Anaplastic carcinoma of the thyroid with rhabdomyosarcomatous differentiation:: a report of two cases

被引:24
作者
Carda, C [1 ]
Ferrer, J [1 ]
Vilanova, M [1 ]
Peydrö, A [1 ]
Llombart-Bosch, A [1 ]
机构
[1] Univ Valencia, Fac Med, Dept Pathol, Valencia 46010, Spain
关键词
anaplastic carcinoma thyroid; rhabdomyosarcomatous differentiation; immunohistochemistry; electron microscopy;
D O I
10.1007/s00428-004-1123-0
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Anaplastic carcinoma of the thyroid gland (ACT) is a highly malignant tumor that is almost invariably associated with a fatal outcome. It demonstrates a variety of peculiar histological features, with squamoid, giant cell and spindle cell growth patterns. The spindle cell variant of ACT is usually indistinguishable from a true sarcoma and it can simulate fibrosarcoma, malignant fibrous histiocytoma (MFH), hemangiopericytoma and angiosarcoma or rhabdomyosarcoma. Although a rhabdomyosarcomatous appearance has sometimes been mentioned in the literature, true skeletal muscle differentiation has never been consistently proved. We report two cases of ACT with rhabdomyosarcomatous differentiation, as demonstrated by means of immunohistochemistry and electron microscopy. Both cases disclosed a very similar histological appearance, with a main population of small, pleomorphic, round-to-oval cells arranged in a storiform pattern, admixed with scattered pleomorphic giant cells, an image similar to that of the usual type of MFH. Stains for epithelial markers showed only few, scattered, weakly positive cells. Thyroglobulin and calcitonin were negative in tumor cells in both cases. On the contrary, positivity to vimentin was strong and generalized. Immunomarkers of muscular differentiation showed a consistent positivity. At the ultrastructural level, the cells disclosed the same spindle and pleomorphic morphology, with large, bizarre nuclei and cytoplasm with abundant mitochondria, rough endoplasmic reticulum, secretory granules and lipid droplets. There were also cells with wide cytoplasm filled with filamentous material, either of actin or myosin, as well as Z-band material. In conclusion, the cases reported here show a clear-cut rhabdomyosarcomatous differentiation of ACT, confirmed both immunohistochemically and ultrastructurally, a feature not previously reported in the literature. These findings may contribute to the broadening of the differentiation spectrum of this unusual neoplasm.
引用
收藏
页码:46 / 51
页数:6
相关论文
共 33 条
[1]  
ALDINGER KA, 1978, CANCER-AM CANCER SOC, V41, P2267, DOI 10.1002/1097-0142(197806)41:6<2267::AID-CNCR2820410627>3.0.CO
[2]  
2-7
[3]  
[Anonymous], 1992, ATLAS TUMOR PATHOL
[4]  
BELTRAMI C A, 1989, Applied Pathology, V7, P122
[5]   ANAPLASTIC THYROID-CARCINOMA - A STUDY OF 70 CASES [J].
CARCANGIU, ML ;
STEEPER, T ;
ZAMPI, G ;
ROSAI, J .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1985, 83 (02) :135-158
[6]   Are myogenin and MyoD1 expression specific for rhabdomyosarcoma? A study of 150 cases, with emphasis on spindle cell mimics [J].
Cessna, MH ;
Zhou, H ;
Perkins, SL ;
Tripp, SR ;
Layfield, L ;
Daines, C ;
Coffin, CM .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2001, 25 (09) :1150-1157
[7]   LEIOMYOSARCOMA OF THE THYROID - IMMUNOHISTOCHEMICAL AND ULTRASTRUCTURAL-STUDY [J].
CHETTY, R ;
CLARK, SP ;
DOWLING, JP .
PATHOLOGY, 1993, 25 (02) :203-205
[8]  
DIAS P, 1994, SEMIN DIAGN PATHOL, V11, P3
[9]  
DONNELL CA, 1987, ARCH PATHOL LAB MED, V111, P1169
[10]   KERATIN-POSITIVE EPITHELIOID ANGIOSARCOMA OF THYROID - A REPORT OF 4 CASES [J].
EUSEBI, V ;
CARCANGIU, ML ;
DINA, R ;
ROSAI, J .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1990, 14 (08) :737-747