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Gupta, et al.: ISNO consensus guidelines for management of medulloblastoma
postoperative chemotherapy alone. N Engl J Med 2005;352:978‑86.
72. von Bueren AO, von Hoff K, Pietsch T, Gerber NU, Warmuth‑Metz M,
Deinlein F, et al. Treatment of young children with localized
medulloblastoma by chemotherapy alone: Results of the prospective
multicenter trial HIT 2000 confirming the prognostic impact of
histology. Neuro Oncol 2011;13:669‑79.
73. Jakacki RI, Burger PC, Zhou T, Holmes EJ, Kocak M, Onar A, et al.
Outcome of children with metastatic medulloblastoma treated with
carboplatin during craniospinal radiotherapy: A Children’s Oncology
Group phase I/II study. J Clin Oncol 2012;30:2648‑53.
74. Frange P, Alapetite C, Gaboriaud G, Bours D, Zucker JM,
Zerah M, et al. From childhood to adulthood: Long‑term outcome
of medulloblastoma patients. The Institute Curie experience
(1980–2000). J Neurooncol 2009;95:271‑9.
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Supplementary File S1
junction is the line of attachment of the tela choroidea with
the inferior medullary velum. The inferior half of the roof of
fourth ventricle (starting from the fastigium, the apex of fourth
ventricle) is formed by two structures. The inferior medullary
velum forms the cranial half and tela choroidea the caudal
half. The inferior medullary velum appears like two wings of
a butterfly starting from the nodule in the midline connecting to
the flocculus laterally. The tela choroidea is a semi-transparent
structure and the choroid plexus arises from its ventricular
surface. The tela choroidea is attached to the telovelar junction
cranially and the tinea which is a ridge along the inferolateral
edge of the floor of fourth ventricle. In telovelar approach to
the tumor, the cerebello-medullary fissure is accessed, which
is considered as one of the most complex fissures in the brain.
This fissure is between the tonsillar part of the cerebellum and
the postero-medial part of the medulla through which the PICA
vessels pass to supply the suboccipital surface of the cerebellum.
The arachnoid in this fissure is dissected and the telovelar
junction is exposed by gently retracting the medial wall of the
tonsil away from the lateral wall of the uvula. Then, the tela
choroidea is incised starting from the foramen of Magendie to
the telovelar junction, which gives access to the floor of fourth
ventricle from the obex to aqueduct in most cases. If additional
exposure of the superolateral recess or the floor are required,
the incision is extended on to the inferior medullary velum.
Surgical Approaches for a Medulloblastoma
Confined to the Fourth Ventricle
Transvermian approach
Medulloblastomas are traditionally approached by the
transvermian route by splitting the inferior vermis. After
opening the dura, the arachnoid over the cisterna magna
and foramen of Magendie are opened. The tonsils with the
posterior inferior cerebellar artery (PICA) are retracted to
expose the inferior vermis. The retraction of tonsils can be done
by two retractor blades on a Greenberg clamp. However, more
recently, a dynamic retraction technique is being adopted using
the surgeon’s suction tubing and bipolar forceps in an area
of interest, with an additional assistance for retraction being
provided by the brain retractor. This intermittent rather than
fixed retraction reduces the risk of retraction-related injury
to tonsils and PICA. Once the inferior vermis is exposed,
cortisectomy is done and is deepened by suction and bipolar.
The next structure that is found deep to the inferior vermis is
the nodule. The tumor is generally encountered after dissecting
through the nodule. If the tumor is small and is not seen at
this stage, the vermis is split and the tonsils are retracted to
expose the telovelar segment of PICA, which are followed to
identify the inferior medullary velum and tela choroidea. The
latter sturcutres are opened in the midline to gain access to
the full length of the fourth ventricle. In a sagittal plane, the
main structure limiting the exposure is the superior medullary
velum; and, along the horizontal plane, it is difficult to go
beyond the foramen of Luschka. Although the transvermian
approach has remained the workhorse among different
approaches to the fourth ventricle, its main disadvantage is
the occurrence of the vermian split syndrome with multitude
of manifestations, most important of which are gait ataxia and
cerebellar mutism. It is very important to limit the vermian
incision to the smallest possible length to reduce the severity
of this postulated syndrome.
Lateral telovelar approach
This approach was required due to the complications
encountered during the transvermian approach related to
the sectioning of normal cerebellum. The advantage of this
approach is that this gives exposure to the lateral recesses of
the fourth ventricle from the midline to the foramen of Luschka.
It also provides a cranio-caudal exposure from the obex to the
aqueduct by opening the natural clefts and fissures. It also avoids the removal of normal cerebellar tissue. However,
the normal anatomy in this area is fairly complex, which is
further complicated in cases of fourth ventricular tumors due
to distortion of normal anatomical landmarks. The telovelar
330
With these approaches, the tumor is exposed and after an
adequate biopsy is taken, the tumor is internally decompressed
using suction and ultrasonic aspirator. The main concerns
during the surgery are: (i) injury to the structures in the floor
of the fourth ventricle; (ii) excessive blood loss; and, (iii)
inability to establish CSF flow across the aqueduct. The floor
of the fourth ventricle should be identified early during the
surgery from an inferior aspect and protected with gelatin
sponge and patties. No attempt should be made to excise the
tumor infiltrating into the floor of the fourth ventricle. The
tumor is usually solid, vascular, but suckable; being a highgrade tumor, it is easily differentiated from the surrounding
normal cerebellum. Sequential decompression and dissection
is continued until CSF flow from aqueduct is visualized
superiorly, the entire floor of the fourth ventricle is seen
ventrally and the obex is visualised inferiorly. Bleeding should
be controlled with bipolar coagulation, gelatin sponge and
compression, with excessive blood loss mandating appropriate
replacement with transfusion of blood/blood components. It is
important to prevent spillage of blood into the third ventricle
through the aqueduct as this increases the chances of postoperative worsening of hydrocephalus and may necessitate a
shunt in spite of a radical excision. This can be prevented by
plugging the aqueduct carefully with a pad of gelatin sponge
covered by a cotton patty.
Neurology India | Volume 65 | Issue 2 | March-April 2017