Fine-Needle Aspiration of Renal and Extrarenal Rhabdoid Tumors The Experience of the Institut Curie Regarding 20 Tumors in 13 Patients

被引:20
|
作者
Thomson, Thomas A. [2 ]
Klijanienko, Jerzy [1 ]
Couturier, Jerome [1 ]
Brisse, Herve [3 ]
Pierron, Gaelle [4 ]
Freneaux, Paul [1 ]
Sastre-Garau, Xavier [1 ]
Lagace, Real [6 ]
Bourdeaut, Franck [5 ]
机构
[1] Inst Curie, Dept Pathol, F-75005 Paris, France
[2] British Columbia Canc Agcy, Lab Med, Vancouver, BC V5Z 4E6, Canada
[3] Inst Curie, Dept Radiol, F-75005 Paris, France
[4] Inst Curie, Dept Genet & Biol Canc, INSERM, U830, F-75005 Paris, France
[5] Inst Curie, Dept Pediat Oncol, F-75005 Paris, France
[6] Univ Hosp Quebec, Dept Pathol, Quebec City, PQ, Canada
关键词
rhabdoid tumor; fine-needle aspiration; karyotyping; molecular biology; diagnosis; SOFT-TISSUE SARCOMAS; NATIONAL WILMS-TUMOR; EPITHELIOID SARCOMA; INI1; EXPRESSION; SMARCB1/INI1; PROTEIN; AGGRESSIVE-BEHAVIOR; CYTOLOGY; KIDNEY; DIAGNOSIS; FEATURES;
D O I
10.1002/cncy.20121
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Rhabdoid tumors (RT) are rare, renal or extrarenal, high-grade malignancies. The cytologic diagnosis may be confirmed if combined with genomic results. In the current study, the authors present the cytologic and ancillary techniques used to diagnose RT in their series of 20 tumors in 13 patients. METHODS: Clinical charts as well as cytologic, histologic, karyotypic, and molecular biology results were reviewed. RESULTS: Twelve fine-needle aspirations (FNAs) were performed for primary diagnosis, 7 were to confirm a metastasis, and 1 was to confirm local recurrence. Primary tumors were in the kidney in 7 cases and 13 were extrarenal. Patient age ranged from 5 months to 26 years. There were 7 females and 6 males. FNAs were cell-rich in 16 cases and cell-poor in 4 cases and revealed a mix of atypical spindleshaped, round, rhabdoid, or epithelioid cells, singly or in clusters. Mitosis and necrosis occasionally were present. The original cytologic diagnosis was malignant in all cases. There were no unsatisfactory or false-negative samples. In the 12 primary tumors, the preliminary FNA diagnosis was RI in 7 cases (58%), rhabdomyosarcoma in 4 cases (33%), and malignant peripheral nerve sheath tumor in 1 case (8%). Karyotypes were available in 6 cases, 3 of which demonstrated chromosome 22 changes. Fluorescence in situ hybridization revealed loss of probe signals for the SMARCB1 gene locus in 5 cases; DNA sequence analysis performed in 9 cases revealed deletions in codons of the SMARCB7 gene in 7 cases and a mutation in 2 cases. CONCLUSIONS: The primary diagnosis of RT is possible on FNA. In the current study, 12 of 13 cases were diagnosed by FNA with a combination of clinical information, immunocytochemistry, and molecular analysis. Cancer (Cancer Cytopathol) 2011;119:49-57. (C) 2010 American Cancer Society
引用
收藏
页码:49 / 57
页数:9
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