Grajales-Cruz Ariel, Baco-Viera Francis, Rive-Mora Ernesto, Ramirez-Tanchez Carlos, Tasso David, Arroyo-Portela Norma, Calderon Elizabeth, Padua-Octaviani Ilean Joan, Caceres-Perkins William
Veterans Affairs Caribbean Healthcare System, San Juan, Puerto Rico.
Cancer Control. 2017 Apr;24(2):198-201. doi: 10.1177/107327481702400213.
A man aged 69 years presented with acute right flank pain secondary to a hemorrhagic large adrenal tumor. En bloc resection was performed to repair the inferior vena cava. Immunoperoxidase levels in the tumor were positive for factor VIII and CD31 and negative for S100, protein Melan-A, CD34, synaptophysin, chromogranin, desmin, muscle specific actin, ETFA (EMA), KRT20 (CK20), CDX2, TTF1, LNPEP (PLAP), inhibin, ?-fetoprotein, CD30, hepatocyte paraffin, and aberrant expression of cytokeratin 7 and pankeratin. The pathological diagnosis was consistent with adrenal angiosarcoma. Obtaining appropriate immunoperoxidase stains and multidisciplinary evaluation helped make the diagnosis of this rare adrenal tumor and determine its management. The patient had an uneventful postoperative course and completed 4 cycles of adjuvant chemotherapy with doxorubicin/ifosfamide and adequately tolerated the treatment. However, positive surgical margins were found, so he was referred to radiation oncology specialists for possible adjuvant radiotherapy to the surgical bed. Weeks after the first initiation of therapy, the patient presented to the emergency department complaining of shortness of breath, fatigue, and generalized weakness for 3 days. He was admitted and found to have new-onset anemia and a new-onset, large, right pleural effusion. Thoracentesis performed showed sanguinolent fluid that, after microscopic evaluation, was suggestive of recurrent malignancy. Thoracic aortography performed with subselective catheterization to several arteries (right bronchial, right phrenic, and right renal arteries) did not show any active bleeding. However, the right inferior intercostal and adrenal arteries were presumed to be the reason for the bleeding event, so they were embolized until stasis. The patient remained hemodynamically unstable but eventually experienced multiorgan failure. In spite of aggressive measures, he died 10 days after admission to the hospital.
一名69岁男性因出血性肾上腺大肿瘤继发急性右侧腰痛就诊。进行了整块切除以修复下腔静脉。肿瘤免疫过氧化物酶水平VIII因子和CD31呈阳性,S100、黑色素A蛋白、CD34、突触素、嗜铬粒蛋白、结蛋白、肌肉特异性肌动蛋白、ETFA(上皮膜抗原)、KRT20(细胞角蛋白20)、CDX2、TTF1、LNPEP(胎盘碱性磷酸酶)、抑制素、甲胎蛋白、CD30、肝细胞石蜡以及细胞角蛋白7和全角蛋白异常表达呈阴性。病理诊断为肾上腺血管肉瘤。进行适当的免疫过氧化物酶染色和多学科评估有助于诊断这种罕见的肾上腺肿瘤并确定其治疗方案。患者术后恢复顺利,完成了4个周期的阿霉素/异环磷酰胺辅助化疗,且对治疗耐受性良好。然而,发现手术切缘阳性,因此他被转介给放射肿瘤学专家,考虑对手术床进行辅助放疗。首次开始治疗数周后,患者因气促、乏力和全身虚弱3天就诊于急诊科。他入院后被发现出现新发贫血和新发的右侧大量胸腔积液。胸腔穿刺抽出的血性液体经显微镜检查提示为复发性恶性肿瘤。对多条动脉(右支气管动脉、右膈动脉和右肾动脉)进行选择性亚插管的胸主动脉造影未显示任何活动性出血。然而,推测右下肋间动脉和肾上腺动脉是出血原因,因此对其进行栓塞直至血流停滞。患者血流动力学仍不稳定,但最终出现多器官功能衰竭。尽管采取了积极措施,他在入院10天后死亡。