发生,不寻常的症状,组织学上的上皮样和肉瘤样成分对肾上腺源性肉瘤样癌的诊断都是一个挑战。大多数患者在患有转移性疾病的较晚阶段被诊断出来,由于疾病的侵袭性,在诊断后几个月内因疾病而死亡。可能是由于诊断时疾病进展较晚;诊断为肾上腺肉瘤样肿瘤的患者预后非常差。对于非转移性疾病,建议在肿瘤切除后进行辅助化疗。早期诊断这些肿瘤以有效的治疗方式治疗是至关重要的。本研究报告一例罕见的肉瘤样癌累及双侧肾上腺,并转移到骨骼、淋巴结和胸膜,通过18F-FDG PET/CT进行评估。
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来源期刊
Asia Oceania Journal of Nuclear Medicine and Biology
Asia Oceania Journal of Nuclear Medicine and Biology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.80
自引率
0.00%
发文量
28
审稿时长
12 weeks
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