1.Dyskinesia-hyperpyrexia syndrome with syndrome of inappropriate secretion of antidiuretic hormone in Parkinson disease: A case report
Congcong GAO ; Fei GAO ; Lifei TAN
Journal of Apoplexy and Nervous Diseases 2025;42(6):550-553
Dyskinesia-hyperpyrexia syndrome(DHS)is an acute hyperpyrexia syndrome that is different from Parkinsonism-hyperpyrexia syndrome and serotonin syndrome in patients with advanced Parkinson's disease(PD),with the main symptoms of high fever,disturbance of consciousness,elevated creatine kinase,and dyskinesia. Syndrome of inappropriate secretion of antidiuretic hormone(SIADH)is a clinical syndrome caused by excessive secretion of antidiuretic hormone,which leads to the symptoms of dilutional hyponatremia,water retention,and increases in urine sodium and urine osmotic pressure. DHS has not received widespread attention in clinical practice,and there are rare reports of DHS comorbid with SIADH. This article reports the diagnosis and treatment processes of a case of DHS comorbid with SIADH and reviews the relevant literature,in order to guide the diagnosis and treatment of PD-related critical diseases.
Hyponatremia
2.Neonatal systemic pseudohypoaldosteronism type I.
Xin-Cheng CAO ; Yuan-Yuan CHEN ; Ke ZHANG ; Xun-Jie ZHANG ; Lin YANG ; Zhi-Hua LI
Chinese Journal of Contemporary Pediatrics 2023;25(7):774-778
An 18-day-old male infant was admitted to the hospital due to recurrent hyperkalemia for more than 10 days. The neonate had milk refusal and dyspnea. The blood gas analysis revealed recurrent hyperkalemia, hyponatremia and metabolic acidosis. Adrenocortical hormone replacement therapy was ineffective. Additional tests showed a significant increase in aldosterone levels. Family whole exome sequencing revealed that the infant had compound heterozygous in the SCNNIA gene, inherited from both parents. The infant was diagnosed with neonatal systemic pseudohypoaldosteronism type I. The infant's electrolyte levels were stabilized through treatment with sodium polystyrene sulfonate and sodium supplement. The infant was discharged upon clinical recovery. This study provides a focused description of differential diagnosis of salt-losing syndrome in infants and introduces the multidisciplinary management of neonatal systemic pseudohypoaldosteronism type I.
Infant
;
Infant, Newborn
;
Humans
;
Male
;
Pseudohypoaldosteronism/genetics*
;
Hyperkalemia/etiology*
;
Hyponatremia/diagnosis*
;
Diagnosis, Differential
3.Thermal strain and fluid balance during a 72-km military route march in a field setting.
Beng Hoong POON ; Suriya PRAKAASH ; Ya Shi TEO ; Priscilla Weiping FAN ; Jason Kai WEI LEE
Singapore medical journal 2022;63(9):497-502
INTRODUCTION:
A physiological profiling study was conducted to evaluate thermal strain as well as fluid and electrolyte balances on heat-acclimatised men performing a 72-km route march in a field setting.
METHODS:
38 male soldiers (age range 18-23 years) participated in the study, as part of a cohort that marched for 72 km, with loads for about 26 hours. Core temperature and heart rate sensors were used for the duration of the march. Fluid and food intake and output were monitored for the duration of the march. Blood samples were taken one day before the march (pre-march), immediately after the march (Post 1) and on the 15th day after the march to ascertain recovery (Post 2) to assess fluid and electrolyte profiles.
RESULTS:
Mean core temperature was within safe limits, ranging from 37.1 to 38.1°C throughout the march. There was an overall decrease in serum sodium levels, a decline in serum sodium concentration in 28 participants and three instances of hyponatraemia (serum sodium concentration <135 mmol/L).
CONCLUSION
Our study found low thermal strain heat-acclimatised individuals during a 72-km route march. However, there was an overall decrease in serum sodium levels, even when the participants were allowed to drink ad libitum. Challenges of exercise-associated hyponatraemia during prolonged activities remain to be addressed.
