• 文章类型: Case Reports
    低钠血症是一种常见的电解质异常。
    我们报告了一例低钠血症患者,诊断为转移到下丘脑和垂体的小细胞肺癌。
    一名68岁男性患者因发热、咳嗽和肺炎入院。血清钠水平为113mmol/L考虑ADH不当综合征(SIADH)。甲状腺功能检查和皮质醇水平指出了两个轴的中枢缺陷。进行垂体MRI检查,观察下丘脑和垂体肿块。开始泼尼松龙治疗,然后进行L甲状腺素替代。2周后进行胸部计算机断层扫描(CT),发现肿块病变。进行支气管镜活检,组织病理学诊断为小细胞肺癌。
    许多机制被认为是我们患者低钠血症的原因。SIADH,继发性肾上腺功能不全和垂体转移引起的继发性甲状腺功能减退是可能的原因。
    低钠血症的原因有时很复杂。当低钠血症的根本原因没有详细评估时,许多诊断可能会错过。
    UNASSIGNED: Hyponatremia is a common electrolyte abnormality.
    UNASSIGNED: We report a patient who presented with hyponatremia and diagnosed as small cell lung cancer metastatic to hypothalamus and pituitary.
    UNASSIGNED: A 68 year old male patient was admitted with fever and cough and pneumonia was considered. Serum sodium level was 113 mmol/L. Syndrome of inappropriate ADH (SIADH) is considered. Thyroid function tests and cortisol levels pointed out a central deficiency in both axes. Pituitary MRI was performed and a hypothalamic and pituitary mass were observed. Prednisolone therapy was started followed by L thyroxine replacement. A chest computer tomography (CT) was taken 2 weeks later revealed a mass lesion. Bronchoscopic biopsy was performed and histopathological diagnosis of the tumor was reported as small cell lung cancer.
    UNASSIGNED: Many mechanisms were considered as the cause of hyponatremia in our patient. SIADH, secondary adrenal insufficiency and secondary hypothyroidism due to pituitary metastasis are possible causes.
    UNASSIGNED: The reason of hyponatremia is sometimes complex. When the underlying causes of hyponatremia are not evaluated in detail, many diagnoses can be missed.
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  • 文章类型: Case Reports
    This report aims to present an elderly woman with persistent delirium after hospitalization for lethargy secondary to hyponatremia. The diagnosis of pontine myelinolysis was made and there were no characteristic neurological manifestations such as pupillary changes or spastic tetraparesis. Hallucinations and personality changes were the clues to the diagnosis and should be considered an atypical manifestation of pontine myelinolysis.
    O objetivo deste relato é apresentar uma idosa que apresentou, após internação por letargia secundária à hiponatremia, delirium persistente depois da alta hospitalar. O diagnóstico de mielinólise pontina foi feito após a alta hospitalar e não houve manifestações neurológicas características, como alterações pupilares ou tetraparesia espástica. Alucinações e mudança de personalidade foram as pistas para o diagnóstico e devem ser consideradas como uma manifestação atípica de mielinólise pontina.
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  • 文章类型: Journal Article
    背景:低钠血症很常见,尤其是老年人。复位渗透压(RO)可作为不适当利尿(SIAD)综合征的替代诊断。关于门诊诊所和医院病房中RO患病率的信息有限。水稀释试验被认为是诊断RO的金标准。最近对和肽素的鉴定提供了额外的诊断标志物,以及尿酸排泄分数的利用。方法:这种单中心,prospective,观察性研究包括8例患者,他们在2年的研究期间接受了水稀释试验.结果:在50%的病例中诊断出复位渗透压,而SIAD在一名患者中得到证实。其余三名患者的测试尚无定论。结论:我们的研究结果表明,重置渗透压,尽管它很罕见,是慢性低钠血症的合理诊断。在这项研究中无法证实和肽素的相关性。此外,在诊断复位渗透压时,尿酸排泄分数可能与水稀释试验一样有效.
    Background: Hyponatremia is common, particularly among the elderly. Reset osmostat (RO) serves as an alternative diagnosis to the syndrome of inappropriate antidiuresis (SIAD). There is limited information available regarding the prevalence of RO in outpatient clinics and hospital wards. The water-diluting test is considered the gold standard for the diagnosis of RO. The recent identification of copeptin provides an additional diagnostic marker alongside the utilization of fractional uric acid excretion. Methods: This single-center, prospective, observational study involved eight patients undergoing a water-diluting test over a study period of 2 years. Results: Reset osmostat was diagnosed in 50% of cases, while SIAD was confirmed in one patient. The tests were inconclusive for the remaining three patients. Conclusions: Our findings suggest that reset osmostat, despite its rarity, is a plausible diagnosis in chronic hyponatremia. The relevance of copeptin could not be confirmed in this study. Moreover, fractional uric acid excretion might be as effective as the water-diluting test in diagnosing reset osmostat.
