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Updated: Aug 2, 2025

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Clinical Features of Pituitary or Parasellar Tumor Onset with Cranial Nerve Palsy: Surgical Intervention
Yuichi Oda1, Kosaku Amano1, Kenta Masui2
1Department of Neurosurgery, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.
Objective:
This study aimed to clarify the symptoms of pituitary or parasellar tumor onset with cranial nerve palsy (CNP) and to improve our knowledge of this rare symptom and its most appropriate treatment.
Methods:
Among 1281 patients with pituitary or parasellar tumors surgically treated from 2003 to 2020, 30 cases (2.34%; 15 men and 15 women; mean age: 55.6 years, range: 6-83 years) first presenting with CNP were reviewed to evaluate the neurological symptoms, histological diagnosis, interval from onset to surgery, and time before complete CNP recovery.
Results:
Pathological diagnoses comprised 17 pituitary adenomas, including 10 pituitary apoplexies and 4 adrenocorticotropic hormone-positive adenomas, and 13 other tumors, including 3 chordomas, 2 xanthogranulomas, 2 malignant lymphomas, 2 metastatic tumors, 1 Rathke cleft cyst, 1 plasmacytoma, 1 craniopharyngioma, and 1 neuroendocrine carcinoma. The mechanisms causing CNP were pituitary apoplexy (n = 10), cranial nerve compression or involvement (n = 17), and inflammatory changes (n = 9). As the first manifestation, 20 (66.7%) patients presented with oculomotor nerve palsy, 2 (6.7%) with trochlear nerve palsy, and 13 (43.3%) with abducens nerve palsy. Full recovery of CNP was obtained in 25 patients (83.3%) after surgery alone and in 2 patients (6.7%) after adjuvant therapy. Early surgery provided no significant difference in full recovery rates although it reduced the time to reach full recovery.
Conclusions:
It is critical to determine the mechanisms of CNP and intervene surgically to improve symptoms, shorten the duration of the disorder, prevent relapses, and obtain the correct pathological diagnosis to select the proper adjuvant therapy.
Insights
Pituitary tumors can cause cranial nerve palsy (CNP). Surgical intervention for these rare tumors improves symptoms and recovery time, with most patients experiencing full recovery.
Area of Science:
- Neurosurgery
- Neurology
- Endocrinology
Background:
- Pituitary and parasellar tumors are rare.
- Cranial nerve palsy (CNP) is an uncommon presenting symptom of these tumors.
- Understanding the mechanisms and optimal treatment for CNP in this context is crucial.
Purpose of the Study:
- To clarify the symptoms associated with pituitary or parasellar tumors presenting with CNP.
- To enhance knowledge regarding this rare symptom and its most effective treatment strategies.
- To evaluate the neurological symptoms, pathological diagnoses, and recovery outcomes in patients with CNP due to pituitary/parasellar tumors.
Main Methods:
- Retrospective review of 1281 surgically treated pituitary/parasellar tumors (2003-2020).
- Analysis of 30 cases presenting initially with CNP.
- Evaluation of neurological symptoms, histological diagnosis, surgical timing, and CNP recovery.
Main Results:
- CNP was the initial presentation in 2.34% of patients.
- Common causes included pituitary apoplexy, nerve compression, and inflammation.
- Oculomotor nerve palsy was most frequent (66.7%), followed by abducens (43.3%) and trochlear (6.7%).
- Complete CNP recovery occurred in 83.3% after surgery alone.
- Early surgery did not impact recovery rates but reduced recovery time.
Conclusions:
- Determining the mechanism of CNP is critical for effective intervention.
- Surgical treatment improves symptoms, shortens recovery duration, and prevents relapses.
- Accurate pathological diagnosis guides appropriate adjuvant therapy selection.
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