HIV related neuropathologic changes in children
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Parenchymal
changes
HIV encephalitis
HIV leucoencephalopathy
Myelin loss
Microcephaly and brain atrophy
Basal ganglia mineralization
Vascular
changes
Vasculitis (small arteries and venues)
Vasculopathy (medium to larger arteries)
Hemorrhages
Infarcts/Leigh disease-like changes
Infections
CMV encephalitis
Measles encephalitis
Adenovirus encephalitis
Mycobacterium avium intracellular (MAI)
Aspergillosis
Toxoplasmosis
Neoplasm
Lymphomas
HIV myelitis
Cortico-spinal tract degeneration
Vacuolar myelopathy
HIV leucoencephalopathy: this refers to condition characterized by the
presence of multinucleated giant cells, a relatively diffuse form of myelin
loss, reactive gliosis, and little or no inflammation.
Myelin loss: this is seen in over 50% of cases and range from
focal myelin loss, usually associated with foci of inflammation (HIV
encephalitis), to diffuse myelin pallor with gliosis involving central and gyral
myelin.
Microcephaly and brain
atrophy: brain atrophy is seen in over half of all
pediatric CNS HIV cases. Microcephaly and brain atrophy, however, do not
necessary to co-exist with HIV encephalitis.
Basal ganglia mineralization: mineralizations are present as parenchymal
deposits (calcospherites) or as vascular deposits (calcific vasopathy or small
blood vessels) in basal ganglia. In many cases, there are enough calcium to be
detected by CT scan. Kids with such depositions characteristically loss the
ability to walk, acquired during the earlier course of the disease, and with
progressive neurologic deterioration.
Vasculitis: vasculitis and perivasculitis affect primarily
small parenchymal arteries and small venules. In addition to lymphocytic
infiltration, multinucleated giant cells may be seen in the adjacent parenchyma.
Usually associated with encephalitis but may exist as an independent condition.
It can co-exist with vasculopathy. In contrast to vasculopathy, vasculitis is
seen only in the brain.
Vaculopathy: usually the medium to large arteries are affected.
Histologically, there is intimal fibroblastic proliferation, perivascular
fibrosis, and fragmentation of elastic lamina, sometimes with aneurysmal
dilatation and endothelial cell hypertrophy. It appears to be a part of a
process of the systemic vasculopathy involving small- and medium sized arteries
in many internal organs.