Kopel Jonathan, Moreno Tanir, Singh Simran, Van-Spronsen Nicole, Sorensen Grant, Griswold John
Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Timothy J. Harnar Burn Center, Lubbock, Texas, USA.
Scars Burn Heal. 2022 Oct 19;8:20595131221122312. doi: 10.1177/20595131221122312. eCollection 2022 Jan-Dec.
Diabetes insipidus (DI) is characterized by polyuria and polydipsia. In most cases, the condition results from either an inadequate release or resistance to the activity of antidiuretic hormone in the renal collecting tubules. The underlying pathophysiology may be related to destruction the destruction or degeneration of neurons from inflammatory, autoimmune diseases, vascular diseases, Langerhans cell histiocytosis, sarcoidosis, or trauma. However, a large majority of diabetes insipidus cases (50%) are considered idiopathic. An exceedingly rare cause of idiopathic central DI occurs in burn injuries, which has only been reported in eight cases. We present an extremely rare case of idiopathic DI in a 15-year-old male with 76% total body surface area (TBSA) burns with the development of idiopathic central DI. An extensive literature review was accomplished to compare this case with the small number of previously reported case reports of idiopathic DI in burn patients.
Diabetes insipidus (DI) is a rare complication of burn injuries that results from the destruction of neurons involved in the secretion of antidiuretic hormone from the pituitary gland. Only eight cases of DI have been reported in the literature in association to burn injuries. The patient in this case report received immediate fluid resuscitation, burn treatment, and intensive observation after the initial burn injury. The rapid response was likely the main reason for the absence of neurological damage as reported in the CT image. Therefore, the treatment of burn injuries remains an important step for reducing neurological damage and hormonal dysregulation leading to diabetes insipidus.
尿崩症(DI)的特征是多尿和烦渴。在大多数情况下,这种情况是由于抗利尿激素在肾集合管中的释放不足或对其活性产生抵抗所致。潜在的病理生理学可能与炎症、自身免疫性疾病、血管疾病、朗格汉斯细胞组织细胞增多症、结节病或创伤导致的神经元破坏或变性有关。然而,大多数尿崩症病例(50%)被认为是特发性的。特发性中枢性尿崩症极其罕见的一个病因是烧伤,仅报告过8例。我们报告一例极为罕见的特发性尿崩症病例,患者为一名15岁男性,全身表面积(TBSA)76%烧伤,并出现了特发性中枢性尿崩症。我们进行了广泛的文献综述,以将此病例与之前报道的少数烧伤患者特发性尿崩症病例报告进行比较。
尿崩症(DI)是烧伤的一种罕见并发症,由参与垂体抗利尿激素分泌的神经元破坏引起。文献中仅报道过8例与烧伤相关的尿崩症病例。本病例报告中的患者在初次烧伤后立即接受了液体复苏、烧伤治疗和密切观察护理。快速反应可能是CT图像中未出现神经损伤报告的主要原因。因此,烧伤治疗仍然是减少导致尿崩症的神经损伤和激素失调的重要步骤。