Liver Transplant as Treatment Modality for Inflammatory Myofibroblastic Tumor of the Liver

A. Setya
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引用次数: 1

Abstract

A 3-year-old African female child with a noncontributory birth, past and family history presented with progressively increasing abdominal distension for 3 months associated with intermittent fever, abdominal pain and cough. On her initial evaluation, contrastenhanced computed tomography (CECT) abdomen revealed a mass in the right hepatic lobe with thrombus in the inferior vena cava (IVC) and right ventricle with enlarged aortocaval, para aortic and celiac lymph nodes with mild ascites. Liver biopsy was deferred, as the patient was sick upon presentation. Suspecting it to be hepatoblastoma, she was given 4 cycles of Doxorubicin and Carboplatin. Tumor markers carcinoembryonic antigen (CEA), Beta human chorionic gonadotropin (hCG) and Alpha-fetoprotein (AFP) were found to be negative. In view of poor response to chemotherapy and persistent symptoms, she was brought to our hospital in New Delhi, India. On presentation, she was hemodynamically stable and had firm hepatomegaly and pallor. Positron emission tomography–computed tomography (PET CT) abdomen revealed hypertrophied left lobe of the liver, 18F-fluorodeoxyglucose (FDG) avid large heterogenous arterial enhancing lesion in the right lobe liver involving segment VII, VIII, VI with extension into IVC, right atrium and ventricle. There was bilateral moderate pleural effusion with atelectasis. She underwent an ultrasound guided biopsy of the lesion which was suggestive of inflammatory Myofibroblastic tumor (bundles of oval to spindle shaped fibroblastic cells in a collagenized stroma with cells showing mild pleomorphism). Immunohistochemical stain for Anaplastic Lymphoma Kinase (ALK) was positive but stain for SMA, CD34 and CD31 were negative. Crizotinib (ALK inhibitor) was started for reduction of the tumor volume and patient improved. *Corresponding author: Aniruddh Setya, Department of Pediatric Gastroenterology, Hepatology and Nutrition, University of Florida, Gainesville, USA. Received Date: March 02, 2020 Published Date: March 12, 2020
肝移植作为肝炎性肌成纤维细胞瘤的治疗方式
一名3岁非洲女性儿童,非自愿出生,既往史和家族史,在3个月内腹胀逐渐加重,伴有间歇性发烧、腹痛和咳嗽。在她的初步评估中,腹部增强计算机断层扫描(CECT)显示右肝叶有一个肿块,下腔静脉(IVC)和右心室有血栓,主动脉腔、主动脉旁和腹腔淋巴结肿大,伴有轻度腹水。肝活检被推迟,因为病人在就诊时生病了。怀疑是肝母细胞瘤,她接受了4个周期的阿霉素和卡铂治疗。肿瘤标志物癌胚抗原(CEA)、β-人绒毛膜促性腺激素(hCG)和甲胎蛋白(AFP)均为阴性。鉴于化疗反应不佳,症状持续,她被送到了我们位于印度新德里的医院。经检查,她血流动力学稳定,肝肿大,面色苍白。正电子发射断层扫描-计算机断层扫描(PET CT)腹部显示肝脏左叶肥大,18F-氟脱氧葡萄糖(FDG)在右叶肝脏中大量非均质动脉增强病变,涉及第VII、VIII、VI节段,并延伸至IVC、右心房和心室。双侧中度胸腔积液伴肺不张。她接受了超声引导下的病变活检,该病变提示为炎性肌成纤维细胞瘤(胶原化基质中的椭圆形至纺锤形成纤维细胞束,细胞显示轻度多形性)。间变性淋巴瘤激酶(ALK)的免疫组织化学染色为阳性,但SMA、CD34和CD31的染色为阴性。开始使用克唑替尼(ALK抑制剂)以减少肿瘤体积,患者病情得到改善*通讯作者:Aniruddh Setya,美国盖恩斯维尔佛罗里达大学儿科胃肠病、肝病和营养系。接收日期:2020年3月2日发布日期:2020月12日
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