Pituitary apoplexy

Case contributed by Olumuyiwa Ifedayo Ajayi
Diagnosis certain

Presentation

Worsening severe headache with orbital pain.

Patient Data

Age: 35 years
Gender: Female
ct
This study is a stack
Axial
non-contrast
This study is a stack
Axial C+
arterial phase
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Info

Un-enhanced CT scan of the brain shows a heterogeneous intrasellar mass with central hyperdensity. No obvious enhancement is demonstrated post intravenous contrast injection.

mri
This study is a stack
Axial
T1
This study is a stack
Axial
FLAIR
This study is a stack
Sagittal
T1
This study is a stack
Coronal
T1
This study is a stack
Axial
Gradient Echo
This study is a stack
Sagittal
T2
This study is a stack
Axial T1
C+ fat sat
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Info

Pre-contrast T1W of brain demonstrates a circumscribed intrasellar mass with areas of intrinsic hyper intense T1 signal. The mass is heterogeneous on T2W/ FLAIR with hypointense area. The lesion is expanding the sellar and shows suprasellar extension. There is blooming related to blood products on gradient echo image corresponding to haemorrhage. Mild peripheral enhancement is observed.

Case Discussion

Pituitary apoplexy is an acute clinical syndrome caused by necrosis of the pituitary gland. The necrosis may be haemorrhagic or non-haemorrhagic.  Clinical manifestations may be variable, though typically include headache, visual deficits, orbital pain and altered mental status. Pre-existing pituitary macroadenoma is usually present (60-90%) but it can occur also in healthy glands in a few isolated cases.

The diagnosis of pituitary apoplexy can be made only when haemorrhagic infarction of the pituitary gland leads to the above mentioned clinical syndrome.

Close differential diagnoses are necrotic/haemorrhagic pituitary macroadenoma and adamantinomatous craniopharyngioma in children.

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