Humans
;
Male
;
Adolescent
;
Young Adult
;
Adult
;
Military Personnel
;
Hyponatremia
;
Water-Electrolyte Balance/physiology*
;
Exercise/physiology*
;
Sodium
4.Online Team-Based Learning in Teaching Hyponatremia Among Medical Clerks of the University of Santo Tomas Faculty of Medicine and Surgery, Philippines
Journal of Medicine University of Santo Tomas 2022;6(S1):103-113
Education, Distance
;
COVID-19
;
Hyponatremia
5.Pituitary immune-related adverse events induced by programmed cell death protein 1 inhibitors in advanced lung cancer patients: A report of 3 cases.
Yang Chun GU ; Ying LIU ; Chao XIE ; Bao Shan CAO
Journal of Peking University(Health Sciences) 2022;54(2):369-375
Pituitary immune-related adverse events induced by programmed cell death protein 1 inhibitors in advanced lung cancer patients: A report of 3 cases SUMMARY Programmed cell death protein 1 (PD-1) and its ligand 1 (PD-L1) have been widely used in lung cancer treatment, but their immune-related adverse events (irAEs) require intensive attention. Pituitary irAEs, including hypophysitis and hypopituitarism, are commonly induced by cytotoxic T lymphocyte antigen 4 inhibitors, but rarely by PD-1/PD-L1 inhibitors. Isolated adrenocorticotropic hormone(ACTH) deficiency (IAD) is a special subtype of pituitary irAEs, without any other pituitary hormone dysfunction, and with no enlargement of pituitary gland, either. Here, we described three patients with advanced lung cancer who developed IAD and other irAEs, after PD-1 inhibitor treatment. Case 1 was a 68-year-old male diagnosed with metastatic lung adenocarcinoma with high expression of PD-L1. He was treated with pembrolizumab monotherapy, and developed immune-related hepatitis, which was cured by high-dose methylprednisolone [0.5-1.0 mg/(kg·d)]. Eleven months later, the patient was diagnosed with primary gastric adenocarcinoma, and was treated with apatinib, in addition to pembrolizumab. After 17 doses of pembrolizumab, he developed severe nausea and asthenia, when methylprednisolone had been stopped for 10 months. His blood tests showed severe hyponatremia (121 mmol/L, reference 137-147 mmol/L, the same below), low levels of 8:00 a.m. cortisol (< 1 μg/dL, reference 5-25 μg/dL, the same below) and ACTH (2.2 ng/L, reference 7.2-63.3 ng/L, the same below), and normal thyroid function, sex hormone and prolactin. Meanwhile, both his lung cancer and gastric cancer remained under good control. Case 2 was a 66-year-old male with metastatic lung adenocarcinoma, who was treated with a new PD-1 inhibitor, HX008, combined with chemotherapy (clinical trial number: CTR20202387). After 5 months of treatment (7 doses in total), his cancer exhibited partial response, but his nausea and vomiting suddenly exacerbated, with mild dyspnea and weakness in his lower limbs. His blood tests showed mild hyponatremia (135 mmol/L), low levels of 8:00 a.m. cortisol (4.3 μg/dL) and ACTH (1.5 ng/L), and normal thyroid function. His thoracic computed tomography revealed moderate immune-related pneumonitis simultaneously. Case 3 was a 63-year-old male with locally advanced squamous cell carcinoma. He was treated with first-line sintilimab combined with chemotherapy, which resulted in partial response, with mild immune-related rash. His cancer progressed after 5 cycles of treatment, and sintilimab was discontinued. Six months later, he developed asymptomatic hypoadrenocorticism, with low level of cortisol (1.5 μg/dL) at 8:00 a.m. and unresponsive ACTH (8.0 ng/L). After being rechallenged with another PD-1 inhibitor, teslelizumab, combined with chemotherapy, he had pulmonary infection, persistent low-grade fever, moderate asthenia, and severe hyponatremia (116 mmol/L). Meanwhile, his blood levels of 8:00 a.m. cortisol and ACTH were 3.1 μg/dL and 7.2 ng/L, respectively, with normal thyroid function, sex hormone and prolactin. All of the three patients had no headache or visual disturbance. Their pituitary magnetic resonance image showed no pituitary enlargement or stalk thickening, and no dynamic changes. They were all on hormone replacement therapy (HRT) with prednisone (2.5-5.0 mg/d), and resumed the PD-1 inhibitor treatment when symptoms relieved. In particular, Case 2 started with high-dose prednisone [1 mg/(kg·d)] because of simultaneous immune-related pneumonitis, and then tapered it to the HRT dose. His cortisol and ACTH levels returned to and stayed normal. However, the other two patients' hypopituitarism did not recover. In summary, these cases demonstrated that the pituitary irAEs induced by PD-1 inhibitors could present as IAD, with a large time span of onset, non-specific clinical presentation, and different recovery patterns. Clinicians should monitor patients' pituitary hormone regularly, during and at least 6 months after PD-1 inhibitor treatment, especially in patients with good oncological response to the treatment.
