Pituitary hyperplasia resulting from primary hypothyroidism

We report an unusual case of pituitary hyperplasia secondary to primary hypothyroidism clinically masquerading pituitary apoplexy. A 22-year-old female presented with intermittent headache, easy fatigability, facial puffiness, coarseness of facial features, and hoarseness of voice for six months duration. Diplopia and diminution of vision was also observed for the last 15 days. Brain imaging findings showed pituitary enlargement, the thyroid function test were suggestive of primary hypothyroidism. Patient did well with thyroid hormone replacement therapy.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Pituitary hyperplasia resulting from primary hypothyroidism ; volume:6 ; number:02 ; year:2011 ; pages:99-100
Asian journal of neurosurgery ; 6, Heft 02 (2011), 99-100

Contributor
Agrawal, Amit
Diwan, S.

DOI
10.4103/1793-5482.92171
URN
urn:nbn:de:101:1-2022120112430933547092
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:27 AM CEST

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Associated

  • Agrawal, Amit
  • Diwan, S.

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