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Biomedical subjects

Alan L Diamond

Publications and source records attributed to Alan L Diamond.

4 recordsLinked to original sources

Primary central white matter hypoplasia of the neocortex.

Leukodystrophies, or diseases of the white matter, represent acute or ongoing damage to the oligodendrocytes of the central nervous system. Early childhood white matter disease is most commonly observed after hypoxic ischemic insults, with acute magnetic resonance imaging changes followed by atrophy or periventricular leukomalacia. Dysmyelination occurring in the setting of inborn errors of metabolism is characterized by progressive changes with high signal intensity in white matter on magnetic resonance imaging. This report presents a patient whose magnetic resonance imaging scans demonstrated hypoplasia of myelin in the telencephalon, without clinical or magnetic resonance imaging evidence of inflammatory dysmyelination. Clinical features included intractable seizures, severe hypotonia, and dysmorphic facial features coupled with a static failure to gain developmental milestones. Together, the clinical and magnetic resonance imaging findings are evidence of a primary failure of myelination in the neocortex.

Abnormalities, Multiple↗

Cerebral air embolism secondary to intra-aortic balloon pump rupture.

INTRODUCTION: Cerebral air embolism is a neurological emergency. It has been reported following cardiac catheterization, central venous catheter insertion, and cardiothoracic surgery. METHODS AND RESULTS: We report a case of massive cerebral air embolism secondary to intra-aortic balloon pump (IABP) rupture. Computed tomography (CT) of the brain showed serpiginous hypodensities following the sulci associated with hypodense brain parenchymal lesions. CONCLUSION: The prompt recognition of cerebral air embolism secondary to IABP rupture requires a high level of suspicion and is confirmed by head CT.

Embolism, Air↗

Paroxysmal sympathetic storm.

INTRODUCTION: Paroxysmal sympathetic storm (PSS) is a rare syndrome characterized by episodic hypertension, hyperhydrosis, hyperthermia, tachycardia, tachypnea, and extensor posturing. CASE REPORTS: This article describes two cases of PSS: one following traumatic brain injury and the other following cardiac arrest. DISCUSSION: The first responded to labetalol, morphine, and codeine, whereas the second responded to labetalol. CONCLUSION: These observations underscore the importance of central opioid receptors and nonselective beta-adrenergic antagonists in modulating catecholamine pathways.

Adrenergic beta-Antagonists↗

"Whippets"-induced cobalamin deficiency manifesting as cervical myelopathy.

BACKGROUND: Nitrous oxide (N2O) is inhaled in anesthesia and as a recreational drug from whipped cream dispensers. Its abuse reaches approximately 10% in some age groups. By inactivating cobalamin (Cbl) (vitamin B12), N2O can cause neurologic and hematologic manifestations. We present a case of N2O-induced Cbl deficiency presenting as cervical myelopathy. CASE HISTORY: After regularly inhaling N2O for many months, a 31-year-old man developed limb paresthesiae and ataxia over 3 months. Examination revealed finger pseudoathetosis, hyporeflexia, decreased sensation, and gait ataxia. Brain magnetic resonance imaging (MRI) was normal, but the posterior columns of the cervical and upper thoracic cord revealed patchy nonenhancing hyperintense lesions. Serum Cbl was 98 pg/mL (normal = 170-900 pg/mL). Cbl replacement led to recovery within 3 months. DISCUSSION: This patient presented with the symptoms and signs of Cbl deficiency. The MRI lesions in the posterior columns aided the diagnosis. Physicians need to have a high level of suspicion in cases of unexplained Cbl deficiency and myelopathy.

Adult↗