Volume 9, Issue 28 (6-2002)
RJMS 2002, 9(28): 45-50 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Setarehshenas R, Rakhshani N. INTRANODAL PALISADED MYOFIBROBLASTOMA IN RIGHT ARM IN 13 YEARS OLD BOY “A CASE REPORT”. RJMS 2002; 9 (28) :45-50
URL: http://rjms.iums.ac.ir/article-1-251-en.html
URL: http://rjms.iums.ac.ir/article-1-251-en.html
Abstract: (10063 Views)
ABSTRACT
Intranodal palisaded myofibroblastoma (IPM) is a rare primary nonlymphoid Tumor of the lymph node, which can easily be mistaken for other spindle cell tumors. Intranodal palisaded myofibroblastoma is thought to arise from intranodal myofibroblasts. We describe a 13 year Iranian boy with IPM arose in the right arm. The tumor was well-demarcated and composed of a fascicular proliferation of spindle cells with focal nuclear palisading and acellular stellate shaped collagen-rich areas. Histologically and immunohistochemically myofibroblastic differentiation was confirmed. To our knowledge this case represents only the first case of IPMin the lymph node of arm.
Keywords: 1) Myofibroblastoma 2) Lymph node 3) Arm
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