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  • 文章类型: Journal Article
    背景与目的:组氨酸-色氨酸-酮戊二酸(HTK)诱导的低钠血症与成人心脏手术患者脑损伤的关系尚不清楚。本研究分析了术中输注HTK心脏停搏液后的神经系统转归。材料和方法:对60例接受体外循环心脏手术的成年患者进行了前瞻性队列研究。在这些病人中,13和47接受了HTK输注和常规高钾血症性心脏停搏液,分别。患者的基线特征,术中数据,脑损伤标记物,简易精神状态检查(MMSE)成绩,并收集了定量脑电图(qEEG)数据。体外循环期间的电解质变化,低钠血症的程度,和任何相关的脑损伤进行了评估。结果:HTK组在体外循环期间出现急性低钠血症,术中通过超滤和生理盐水给药进行校正。HTK组术后钠水平高于常规心脏停搏组。体外循环后,HTK组的神经元特异性烯醇化酶水平变化明显更高(p=0.043)。使用病例对照匹配,变化没有显着差异。qEEG分析显示HTK组在术后第7天(POD)显著增加(p=0.018);POD60无明显变化.两组在POD7和POD60上的MMSE评分没有显着差异。结论:在成人心脏手术中,HTK引起的急性低钠血症和生理盐水的快速矫正与潜在的短期但不是长期的神经系统影响有关。需要进一步的研究来确定纠正HTK引起的低钠血症的必要性。
    Background and Objectives: The relationship between histidine-tryptophan-ketoglutarate (HTK)-induced hyponatremia and brain injury in adult cardiac surgery patients is unclear. This study analyzed postoperative neurological outcomes after intraoperative HTK cardioplegia infusion. Materials and Methods: A prospective cohort study was conducted on 60 adult patients who underwent cardiac surgery with cardiopulmonary bypass. Of these patients, 13 and 47 received HTK infusion and conventional hyperkalemic cardioplegia, respectively. The patients\' baseline characteristics, intraoperative data, brain injury markers, Mini-Mental State Examination (MMSE) scores, and quantitative electroencephalography (qEEG) data were collected. Electrolyte changes during cardiopulmonary bypass, the degree of hyponatremia, and any associated brain insults were evaluated. Results: The HTK group presented with acute hyponatremia during cardiopulmonary bypass, which was intraoperatively corrected through ultrafiltration and normal saline administration. Postoperative sodium levels were higher in the HTK group than in the conventional cardioplegia group. The change in neuron-specific enolase levels after cardiopulmonary bypass was significantly higher in the HTK group (p = 0.043). The changes showed no significant differences using case-control matching. qEEG analysis revealed a significant increase in relative delta power in the HTK group on postoperative day (POD) 7 (p = 0.018); however, no significant changes were noted on POD 60. The MMSE scores were not significantly different between the two groups on POD 7 and POD 60. Conclusions: HTK-induced acute hyponatremia and rapid correction with normal saline during adult cardiac surgeries were associated with a potential short-term but not long-term neurological impact. Further studies are required to determine the necessity of correction for HTK-induced hyponatremia.
