Secondary normal pressure hydrocephalus following pituitary apoplexy: a case report.

Author:

Tomita Yusuke1ORCID,Fukuda Shoichi1,Kobasi Aiko1,Okada Yoshihiro1,Makino Keigo1,Kidani Naoya1,Muraoka Kenichiro1,Hirotsune Nobuyuki1,Nishino Shigeki1

Affiliation:

1. Hiroshima City Hiroshima Citizens Hospital: Hiroshima Shiritsu Hiroshima Shimin Byoin

Abstract

Abstract Introduction: Although secondary normal pressure hydrocephalus (sNPH) can occur in various central nervous system diseases, there are no reports of sNPH caused by pituitary lesions. Herein, we present a unique case of sNPH caused by pituitary apoplexy. Case Presentation: A 70-year-old man was transferred to our hospital because of sudden onset of headache and loss of consciousness. Cerebrospinal fluid (CSF) test showed slightly elevated cell counts and protein levels, but a negative CSF culture test. Magnetic resonance imaging showed a dumbbell-like cystic lesion with hemorrhagic changeat the sella turcica. From the above, the patient was diagnosed with aseptic meningitis caused by pituitary apoplexy. Pituitary hormone replacement therapy was undertaken and his symptoms fully improved. However, 2 months later he complained of a gait disturbance and incontinence that had gradually appeared. Brain imaging with computed tomography showed no ventricular enlargement compared with initial images, although the lateral ventricles were slightly enlarged. As a CSF drainage test improved his symptoms temporarily, sNPH with possible longstanding overt ventriculomegaly in adults (LOVA) background was suspected. We performed a lumbo-peritoneal shunt placement, which improved his symptoms. Conclusions: This case suggestes that sNPH can develop even after a small subarachnoid hemorrhage caused by a pituitary apoplexy in LOVA patients. If the aqueduct of Silvius is open, sNPH with a LOVA background can be successfully treated with lumbo-peritoneal shunt placement.

Publisher

Research Square Platform LLC

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