A 20-Year Prospective Study of Wilms Tumor and Other Kidney Tumors: A Report From Hong Kong Pediatric Hematology and Oncology Study Group

被引:12
|
作者
Chan, Ching Ching [1 ]
To, Ka Fai [2 ]
Yuen, Hui Leung [3 ]
Chiang, Alan Kwok Shing [4 ]
Ling, Siu Cheung [5 ]
Li, Chak Ho [6 ]
Cheuk, Daniel Ka Leung [4 ]
Li, Chi Kong [1 ]
Shing, Matthew Ming Kong [1 ]
机构
[1] Chinese Univ Hong Kong, Dept Pediat, Lady Pao Childrens Canc Ctr, Prince Wales Hosp, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Dept Anat & Cellular Pathol, Prince Wales Hosp, Shatin, Hong Kong, Peoples R China
[3] Queen Elizabeth Hosp, Dept Pediat, Hong Kong, Hong Kong, Peoples R China
[4] Queen Mary Hosp, Dept Pediat & Adolescent Med, Hong Kong, Hong Kong, Peoples R China
[5] Princess Margaret Hosp, Dept Pediat & Adolescent Med, Hong Kong, Hong Kong, Peoples R China
[6] Tuen Mun Hospita, Dept Pediat, Hong Kong, Hong Kong, Peoples R China
关键词
renal tumor; Wilms tumor; clear cell sacroma; CLEAR-CELL SARCOMA; PROGNOSTIC-FACTORS; LATE MORTALITY; RENAL TUMORS; CHILDREN; CANCER; EPIDEMIOLOGY; CHILDHOOD; DIAGNOSIS; 2ND;
D O I
10.1097/MPH.0000000000000018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Renal tumors are one of the most common tumors in children. We aim at evaluating the characteristics and the outcome of Wilms tumor and other malignant kidney tumors in Hong Kong. Procedure: Between January 1990 to December 2010, 68 patients under the age of 18 with malignant renal tumors were diagnosed and received treatment in Hong Kong. Clinical records were updated regularly. Prognostic factors and survival rate were evaluated. Results: Fifty-four patients were diagnosed with Wilms tumor. The annual incidence was estimated to be 2.29 per million. The mean age was 38 months. Median follow-up was 9.2 years. The event-free survival and overall survival rate at 10 years were 85.2% and 92.6%, respectively. A pair of siblings with familial extrarenal Wilms tumor was included. Pulmonary metastasis did exhibit a significant difference in survival rate. Eight cases of clear cell sarcoma of the kidneys were reported and the survival rate was 100%. Conclusions: The clinical characteristics and outcome of the patients diagnosed Wilms tumor were comparable with other developed countries. Relatively high proportion and excellent outcome were found in clear cell sarcoma of the kidneys.
引用
收藏
页码:445 / 450
页数:6
相关论文
共 50 条
  • [1] TREATMENT OF WILMS TUMOR: A Report from the Turkish Pediatric Oncology Group (TPOG)
    Akyuz, Canan
    Yalcin, Bilgehan
    Yildiz, Inci
    Hazar, Volkan
    Yoruk, Asim
    Tokuc, Guelnur
    Akici, Ferhan
    Buyukpamukcu, Nebil
    Kale, Guelsev
    Atahan, Lale
    Buyukunal, Cenk
    Dervisoglu, Serguelen
    Atkovar, Guelyuez Akyil
    Melikoglu, Mustafa
    Karpuzoglu, Guelten
    Olgun, Nur
    Ayan, Inci
    Oguz, Aynur
    Yaris, Nilguen
    Dagdemir, Ayhan
    Darendeliler, Emin
    Sander, Serdar
    Kuyumcuoglu, Ugur
    Ozseker, Naciye
    Corapcioglu, Funda
    Tanyeli, Atilla
    Duezovali, Oeznur
    Aydin, G. Burca
    Buyukpamukcu, Muenevver
    PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2010, 27 (03) : 161 - 178
  • [2] Prognosis and outcome of relapsed acute lymphoblastic leukemia: A Hong Kong pediatric hematology and Oncology Study Group report
    Leung, Alex Wing Kwan
    Vincent, Lee
    Chiang, Alan Kwok Shing
    Lee, Anselm Chi Wai
    Cheng, Frankie Wai Tsoi
    Cheuk, Daniel Ka Leung
    Luk, Chung Wing
    Ling, Siu Cheung
    Li, Chi Kong
    PEDIATRIC BLOOD & CANCER, 2012, 59 (03) : 454 - 460
  • [3] Tumors of the Pediatric Maxillofacial Skeleton A 20-Year Clinical Study
    Perry, Katherine S.
