Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression

We present a case of a 17-year-old Hispanic male with Arnold-Chiari Type 1 [AC-Type 1] with syringomyelia, status post decompression, who complains of exercise intolerance, headaches, and fatigue with exertion. The patient was found to have diurnal hypercapnia and nocturnal alveolar hypoventilation....

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Main Authors: Keely Smith, Ana M. Gomez-Rubio, Tomika S. Harris, Lauren E. Brooks, Ricardo A. Mosquera
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Case Reports in Pediatrics
Online Access:http://dx.doi.org/10.1155/2016/8359838
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author Keely Smith
Ana M. Gomez-Rubio
Tomika S. Harris
Lauren E. Brooks
Ricardo A. Mosquera
author_facet Keely Smith
Ana M. Gomez-Rubio
Tomika S. Harris
Lauren E. Brooks
Ricardo A. Mosquera
author_sort Keely Smith
collection DOAJ
description We present a case of a 17-year-old Hispanic male with Arnold-Chiari Type 1 [AC-Type 1] with syringomyelia, status post decompression, who complains of exercise intolerance, headaches, and fatigue with exertion. The patient was found to have diurnal hypercapnia and nocturnal alveolar hypoventilation. Cardiopulmonary testing revealed blunting of the ventilatory response to the rise in carbon dioxide (CO2) resulting in failure of the parallel correlation between increased CO2 levels and ventilation; the expected vertical relationship between PETCO2 and minute ventilation during exercise was replaced with an almost horizontal relationship. No new pathology of the brainstem was discovered by MRI or neurological evaluation to explain this phenomenon. The patient was placed on continuous noninvasive open ventilation (NIOV) during the day and CPAP at night for a period of 6 months. His pCO2 level decreased to normal limits and his symptoms improved; specifically, he experienced less headaches and fatigue during exercise. In this report, we describe the abnormal response to exercise that patients with AC-Type 1 could potentially experience, even after decompression, characterized by the impairment of ventilator response to hypercapnia during exertion, reflecting a complete loss of chemical influence on breathing with no evidence of abnormality in the corticospinal pathway.
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spelling doaj-art-72ba0b571d4f49489f24cbdc7c7047ac2025-02-03T01:20:25ZengWileyCase Reports in Pediatrics2090-68032090-68112016-01-01201610.1155/2016/83598388359838Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa DecompressionKeely Smith0Ana M. Gomez-Rubio1Tomika S. Harris2Lauren E. Brooks3Ricardo A. Mosquera4Department of Pediatrics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USADepartment of Pediatrics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USADepartment of Pediatrics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USAMcGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USADepartment of Pediatrics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX 77030, USAWe present a case of a 17-year-old Hispanic male with Arnold-Chiari Type 1 [AC-Type 1] with syringomyelia, status post decompression, who complains of exercise intolerance, headaches, and fatigue with exertion. The patient was found to have diurnal hypercapnia and nocturnal alveolar hypoventilation. Cardiopulmonary testing revealed blunting of the ventilatory response to the rise in carbon dioxide (CO2) resulting in failure of the parallel correlation between increased CO2 levels and ventilation; the expected vertical relationship between PETCO2 and minute ventilation during exercise was replaced with an almost horizontal relationship. No new pathology of the brainstem was discovered by MRI or neurological evaluation to explain this phenomenon. The patient was placed on continuous noninvasive open ventilation (NIOV) during the day and CPAP at night for a period of 6 months. His pCO2 level decreased to normal limits and his symptoms improved; specifically, he experienced less headaches and fatigue during exercise. In this report, we describe the abnormal response to exercise that patients with AC-Type 1 could potentially experience, even after decompression, characterized by the impairment of ventilator response to hypercapnia during exertion, reflecting a complete loss of chemical influence on breathing with no evidence of abnormality in the corticospinal pathway.http://dx.doi.org/10.1155/2016/8359838
spellingShingle Keely Smith
Ana M. Gomez-Rubio
Tomika S. Harris
Lauren E. Brooks
Ricardo A. Mosquera
Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression
Case Reports in Pediatrics
title Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression
title_full Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression
title_fullStr Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression
title_full_unstemmed Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression
title_short Unusual Ventilatory Response to Exercise in Patient with Arnold-Chiari Type 1 Malformation after Posterior Fossa Decompression
title_sort unusual ventilatory response to exercise in patient with arnold chiari type 1 malformation after posterior fossa decompression
url http://dx.doi.org/10.1155/2016/8359838
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