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Accès ouvert déclaré 2025 article

Computed tomographic features of pituitary apoplexy in a cat

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1Pays d’affiliation déclarés

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Le résumé fourni par la source

An 11-year-old, female neutered domestic long hair cat was presented, following a peracute onset of agitation, ataxia, and vocalisation progressing over three days to obtundation. Neurological examination showed severe obtundation, ambulatory tetraparesis, and compulsive circling to the left. Postural reactions were decreased on the right thoracic and pelvic limbs. There was an absent left menace response with a normal pupillary light reflex. The left eye was miotic secondary to an anterior reflex uveitis caused by a superficial corneal ulcer. The remainder of the neurological examination was unremarkable. Neuroanatomical localisation was multifocal with forebrain and brainstem lesions. Pre-contrast computed tomography (CT) demonstrated an ovoid, slightly left lateralised hyperattenuating (~100 HU) suprasellar mass (Fig 1). Rostrally and to the right of (and confluent with) the mass was an irregularly marginated area of tissue (57 HU) that was hypoattenuating to the mass but hyperattenuating to normal brain parenchyma—this region was most consistent with recent haemorrhage. The lesions resulted in a mild mass effect on the third ventricle, hypothalamus, and midbrain, displacing them dorsally. The mass and region of suspected haemorrhage measured 7.6 mm (H) × 9 mm (W) × 5.5 mm (L). The pituitary height to brain ratio was 0.52 (reference range 0.28 ± 0.05). No CT evidence of oedema, CSF obstruction, or brain herniation was associated with the mass. Pituitary apoplexy (PA) associated with a pituitary tumour was suspected. A diffuse hepatopathy and bilateral adenomegaly were evident on abdominal ultrasound, consistent with pituitary-dependent hyperadrenocorticism. Despite supportive treatment, the cat failed to improve, and the owner elected euthanasia. Post-mortem examination and histopathology findings revealed a pituitary adenoma with locally extensive haemorrhage, confirming a diagnosis of PA. This case demonstrates CT imaging features of PA in a cat not previously described. W. Swan: Writing – original draft; writing – review and editing. M. Taylor: Writing – original draft; writing – review and editing. I. Orgonikova: Writing – original draft; writing – review and editing. J. M. De Frias: Supervision; writing – review and editing; writing – original draft; conceptualization. No conflicts of interest have been declared.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Computed tomographic features of pituitary apoplexy in a cat
Date Crossref
19/06/2025
Éditeur
Wiley
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Où se fait cette recherche

  • Roslin Institute pays non établi dans la notice
    Structure de recherche
  • Royal Edinburgh Hospital pays non établi dans la notice
    Établissement de santé
  • University of Edinburgh Hospital for Small Animals pays non établi dans la notice
    Université ou école supérieure
  • The Royal (Dick) School of Veterinary Studies Hospital for Small Animals pays non établi dans la notice
    Université ou école supérieure

Roslin Institute, Royal Edinburgh Hospital et Hospital for Small Animals — University of Edinburgh, avec 1 autre affiliation.

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Pituitary Gland Disorders and TreatmentsGrowth Hormone and Insulin-like Growth FactorsVeterinary Medicine and Surgery

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