Notochordal Tumor

Known as: Notochordal Neoplasm 
A bone tumor arising from the remnants of the fetal notochord. This category includes the chordoma and benign notochordal cell tumor.
National Institutes of Health

Topic mentions per year

Topic mentions per year

2010-2017
02420102017

Papers overview

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2017
2017
By the current WHO classification, benign notochordal cell tumor (BNCT) and chordoma comprise the entire spectrum of notochordal… (More)
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2017
2017
This case reports a 25-year-old woman initially diagnosed with adjacent benign notochordal cell tumors (BNCTs) of L3 and L4 based… (More)
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Review
2017
Review
2017
Chordomas are rare, locally aggressive notochordal tumors, which most frequently occur in the neuraxis. We describe the case of a… (More)
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Review
2017
Review
2017
Benigne notochordale Tumoren (BNCT) und Chordome sind primäre intraossäre Tumoren, die entlang des Achsenskeletts entstehen und… (More)
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2015
2015
Benign notochordal cell tumors (BNCTs) are tumors originating in the axial skeleton, where chordomas occur. Although very rare… (More)
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2014
2014
Chordoma is a malignant tumor thought to arise from remnants of the embryonic notochord, with its origin in the bones of the… (More)
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Review
2012
Review
2012
STUDY DESIGN Clinical case series. OBJECTIVE To describe the clinical, radiological, and histological presentation of a series… (More)
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Review
2011
Review
2011
BACKGROUND AND IMPORTANCE Chordomas are relatively rare tumors that arise from the neuraxis. Most often, chordomas are single… (More)
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2010
2010
CONTEXT Chordoma is a rare, notochordal tumor with a characteristic histomorphology and immunohistochemical profile. At times, it… (More)
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2010
2010
This manual is the 19th volume of a series untitled: ‘‘Monographs in Clinical Cytology’’, edited by S. R. Orell. The purpose of… (More)
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