Abstract
Pituitary apoplexy is a clinical syndrome of hemorrhage or infarction of a pituitary adenoma. It has classically been associated with pituitary macroadenomas. The authors report three cases of pituitary apoplexy that occurred in patients with pituitary microadenomas. The presentation, endocrine results, and radiological and clinical outcome of each patient are described. In each of these cases of pituitary apoplexy due to microadenoma, the presenting headache was mistakenly attributed to a different diagnosis. The authors propose that pituitary apoplexy associated with a microadenoma may be much more common than appreciated and could be misdiagnosed as headache of alternative cause. Clinicians and radiologists should be aware of this clinical presentation.
References
Binning MJ, Liu JK, Gannon J, Osborn AG, Couldwell WT (2008) Hemorrhagic and nonhemorrhagic Rathke cleft cysts mimicking pituitary apoplexy. J Neurosurg 108:3–8
Corkill G, Hanson F, Sobel R, Keller T (1981) Apoplexy in a prolactin microadenoma leading to remission of galactorrhea and amenorrhea. Surg Neurol 15:114–115
Liu JK, Couldwell WT (2006) Pituitary apoplexy in the magnetic resonance imaging era: clinical significance of sphenoid sinus mucosal thickening. J Neurosurg 104:892–898
Liu JK, Rovit R, Couldwell WT (2001) Pituitary apoplexy. Semin Neurosurg 12:315–320
Nawar R, AbdelMannan D, Selman W, Arafah B (2008) Pituitary tumor apoplexy: a review. J Intensive Care Med 23:75–90
Semple P, Webb M, de Villiers J, Laws EJ (2005) Pituitary apoplexy. Neurosurgery 56:65–72, discussion 72-63
Verrees M, Arafah B, Selman W (2004) Pituitary tumor apoplexy: characteristics, treatment, and outcomes. Neurosurg Focus 16(4):E6
Acknowledgments
The authors thank Kristin Kraus, M.Sc., for editorial assistance preparing this paper.
Disclosure
The authors do not report any conflict of interest concerning the cases outlined in the paper.
Author information
Authors and Affiliations
Corresponding author
Additional information
Comment
This straightforward presentation of three cases of pituitary apoplexy in microadenomas encourages rethinking of patients during the daily work. Headaches with sudden onset in young women demand to rule out subarachnoid hemorrhage, but hemorrhage into another compartment of the skull is also a differential diagnosis. Hypopituitarism may develop in these patients. Minor deficits may only be detected in the blood workup and not present with clinical signs.
Jens Lehmberg
Munich, Germany
A timely reminder that small pituitary lesions can undergo apoplexy.
Michael Powell
London, UK
Rights and permissions
About this article
Cite this article
Randall, B.R., Couldwell, W.T. Apoplexy in pituitary microadenomas. Acta Neurochir 152, 1737–1740 (2010). https://doi.org/10.1007/s00701-010-0706-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00701-010-0706-6