Large solitary fibrous tumor of the kidney - Report of two cases and review of the literature

被引:40
作者
Wang, J
Arber, DA
Frankel, K
Weiss, LM
机构
[1] Loma Linda Univ, Med Ctr, Dept Pathol & Lab Med, Loma Linda, CA 92354 USA
[2] City Hope Natl Med Ctr, Dept Anat Pathol, Duarte, CA 91010 USA
[3] Citrus Valley Med Ctr, Dept Anat & Clin Pathol, Covina, CA USA
关键词
solitary fibrous tumor; kidney; CD34; bcl-2; protein;
D O I
10.1097/00000478-200109000-00011
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Solitary fibrous tumors are spindle cell neoplasms frequently arising in the serosal surface as well as a variety of other sites. We report two cases of large solitary fibrous tumor arising in the kidney, clinically thought to be renal cell carcinoma, in 41- and 72-year-old men. Although large in size (13.0 and 14.0 cm in greatest dimension, respectively), both lesions were well circumscribed and composed of a mixture of spindle cells and dense collagenous bands with no areas of necrosis or cystic changes noted macroscopically or microscopically. Immunohistochemical studies revealed reactivity for vimentin, CD34, collagen IV, and bcl-2 protein in both cases, with no staining for keratin, S-100 protein, or muscle markers, confirming the diagnosis of solitary fibrous tumor of the kidney. Solitary fibrous tumor of the kidney is rare but may present as a large mass that may be clinically confused with carcinoma or sarcoma.
引用
收藏
页码:1194 / 1199
页数:6
相关论文
共 48 条
  • [1] Primary renal synovial sarcoma - Molecular and morphologic delineation of an entity previously included among embryonal sarcomas of the kidney
    Argani, P
    Faria, PA
    Epstein, JI
    Reuter, VE
    Perlman, EJ
    Beckwith, JB
    Ladanyi, M
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2000, 24 (08) : 1087 - 1096
  • [2] Detection of the ETV6-NTRK3 chimeric RNA of infantile fibrosarcoma/cellular congenital mesoblastic nephroma in paraffin-embedded tissue: Application to challenging pediatric renal stromal tumors
    Argani, P
    Fritsch, M
    Kadkol, SS
    Schuster, A
    Beckwith, JB
    Perlman, EJ
    [J]. MODERN PATHOLOGY, 2000, 13 (01) : 29 - 36
  • [3] BATTIFFORA H, 1995, ATLAS TUMOR PATHOLOG
  • [4] BENISCH B, 1981, CANCER, V47, P731, DOI 10.1002/1097-0142(19810215)47:4<731::AID-CNCR2820470418>3.0.CO
  • [5] 2-7
  • [6] Congenital mesoblastic nephroma: Report of a case with review of the most significant literature
    Bisceglia, M
    Carosi, I
    Vairo, M
    Zaffarano, L
    Bisceglia, M
    Creti, G
    [J]. PATHOLOGY RESEARCH AND PRACTICE, 2000, 196 (03) : 199 - 204
  • [7] Ceballos KM, 1999, ARCH PATHOL LAB MED, V123, P941
  • [8] Chu P G, 1999, Ann Diagn Pathol, V3, P104, DOI 10.1016/S1092-9134(99)80038-0
  • [9] DALTON WT, 1979, CANCER, V44, P1465, DOI 10.1002/1097-0142(197910)44:4<1465::AID-CNCR2820440441>3.0.CO
  • [10] 2-Y