Computed tomographic features of pituitary apoplexy in a cat

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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Publication Details

Journal
Journal of Small Animal Practice
Published
2025-06-19
DOI
https://doi.org/10.1111/jsap.13898
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
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article

Computed tomographic features of pituitary apoplexy in a cat

Ivona Orgonikova, João Miguel De Frias, M. Taylor, Will Howard Swan
2 links
Journal of Small Animal Practice
Pituitary Gland Disorders and Treatments
article

Computed tomographic features of pituitary apoplexy in a cat

Ivona Orgonikova, João Miguel De Frias, M. Taylor, Will Howard Swan
article en

Abstract

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.

Journal of Small Animal PracticeVol. 66(11)
Roslin Institute (GB), Royal Edinburgh Hospital (GB), University of Edinburgh (GB)
Zero hunger
Openalex Percentile: Top 79%
Pituitary Gland Disorders and Treatments
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