Adenocarcinoma of Lung/drug therapy*
;
Adrenocorticotropic Hormone/therapeutic use*
;
Aged
;
B7-H1 Antigen/therapeutic use*
;
Humans
;
Hydrocortisone/therapeutic use*
;
Hyponatremia/drug therapy*
;
Hypopituitarism/drug therapy*
;
Immune Checkpoint Inhibitors
;
Lung Neoplasms/pathology*
;
Male
;
Methylprednisolone/therapeutic use*
;
Middle Aged
;
Nausea/drug therapy*
;
Pituitary Gland/pathology*
;
Pneumonia
;
Prednisone/therapeutic use*
;
Programmed Cell Death 1 Receptor/therapeutic use*
;
Prolactin/therapeutic use*
6.Clinical characteristics of hospitalized patients with 2019 novel coronavirus disease indicate potential proximal tubular dysfunction.
Liu LIU ; Fan HE ; Si-Si CAI ; Kai-Li HU ; Chong YU ; Yi HUANG ; Rui ZENG ; Gang XU
Chinese Medical Journal 2020;133(16):1983-1985
Adult
;
Aged
;
Aged, 80 and over
;
Betacoronavirus
;
Coronavirus Infections
;
complications
;
Female
;
Glomerular Filtration Rate
;
Glycosuria
;
epidemiology
;
Hospitalization
;
Humans
;
Hyponatremia
;
epidemiology
;
Kidney Tubules, Proximal
;
physiopathology
;
Male
;
Middle Aged
;
Pandemics
;
Pneumonia, Viral
;
complications
;
Retrospective Studies
7.Transient Pseudohypoaldosteronism in a 5-Month-old Infant Manifested as a Failure to Thrive.
Jung Won LEE ; Su Jin CHO ; Hae Soon KIM
The Ewha Medical Journal 2019;42(1):6-9
Pseudohypoaldosteronism (PHA) in infants is manifested by presence of hyperkalemia, hyponatremia, and metabolic acidosis. At initial stages, PAH is generally suspected as congenital adrenal hyperplasia. Transient PHA has been reported in infants with urinary tract infection and urinary tract malformation. We report a case of 5-month-old infant with failure to thrive and finally diagnosed with transient PHA due to urinary tract infection with vesicoureteral reflux.
Acidosis
;
Adrenal Hyperplasia, Congenital
;
Failure to Thrive*
;
Humans
;
Hyperkalemia
;
Hyponatremia
;
Infant*
;
Pseudohypoaldosteronism*
;
Urinary Tract
;
Urinary Tract Infections
;
Vesico-Ureteral Reflux
8.Clinical Characteristics of Brucellosis Complicated by Syndrome of Inappropriate Secretion of Antidiuresis.
Xing Yu ZHAO ; Juan Hui ZHU ; Li An TONG ; Peng XIA ; Jie Lin WANG
Acta Academiae Medicinae Sinicae 2019;41(6):787-792
To summarize and analyze the causes of hyponatremia in patients with brucellosis and explore the clinical manifestations of syndrome of inappropriate antidiuresis(SIAD)in patients with brucellosis. The clinical data of 111 patients with acute brucellosis who were treated in Peking Union Medical College Hospital from September 2011 to December 2017 were retrospectively reviewed.Hyponatremia was defined by serum sodium level lower than 135 mmol/L.Clinical characteristics including medical histories,vital signs,and laboratory test findings were collected and analyzed. Hyponatremia was found in 14(12.6%)of 111 patients with brucellosis,among whom 3 patients were confirmed to be with SIAD,10 were suspected as SIAD,and 1 was diagnosis as hypopituitarism.Hypoalbuminemia,elevation of erythrocyte sedimentation rate,and high sensitivity C reactive protein were found in brucellosis patients with SIAD,along with severe complications such as infective endocarditis,septic shock,and anemia. Hyponatremia is not a rare condition in brucellosis patients and may be caused by SIAD.
