Diagnosis and Therapy of Primary Hepatic Neuroendocrine Carcinoma: Clinical Analysis of 10 Cases

被引:15
作者
Wang, Li-Ming
An, Song-Lin
Wu, Jian-Xiong [1 ]
机构
[1] Chinese Acad Med Sci, Canc Inst & Hosp, Dept Abdominal Surg, Beijing 100730, Peoples R China
关键词
Neuroendocrine carcinoma; carcinoid tumor; diagnosis; therapy; HEPATOCELLULAR-CARCINOMA; TUMOR; LIVER; EMPHASIS;
D O I
10.7314/APJCP.2014.15.6.2541
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Primary hepatic neuroendocrine carcinoma (PHNEC) is rarer than extrahepatic gastrointestinal neuroendocrine carcinoma (NEC). It is difficult to make a correct diagnosis and poses a challenge for management. Materials and Methods: Ten PHNEC patients were admitted to our hospital from June 2006 to June 2011. Laboratory tests and imaging scans were performed for diagnosis and exclusion of extrahepatic NEC. All patients were AFP - and CA199-. Seven patients had solid tumors with cystic changes on ultrasonography, CT and/or MRI. For the initial treatment, four patients received combined-therapy and six monotherapy. Considering overall treatment, six patients received combined-therapy and four patients monotherapy. Staging criteria of primary hepatocellular carcinoma (PHC, AJCC 7th edition) were used to differentiate the stage of all patients: 3 patients were stage I, 2 stageII, 4 patients stageIII and 1 stageIV. All patients were followed up and clinical data were gathered. Results: The median follow-up duration was 38.5 months. The 1-year, 2-year, 3-year and 6-year disease-free survival was 80.0%, 46.2% and 46.2% and 0% respectively. The overall survival rates were 100%, 67.1%, 67.1% and 33.6% respectively. Patients in early-stages (I/II) had similar disease-free and overall survival as those in advanced-stages (III/IV). Patients with monotherapy had significant shorter disease-free and overall survival than the patients with combination-therapy. Conclusions: PHNEC has a unique specificity during its occurrence and development. The staging criteria of PHC might not be suitable for the PHENT. More convenient and effective features need to be found in imaging and laboratory detection. Surgical resection, TACE, chemotherapy and radiofrequency ablation should be performed in combination and actively for patients with PHNEC or recurrence to get the best effectiveness; they might extend the disease-free and overall survival.
引用
收藏
页码:2541 / 2546
页数:6
相关论文
共 25 条
[11]   Primary hepatic neuroendocrine carcinoma: MR imaging findings including preliminary observation on diffusion-weighted imaging [J].
Li, Ruo-Kun ;
Zhao, Jing ;
Rao, Sheng-Xiang ;
Chen, Cai-Zhong ;
Zeng, Meng-Su ;
Qiang, Jin-Wei .
ABDOMINAL IMAGING, 2013, 38 (06) :1269-1276
[12]  
Lin Chih-Wen, 2009, Cases J, V2, P90, DOI 10.1186/1757-1626-2-90
[13]   Gastrointestinal neuroendocrine (carcinoid) tumours: current diagnosis and management [J].
Modlin, Irvin M. ;
Moss, Steven F. ;
Oberg, Kjell ;
Padbury, Robert ;
Hicks, Rodney J. ;
Gustafsson, Bjorn I. ;
Wright, Nicholas A. ;
Kidd, Mark .
MEDICAL JOURNAL OF AUSTRALIA, 2010, 193 (01) :46-52
[14]   Nuclear medicine in the detection, staging and treatment of gastrointestinal carcinoid tumours [J].
Öberg, K ;
Eriksson, B .
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 19 (02) :265-276
[15]   Whole-body 11C-5-hydroxytryptophan positron emission tomography as a universal imaging technique for neuroendocrine tumors:: Comparison with somatostatin receptor scintigraphy and computed tomography [J].
Orlefors, H ;
Sundin, A ;
Garske, U ;
Juhlin, C ;
Oberg, K ;
Skogseid, B ;
Langstrom, B ;
Bergstrom, M ;
Eriksson, B .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (06) :3392-3400
[16]  
Rascarachi Gabriela, 2009, Cases J, V2, P6346, DOI 10.4076/1757-1626-2-6346
[17]  
Shinkawa Hiroji, 2013, Osaka City Med J, V59, P105
[18]   Primary Hepatic Neuroendocrine Tumor with Exophytic Growth Report of a Case with Diagnosis by Fine Needle Aspiration Biopsy [J].
Skagias, Lazaros ;
Vasou, Olympia ;
Ntinis, Apostolos ;
Kondi-Pafiti, Agathi ;
Koureas, Andreas ;
Politi, Ekaterini .
ACTA CYTOLOGICA, 2010, 54 (02) :202-204
[19]  
Soga J, 2002, J EXP CLIN CANC RES, V21, P457
[20]  
Sotiropoulos GC, 2013, J GASTROINTEST SURG