Lymphocytic hypophysitis

Case contributed by Dalia Ibrahim

Presentation

2 months postpartum presented with polyuria, dehydration, and seizures. Her laboratory work-up revealed hypokalaemia. Her hormonal profile revealed reduced ADH, FSH & LH levels. Normal ACTH and TSH levels.

Patient Data

Age: 25 years
Gender: Female
mri
This study is a stack
Sagittal
T2
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Coronal
T2
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Coronal
T1
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Coronal
T1 C+
This study is a stack
Sagittal
T1 C+
This study is a stack
Axial
FLAIR
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Info
  • absent high T1 signal of the posterior pituitary gland
  • enlarged avidly enhancing pituitary
  • thickened intensely enhancing infundibulum with loss of its inferior tapering.
  • incidental finding - pineal cyst

Case Discussion

Diagnosis, in this case, is presumptive depending on the clinical, laboratory, and radiological features of the disease. The patient reported a dramatic clinical improvement after corticosteroid treatment.

Radiological features which could differentiate lymphocytic hypophysitis from pituitary adenoma:

  • absent posterior pituitary high signal on non-contrast T1 WI
  • thickened enhancing pituitary stalk
  • bulky pituitary gland showing homogenous enhancement with no focal lesions
  • dural tail sign
  • parasellar dark signal encasing the pituitary

Differential diagnosis

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