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Rathke's cleft cyst with pituitary apoplexy: case report.

H Nishioka1, H Ito, T Miki

  • 1Department of Neurosurgery, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan.

Neuroradiology
|December 22, 1999
PubMed
Summary

A rare case of Rathke's cleft cyst presented as pituitary apoplexy, causing sudden headache and vision loss. The cyst, initially showing a hematoma, spontaneously regressed on MRI scans.

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Area of Science:

  • Endocrinology
  • Neurosurgery
  • Radiology

Background:

  • Rathke's cleft cysts are typically benign cystic lesions arising from remnants of the Rathke's pouch.
  • Pituitary apoplexy is a clinical syndrome characterized by sudden onset of severe headache, visual impairment, and ophthalmoplegia, usually due to pituitary infarction or hemorrhage.

Observation:

  • A 46-year-old woman presented with acute headache and visual loss, indicative of pituitary apoplexy.
  • Magnetic resonance imaging (MRI) revealed a cystic lesion between the anterior and posterior pituitary lobes with internal high-signal intensity, consistent with a hematoma.
  • Serial imaging demonstrated spontaneous regression of the lesion over three weeks.

Findings:

  • The patient's symptoms and imaging findings were attributed to a Rathke's cleft cyst complicated by a pituitary apoplectic event.

Related Experiment Videos

  • Histopathological examination following trans-sphenoidal surgery confirmed the presence of a Rathke's cleft cyst containing a hematoma.
  • Implications:

    • This case highlights an unusual presentation of Rathke's cleft cyst, emphasizing the importance of considering this diagnosis in pituitary apoplexy.
    • The spontaneous regression observed suggests a potential natural course for some Rathke's cleft cysts with intralesional hemorrhage.
    • Understanding such rare presentations aids in accurate diagnosis and management of sellar region pathologies.