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Neuropathology
A.
Autopsy
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Prior to starting
the autopsy, determine, from the clinical history, the presences
or absence of neurological manifestations.. This will help you
to plan re: taking tissue for special studies, giving tissue
for research, and in examining the brain and spinal cord for clinically
relevant findings. (See section below for discussion of brain
removal in cases with infections or other hazards.)
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Brain removal,
while generally done by the morgue attendant, should be learned
by the resident as well.
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Prior to fixation,
weigh the brain:
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Look for
evidence of meningeal infection and culture as needed. Look
for abscess exposed to the brain's surface and culture as
needed. Look at the base of the skull for evidence of meningiomas
and sample and photograph.
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Consider
whether the pituitary gland would be of diagnostic interest
in your case.
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The brain
should be floated in 20% formalin, suspended by a string going
under the basilar artery.
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The brain
must fix for 2 weeks in 20% formalin before it is cut. It must
be rinsed for 24 hours prior to brain cutting conference.
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There are
standard description forms for both demented and non-demented
patients.
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Neuropathology
brain cutting: Every week.
(Appendix XI)
B. Neuropathology
Surgicals
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Neuropathology
surgical specimens (in-house, submitted) interpretation performed
by the neuropathologist.
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Frozen sections
are done in consultation with the neuropathologist.
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Nerve:
The nerve should be received in saline moistened gauze,
not in fixative!
Fresh peripheral
nerve that is for a diagnosis of a neurologic illness (the excludes
vagotomies) must be divided as follows:
One cm of nerve
should be laid out on a piece of a 3x5 card and emmersed in glutaraldehyde
to allow for both cross section and longitudinal section embedding
for electron microscopy. An additional1 cm should be fixed
in glutaraldehyde for nerve testing if demyelination is suspected.
Two small pieces, approximately 0.3 cm each should be fixed
in formalin for cross section and longitudinal section evaluation
at the light microscope. A section of the nerve must be frozen
if there is evaluation at the light microscope. A section
of the nerve must be frozen if there is any suspicion of
paraneoplastic disease, to allow for immunofluorescence for immunoglobulin
depostition. See Appendix XXXI (pages from Dyck Peripheral Neuropathy
on nerve biopsies)
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Muscle
and Fascia: The
muscle should be receieved in a muscle clamp, fresh from surgery,
without any fixative. It may be wrapped in saline moistened
gauze until it is ready for processing. The muscle must then
be divided for different methods of processing. The muscle inside
the clamp (between the teeth) must be used for snap frozen section
for histochemistry (dipped in isopentane, suspended in liquid
nitrogen, on a cork base with a touch of OCT to hold it down--DO
NOT COVER WITH OCT AS THIS WILL DELAY FREEZING). The muscle
outside the clamp's teeth is to be used both for electron microscopy
and paraffin embedding. This tissue can be divided with a few
small pieces of unadulterated muscles going into glutaraldehyde
(usually cut into pieces measuring 1x1x2mm each). A larger piece
should be submitted for routine H&E staining and trichrome
and should be sufficient to allow for embedding longitudinally
and cross-section. The stains ordered routinely should include:
H&E on both paraffin and frozen, On snap frozen tissue: Trichrome,
ATPase at pH4.3 and 10.4, NADH, PAS, fat cytochrome C (and dystrophin
for all patients less than 20 years of age). Cytochrome C and
dystrophin are immunohistochemical stains, the remainder are histochemical
(NAD & ATPase are enzyme histochemistry). See Appendix XXXI
from Muscle Biopsy: A Laboratory Investigation by Mike
Loughlin.
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Pituitaries
need
only one H&E and one reticulin on each specimen submitted.
If the tumor is grossly obvious, the immunohistochemical stains
for the purported syndrome may be ordered at the time that the
specimen is received, as follows:
For
technical preparation, see Surgical Pathology Section.
Last Updated 1/12/2009 3:42:54 PM
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