Type I Arnold-Chiari malformation with bronchiectasis, respiratory failure, and sleep disordered breathing: a case report
© Campisi et al; licensee BioMed Central Ltd. 2013
Received: 13 December 2012
Accepted: 28 January 2013
Published: 22 February 2013
Arnold Chiari Malformation (ACM) is defined as a condition where part of the cerebellar tissue herniates into the cervical canal toward the medulla and spinal cord resulting in a number of clinical manifestations. Type I ACM consists of variable displacement of the medulla throughout the formamen magnum into the cervical canal, with prominent cerebellar herniation.
Type I ACM is characterized by symptoms related to the compression of craniovertebral junction, including ataxia, dysphagia, nistagmus, headache, dizziness, and sleep disordered breathing. We report a case of a life-long non-smoker, 54 years old woman who presented these symptoms associated with bronchiectasis secondary to recurrent inhalation pneumonia, hypercapnic respiratory failure, and central sleep apnea (CSA).
CSA was first unsuccessfully treated with nocturnal c-PAP. The subsequent treatment with low flow oxygen led to breathing pattern stabilization with resolution of CSA and related clinical symptoms during sleep. We suggest that in patients with type I ACM the presence of pulmonary manifestations aggravating other respiratory disturbances including sleep disordered breathing (SDB) should be actively investigated. The early diagnosis is desirable in order to avoid serious and/or poorly reversible damages.
KeywordsArnold-Chiari malformation Bronchiectasis Central sleep apnea Oxygen therapy Respiratory failure Sleep disordered breathing
Arnold-Chiari malformation (ACM) is a complex syndrome in which the brainstem medulla, and the cerebellar tonsils and vermis herniate throughout the foramen magnum. Type I ACM is defined by the herniation of only the medulla and cerebellar tonsils whereas type II ACM is also characterized by caudal displacement of the cerebellar vermis. The main symptoms include ataxia, dizziness, chronic headache, nystagmus, twitching, oropharyngeal dysfunction, recurrent respiratory infections, paresthesia, pyramidal signs and sleep disordered breathing (SDB) encompassing a number of sleep disturbances characterized by apneas or hypopneas, intermittent hypoxaemia, microarousals, and disruption of sleep continuity. All these disturbances are related to the compression of respiratory centers and their neural pathways related to herniation. We report a case of type I ACM with recurrent aspiration-induced pneumonia, secondary bronchiectasis, respiratory failure, and central sleep apneas.
Polysomnographic data at baseline, during C-PAP breathing, and during continuous oxygen administration
Total Sleep Time
7 h 03 m
7 h 40 m
7 h 30 m
Sleep onset latency
% Sleep efficiency
% Slow Wave Sleep
This case presentation offers the opportunity to speculate about the occurrence of respiratory involvement and its mechanisms in patients with type I ACM. Sleep disordered breathing is associated with ACM and generally ascribed to two types of abnormalities: upper airway dysfunctionwhich is associated with obstructive apneas, and abnormalities of respiratory controlwhich is presumably involved in the pathophisiology of central sleep apneas[4, 7]. The latter are characterized by transient cessation of neural respiratory output during sleep resulting in poor ventilation and impaired gas exchange. The transient cessation of respiratory drive could be due to: firstly, an outright defect in respiratory drive; secondly, a transient instability in an otherwise intact respiratory control system; and thirdly, a transient active inhibition of respiratory motor drive. In addition, patients may be either hypercapnic or non-hypercapnic. The hypercapnic group, which includes patients with central hypoventilation and a number of neurological syndromes, is consistent with the first pathophysiological mechanism. The non-hypercapnic group includes patients with idiopathic hyperventilation and periodic breathing. Pathophysiologically this group is consistent with the second or third mechanism. These patients typically have a low or normal awake pCO2. In OSA, pharyngeal anatomy, upper airway muscles responsiveness during sleep, arousal threshold, and loop gain may all contribute to the occurrence of apnea presence and severity of central apneas. During sleep reflex muscles activation is reduced and if the airway anatomy is quite deficient will likely lead to substantial or complete airflow obstruction, yielding a hypopnoea or apnea. The patient had the hypercanic form of CSA The risk of apnoea resulted from both obstructive (short neck, limited mobility of soft palate and tongue) and central causes. Central causes may include: 1) compromised vascular supply to the brainstem due to compression; 2) insensitivity of peripheral