    Tkaczuk, Andrew T.
    Caccamese, John F., Jr.
    Ord, Robert A.
    Pereira, Kevin D.
    JAMA OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2015, 141 (01) : 40 - 44
  • [4] The prognostic significance of blastemal predominant histology in initially resected Wilms' tumors: A report from the Study Group for Pediatric Solid Tumors in the Kyushu Area, Japan
    Kinoshita, Yoshiaki
    Suminoe, Aiko
    Inada, Hiroko
    Yagi, Minoru
    Yanai, Fumio
    Zaizen, Yoshio
    Nishi, Masanori
    Inomata, Yukihiro
    Kawakami, Kiyoshi
    Matsufuji, Hiroshi
    Suenobu, Souichi
    Handa, Noritoshi
    Kohashi, Kenichi
    Oda, Yoshinao
    Hara, Toshiro
    Taguchi, Tomoaki
    JOURNAL OF PEDIATRIC SURGERY, 2012, 47 (12) : 2205 - 2209
  • [5] B-NHL Cases in a Tertiary Pediatric Hematology-Oncology Department: A 20-Year Retrospective Cohort Study
    Kyriakidis, Ioannis
    Pelagiadis, Iordanis
    Stratigaki, Maria
    Katzilakis, Nikolaos
    Stiakaki, Eftichia
    LIFE-BASEL, 2024, 14 (05):
  • [6] Clinical Factors in Relapses of Wilms' Tumor - Results for the Polish Pediatric Solid Tumors Study Group
    Niedzielska, Ewa
    Bronowicki, Krzysztof
    Pietras, Wojciech
    Sawicz-Birkowska, Krystyna
    Trybucka, Katarzyna
    Rapala, Malgorzata
    Karpinska-Derda, Irena
    Kurylak, Andrzej
    Marciniak-Stepak, Patrycja
    Panasiuk, Anna
    Nurzynska-Flak, Joanna
    Peregud-Pogorzelski, Jaroslaw
    Pietrys, Danuta
    Ruranska, Iwona
    Sobol, Grazyna
    Stefanowicz, Joanna
    Szymik-Kantorowicz, Sabina
    Zubowska, Malgorzata
    Godzinski, Jan
    ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2014, 23 (06): : 925 - 931
  • [7] Epidemiology, clinical features and treatment outcome of Wilms' tumor in Taiwan: A report from Taiwan Pediatric Oncology Group
    Hung, IJ
    Chang, WH
    Yang, CP
    Jaing, TH
    Liang, DC
    Lin, KH
    Lin, DT
    Hsiao, CC
    Hsieh, YL
    Chen, JS
    Chang, TT
    Peng, CT
    Shu, SG
    Lin, MT
    Chen, BW
    Lin, KS
    JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION, 2004, 103 (02) : 104 - 111
  • [8] Results of Therapy for Wilms Tumor and Other Malignant Kidney Tumors: A Report From the Chilean Pediatric National Cancer Program (PINDA)
    Joannon, Pilar
    Becker, Ana
    Kabalan, Paola
    Concha, Emma
    Beresi, Victoria
    Salgado, Carmen
    Martinez, Pilar
    Olate, Paola
    Arriagada, Monica
    Espinoza, Felipe
    Varas, Monica
    Benavides, Pablo
    Valero, Miguel
    Reyes, Mauricio
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2016, 38 (05) : 372 - 377
  • [9] Renal failure in Wilms' tumor patients: A report from the National Wilms' Tumor Study group
    Ritchey, ML
    Green, DM
    Thomas, PRM
    Smith, GR
    Haase, G
    Shochat, S
    Moksness, J
    Breslow, NE
    MEDICAL AND PEDIATRIC ONCOLOGY, 1996, 26 (02): : 75 - 80
  • [10] Ureteral extension in Wilms' tumor: a report from the National Wilms' Tumor Study Group (NWTSG)
    Ritchey, Michael
    Daley, Shane
    Shamberger, Robert C.
    Ehlrich, Peter
    Hamilton, Thomas
    Haase, Gerald
    Sawin, Robert
    JOURNAL OF PEDIATRIC SURGERY, 2008, 43 (09) : 1625 - 1629