Angiomatoid malignant fibrous histiocytoma: Report of an unusual case with highly aggressive clinical course

1998 ◽  
Vol 37 (3) ◽  
pp. 235-238 ◽  
Author(s):  
Louis T.C. Chow ◽  
Philip W. Allen ◽  
S.M. Kumta ◽  
J. Griffith ◽  
C.K. Li ◽  
...  
2009 ◽  
Vol 395 (3) ◽  
pp. 261-275 ◽  
Author(s):  
Daigeler Adrien ◽  
Klein-Hitpass Ludger ◽  
Stricker Ingo ◽  
Müller Oliver ◽  
Kuhnen Cornelius ◽  
...  

2004 ◽  
Vol 128 (4) ◽  
pp. 456-459
Author(s):  
Beverly Y. Wang ◽  
Alexander H. Boag ◽  
Muhammad Idrees ◽  
Iain D. Young ◽  
Pamela D. Unger

Abstract Pathologic processes involving the urachus are usually related to inflammatory or sinofistular conditions. Neoplasms rarely arise within this structure, and when they do occur, they are typically epithelial, with mucinous adenocarcinoma being the most common. Mesenchymal lesions, both benign and malignant, have rarely been described in this location. We report the case of a 66-year-old white man who presented with a primary urachal malignant fibrous histiocytoma and died of metastatic disease 20 months after the initial diagnosis. This is an unusual case of malignant fibrous histiocytoma arising in a urachal remnant.


1996 ◽  
Vol 37 (1P1) ◽  
pp. 321-322
Author(s):  
A. K. Sharma

Malignant fibrous histiocytoma is a rare lesion, most often occurring in the elderly. A very unusual case in a 15-year-old boy diagnosed by CT and confirmed at histopathology is presented.


2009 ◽  
Vol 394 (3) ◽  
pp. 589-589
Author(s):  
Adrien Daigeler ◽  
Ludger Klein-Hitpass ◽  
Ingo Stricker ◽  
Oliver Müller ◽  
Cornelius Kuhnen ◽  
...  

2020 ◽  
pp. 106689692094040
Author(s):  
Vidya Rao ◽  
Santosh Menon ◽  
Ganesh Bakshi ◽  
Gagan Prakash ◽  
Archi Agarwal ◽  
...  

Thyroid-like follicular carcinoma of the kidney (TLFCK) is a rare subtype of renal cell carcinoma, which closely resembles follicular neoplasms of the thyroid and has a distinctive indolent clinical behavior. Until now, a single case of TLFCK with extensive sarcomatoid differentiation has been documented with aggressive clinical course. We present an unusual case of sarcomatoid TLFCK with a low-grade spindle cell component in a 34-year-old male patient, with an indolent course following radical nephrectomy and regional node dissection.


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