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Xanthogranuloma of the Sellar Region

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Atlas of Sellar and Parasellar Lesions

Abstract

This lesion is also called a “cholesterol granuloma.” (See also the next Chap. 24.)

They have been reported to comprise a subset of lesions (up to 34 %) initially thought to be adamantinomatous craniopharyngiomas or Rathke’s cleft cysts.

They are likely to originate from Rathke’s cleft cysts or pituitary adenomas with internal hemorrhage, inflammation, or both.

They tend to occur in younger adult patients (mean, 27 years).

In some patients, the lesion may be part of the Erdheim-Chester disease.

They belong to a spectrum of disease that includes xanthogranulomas, xanthomatous hypophysitis, and xanthogranulomatous hypophysitis. (See “Inflammatory Hypophysitis” in Chap. 56.)

Patients have a relatively high incidence of hypopituitarism and diabetes insipidus.

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References

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Correspondence to Gabriel Zada MD, MS .

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Zada, G., Lopes, M.B.S., Mukundan, S., Laws, E. (2016). Xanthogranuloma of the Sellar Region. In: Zada, G., Lopes, M., Mukundan Jr., S., Laws Jr., E. (eds) Atlas of Sellar and Parasellar Lesions. Springer, Cham. https://doi.org/10.1007/978-3-319-22855-6_23

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  • DOI: https://doi.org/10.1007/978-3-319-22855-6_23

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-22854-9

  • Online ISBN: 978-3-319-22855-6

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