2022, Number 1
Diagnosis of a Morgagni-Stewart-Morel Syndrome in a Patient with Ischemic Stroke. Report of a Case
Valladares VM, García LJI, Sánchez LA
Language: Spanish
References: 8
Page: 100-105
PDF size: 207.38 Kb.
ABSTRACT
Morgagni-Stewart-Morel syndrome is a rare disease characterized by bilateral internal frontal hyperostosis associated with metabolic and psychiatric disorders, arterial hypertension, and dysfunction of the cranial nerves of undefined etiology. The case of a 77-year-old patient with a history of type 2 diabetes mellitus, systemic arterial hypertension and psychiatric disorder, who was admitted to the Neurology Service of the Dr. Gustavo Aldereguía Lima University Hospital in Cienfuegos with dysarthria and right hemiparesis is presented. Diagnostic skull imaging studies were performed where the presence of extensive internal frontal hyperostosis, cortical atrophy and a left thalamic infarction was observed. During his hospital stay, the presence of grade I obesity, hirsutism and hypercholesterolemia was documented. The patient met the criteria for Morgagni-Stewart-Morel syndrome by manifesting the presence of internal frontal hyperostosis with endocrinological and neuropsychiatric manifestations. The case is presented in order to demonstrate the diagnosis of a low incidence disease in ischemic cerebrovascular patients with the presence of symptoms that include several well-documented vascular risk factors.REFERENCES
Subirana M, Ortega M, Galtés J, Castellà J. Hallazgo incidental de hiperostosis frontal interna o síndrome de Morgagni asociado a meningiomas. Cuad Med Forense[Internet]. 2012[citado 23 Sep 2020];18(2):[aprox. 5p.]. Disponible en: https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1135-76062012000200006.