chemo-receptors, due to brainstem involvement; 3) direct compression of the respiratory centre. In our case both central and obstructive apneas was confirmed with polysomnography. Nasal c-PAP (9 cmH2O), after proper titration, was partially effective in improving the AHI and apnea duration, but limited compliance to the treatment. Polysomnography was repeated during low flow oxygen administration resulting in a significant reduction in both number and duration of CSA and an increase in SpO2 (average apnea duration in baseline condition 16.5 seconds; after low flow oxygen administration 11.2 sec). The use of supplemental low flow oxygen, as mentioned in another case report of a patient with primary alveolar hypoventilation, chronic hypercapnia and CSA, led to a decrease in number and duration of central apneas[11, 12]. The improvement produced by oxygen may have been due to the fact that the patient had no demonstrable ventilatory response to hypoxia during wakefulness, and therefore may have developed hypoxic brainstem depression during sleep. The findings suggest that oxygen therapy during sleep may be beneficial in patients with primary alveolar hypoventilation and CSA leading to significant improvement of SDB and all related symptoms. Oxygen administration during sleep has been associated with reproducible reduction of AHI [Table 1] Type I ACM, whether alone or in combination with syringomyelia, can cause a great number of progressive disorders such as dysphagia, alveolar hypoventilation, inhalation pneumonia, and respiratory failure. In our patient recurrent aspirations with consequent inhalation pneumonia occurred. The most important mechanism of recurrent aspiration pneumonia was dysphagia. The alterations underlying dysphagia are stretch injury to the lower cranial nerves caused by caudal displacement of the medulla or compression of the swallowing centres in the brainstem. Probably the pressure determined by the cerebellar tonsils on the hypoglossal nuclei and other swallowing centres located in the medulla is tough to be the leading cause of the dysphagia. Recurrent aspirations result in several respiratory infections which may lead both to post-inflammatory bronchiectasis and lung parenchymal damage, causing chronic respiratory failure (CRF)[17, 18]. Respiratory failure as the early manifestation in type I ACM is uncommon and, generally, is the result of postoperative conditions. Cylindrical bronchiectasis, as documented in Figure 2, have become a source of repeated infections with recurrent exacerbations of CRF, chronic cough, intense dyspnoea and fever treated with antibiotics and often requiring hospitalization. Respiratory failure probably has been caused not only by neuromuscular disorders affecting the diaphragm due to compression of neural centers in the brainstem, but also resulted from swallowing disturbances and dysphagia further complicated by recurrent aspiration pneumonia.
This case report suggests that a neurologic cause can always be considered for recurrent aspiration pneumonia and progressive dysphagia, even in absence of prominent signs and symptoms. The high prevalence of sleep apnoea syndrome in patients with neurological disorders indicates that respiratory disturbances during sleep should be systematically screened even in ACM patients, in order to prevent nocturnal respiratory failure and all the risks associated with nocturnal intermittent hypoxia. In summary, central sleep apnoea can be the typical manifestation of ACM and may be a life-threatening condition. The severity of CSA may explain the reported increased incidence of death during sleep in ACM patients. Using a low flow oxygen during sleep, even in hypercanic patients, avoids mechanical ventilation that is often not well tolerated. Oxygen administration allows to solve CSA and all related cerebrovascular risks associated with nocturnal respiratory failure and sleep fragmentation, improving quality of life. Oxygen therapy can generate potentially deprimental effects. The most relevant of these is the worsening of hypercapnia, which is mediated by mechanisms such as hypoventilation and ventilation-perfusion redistribution. Particularly sleep itself generates ventilatory alterations that include an increase in airway resistance and decreased sensitivity of respiratory centers. Arterial blood gases samples should be periodically taken at awakening to assess pCO2 in order to prevent hypoventilation from the oxygen therapy[21, 22]. The availability of further clinical studies for the treatment of CSA with low flow oxygen in hypercapnic patients is desiderable to avoid serious and irreversible damage.
"Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal."
Arnold Chiari Malformation
Chronic Respiratory Failure
Central Sleep Apnea
Obstructive Sleep Apnea
Sleep Disordered Breathing
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