3.8 Article

Value of fine needle aspiration biopsy in childhood rhabdomyosarcoma: Twenty-six years of experience in Slovenia

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MEDICAL AND PEDIATRIC ONCOLOGY
卷 38, 期 6, 页码 416-420

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WILEY-LISS
DOI: 10.1002/mpo.10075

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rhabdomyosarcoma; fine needle aspiration biopsy; cytology; childhood cancer; needle biopsy

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Background. Chemotherapy (Cht) for rhabdomyosarcoma (RMS) given before local treatment can prevent mutilating surgery and high-dose irradiation (RT). Fine needle aspiration biopsy (FNAB) can confirm the diagnosis and neoadjuvant treatment can start without delay. The purpose of our study was to assess the role of FNAB in the management of childhood RMS in Slovenia, Procedure. A total of 78 children and young adults were included. FNAB provided the pre-treatment diagnosis in 37 and surgical biopsy in 41 patients. In 61 cases recurrent/metastatic disease was aspirated. Cytological diagnoses were compared to the original histological diagnoses. All case histories, cytological and histological material were reviewed and immunocytochemical staining performed when necessary. Results. FNAB provided a correct diagnosis of malignancy in all 37 primary tumours, a specific diagnosis of RMS was given in 29 (78%). With the use of immunocytochemistry during the last 15 years, the accuracy has risen to 87%. FNAB provided the diagnosis of recurrence/metastasis in 57/61 cases. No complications of FNAB were noted. Review of histology reclassified five original diagnoses of RMS into one malignant rhabdoid tumour and four sarcomas NOS. in review of cytology we were able to sub classify 80% of RMS. Conclusions. FNAB is a safe method, which enables us to establish the pre-treatment diagnosis of RMS, and to some extent even its type, without delay. In our study, FNAB successfully replaced surgical biopsy in 87% of RMS patients during the last 15 years. Neoadjuvant Cht was started immediately, surgery was delayed and more conservative. Consequently, the risk for treatment sequelae was considerably reduced. Med Pediatr Oncol 2002;38: 416-420. (C) 2002 Wiley-Liss, Inc.

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