Enterogenous cyst from craniovertebral junction to D2 – Rare presentation

2018 ◽  
Vol 15 (4) ◽  
pp. 186
Author(s):  
Kodeeswaran Marappan ◽  
Saravanan Ramamurthy ◽  
JSharmila Beevi
Keyword(s):  
Craniovertebral Junction ◽  
Enterogenous Cyst ◽  
Rare Presentation

scholarly journals Klippel-Feil syndrome with multiple skeletal anomalies, Dandy-Walker spectrum, and occipital cephalocele—a rare presentation

2021 ◽  
Vol 52 (1) ◽  
Author(s):  
Mohammad Shoaib ◽  
M. Sarthak Swarup ◽  
Gaurav Pradhan
Keyword(s):  
Spina Bifida ◽  
Congenital Malformation ◽  
Cervical Vertebrae ◽  
Craniovertebral Junction ◽  
Spina Bifida Occulta ◽  
Short Neck ◽  
Rare Presentation ◽  
Case Presentation ◽  
Skeletal Anomalies ◽  
Rib Anomalies

Abstract Background Klippel-Feil syndrome (KFS) is a congenital malformation causing fusion of at least two cervical vertebrae and characterized clinically by presence of triad of short neck, limited neck movements, and low posterior hair line. Various skeletal and non-skeletal anomalies may be seen in association with KFS. Case presentation We present a case of 6-year-old boy of KFS with various skeletal anomalies such as multiple segmentation and formation anomalies of the spine including anomalies of craniovertebral junction (CVJ), spina bifida occulta, scoliosis, Sprengel deformity of right shoulder, and multiple rib anomalies, as well as neurological anomalies like Dandy-Walker spectrum and atretic occipital cephalocele. Conclusion To the best of our knowledge, association of such extensive skeletal anomalies and Dandy-Walker spectrum with KFS has been uncommonly reported in the literature. This case highlights the importance of knowledge of various common and uncommon associations of KFS to avoid missing significant anomalies.

A Rare Presentation of an Enterogenous Cyst as an Intra-Axial Pontine Lesion

2017 ◽  
Vol 100 ◽  
pp. 707.e1-707.e3 ◽  
Author(s):  
Tengfei Li ◽  
Xia Wu ◽  
Yuekang Zhang
Keyword(s):  
Enterogenous Cyst ◽  
Rare Presentation ◽  
Pontine Lesion

Abstract #842 Partial Hypopituitarism Following Miscarriage- A Rare Presentation

2018 ◽  
Vol 24 ◽  
pp. 195
Author(s):  
Monisha Priyadarshini Kumar ◽  
Irtsam Shahid ◽  
Daniela Ciltea
Keyword(s):  
Rare Presentation

Abstract #255: Kenny-Caffey Syndrome: A Rare Presentation of a Rare Disease

2006 ◽  
Vol 12 ◽  
pp. 93-94
Author(s):  
Khurshid Ahmad Khan ◽  
Stephen A. Brietzke
Keyword(s):  
Rare Disease ◽  
Rare Presentation
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