Brucellosis
;
Humans
;
Hyponatremia
;
Inappropriate ADH Syndrome
;
Retrospective Studies
9.Small bowel obstruction by water beads in a 12-month-old girl presenting with acute hyponatremia with seizure
Na Ra LEE ; Hyun Beak SHIN ; Yeon Jun JEONG ; Sun Jun KIM
Pediatric Emergency Medicine Journal 2019;6(2):86-91
Although foreign body ingestion is relatively common in children aged 6 months-3 years, small bowel obstruction rarely develops, and few cases require surgical interventions. We report a case of 12-month-old girl who presented to the emergency department with new-onset seizure after projectile bilious vomiting. The initial diagnosis was seizure caused by hyponatremia based on laboratory findings, plain abdominal radiograph, brain magnetic resonance imaging, and electroencephalography. Despite fluid resuscitation, clinical manifestations did not improve, and severe ileal obstruction was found on computed tomography. Emergency laparoscopy showed a foreign body (a water bead [superabsorbent polymer], 3 cm in diameter) that was subsequently removed by enterotomy. After the surgery, bilious vomiting continued, and gastrografin did not pass on fluoroscopy. The second laparoscopy showed a residual foreign body that was crushed and then removed by minimal enterotomy. She was discharged in good condition 5 days after the second surgery. This case suggests a particular danger of water beads as foreign bodies and the need for differential diagnosis of multiple foreign bodies in children with poor communication skills.
Brain
;
Child
;
Diagnosis
;
Diagnosis, Differential
;
Diatrizoate Meglumine
;
Eating
;
Electroencephalography
;
Emergencies
;
Emergency Service, Hospital
;
Female
;
Fluoroscopy
;
Foreign Bodies
;
Humans
;
Hyponatremia
;
Infant
;
Intestinal Obstruction
;
Laparoscopy
;
Magnetic Resonance Imaging
;
Resuscitation
;
Seizures
;
Vomiting
;
Water
10.Diagnosis and Clinical Progress in a Case of Dementia with Lewy Bodies
Journal of the Korean Society of Biological Therapies in Psychiatry 2019;25(1):60-68
Dementia with Lewy bodies(DLB) is the second most common neurodegenerative disease. However, DLB might not be adequately diagnosed due to its variety of clinical symptoms. The authors present 65-year-old Mrs. A. who showed Parkinson's movement, cognitive decline, psychological symptoms, and autonomic dysfunction. According to the clinical features and biological markers in the recently revised DLB criteria, Mrs. A. was diagnosed with probable DLB. Differential diagnoses of delirium, Parkinson's dementia, and Alzheimer's dementia were discussed. Psychopharmacological treatments of antidepressants or anxiolytics caused intolerable side effects and showed little efficacy to Mrs. A. She experienced two episodes of hyponatremia during her one-year treatment. Recovery from neurological symptoms due to the first hyponatremia was time-consuming, and in the second, it was associated with changes in the level of consciousness despite relatively mild hyponatremia. A fall that occurred in the latter part of treatment triggered remarkable deterioration of DLB symptoms and daily life function. Prevention of falls is important for maintaining the quality of life of patients with DLB.
Accidental Falls
;
Aged
;
alpha-Synuclein
;
Anti-Anxiety Agents
;
Antidepressive Agents
;
Biomarkers
;
Consciousness
;
Delirium
;
Dementia
;
Diagnosis
;
Diagnosis, Differential
;
Humans
;
Hyponatremia
;
Lewy Bodies
;
Neurodegenerative Diseases
;
Quality of Life


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