Falcine Chondrosarcoma: Case Report and Literature Review

Neurosurgery ◽  
1985 ◽  
Vol 16 (3) ◽  
pp. 412-415 ◽  
Author(s):  
George R. Cybulski ◽  
Eric J. Russell ◽  
Charles M. D'Angelo ◽  
Orville T. Bailey
Keyword(s):  
Case Report ◽  
Natural History ◽  
Literature Review ◽  
Rare Tumor ◽  
Intracranial Tumors ◽  
History Of ◽  
Distinguishing Features

Abstract We present a case of falcine chondrosarcoma in a 58-year-old man. Only a few other examples of chondrosarcomas in this location and a total of approximately 50 intracranial cases have been reported. Because its rarity prevents any group of neurosurgeons from collecting a large experience in managing this tumor, we reviewed descriptions of previous cases to determine the natural history of intracranial chondrosarcomas. The distinguishing features of this rare tumor are compared with previous examples of intracranial tumors derived from cartilage and more common tumors in the parasagittal region, such as meningioma.

Natural History of a Patient with Sacral Chordoma: Case Report and Literature Review

2020 ◽  
Vol 139 ◽  
pp. 132-135
Author(s):  
Brooke T. Kennamer ◽  
Daniel G. Gridley ◽  
Laurence D. Rhines ◽  
Geetha R. Nair ◽  
Salvatore C. Lettieri ◽  
...  
Keyword(s):  
Case Report ◽  
Natural History ◽  
Literature Review ◽  
Sacral Chordoma ◽  
History Of

Malignant Peritoneal Mesothelioma in a Hemodialysis Patient with Familial Mediterranean Fever: A Case Report and Literature Review

2008 ◽  
Vol 53 (4) ◽  
pp. 1-3
Author(s):  
E Sengul ◽  
K Yildiz ◽  
Y Topcu ◽  
A Yilmaz
Keyword(s):  
Case Report ◽  
Familial Mediterranean Fever ◽  
Literature Review ◽  
Medical Literature ◽  
Hemodialysis Patient ◽  
Peritoneal Mesothelioma ◽  
Rare Tumor ◽  
Malignant Peritoneal Mesothelioma ◽  
History Of ◽  
Mediterranean Fever

Malignant mesothelioma is a rare tumor. The most common localization of mesothelioma is pleura. It rarely arises from the peritoneum. It has been suggested that familial Mediterranean fever (FMF) may cause the development of peritoneal mesothelioma. We describe a case of malignant peritoneal mesothelioma in a hemodialysis patient with FMF. The patient was a 56 year old female. A history of FMF was present since her childhood. She did not use colchicine and suffered from recurrent ascites. To the best of our knowledge, this is the seventh case of FMF diagnosed as having malignant peritoneal mesothelioma in the medical literature.

Natural history of Kindler syndrome and propensity for skin cancer - case report and literature review

2018 ◽  
Vol 16 (3) ◽  
pp. 338-341 ◽  
Author(s):  
Mina Saleva ◽  
Cristina Has ◽  
Yinghong He ◽  
Snejina Vassileva ◽  
Maria Balabanova ◽  
...  
Keyword(s):  
Case Report ◽  
Skin Cancer ◽  
Natural History ◽  
Literature Review ◽  
Cancer Case ◽  
Kindler Syndrome ◽  
History Of

scholarly journals Natural history of cranial fibrous dysplasia revealed during long-term follow-up: Case report and literature review

2017 ◽  
Vol 8 (1) ◽  
pp. 209 ◽  
Author(s):  
IanF Dunn ◽  
DavidL Penn ◽  
RichardJ Tartarini ◽  
CarolynH Glass ◽  
Umberto De Girolami ◽  
...  
Keyword(s):  
Case Report ◽  
Natural History ◽  
Literature Review ◽  
Fibrous Dysplasia ◽  
Long Term Follow Up ◽  
History Of

scholarly journals Natural History of Early Gastric Cancer: a Case Report and Literature Review

2017 ◽  
Vol 17 (1) ◽  
pp. 88 ◽  
Author(s):  
Tomohiro Iwai ◽  
Masao Yoshida ◽  
Hiroyuki Ono ◽  
Naomi Kakushima ◽  
Kohei Takizawa ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Case Report ◽  
Early Gastric Cancer ◽  
Natural History ◽  
Literature Review ◽  
History Of

scholarly journals Esthesioneuroblastoma: case report

2002 ◽  
Vol 60 (2A) ◽  
pp. 303-307 ◽  
Author(s):  
Jackson Gondim ◽  
Francisco Ramos Jr ◽  
Jorge Azevedo ◽  
Fernando Porto Carrero Jr ◽  
Oswaldo Inácio Tella Jr
Keyword(s):  
Case Report ◽  
Natural History ◽  
Literature Review ◽  
Olfactory Epithelium ◽  
Age Distribution ◽  
Cranial Base ◽  
Rare Tumor ◽  
Craniofacial Resection ◽  
Nasal Vault ◽  
Head Neck

Esthesioneuroblatoma (ENB) is a rare tumor arising from the olfactory epithelium of the nasal vault which frequently invades the cranial base, cranial vault and orbit. ENB has a bimodal age distribution between 11 and 20 years and between 51 and 60 years. ENB accounts for approximately 1 to 5% of intranasal cancers and no consensus has been reached regarding treatment of this tumor. We report on a 66 year old female patient with a Kadish stage C tumor with frontal lobe invasion submitted a total craniofacial resection with a combined head neck and neurosurgeon team. The purpose of this study is to analyze the natural history, treatment and prognosis of this tumor, based on the literature review.

scholarly journals Natural history of an early diagnosed retinocytoma: case report and literature review

2012 ◽  
Vol 90 ◽  
pp. 0-0
Author(s):  
S DE FRANCESCO ◽  
P GALLUZZI ◽  
A RENIERI ◽  
M BORRI ◽  
L MAZZERA ◽  
...  
Keyword(s):  
Case Report ◽  
Natural History ◽  
Literature Review ◽  
History Of
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