scholarly journals Invasive Recurrence of an Intestinal-Type Mucinous Epithelial Neoplasm of Low Malignant Potential: Case Report and Review of the Literature

2011 ◽  
Vol 4 (2) ◽  
pp. 426-432
Author(s):  
S. Cosyns ◽  
M. Leyder ◽  
C. Bourgain ◽  
P. De Sutter
Keyword(s):  
Case Report ◽  
Malignant Potential ◽  
Intestinal Type ◽  
Review Of The Literature ◽  
Low Malignant Potential ◽  
Potential Case ◽  
Epithelial Neoplasm

scholarly journals Soft tissue giant cell tumor of low malignant potential of the neck: a case report and review of the literature

2014 ◽  
Vol 30 (1) ◽  
pp. 73 ◽  
Author(s):  
Aylin Orgen Calli ◽  
Mine Tunakan ◽  
Huseyin Katilmis ◽  
Sevil Kilciksiz ◽  
Sedat Ozturkcan
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Giant Cell Tumor ◽  
Giant Cell ◽  
Malignant Potential ◽  
Cell Tumor ◽  
Review Of The Literature ◽  
Low Malignant Potential

scholarly journals Relapsed papillary urothelial neoplasm of low malignant potential (PUNLMP) of the young age: a case report and a review of the literature

BMC Urology ◽  
2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Palma Maurizi ◽  
Michele Antonio Capozza ◽  
Silvia Triarico ◽  
Maria Luisa Perrotta ◽  
Vito Briganti ◽  
...  
Keyword(s):  
Case Report ◽  
Malignant Potential ◽  
Young Age ◽  
Review Of The Literature ◽  
Low Malignant Potential ◽  
Urothelial Neoplasm

scholarly journals Mediastinal smooth muscle tumor of uncertain malignant potential: case report and literature review

2019 ◽  
Vol 55 (1) ◽  
pp. 89-94
Author(s):  
Veljko Flego ◽  
Darian Volarić ◽  
Koviljka Matušan Ilijaš ◽  
Ljiljana Bulat-Kardum
Keyword(s):  
Smooth Muscle ◽  
Case Report ◽  
Literature Review ◽  
Smooth Muscle Tumor ◽  
Malignant Potential ◽  
Uncertain Malignant Potential ◽  
Potential Case ◽  
Muscle Tumor

scholarly journals Malignant potential of intrahepatic biliary papillomatosis: a case report and review of the literature

2006 ◽  
Vol 4 (1) ◽  
Author(s):  
Ioannis Vassiliou ◽  
Evi Kairi-Vassilatou ◽  
Athanasios Marinis ◽  
Theodosios Theodosopoulos ◽  
Nikolaos Arkadopoulos ◽  
...  
Keyword(s):  
Case Report ◽  
Malignant Potential ◽  
Review Of The Literature ◽  
Biliary Papillomatosis

Testicular Papillary Cystadenomatous Tumor of Low Malignant Potential: A Case Report and Discussion of the Literature

1988 ◽  
Vol 139 (2) ◽  
pp. 378-379 ◽  
Author(s):  
C. Gilberto Brito ◽  
Ted Bloch ◽  
Richard S. Foster ◽  
Richard Bihrle
Keyword(s):  
Case Report ◽  
Malignant Potential ◽  
Low Malignant Potential

Primary Intradural Classic Chondrosarcoma: Case Report and Literature Review

Neurosurgery ◽  
2001 ◽  
Vol 48 (2) ◽  
pp. 420-423 ◽  
Author(s):  
Jark Jan Daniël Bosma ◽  
Ramez Wadie Kirollos ◽  
John Broome ◽  
Paul Richard Eldridge
Keyword(s):  
Case Report ◽  
Adjuvant Radiotherapy ◽  
Clinical Presentation ◽  
Malignant Potential ◽  
Review Of The Literature ◽  
Resonance Imaging ◽  
Image Guided ◽  
History Of ◽  
Grade Ii ◽  
Exact Origin

Abstract OBJECTIVE AND IMPORTANCE The exact origin of rare intradural chondrosarcomas remains obscure. We present a case report of an intradural classic chondrosarcoma (a very rare subtype of chondrosarcoma in this location), with a review of the literature, in an attempt to clarify the histogenesis of these tumors. CLINICAL PRESENTATION A 48-year-old man presented with a 12-month history of progressive right hemiparesis. Computed tomography and magnetic resonance imaging demonstrated a left parietal space-occupying lesion. INTERVENTION The patient underwent an image-guided, left parietal parasagittal craniotomy. An extrinsic tumor, which seemed to arise from the dura, was macroscopically removed. There was no bone involvement. The histological examination revealed a Grade II classic chondrosarcoma with tumor infiltration into the dura. Adjuvant radiotherapy was administered. CONCLUSION Intradural chondrosarcomas are rare tumors, the majority of which are mesenchymal. Classic chondrosarcomas in this location are much rarer. Their histogenesis is uncertain. In this case, the origin seems to be from the dura. Because of the malignant potential of these tumors, radical extirpation whenever possible, followed by radiotherapy, is indicated.

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