scholarly journals Low-Grade Adenosquamous Carcinoma of the Axilla of Breast Origin in a Male: A Case Report and Literature Review

2020 ◽  
Vol 10 ◽  
Author(s):  
Xingqiang Yan ◽  
Fanshuang Zhu ◽  
Qiupeng Wang ◽  
Lijie Chen ◽  
Yixing Zhou ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Adenosquamous Carcinoma ◽  
Low Grade

scholarly journals MRI findings of low-grade fibromyxoid sarcoma: a case report and literature review

2018 ◽  
Vol 19 (1) ◽  
Author(s):  
Yali Yue ◽  
Yongkang Liu ◽  
Lina Song ◽  
Xiao Chen ◽  
Yaohui Wang ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Low Grade ◽  
Mri Findings ◽  
Fibromyxoid Sarcoma

scholarly journals Thyroid-like low-grade nasopharyngeal papillary adenocarcinoma: a case report and literature review

2020 ◽  
Vol 9 (7) ◽  
pp. 4457-4463
Author(s):  
Jun Wang ◽  
Zhao-Zhen Chen ◽  
Chen-Lu Lian ◽  
Qin Lin ◽  
San-Gang Wu
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Papillary Adenocarcinoma ◽  
Low Grade

scholarly journals Limbal, low-grade myofibroblastic sarcoma: Case report and literature review

2020 ◽  
Vol 68 (11) ◽  
pp. 2538
Author(s):  
Kaustubh Mulay ◽  
Mrittika Sen ◽  
SantoshG Honavar
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Low Grade ◽  
Myofibroblastic Sarcoma

Mesenteric Fibromatosis in a Patient with Camurati-Engelmann Disease. A Case Report and Literature Review

2005 ◽  
Vol 91 (6) ◽  
pp. 552-554 ◽  
Author(s):  
Pierluigi Ballardini ◽  
Loretta Gulmini ◽  
Guido Margutti ◽  
Giorgio Lelli
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Diseases ◽  
Bone Dysplasia ◽  
Low Grade ◽  
Long Bones ◽  
Rare Form ◽  
Rare Type ◽  
Mesenteric Fibromatosis ◽  
Engelmann Disease

Mesenteric fibromatosis is a rare type of desmoid tumor characterized by local aggressiveness and a tendency to relapse. In view of these characteristics it may be considered a low-grade fibrosarcoma. Camurati-Engelmann disease is a very rare form of bone dysplasia characterized by osteosclerosis of the diaphyses of the long bones. Here we describe the case of a male patient affected by these two rare diseases in association with chronic inflammatory intestinal disease.

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