Lamou Hayat, Grassmann Jan-Peter, Betsch Marcel, Wild Michael, Hakimi Mohssen, Windolf Joachim, Jungbluth Pascal
Department of Trauma and Handsurgery, Heinrich Heine University Hospital Düsseldorf, Moorenstr, 5, 40225 Düsseldorf, Germany.
J Med Case Rep. 2014 Jun 16;8:196. doi: 10.1186/1752-1947-8-196.
Systemic capillary leak syndrome is a rare and life threatening disease characterized by periodic episodes of hypovolemic shock due to leakage of plasma from the intravascular to the extravascular space. It is associated with hemoconcentration, hypoalbuminemia, and generalized edema. We report the case of a patient with idiopathic systemic capillary leak syndrome who developed an unexpected and potentially fatal abdominal and four-limb compartment syndrome. This was successfully treated with fasciotomies and medical treatment including terbutaline, theophylline, and corticosteroids. To the best of our knowledge this is the first report of this kind in the literature.
A previously healthy 54-year-old Caucasian man presented to the emergency department of our internal medicine ward with a medical history of aggravation of general health related to dizziness, weight gain, and two syncopal attacks. Due to a massive emission of fluids and proteins from the intravascular to the extracellular compartments, he developed compartment syndromes in his upper and lower limbs and the abdominal compartment. The abdomen and all four limbs required decompression by a fasciotomy of both forearms, both thighs, both lower legs, and the abdomen within 24 hours after admission. After 60 days of treatment he was dismissed from the clinic. He was able to return to his previous occupation and reached the same level of athletic activity as before the illness.
Systemic capillary leak syndrome is a very rare disease that can lead to a fatal clinical outcome. It is important to be aware of the fatal complications that can be caused by this disease. Despite the fact that systemic capillary leak syndrome represents a very rare disease it is still important to be aware of life threatening complications, like compartment syndromes, which need surgical intervention. However, early diagnosis and interdisciplinary treatment can lead to a good clinical outcome.
系统性毛细血管渗漏综合征是一种罕见且危及生命的疾病,其特征为由于血浆从血管内渗漏至血管外间隙而导致周期性低血容量性休克发作。它与血液浓缩、低白蛋白血症及全身性水肿相关。我们报告一例特发性系统性毛细血管渗漏综合征患者,该患者出现了意外且可能致命的腹部及四肢骨筋膜室综合征。通过筋膜切开术及包括特布他林、茶碱和皮质类固醇在内的药物治疗,该患者获得成功救治。据我们所知,这是文献中此类报告的首例。
一名既往健康的54岁白种男性因与头晕、体重增加及两次晕厥发作相关的全身健康状况恶化而就诊于我们内科病房的急诊科。由于大量液体和蛋白质从血管内渗漏至细胞外间隙,他的上肢、下肢及腹部均出现了骨筋膜室综合征。入院后24小时内,患者的双侧前臂、双侧大腿、双侧小腿及腹部均需通过筋膜切开术进行减压。经过60天的治疗,他出院了。他能够重返之前的工作岗位,并恢复到患病前的运动水平。
系统性毛细血管渗漏综合征是一种非常罕见的疾病,可导致致命的临床结局。认识到该疾病可能引发的致命并发症很重要。尽管系统性毛细血管渗漏综合征是一种非常罕见的疾病,但认识到诸如骨筋膜室综合征等需要手术干预的危及生命的并发症仍然很重要。然而,早期诊断和多学科治疗可带来良好的临床结局。