A de novo desmoid tumor of the surgical site following foramen magnum meningioma resection in a patient with Gardner’s Syndrome: a case report and review of the literature

2008 ◽  
Vol 91 (1) ◽  
pp. 107-111 ◽  
Author(s):  
Tyler James Kenning ◽  
Vikramjit S. Kanwar ◽  
Jiang Qian ◽  
Eric M. Deshaies
2018 ◽  
Vol 07 (11) ◽  
pp. 533-540
Author(s):  
Olfa Zoukar ◽  
Amel Khaskhoussy ◽  
Sonia Hammami ◽  
Sandra Zribi ◽  
Awatef Hajjajji ◽  
...  

2021 ◽  
pp. 1071-1079
Author(s):  
Jennifer Y. Ge ◽  
Beth Overmoyer

Inflammatory breast cancer (IBC) is a rare type of breast cancer that is associated with poor outcomes compared with non-IBC. Overexpression of HER2 is enriched in IBC, and those with HER2-positive disease have a relatively favorable prognosis, with improved survival over the last two decades driven by the advent of novel targeted therapies. Here, we present two patients who have survived for over 10 years after being diagnosed with de novo metastatic HER2-positive IBC. We review the data for the treatments available for metastatic HER2-positive IBC and the evolving treatment recommendations for this disease.


Author(s):  
Murat Sakir Eksi ◽  
Huseyin Kemal Turkoz ◽  
Emel Ece Ozcan Eksi ◽  
Akin Akakin ◽  
Zafer Orkun Toktas ◽  
...  

2021 ◽  
Author(s):  
J Sollors ◽  
B Kallinowski ◽  
T Gaiser ◽  
C Antoni ◽  
M Ebert ◽  
...  

2020 ◽  
Author(s):  
Raffaele Vitiello ◽  
Tommaso Greco ◽  
Luigi Cianni ◽  
Silvia Careri ◽  
Maria Serena Oliva ◽  
...  

Osteoma is a benign, slowly growing, asymptomatic, bone-forming tumor arising from cancellous or compact bone. Osteoma usually is a solitary lesion, but in patients with Gardner’s Syndrome it may be multiple. osteoma may rarely have a parosteal localization. Parosteal osteoma has peculiar radiographic, histologic and clinical features. We describe a case report of a 51- years old man with a bifocal parosteal osteoma of the femur in a non-syndromic patient. This is the first described patient with a bifocal lesion. In literature only 24 cases of paraosteal osteoma are found. Our patient underwent surgery and the lesions were fully excised. At one year follow-up there was no evidence of recurrence.


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