Wong Poh Shean, Rajoo Subashini, Achmad Sankala Hairuddin, Long Bidin Mohamed Badrulnizam
Endocrine Unit, Medical Department, Hospital Kuala Lumpur, Malaysia.
Radiology Department, Hospital Kuala Lumpur, Malaysia.
Endocr Oncol. 2022 Sep 6;2(1):K15-K20. doi: 10.1530/EO-22-0064. eCollection 2022 Jan.
Pituitary metastasis (PM) is a rare complication of an advanced malignancy. Albeit rare, PM can be more detected and achieve a longer survival rate through frequent neuroimaging and newer oncology therapies. Lung cancer is the most frequent primary site, followed by breast and kidney cancers. Patients with lung cancer generally present with respiratory symptoms and are commonly diagnosed at an advanced stage already. Nevertheless, physicians should be mindful of other systemic manifestations as well as signs and symptoms related to metastatic spread and paraneoplastic syndromes. Herein, we report the case of a 53-year-old woman who presented with PM as the first sign of an undiagnosed lung cancer. Initially, her condition was a challenging diagnosis and was even complicated with diabetes insipidus (DI), which can present as severe hyponatremia when coexisting with adrenal insufficiency. This case also highlights that treating DI with antidiuretic hormone (ADH) replacement was complicated by extreme difficulties in attaining satisfactory sodium and water balance during the clinical course, with the possibility of coexistent DI and syndrome of inappropriate ADH secretion because of the underlying lung cancer.
When patients present with pituitary mass and diabetes insipidus (DI), pituitary metastasis should be considered as an initial differential diagnosis. DI caused by pituitary adenoma is rare and is typically a late finding.DI can present as severe hyponatremia when coexisting with adrenal insufficiency.Cortisol can directly inhibit endogenous antidiuretic hormone (ADH) secretion. Patients with adrenocorticotropic hormone deficiency will have increased tonic ADH activity and subsequently reduced capacity for free-water excretion. However, when on steroid therapy, patients should be monitored for possible DI because steroids can restore free-water excretion.A substantial change in serum sodium after desmopressin treatment should eliminate the possibility of desmopressin overdose or coexistence of DI and syndrome of inappropriate ADH secretion in patients with lung cancer. Therefore, frequent monitoring of serum sodium concentrations is crucial.
垂体转移瘤(PM)是晚期恶性肿瘤的一种罕见并发症。尽管罕见,但通过频繁的神经影像学检查和更新的肿瘤治疗方法,PM能够被更多地检测出来并获得更长的生存率。肺癌是最常见的原发部位,其次是乳腺癌和肾癌。肺癌患者通常表现出呼吸道症状,且通常在晚期才被诊断出来。然而,医生也应留意其他全身表现以及与转移扩散和副肿瘤综合征相关的体征和症状。在此,我们报告一例53岁女性病例,该患者以垂体转移瘤作为未确诊肺癌的首发症状。最初,她的病情诊断颇具挑战性,甚至并发了尿崩症(DI),当与肾上腺功能不全并存时,可表现为严重低钠血症。该病例还凸显出,在临床过程中,用抗利尿激素(ADH)替代疗法治疗尿崩症时,要达到满意的钠和水平衡极其困难,且由于潜在的肺癌,可能并存尿崩症和抗利尿激素分泌不当综合征。
当患者出现垂体肿块和尿崩症(DI)时,应将垂体转移瘤作为初步鉴别诊断。垂体腺瘤引起的尿崩症罕见,通常是晚期表现。尿崩症与肾上腺功能不全并存时可表现为严重低钠血症。皮质醇可直接抑制内源性抗利尿激素(ADH)分泌。促肾上腺皮质激素缺乏的患者会有增强的持续性ADH活性,随后自由水排泄能力降低。然而,在接受类固醇治疗时,应监测患者是否可能出现尿崩症,因为类固醇可恢复自由水排泄。去氨加压素治疗后血清钠的大幅变化应可排除肺癌患者去氨加压素过量或并存尿崩症和抗利尿激素分泌不当综合征的可能性。因此,频繁监测血清钠浓度至关重要。