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  • 文章类型: Journal Article
    低钠血症是最常见的电解质失衡障碍。有必要开发新型利尿剂来治疗低钠血症而不损失电解质。尿素转运蛋白(UT)在尿液浓缩过程中起着重要作用,已被证明是一种新型的利尿剂靶标。在这项研究中,我们构建并分析了抗利尿激素分泌异常综合征(SIADH)大鼠和小鼠模型,以确定UTs是否是治疗低钠血症的有希望的药物靶点.实验结果表明,100mg/kgUT抑制剂25a可显著增加低钠血症大鼠的血清渗透压浓度(从249.83±5.95到294.33±3.90mOsm/kg)和血清钠(从114±2.07到136.67±3.82mmol/L)。血清化学检查显示25a既没有引起另一种电解质失衡,也没有影响脂质代谢。使用UT-A1和UT-B敲除小鼠SIADH模型,发现UT-A1敲除小鼠的血清渗透压和血清钠的降低比UT-B敲除小鼠的低得多,这表明UT-A1是比UT-B更好的治疗低钠血症的治疗靶点。这项研究证明了UT-A1是SIADH诱导的低钠血症的利尿剂靶标,UT-A1抑制剂可能会发展成为治疗低钠血症的新利尿剂。
    Hyponatremia is the most common disorder of electrolyte imbalances. It is necessary to develop new type of diuretics to treat hyponatremia without losing electrolytes. Urea transporters (UT) play an important role in the urine concentrating process and have been proved as a novel diuretic target. In this study, rat and mouse syndromes of inappropriate antidiuretic hormone secretion (SIADH) models were constructed and analyzed to determine if UTs are a promising drug target for treating hyponatremia. Experimental results showed that 100 mg/kg UT inhibitor 25a significantly increased serum osmolality (from 249.83 ± 5.95 to 294.33 ± 3.90 mOsm/kg) and serum sodium (from 114 ± 2.07 to 136.67 ± 3.82 mmol/L) respectively in hyponatremia rats by diuresis. Serum chemical examination showed that 25a neither caused another electrolyte imbalance nor influenced the lipid metabolism. Using UT-A1 and UT-B knockout mouse SIADH model, it was found that serum osmolality and serum sodium were lowered much less in UT-A1 knockout mice than in UT-B knockout mice, which suggest UT-A1 is a better therapeutic target than UT-B to treat hyponatremia. This study provides a proof of concept that UT-A1 is a diuretic target for SIADH-induced hyponatremia and UT-A1 inhibitors might be developed into new diuretics to treat hyponatremia.
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  • 文章类型: Case Reports
    Boswelliaserrata是一种来自Boswelliaserrata树的草药提取物,具有抗炎和镇痛特性,并减轻类风湿性关节炎引起的疼痛,痛风,骨关节炎,和坐骨神经痛.抗利尿激素分泌不当综合征伴有低钠血症,癫痫发作,以前没有报道过横纹肌溶解症作为锯缘乳香中毒的表现。一名38岁的女性患有临床孤立综合征,此后一直定期服用蛇床子胶囊(200mg/d)以增强其免疫系统。她对光过敏,眼痛,恶心,头晕,在接受她的第一个BNT162b2疫苗剂量四天后,下肢无力,接种后一周,她将锯缘双歧杆菌的剂量增加到5粒胶囊(1000mg/d)。以1000mg/d的剂量连续3周后,她因为第一次入住重症监护室,无缘无故的全身性强直-阵挛性癫痫发作。病人的检查显示了抗利尿激素分泌不当综合征,在治疗和停药锯缘芽孢杆菌后完全解决。总之,当高剂量服用时,锯齿芽孢杆菌可能会导致抗利尿激素分泌不当综合征。患者不应自行用药。
    Boswellia serrata is an herbal extract from the Boswellia serrata tree that has anti-inflammatory and analgesic properties and alleviates pain caused by rheumatoid arthritis, gout, osteoarthritis, and sciatica. Syndrome of inappropriate antidiuretic hormone secretion accompanied by hyponatremia, seizures, and rhabdomyolysis as a manifestation of Boswellia serrata intoxication has not been reported previously. A 38-year-old female suffered clinically isolated syndrome and has since been regularly taking B. serrata capsules (200mg/d) to strengthen her immune system. She experienced hypersensitivity to light, ocular pain, nausea, dizziness, and lower limb weakness four days after receiving her first BNT162b2 vaccine dose, and she increased the dosage of B. serrata to five capsules (1000mg/d) one week after vaccination. After taking B. serrata at a dosage of 1000mg/d for 3 weeks, she was admitted to the intensive care unit because of a first, unprovoked generalized tonic-clonic seizure. The patient\'s workup revealed syndrome of inappropriate antidiuretic hormone secretion, which resolved completely upon treatment and discontinuation of B. serrata. In summary, B. serrata potentially causes syndrome of inappropriate antidiuretic hormone secretion when it is taken at high doses. Patients should not self-medicate.
