Neurosyphilis : $b Modern systematic diagnosis and treatment presented in one hundred and thirty-seven case historiesSouthard, Elmer Ernest
Science
Neurosyphilis : $b Modern systematic diagnosis and treatment presented in one hundred and thirty-seven case histories
Southard, Elmer Ernest
Neurosyphilis
The =calvarium= was dense and the =dura mater= everywhere adherent. The
=arachnoidal villi= were but slightly developed, but there was one small
focus of cortical herniation through the dura mater of the left middle
cranial fossa. The =pia mater= was delicate except for slight opacities
along sulci. There was some pial thickening over the region of the
interparietal sulci on both sides. There was pial pigmentation
anteriorly and superiorly.
There is no gross evidence of intracranial arteriosclerosis, except (1)
that afforded by the lesions of the dentate nuclei of the cerebellum
mentioned below and (2) the swerving to the right of the basilar artery,
possibly due not to arteriosclerotic lengthening of the artery but to an
unusual shape of the pons (see below).
The =brain= weighed 1245 grams (cerebellum and pons 165 grams). =The
anatomical diagnoses of central nervous system= were:
Slight general encephalomalacia (post mortem imbibition of fluid, 31
hours). Slight gliosis of right prefrontal and frontal gyri. Slight
gliosis of right optic thalamus. Generalized granular ependymitis,
especially near fornix and about foramina of Monro. Anomaly of pons (not
gliotic, but possessing far more white matter on the left side than the
right). Severe arteriosclerosis confined to the dentate nuclei of the
cerebellum.
As we now look over the data in Cases 40 and 41 we are inclined to ask
the question, whether modern systematic diagnosis would not have shown
these cases to be NEUROSYPHILITIC? One is inclined to answer this
question in the affirmative, on the basis that Case 40 showed somewhat
questionable Argyll-Robertson pupils, and Case 41 showed unilateral
Argyll-Robertson effect. Both cases showed Romberg sign, but the dentate
nucleus and other cerebellar disease in each case may in some way have
contributed to or imitated this phenomenon. Whether Case 40 was a
tabetic must remain a question, but Case 41 must be regarded as a case
with spinal and meningeal changes highly characteristic of syphilis.
=VASCULAR NEUROSYPHILIS plus TABETIC NEUROSYPHILIS (“tabes
dorsalis”) simulating paretic neurosyphilis (“general paresis”).
Autopsy.=
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