Abstract：
:Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood, while RMS from the urinary tract has rarely been reported. Aspects of the manifestation, diagnosis, and treatment of these tumors are discussed in the case of a girl with rapidly progressive RMS from the urethral tract. She was treated with a two-stage surgical procedure and chemotherapy. At the latest follow-up visit at 18 months after treatment, the patient had no evidence of disease on clinical examination or imaging studies. The present case underscores that careful history, physical examination, and laboratory tests should be performed, in additional to using adequate tissue for routine pathologic examination, before making the diagnosis. A combined approach to treating RMS using multidrug chemotherapy and surgery has markedly improved survival.
journal_name
Urologyjournal_title
Urologyauthors
Liu AX,Zhou JH,Jin HM,Zhu CK,Cheng XDdoi
10.1016/j.urology.2007.03.022subject
Has Abstractpub_date
2007-06-01 00:00:00pages
1208.e17-9issue
6eissn
0090-4295issn
1527-9995pii
S0090-4295(07)00367-6journal_volume
69pub_type
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