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[Diagnosis and treatment of Wilms' tumor].
Gan To Kagaku Ryoho 1983; 10(10):2117-24GT

Abstract

Recent advances in the diagnosis and treatment of Wilms' tumor are reviewed. Our study disclosed that principal clinical and pathological features of Wilms' tumor are as follows: (1) It occurs in young infants and children under 5 years of age; (2) It is frequently associated with other congenital anomalies; (3) Deletion of a portion of short arm of chromosome 11 can be closely related to the tumor genesis of nephroblastoma; (4) The occurrence of distant metastases is rare at diagnosis; (5) Differential diagnosis between Wilms' tumor and neuroblastoma is occasionally quite difficult; (6) There is no good tumor marker specific to Wilms' tumor; and (7) Two-year survival rate is about 90% at present.

Authors

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Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

jpn

PubMed ID

6137999

Citation

Tsuchida, Y, et al. "[Diagnosis and Treatment of Wilms' Tumor]." Gan to Kagaku Ryoho. Cancer & Chemotherapy, vol. 10, no. 10, 1983, pp. 2117-24.
Tsuchida Y, Saito S, Honna T, et al. [Diagnosis and treatment of Wilms' tumor]. Gan To Kagaku Ryoho. 1983;10(10):2117-24.
Tsuchida, Y., Saito, S., Honna, T., Makino, S., & Iwanaka, T. (1983). [Diagnosis and treatment of Wilms' tumor]. Gan to Kagaku Ryoho. Cancer & Chemotherapy, 10(10), pp. 2117-24.
Tsuchida Y, et al. [Diagnosis and Treatment of Wilms' Tumor]. Gan To Kagaku Ryoho. 1983;10(10):2117-24. PubMed PMID: 6137999.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Diagnosis and treatment of Wilms' tumor]. AU - Tsuchida,Y, AU - Saito,S, AU - Honna,T, AU - Makino,S, AU - Iwanaka,T, PY - 1983/10/1/pubmed PY - 1983/10/1/medline PY - 1983/10/1/entrez SP - 2117 EP - 24 JF - Gan to kagaku ryoho. Cancer & chemotherapy JO - Gan To Kagaku Ryoho VL - 10 IS - 10 N2 - Recent advances in the diagnosis and treatment of Wilms' tumor are reviewed. Our study disclosed that principal clinical and pathological features of Wilms' tumor are as follows: (1) It occurs in young infants and children under 5 years of age; (2) It is frequently associated with other congenital anomalies; (3) Deletion of a portion of short arm of chromosome 11 can be closely related to the tumor genesis of nephroblastoma; (4) The occurrence of distant metastases is rare at diagnosis; (5) Differential diagnosis between Wilms' tumor and neuroblastoma is occasionally quite difficult; (6) There is no good tumor marker specific to Wilms' tumor; and (7) Two-year survival rate is about 90% at present. SN - 0385-0684 UR - https://www.unboundmedicine.com/medline/citation/6137999/[Diagnosis_and_treatment_of_Wilms'_tumor]_ L2 - http://www.diseaseinfosearch.org/result/7505 DB - PRIME DP - Unbound Medicine ER -