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  • 文章类型: Editorial
    暂无摘要。
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  • 文章类型: Case Reports
    肾上腺功能不全(AI)是一种罕见但可能危及生命的内分泌疾病,其特征是产生不足或对肾上腺激素的反应受损。症状可能是以血流动力学休克为表现的急性突发危象,也可能是以非特异性症状逐渐发作为表现的更慢性。这些模糊的症状通常伴随着典型的实验室检查结果,比如低钠血症,低血压,和高钾血症,并指向慢性AI的诊断。在这种情况下,我们证明慢性AI表现为严重低钠血症,这是在回到正常血容量基线后发现的。因为一个阴险的演讲,人工智能既可以是偶然的发现,也很容易被错过。该案例强调了在基线代谢和血液动力学状态下评估可疑AI病例的重要性。包括卷状态。这些患者需要高度的临床怀疑,以避免潜在的紧急肾上腺危象,并在病因确定后提供适当的替代疗法。
    Adrenal insufficiency (AI) is a rare but potentially life-threatening endocrine disorder characterized by inadequate production or impaired response to adrenal hormones. Symptoms may range from acute emergent crisis presenting as hemodynamic shock or may be more chronic in presentation with a gradual onset of nonspecific symptoms. These vague symptoms are often accompanied by typical laboratory findings, such as hyponatremia, hypotension, and hyperkalemia, and point toward a diagnosis of chronic AI. In this case presentation, we demonstrate chronic AI presenting with severe hyponatremia, which was revealed after return to an euvolemic baseline. Because of an insidious presentation, AI can be both an incidental finding and easily missed. This case highlights the importance of evaluating suspected cases of AI at a baseline metabolic and hemodynamic state, including volume status. High clinical suspicion is warranted in these patients to avoid potential emergent adrenal crisis and to provide appropriate replacement therapy once etiology is established.
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  • 文章类型: Case Reports
    随着医学肿瘤学的进步,免疫检查点抑制剂(ICIs)已成为许多恶性肿瘤的一线治疗方法.ICI在改善癌症预后方面发挥着重要作用,但一系列免疫相关的不良事件(irAE),包括与免疫相关的内分泌事件(IREEs),由ICI引起的关注也引起了人们的关注。由ICIs引起的irAE的快速临床鉴定尤为重要。我们描述了子宫内膜癌术后患者PD-1治疗后继发性肾上腺皮质功能不全(AI)的情况。一名73岁的女性患者出现厌食症,恶心,呕吐,萎靡不振,电解质干扰,无效的对症治疗,retifanlimab治疗6个月后血清促肾上腺皮质激素和皮质醇水平下降。呕吐消失了,和电解质水平在糖皮质激素治疗3天后得到纠正(氢化可的松,静脉注射,200毫克/天)。当患者出现胃肠道症状时,比如食欲不振和恶心,不仅需要对症治疗,还需要寻找症状背后的病因,特别是在免疫治疗患者中,应该对内分泌系统进行彻底评估,并警惕肾上腺皮质功能不全。
    With advancements in medical oncology, immune checkpoint inhibitors (ICIs) have become the first-line treatment for many malignancies. ICIs play a significant role in improving cancer prognosis, but a series of immune-related adverse events (irAEs), including immune-related endocrine events (irEEs), caused by ICIs have also aroused concerns. Rapid clinical identification of irAEs caused by ICIs is particularly important. We describe a case of secondary adrenocortical insufficiency (AI) after PD-1 treatment in a postoperative patient with endometrial cancer. A 73-year-old female patient developed anorexia, nausea, vomiting, malaise, electrolyte disturbances, ineffective symptomatic treatment, and decreased serum adrenocorticotropin and cortisol levels six months after retifanlimab treatment. The vomiting resolved, and the electrolyte levels were corrected after 3 days of treatment with glucocorticoids (hydrocortisone, intravenous, 200 mg/day). When patients present with gastrointestinal symptoms, such as poor appetite and nausea, not only symptomatic treatment but also a search for the etiology behind the symptoms is needed, especially in immunotherapy patients who should undergo a thorough evaluation of the endocrine system and be alert for adrenocortical insufficiency.
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  • 文章类型: Case Reports
    一名63岁的男子因精神状态改变和反应性下降而住院,被发现患有严重的症状性低钠血症,钠水平为96mmol/L和肺炎。患者因感染性休克和急性严重低钠血症而被送往重症监护病房。他接受了气管保护的插管,并用3%高渗盐水和抗生素治疗。四天后,钠水平校正为128mmol/L,病人被拔管并降级到医疗层。此病例显示了有史以来记录的最低钠实验室值之一,患者成功治疗并通过适当的门诊预约出院。
    A 63-year-old man who presented to the hospital with altered mental status and decreased responsiveness was found to have severe symptomatic hyponatremia with a sodium level of 96 mmol/L and pneumonia. The patient was admitted to the medical intensive care unit for septic shock and acute severe hyponatremia. He was intubated for airway protection, and treated with 3% hypertonic saline bolus and antibiotics. After four days, sodium levels were corrected to 128 mmol/L, and the patient was extubated and downgraded to the medical floor. This case demonstrates one of the lowest recorded sodium lab values ever and the patient was successfully treated and discharged home with appropriate outpatient appointments.
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