Cargando…
Symptomatic Chiari type 1 malformation associated with acromegaly: A case report
BACKGROUND: Here, we report a patient who presented with both symptomatic acromegaly and symptomatic Chiari I malformation (CM1) with a C2-T5 syrinx. CASE DESCRIPTION: A 63-year-old female presented with bilateral arm dysesthesias and back pain. For approximately the past 30 years, she had chronic s...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247717/ https://www.ncbi.nlm.nih.gov/pubmed/34221614 http://dx.doi.org/10.25259/SNI_332_2021 |
_version_ | 1783716575810945024 |
---|---|
author | Aoki, Takuma Umebayashi, Daisuke Tatsuzawa, Kazunori Hashimoto, Naoya |
author_facet | Aoki, Takuma Umebayashi, Daisuke Tatsuzawa, Kazunori Hashimoto, Naoya |
author_sort | Aoki, Takuma |
collection | PubMed |
description | BACKGROUND: Here, we report a patient who presented with both symptomatic acromegaly and symptomatic Chiari I malformation (CM1) with a C2-T5 syrinx. CASE DESCRIPTION: A 63-year-old female presented with bilateral arm dysesthesias and back pain. For approximately the past 30 years, she had chronic signs of acromegaly (i.e. an enlarged forehead, jaw, and nose, and enlarged hands and feet). When the cervical magnetic resonance showed a CM1 (tonsillar herniation) with C2-T5 syringomyelia, she underwent foramen magnum decompression and C1 posterior arch resection. Postoperatively, she was asymptomatic. The added finding of a growth hormone (GH)-producing pituitary lesion was treated medically with endocrine therapy, as she had incidentally required surgery/chemotherapy for a newly diagnosed colon cancer. CONCLUSION: Symptomatic CM1, syrinx, and acromegaly may occur together. Appropriately treatment may include a suboccipital decompression, and C1 arch resection surgery, followed by either surgical or medical treatment for the GH-producing pituitary adenoma. |
format | Online Article Text |
id | pubmed-8247717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-82477172021-07-02 Symptomatic Chiari type 1 malformation associated with acromegaly: A case report Aoki, Takuma Umebayashi, Daisuke Tatsuzawa, Kazunori Hashimoto, Naoya Surg Neurol Int Case Report BACKGROUND: Here, we report a patient who presented with both symptomatic acromegaly and symptomatic Chiari I malformation (CM1) with a C2-T5 syrinx. CASE DESCRIPTION: A 63-year-old female presented with bilateral arm dysesthesias and back pain. For approximately the past 30 years, she had chronic signs of acromegaly (i.e. an enlarged forehead, jaw, and nose, and enlarged hands and feet). When the cervical magnetic resonance showed a CM1 (tonsillar herniation) with C2-T5 syringomyelia, she underwent foramen magnum decompression and C1 posterior arch resection. Postoperatively, she was asymptomatic. The added finding of a growth hormone (GH)-producing pituitary lesion was treated medically with endocrine therapy, as she had incidentally required surgery/chemotherapy for a newly diagnosed colon cancer. CONCLUSION: Symptomatic CM1, syrinx, and acromegaly may occur together. Appropriately treatment may include a suboccipital decompression, and C1 arch resection surgery, followed by either surgical or medical treatment for the GH-producing pituitary adenoma. Scientific Scholar 2021-06-14 /pmc/articles/PMC8247717/ /pubmed/34221614 http://dx.doi.org/10.25259/SNI_332_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 Aoki, Takuma Umebayashi, Daisuke Tatsuzawa, Kazunori Hashimoto, Naoya Symptomatic Chiari type 1 malformation associated with acromegaly: A case report |
title | Symptomatic Chiari type 1 malformation associated with acromegaly: A case report |
title_full | Symptomatic Chiari type 1 malformation associated with acromegaly: A case report |
title_fullStr | Symptomatic Chiari type 1 malformation associated with acromegaly: A case report |
title_full_unstemmed | Symptomatic Chiari type 1 malformation associated with acromegaly: A case report |
title_short | Symptomatic Chiari type 1 malformation associated with acromegaly: A case report |
title_sort | symptomatic chiari type 1 malformation associated with acromegaly: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247717/ https://www.ncbi.nlm.nih.gov/pubmed/34221614 http://dx.doi.org/10.25259/SNI_332_2021 |
work_keys_str_mv | AT aokitakuma symptomaticchiaritype1malformationassociatedwithacromegalyacasereport AT umebayashidaisuke symptomaticchiaritype1malformationassociatedwithacromegalyacasereport AT tatsuzawakazunori symptomaticchiaritype1malformationassociatedwithacromegalyacasereport AT hashimotonaoya symptomaticchiaritype1malformationassociatedwithacromegalyacasereport |