Syndrome of inappropriate secretion of antidiuretic hormone (SIADH) in a patient with multiple sclerosis
E Ishikawa1, S Ohgo, K Nakatsuru
1Department of Internal Medicine, Miyazaki Medical College, Japan.
Abstract:
Association of the syndrome of inappropriate secretion of antidiuretic hormone (SIADH) with multiple sclerosis (MG) is very rare, although many other disorder of the nervous system have been reported to be associated with this syndrome; there is only one case report in the literature. We describe here a patient with the syndrome associated with MS. A 62-year-old women had a variety of neurologic symptoms, where clinical course was typical of MS. Transient episodes of hyponatremia and disturbance of consciousness occurred repeatedly with deterioration of MS. The concentration of antidiuretic hormone (ADH) was high whereas the plasma osmolality was low in the presence of concentrated urine, during the episodes of hyponatremia. Urinary Na excretions exceeded 20 mEq/day. Computed tomography and magnetic resonance imaging revealed lesions in the brain, especially in the periventricular region. The hypothalamus and pituitary appeared normal by these imaging methods. Since the periventricular region surrounds and may be functionally connected to the hypothalamus which plays the central role in the regulation of ADH secretion, it was concluded that association of SIADH and MS in this patient was not coincidental, and that demyelinating processes in the periventricular region exerted an abnormal influence on ADH secretion resulting in SIADH. Contribution of other mechanisms as increased intrathoracic pressure, however, could not be excluded completely.
Insights
Syndrome of inappropriate antidiuretic hormone secretion (SIADH) is rarely associated with multiple sclerosis (MS). This case report details a patient with MS experiencing SIADH, suggesting a link between demyelination and ADH dysregulation.
Area of Science:
- Neurology
- Endocrinology
Background:
- The syndrome of inappropriate antidiuretic hormone secretion (SIADH) is infrequently associated with neurological disorders.
- Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system.
Observation:
- A 62-year-old female with neurological symptoms consistent with MS experienced recurrent episodes of hyponatremia and altered consciousness.
- Laboratory findings during episodes included high antidiuretic hormone (ADH) levels, low plasma osmolality, concentrated urine, and elevated urinary sodium excretion (>20 mEq/day).
- Brain imaging revealed periventricular lesions typical of MS, with normal appearance of the hypothalamus and pituitary gland.
Findings:
- The patient's clinical presentation and laboratory results were consistent with SIADH.
- The location of MS lesions in the periventricular region, functionally connected to the hypothalamus, suggests a causal link to ADH dysregulation.
- Demyelinating processes in the periventricular region are proposed to abnormally influence ADH secretion, leading to SIADH in this MS patient.
Implications:
- This case suggests a potential pathophysiological mechanism linking MS-related demyelination to SIADH.
- Understanding this association may improve the diagnosis and management of SIADH in multiple sclerosis patients.
- Further research is warranted to elucidate the precise mechanisms and rule out other contributing factors, such as increased intrathoracic pressure.
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