Natural history of pituitary carcinoma with metastasis to the cervical spine: illustrative case
Pituitary carcinoma is a rare tumor of the adenohypophysis with noncontiguous craniospinal dissemination and/or systemic metastases. Given the rarity of this malignancy, there is limited knowledge and consensus regarding its natural history, prognosis, and optimal treatment. The authors present the...
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Published in | Journal of neurosurgery. Case lessons Vol. 5; no. 3 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Association of Neurological Surgeons
16.01.2023
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Subjects | |
Online Access | Get full text |
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Summary: | Pituitary carcinoma is a rare tumor of the adenohypophysis with noncontiguous craniospinal dissemination and/or systemic metastases. Given the rarity of this malignancy, there is limited knowledge and consensus regarding its natural history, prognosis, and optimal treatment.
The authors present the case of a 46-year-old woman initially treated with invasive prolactin-secreting pituitary macroadenoma who developed metastatic disease of the cervical spine 6 years later. The patient presented with acutely worsening compressive cervical myelopathy and required posterior cervical decompression, tumor resection, and instrumented arthrodesis for posterolateral fusion.
This case underscores the importance of long-term monitoring of hormone levels and having a high clinical suspicion for metastatic disease to the spine in patients presenting with acute myelopathy or radiculopathy in the setting of previously treated invasive secreting pituitary adenoma. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Disclosures Dr. Sherrod reported grants from AO Spine Foundation outside the submitted work. Dr. Dailey reported personal fees from Zimmer Biomet and personal fees from AO North America outside the submitted work. No other disclosures were reported. INCLUDE WHEN CITING Published January 16, 2023; DOI: 10.3171/CASE22363. |
ISSN: | 2694-1902 2694-1902 |
DOI: | 10.3171/CASE22363 |