A rare case of hyponatremia from a hypothalamic lesion in a patient with multiple sclerosis

2014 ◽  
Vol 21 (5) ◽  
pp. 662-665 ◽  
Author(s):  
Joseph J Sabatino ◽  
J Kent Werner ◽  
Scott D Newsome

The syndrome of inappropriate antidiuretic hormone secretion (SIADH) can occur from a variety of neurologic and systemic processes; however, it has rarely been seen in multiple sclerosis (MS). We report a case of SIADH in a patient with MS and compare it with previously reported English-only cases. A 32-year-old woman experienced generalized fatigue followed by confusion and was found to have profound hyponatremia. Her work-up demonstrated SIADH secondary to a discrete enhancing hypothalamic lesion. Despite the seldom occurrence of SIADH in MS, hypothalamic lesions are more common than appreciated and should be considered in patients presenting with hyponatremia or endocrinopathy symptoms.

2021 ◽  
Vol 10 (13) ◽  
pp. 986-987
Author(s):  
Shivam Khanna ◽  
Yash Gupte ◽  
Parth Godhiwala ◽  
Sachin Agrawal ◽  
Sunil Kumar

In cancer patients, syndrome of inappropriate antidiuretic hormone secretion (SIADH) is the leading cause of hyponatremia. 1 Hyponatremia is a serious disorder of dyselectrolytemia, linked with neurological symptoms that are life-threatening and it is the most common aetiology of tumour-related electrolyte imbalance.2 The tumours commonly causing hyponatremia of SIADH variety are lung, head-neck and breast tumours. SIADH has been documented in various malignancy types with numerous possible aetiologies apart from active malignancy.2,3 The aetiology distribution of SIADH in tumour patients are not completely known. Secondly, clinically, it is not clear which malignancy is most commonly associated with SIADH.3 Calcified meningioma presenting as SIADH had not been reported so far in the literature. Here a case of an elderly female with clinical features and brain imaging suggestive of meningioma associated with hyponatremia due to SIADH had been highlighted.


2021 ◽  
Vol 49 (2) ◽  
pp. 030006052098565
Author(s):  
Cai-Fu Zhao ◽  
Su-Fen Zhao ◽  
Ze-Qing Du

Small cell carcinoma of the cervix is a rare malignant tumor in the clinical setting. Clinical manifestations of this tumor are mostly similar to those of normal types of cervical cancer. Small cell carcinoma of the cervix only shows symptoms of neuroendocrine tumors, such as syndrome of inappropriate antidiuretic hormone secretion (SIADH). Most of the hyponatremia caused by SIADH can be managed after removal of the cause. Hyponatremia is a predictor of poor prognosis and can be used as an indicator of partial recurrence. We report a case of small cell carcinoma of the cervix complicated by SIADH. Our patient presented with irregular vaginal bleeding after menopause. After one cycle of chemotherapy, there was trembling of the limbs, and a laboratory examination showed low Na+ and low Cl− levels. After limited water intake, intravenous hypertonic saline, and intermittent diuretic treatment, the patient’s blood Na+ levels returned to normal. After a radical operation, the above-mentioned symptoms disappeared.


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