scholarly journals Purely endoscopic resection of a choroid plexus papilloma of the third ventricle: case report

2015 ◽  
Vol 16 (1) ◽  
pp. 54-57 ◽  
Author(s):  
Maria M. Santos ◽  
Mark M. Souweidane

The authors report an illustrative case of a purely endoscopic surgical approach to successfully remove a solid choroid plexus papilloma of the third ventricle in an infant. A 10-week-old male infant first presented with transient episodes of forced downward gaze, divergent macrocephaly, a tense anterior fontanel, diastasis of the cranial sutures, and papilledema. Brain MRI revealed a small, multilobulated contrast-enhancing mass situated within the posterior third ventricle, with resultant obstructive hydrocephalus. A purely endoscopic removal of the tumor was performed through a single right frontal bur hole. Intraoperatively, a unique vascular tributary was recognized coming from the tela choroidea and was controlled with coagulation and sharp dissection. Postoperative MRI confirmed complete tumor removal, and the tumor was classified as a choroid plexus papilloma. There has been no evidence of tumor recurrence over 42 months of follow-up. With this case report the authors intended to show that endoscopic surgery can be an additional tool to consider when planning a choroid plexus tumor approach. It seems to be of particular interest in selected cases in which there are concerns about the patient's total blood volume, as in infants with potential hemorrhagic tumors and when it is possible to preoperatively identify a single vascular pedicle that can be approached early in the surgery.

Neurosurgery ◽  
1983 ◽  
Vol 12 (2) ◽  
pp. 217-220 ◽  
Author(s):  
Wesley C. Gradin ◽  
Charles Taylon ◽  
Alan H. Fruin

Abstract Choroid plexus papilloma (CPP) is a rare intraventricular neoplasm occurring primarily in the lateral ventricles of children and the 4th ventricle of adults. We describe the third reported case of a cystic CPP of the 3rd ventricle and review the pertinent literature.


Neurosurgery ◽  
1983 ◽  
Vol 12 (2) ◽  
pp. 217???20 ◽  
Author(s):  
W C Gradin ◽  
C Taylon ◽  
A H Fruin

2004 ◽  
Vol 40 (6) ◽  
pp. 314-316 ◽  
Author(s):  
Federico Di Rocco ◽  
Massimo Caldarelli ◽  
Giovanni Sabatino ◽  
Gianpiero Tamburrini ◽  
Concezio Di Rocco

2014 ◽  
Vol 21 (7) ◽  
pp. 1263-1266 ◽  
Author(s):  
Charles Kulwin ◽  
David Chan ◽  
Jonathan Ting ◽  
Eyas M. Hattab ◽  
Aaron A. Cohen-Gadol

Neurosurgery ◽  
1997 ◽  
Vol 40 (6) ◽  
pp. 1279-1282 ◽  
Author(s):  
Ichiro Nakano ◽  
Akinori Kondo ◽  
Koichi Iwasaki

2004 ◽  
Vol 100 (2) ◽  
pp. 224-224
Author(s):  
Akio Noguchi ◽  
Yoshiaki Shiokawa ◽  
Keiichi Kobayashi ◽  
Isamu Saito ◽  
Kazuhiro Tsuchiya ◽  
...  

1995 ◽  
Vol 83 (4) ◽  
pp. 729-732 ◽  
Author(s):  
Ian F. Pollack ◽  
Nina F. Schor ◽  
A. Julio Martinez ◽  
Richard Towbin

✓ The authors report an unusual case of a 2-year-old boy with a 3-month history of episodic rightward anterolateral head tilt and large-amplitude positional anteroposterior head bobbing reminiscent of bobble—head doll syndrome. This child experienced a sudden onset of drop attacks and then, within several hours, deep coma. The causative lesion was a contrast-enhancing, partially cystic third ventricular mass, which ultimately obstructed the aqueduct, producing profound obstructive hydrocephalus. An emergency ventriculostomy and endoscopic fenestration of the septum pellucidum was performed. Four days later, the tumor was completely resected by a transcallosal—transforaminal approach. The lesion was freely mobile within the third ventricle and contained a large cyst within its posterior pole; following drainage of the cyst, the lesion was easily delivered through the foramen of Monro. The histopathological diagnosis was choroid plexus papilloma. The child's neurological deficits, head tilt, and head bobbing resolved immediately after operation. To the best of the authors' knowledge, this represents the first well-documented report of bobble—head doll syndrome and drop attacks secondary to a choroid plexus papilloma. The highly mobile nature of the cystic lesion presumably led to its intermittent impaction within the foramen of Monro and/or proximal aqueduct; this produced the intermittent head tilt and bobble-head symptoms and, ultimately, resulted in acute obstruction of the aqueduct, causing the child's precipitous neurological decline.


1981 ◽  
Vol 16 (1) ◽  
pp. 69-71 ◽  
Author(s):  
Francesco Tomasello ◽  
Vincenzo Albanese ◽  
Francesco P. Bernini ◽  
Piero Picozzi

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