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Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome

BACKGROUND: This two-patient case series describes a rare sequela of postoperative empty sella syndrome (ESS) following transsphenoidal resection of pituitary macroadenomas. This is characterized by progressive hormone dysfunction, diabetes insipidus (DI), and associated MRI evidence of pituitary st...

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Detalles Bibliográficos
Autores principales: Winograd, Evan, Kortz, Michael W., Lillehei, Kevin O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422539/
https://www.ncbi.nlm.nih.gov/pubmed/34513152
http://dx.doi.org/10.25259/SNI_530_2021
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author Winograd, Evan
Kortz, Michael W.
Lillehei, Kevin O.
author_facet Winograd, Evan
Kortz, Michael W.
Lillehei, Kevin O.
author_sort Winograd, Evan
collection PubMed
description BACKGROUND: This two-patient case series describes a rare sequela of postoperative empty sella syndrome (ESS) following transsphenoidal resection of pituitary macroadenomas. This is characterized by progressive hormone dysfunction, diabetes insipidus (DI), and associated MRI evidence of pituitary stalk disruption. CASE DESCRIPTION: This phenomenon was retrospectively evaluated in a review of 2000 pituitary tumor resections performed by a single neurosurgeon (KOL). Chart review was retrospectively conducted to gather data on demographics, pituitary hormone status, tumor characteristics, and management. We identified 2 (0.1%) cases of progressive pituitary endocrine dysfunction occurring in the postoperative period associated with MRI evidence of pituitary stalk disruption within 6 weeks of discharge from the hospital. This was felt to be caused by the rapid descent of the residual normal pituitary gland down to the floor of the postoperative empty sella, causing relatively swift stalk stretching. Both patients developed DI, and one patient demonstrated increased pituitary hormone dysfunction. CONCLUSION: This phenomenon is a rare manifestation of postoperative ESS, secondary to surgical resection of a pituitary macroadenoma. We discuss the associated potential risk factors and strategies for avoidance in these two cases. Routine instillation of intrasellar fat in patients at risk is felt to be protective.
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spelling pubmed-84225392021-09-09 Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome Winograd, Evan Kortz, Michael W. Lillehei, Kevin O. Surg Neurol Int Case Report BACKGROUND: This two-patient case series describes a rare sequela of postoperative empty sella syndrome (ESS) following transsphenoidal resection of pituitary macroadenomas. This is characterized by progressive hormone dysfunction, diabetes insipidus (DI), and associated MRI evidence of pituitary stalk disruption. CASE DESCRIPTION: This phenomenon was retrospectively evaluated in a review of 2000 pituitary tumor resections performed by a single neurosurgeon (KOL). Chart review was retrospectively conducted to gather data on demographics, pituitary hormone status, tumor characteristics, and management. We identified 2 (0.1%) cases of progressive pituitary endocrine dysfunction occurring in the postoperative period associated with MRI evidence of pituitary stalk disruption within 6 weeks of discharge from the hospital. This was felt to be caused by the rapid descent of the residual normal pituitary gland down to the floor of the postoperative empty sella, causing relatively swift stalk stretching. Both patients developed DI, and one patient demonstrated increased pituitary hormone dysfunction. CONCLUSION: This phenomenon is a rare manifestation of postoperative ESS, secondary to surgical resection of a pituitary macroadenoma. We discuss the associated potential risk factors and strategies for avoidance in these two cases. Routine instillation of intrasellar fat in patients at risk is felt to be protective. Scientific Scholar 2021-08-03 /pmc/articles/PMC8422539/ /pubmed/34513152 http://dx.doi.org/10.25259/SNI_530_2021 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Winograd, Evan
Kortz, Michael W.
Lillehei, Kevin O.
Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome
title Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome
title_full Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome
title_fullStr Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome
title_full_unstemmed Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome
title_short Radiographic pituitary stalk disruption: A rare sequela of secondary empty sella syndrome
title_sort radiographic pituitary stalk disruption: a rare sequela of secondary empty sella syndrome
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422539/
https://www.ncbi.nlm.nih.gov/pubmed/34513152
http://dx.doi.org/10.25259/SNI_530_2021
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