Diffuse axonal injury in infants with nonaccidental craniocerebral trauma - Enhanced detection by beta-amyloid precursor protein immunohistochemical staining
Am. Gleckman et al., Diffuse axonal injury in infants with nonaccidental craniocerebral trauma - Enhanced detection by beta-amyloid precursor protein immunohistochemical staining, ARCH PATH L, 123(2), 1999, pp. 146-151
Citations number
24
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Objective.-Accurate identification of diffuse axonal injury is important in
the forensic investigation of infants who have died from traumatic brain i
njury. beta-Amyloid precursor protein (beta-APP) immunohistochemical staini
ng is highly sensitive in identifying diffuse axonal injury. However the ef
fectiveness of this method in brain-injured infants has not been well estab
lished. The present study was undertaken to assess the utility of beta-APP
immunohistochemistry in detecting diffuse axonal injury in infants with eit
her shaken baby syndrome or blunt head trauma.
Materials and Methods.-Archival formalin-fixed, paraffin-embedded blocks fr
om infants (<1 year old) with shaken baby syndrome (7 cases) and blunt head
trauma (3) and blocks from 7 control cases that included nontraumatic cere
bral edema (1), acute hypoxic-ischemic encephalopathy (1), and normal brain
(5) were immunostained for beta-APP. A semiquantitative assessment of the
severity of axonal staining was made. Corresponding hematoxylin-eosin-stain
ed sections were examined for the presence of axonal swellings.
Results.-Immunostaining for beta-APP identified diffuse axonal injury in 5
of 7 infants with shaken baby syndrome and 2 of 3 infants with blunt head t
rauma. Immunoreactive axons were easily identified and were present in the
majority of the sections examined. By contrast, hematoxylineosin staining r
evealed axonal swellings in only 3 of 7 infants with shaken baby syndrome a
nd 1 of 3 infants with blunt head trauma. Most of these sections had few if
any visible axonal swellings, which were often overlooked on initial revie
w of the slides. No beta-APP immunoreactivity was observed in any of the 7
control cases.
Conclusions.-Immunostaining for beta-APP can easily and reliably identify d
iffuse axonal injury in infants younger than 1 year and is considerably mor
e sensitive than routine hematoxylin-eosin staining. We recommend its use i
n the forensic evaluation of infants with fatal craniocerebral trauma.