Unusual bifrontal cerebral infarction related to pituitary apoplexy. An uncommon presentation and literature review

Author:

Holanda Tiago S. F.1,Pimentel Isnara Mara Freitas2,Araujo Paulo Victor Ferreira Gomes1,da Silva Damasceno Gomes José Ítalo3,de Morais Moreira Vinícius Chagas3,Soares Tito Bastos Siqueira3,de Albuquerque Lucas Alverne Freitas1

Affiliation:

1. Department of Neurosurgery, General Hospital of Fortaleza, Fortaleza, Brazil.

2. Department of Otorhinolaryngology, Leonardo da Vinci Hospital, Fortaleza, Brazil.

3. Department of Medicine, Ceara State University, Fortaleza, Brazil.

Abstract

Background: Pituitary apoplexy (PA) is a syndromic condition described in 1950. The main symptoms are headache, visual impairment, ophthalmoplegia, and hypopituitarism. The relationship between stroke and PA is uncommon and two mechanisms are described: vascular compression and vasospasm. Case Report: A 65-old-year man presented with severe headache, vomiting, ophthalmoplegia, and somnolence. Radiological examinations showed an expansive sellar and suprasellar lesion with a heterogeneous signal, besides Diffusion-weighted imaging (DWI) restriction in the bifrontal area was present. The findings were compatible with PA and stroke. Conclusion: PA leading to cerebral infarction is a rare condition that presents high morbidity and mortality levels. There are two main mechanisms related: direct arterial compression and arterial vasospasm. The cases must be conducted as neuroendocrinological emergencies and surgical management is a key point to better the prognosis of patients.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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5. Acute degenerative changes in adenomas of the pituitary body-with special reference to pituitary apoplexy;Brougham;J Neurosurg,1950

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