Dilrukshi M D S A, Sandakumari G V N, Abeysundara P K, Chang T
University Medical Unit, National Hospital of Sri Lanka, Colombo 10, Sri Lanka.
Department of Clinical Medicine, University of Colombo, Colombo, Sri Lanka.
J Med Case Rep. 2017 Feb 5;11(1):31. doi: 10.1186/s13256-017-1210-x.
Craniopharyngiomas are rare intracranial tumors commonly presenting with neurological symptoms. Reports of severe hyponatremia as a presenting manifestation of a craniopharyngioma and hyponatremia-induced myopathy are rare. We report the case of a patient with craniopharyngioma presenting with severe hyponatremia, panhypopituitarism, and hyponatremia-induced myopathy.
A 52-year-old Sri Lankan man presented with anorexia, nausea, fatigue, generalized muscle weakness, and cramps for 1 week. The onset of his illness had been preceded by vomiting and diarrhea for 1 day which he attributed to food poisoning. On examination, he had an apathetic disposition with a generalized "sallow complexion." He was not dehydrated. Apart from reduced muscle power (4/5) and hyporeflexia, the neurological examination was normal. His serum sodium was 102 mmol/l; potassium 4.1 mmol/l; chloride 63 mmol/l; plasma osmolality 272 mosm/KgHO; urine osmolality 642 mosm/KgHO; and urine sodium 79 mmol/l. His creatine phosphokinase was 12,400 U/l, lactate dehydrogenase 628 U/l, aspartate aminotransferase 360 U/l, and alanine aminotransferase 64 U/l. His hormone profile revealed panhypopituitarism. An electromyogram showed nonspecific abnormalities while a muscle biopsy did not show any pathology. Magnetic resonance imaging of his brain demonstrated a well-defined craniopharyngioma with suprasellar extension. His pituitary gland was compressed and the pituitary stalk was displaced by the tumor. He had marked improvement in muscle power and rapid reduction of serum creatine phosphokinase levels paralleling the correction of severe hyponatremia, even before the initiation of hormone replacement.
This case illustrates the rare presentation of severe hyponatremia and hyponatremia-induced myopathy in patients with craniopharyngioma, awareness of which would facilitate early appropriate investigations and treatment.
颅咽管瘤是罕见的颅内肿瘤,通常伴有神经症状。关于严重低钠血症作为颅咽管瘤的首发表现以及低钠血症诱发肌病的报道罕见。我们报告一例颅咽管瘤患者,其表现为严重低钠血症、全垂体功能减退和低钠血症诱发的肌病。
一名52岁的斯里兰卡男子出现厌食、恶心、疲劳、全身肌肉无力和痉挛1周。发病前1天他有呕吐和腹泻,他认为是食物中毒所致。检查时,他神情淡漠,面色普遍“蜡黄”。他没有脱水。除了肌力减弱(4/5)和反射减弱外,神经系统检查正常。他的血清钠为102 mmol/L;钾4.1 mmol/L;氯63 mmol/L;血浆渗透压272 mosm/KgH₂O;尿渗透压642 mosm/KgH₂O;尿钠79 mmol/L。他的肌酸磷酸激酶为12400 U/L,乳酸脱氢酶628 U/L,天冬氨酸转氨酶360 U/L,丙氨酸转氨酶64 U/L。他的激素检查显示全垂体功能减退。肌电图显示非特异性异常,而肌肉活检未显示任何病理改变。他脑部的磁共振成像显示一个边界清晰的颅咽管瘤,向鞍上延伸。他的垂体被肿瘤压迫,垂体柄被肿瘤移位。在开始激素替代治疗之前,随着严重低钠血症的纠正,他的肌力有明显改善,血清肌酸磷酸激酶水平迅速降低。
该病例说明了颅咽管瘤患者罕见的严重低钠血症和低钠血症诱发肌病的表现,认识到这一点将有助于早期进行适当的检查和治疗。