scholarly journals Primary osteosarcoma of the breast with abundant chondroid matrix and fibroblasts has a good prognosis: A case report and review of the literature

2013 ◽  
Vol 6 (3) ◽  
pp. 745-747 ◽  
Author(s):  
JINGJIE ZHAO ◽  
XUEDONG ZHANG ◽  
JIANWEI LIU ◽  
JIANHUA LI
2007 ◽  
Vol 25 (2) ◽  
pp. 251-255 ◽  
Author(s):  
Rui Niimi ◽  
Akihiko Matsumine ◽  
Katsuyuki Kusuzaki ◽  
Yasuhiro Inada ◽  
Yuya Kato ◽  
...  

2002 ◽  
Vol 52 (2) ◽  
pp. 158-163 ◽  
Author(s):  
Mu Su ◽  
Takuo Tokairin ◽  
Yuji Nishikawa ◽  
Tomomi Yoshioka ◽  
Osamu Takahashi ◽  
...  

2018 ◽  
Vol 10 (1) ◽  
pp. 18-24 ◽  
Author(s):  
José Omar Navarro Fernández ◽  
Alejandro Monroy Sosa ◽  
Bernardo Cacho Díaz ◽  
Víctor Andrés Arrieta ◽  
Ramses Uriel Ortíz Leyva ◽  
...  

Cervical intramedullary schwannomas are extraordinarily rare. Gross total resection is the best therapeutic option for these types of tumors. Although rare, intramedullary schwannomas should be considered as a differential diagnosis of intramedullary lesions since a good prognosis can be guaranteed to the majority of these patients. We present a case of a cervical intramedullary schwannoma surgically treated in a 19-year-old male patient who initially presented with motor neuron disease.


1994 ◽  
Vol 33 (1) ◽  
pp. 74-76 ◽  
Author(s):  
Ulrich Kaiser ◽  
Peter Barth ◽  
Volker Duda ◽  
Karl-Heinz Pflüger ◽  
Klaus Havemann

2019 ◽  
Vol 27 (6) ◽  
pp. 678-683 ◽  
Author(s):  
Taylor M. Jenkins ◽  
Jason Rosenbaum ◽  
Paul J. Zhang ◽  
Lauren E. Schwartz ◽  
Anupma Nayak ◽  
...  

Thyroid-like follicular carcinoma of the kidney (TLFCK) is an extremely rare primary renal malignancy that typically has an indolent course and good prognosis. Histologically, this tumor mimics follicular carcinoma of the thyroid; however, typical thyroid markers are negative. There are fewer than 40 cases reported in the literature, and thus, the prognosis and course of disease is not well understood. Sarcomatoid differentiation has never been reported in a case of TLFCK. We present a case of a 48-year-old woman with an aggressive TLFCK with extensive sarcomatoid differentiation and metastatic disease at presentation. We performed targeted next-generation sequencing of both the thyroid-like component and the poorly differentiated sarcomatoid component using our solid tumor panel to evaluate for any disease-associated mutations and to better understand the molecular profile of these tumors.


1994 ◽  
Vol 23 (2) ◽  
pp. 162-165 ◽  
Author(s):  
Rejin Kebudi ◽  
Inci Ayan ◽  
Emin Darendeliler ◽  
Leyla A??ao??lu ◽  
Çiçek Bayindir ◽  
...  

1990 ◽  
Vol 39 (3) ◽  
pp. 259-263 ◽  
Author(s):  
Jeffrey F. Hines ◽  
David M. Compton ◽  
C.Christopher Stacy ◽  
Mark E. Potter

2003 ◽  
Vol 61 (2A) ◽  
pp. 269-273 ◽  
Author(s):  
Antonio Aversa do Souto ◽  
Flavio S. Domingues ◽  
Leila Chimelli ◽  
Armando M. Lemos

We present a case of a 46-year old woman with a ventral epidural angiolipoma at the lumbosacral level with erosion of the sacrum. About ninety cases of spinal angiolipomas have been previously described in the literature, most of them situated on the thoracic region, dorsal to the dural sac. Angiolipomas can be radically excised with a good prognosis even in the presence of bone erosion. We did not find any other angiolipoma at the sacral level surgically explored in the review of the literature.


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