Journal of Medical Case Reports | |
Postoperative neurological aggravation after anesthesia with sevoflurane in a patient with xeroderma pigmentosum: a case report | |
Nordine Drissi Kamili1  Hicham Azendour1  Elhoucine Boutayeb1  Najib Bouhabba1  Bahija Yafat1  Mustapha Bensghir1  Salaheddine Fjouji1  | |
[1] Department of Anaesthesiology, Military Hospital Med V Rabat, University of Med V Souissi, Rabat, Morocco | |
关键词: Neurological worsening; Sevoflurane; General anesthesia; Xeroderma pigmentosum; | |
Others : 1181246 DOI : 10.1186/1752-1947-7-73 |
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received in 2012-05-13, accepted in 2013-02-14, 发布年份 2013 | |
【 摘 要 】
Introduction
Xeroderma pigmentosum is a rare autosomal recessive disease that causes changes in skin pigmentation, precancerous lesions and neurological abnormalities. It is a defect in the nucleotide excision repair mechanism. It has been reported that volatile anesthetics has a possible genotoxic side effect and deranged nucleotide excision repair in cells obtained from a patient with xeroderma pigmentosum.
We report an unusual case of postoperative neurological aggravation in a patient with xeroderma pigmentosum anesthetized with sevoflurane.
Case presentation
A 24-year-old African woman, who has had xeroderma pigmentosum since childhood, was admitted to our hospital for a femoral neck fracture. A preoperative physical examination revealed that she had a resting tremor with ataxia. She had cutaneous lesions such as keratosis and hyperpigmentation on her face and both hands. There was no major alteration of cognitive function, muscular strength was maintained and her osteotendinous reflexes were preserved. Surgical fixation was performed under general anesthesia after the failure of spinal anesthesia. All parameters were stable during surgery. When she woke up four hours later, the patient presented with confusion and psychomotor agitation, sharpened reflexes and the Babinski reflex was present. Her postoperative test results and a magnetic resonance imaging scan were unremarkable. It was suggested that sevoflurane had had a probable deleterious effect on the neurological status of this patient.
Conclusion
The anesthetizing of a patient with xeroderma pigmentosum is associated with a risk of worsening neurological disorders. At present, there are no clear recommendations to avoid the use of volatile agents in the anesthetic management of patients with xeroderma pigmentosum. More clinical and experimental research is needed to confirm the sensitivity of patients with xeroderma pigmentosum to sevoflurane and other halogenated anesthetics.
【 授权许可】
2013 Fjouji et al.; licensee BioMed Central Ltd.
【 预 览 】
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20150514120541756.pdf | 200KB | download |
【 参考文献 】
- [1]Stefanini M, Kraemer KHK: Xeroderma pigmentosum. In Neurocutaneous Diseases 51st edition. Edited by Ruggieri M, Pascual-Castroviejo I, Di Rocco C. 2008, 771-792.
- [2]Lehmann AR, McGibbon D, Stefanini M: Xeroderma pigmentosum. Orphanet J Rare Dis 2011, 6:70. BioMed Central Full Text
- [3]Brunner T, Jöhr M: Anesthetic management of a child with xeroderma pigmentosum. Paediatr Anaesth 2004, 14:697-698.
- [4]Oliveira CR, Elias L, Barros AC, Conceição DB: Anesthesia in patient with Xeroderma pigmentosum: case report. Rev Bras Anestesiol 2003, 53:46-51.
- [5]Masuda Y, Imaizumi H, Okanuma M, Narimatsu E, Asai Y, Namiki A: Anesthesia for a patient with xeroderma pigmentosum. Masui 2002, 51:169-171.
- [6]Miyazaki R, Nagata T, Kai T, Takahashi S: Anesthesia for a patient with xeroderma pigmentosum. Masui 2007, 56:439-441.
- [7]Reitz M, Lanz E: DNA strand breaks in cells with DNA repair deficiency after halothane exposure in vitro. Arzneimittelforschung 1993, 43:418-420.
- [8]Zuo Z: Are volatile anesthetics neuroprotective or neurotoxic? Med Gas Res 2012, 2:10. BioMed Central Full Text
- [9]Kraemer KH, Lee MM, Scotto J: Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases. Arch Dermatol 1987, 123:241-250.
- [10]Zhang B, Tian M, Zhen Y, Yue Y, Sherman J, Zheng H, Li S, Tanzi RE, Marcantonio ER, Xie Z: The effects of isoflurane and desflurane on cognitive function in humans. Anesth Analg 2012, 114:410-415.
- [11]Bilotta F, Doronzio A, Stazi E, Titi L, Zeppa IO, Cianchi A, Rosa G, Paoloni FP, Bergese S, Asouhidou I, Ioannou P, Abramowicz AE, Spinelli A, Delphin E, Ayrian E, Zelman V, Lumb P: Early postoperative cognitive dysfunction and postoperative delirium after anaesthesia with various hypnotics: study protocol for a randomised controlled trial-the PINOCCHIO trial. Trials 2011, 12:170. BioMed Central Full Text
- [12]Lauta E, Abbinante C, Del Gaudio A, Aloj F, Fanelli M, de Vivo P, Tommasino C, Fiore T: Emergence times are similar with sevoflurane and total intravenous anesthesia: results of a multicenter RCT of patients scheduled for elective supratentorial craniotomy. J Neurosurg Anesthesiol 2010, 22:110-118.
- [13]Rasmussen M, Juul N, Christensen SM, Jónsdóttir KY, Gyldensted C, Vestergaard-Poulsen P, Cold GE, Østergaard L: Cerebral blood flow, blood volume, and mean transit time responses to propofol and indomethacin in peritumor and contralateral brain regions: perioperative perfusion-weighted magnetic resonance imaging in patients with brain tumors. Anesthesiology 2010, 112:50-56.
- [14]Petersen KD, Landsfeldt U, Cold GE, Petersen CB, Mau S, Hauerberg J, Holst P, Olsen K: Intracranial pressure and cerebral hemodynamic in patients with cerebral tumors: a randomized prospective study of patients subjected to craniotomy in propofol-fentanyl, isoflurane-fentanyl, or sevoflurane-fentanyl anesthesia. Anesthesiology 2003, 98:329-336.
- [15]Trescot AM, Datta S, Lee M, Hansen H: Opioid pharmacology. Pain Physician 2008, 11:S133-S153.
- [16]Karabiyik L, Sardaş S, Polat U, KocabaS NA, Karakaya AE: Comparison of genotoxicity of sevoflurane and isoflurane in human lymphocytes studied in vivo using the comet assay. Mutat Res 2001, 492:99-107.