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A Case of Miller Fisher Syndrome, Thromboembolic Disease, and Angioedema: Association or Coincidence?

Patient: Male, 32 Final Diagnosis: Miller Fisher syndrome Symptoms: Ataxia • headache • ophthalmoplegia Medication: — Clinical Procedure: Plasmapheresis Specialty: Neurology OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Miller Fisher Syndrome is characterized by the clinical triad...

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Detalles Bibliográficos
Autores principales: Salehi, Nooshin, Choi, Eric D., Garrison, Roger C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5260666/
https://www.ncbi.nlm.nih.gov/pubmed/28090073
http://dx.doi.org/10.12659/AJCR.901940
Descripción
Sumario:Patient: Male, 32 Final Diagnosis: Miller Fisher syndrome Symptoms: Ataxia • headache • ophthalmoplegia Medication: — Clinical Procedure: Plasmapheresis Specialty: Neurology OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Miller Fisher Syndrome is characterized by the clinical triad of ophthalmoplegia, ataxia, and areflexia, and is considered to be a variant of Guillain-Barre Syndrome. Miller Fisher Syndrome is observed in approximately 1–5% of all Guillain-Barre cases in Western countries. Patients with Miller Fisher Syndrome usually have good recovery without residual deficits. Venous thromboembolism is a common complication of Guillain-Barre Syndrome and has also been reported in Miller Fisher Syndrome, but it has generally been reported in the presence of at least one prothrombotic risk factor such as immobility. A direct correlation between venous thromboembolism and Miller Fisher Syndrome or Guillain-Barre Syndrome has not been previously described. CASE REPORT: We report the case of a 32-year-old Hispanic male who presented with acute, severe thromboembolic disease and concurrently demonstrated characteristic clinical features of Miller Fisher Syndrome including ophthalmoplegia, ataxia, and areflexia. Past medical and family history were negative for thromboembolic disease, and subsequent hypercoagulability workup was unremarkable. During the course of hospitalization, the patient also developed angioedema. CONCLUSIONS: We describe a possible association between Miller Fisher Syndrome, thromboembolic disease, and angioedema.