anesthetic management of patients with klippel-feil syndrome, a case series

نویسندگان

kamran mottaghi anesthesiology research center, shahid beheshti university of medical sciences

farhad safari anesthesiology research center, shahid beheshti university of medical sciences

parisa sezari anesthesiology research center, shahid beheshti university of medical sciences

naeime gholizadeh anesthesiology research center, shahid beheshti university of medical sciences

چکیده

introduction: klippel feil syndrome (kfs) is a rare entity which is characterized by failure of normal segmentation of cervical vertebrae resulting in short neck with restricted movement and cervical instability. this anomaly increases the risk of neurological damage during airway instrumentation like laryngoscopy and positioning for surgery. case rports: we report three patients, a 42 year old male patient with kfs who scheduled for craniocervical fusion under general anesthesia and a 6 year old girl candidate for cleft palate repair and a 26 year old woman candidate for craniocervical fusion. conclusion: all the cases were successfully managed using fiberoptic bronchoscope in first two cases and gum elastic bougie (geb) in the last case. all things together, awake fiberoptic intubation could be the safest technique for airway management.

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منابع مشابه

The Klippel-Feil syndrome: a case report.

Short neck and fusion of cervical vertebrae are observed in several genetic conditions and well-defined syndromes. An 8-year-old boy with a short neck, low-set posterior hairline, deafness and limited neck motion was suspected of having such a condition. Clinical and radiographic examination led to the diagnosis of Klippel-Feil syndrome.

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Klippel-Feil syndrome: a case report.

OBJECTIVE To report the clinical presentation and peculiarity of management of Klippel-Feil syndrome (KFS) at the University of Abuja Teaching Hospital, Gwagwalada. BACKGROUND KFS is a rare pathology that has not been previously reported on in Nigeria. METHODS Case review was employed to report this pathology. RESULT This case is a 10 year old boy with KFS presenting with cosmetic blemish...

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[A case of Klippel-Feil syndrome].

We would like to present a case of Klippel-Feil Syndrome in which it is associated with multiple cervical vertebra synostosis, short neck, cervical rib, congenital sclerosis, platybasia, spina-bifida and deafness. We are revising the case history of this syndrome.

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Klippel Feil Syndrome: A Rare Case Report

INTRODUCTION In Klippel Feil syndrome, classically there is a triad of short neck, a low posterior hairline and a limited range of neck movements especially of lateral bending. In fewer than 50% of cases have all the three elements. CASE REPORT In the present case we have found congenital Scoliosis, Sprengel deformity and there were no evidence of renal disease, congenital heart disease and n...

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Klippel Feil syndrome

In 1912, Klippel and Feil (1) first reported on a patient with a short neck, a low posterior hairline, and severe restriction of neck movements due to complete fusion of the cervical spine, the classic clinical triad which is the hallmark of Klippel-Feil syndrome (KFS). It is estimated to occur in 1 in 40,000 to 42,000 newborns worldwide. Mutations in the GDF6 and GDF3 genes can cause KFS (2). ...

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ANESTHETIC MANAGEMENT IN A CASE OF KLIPPEL-FElL SYNDROME AND LITERATURE REVIEW

Klippel-Feil syndrome is known by the classic triad of shortness of the neck , limitation of neck movements, and a low posterior hairline. There are often accompanying cervical spinal abnormalities such as kyphoscoliosis as well as urogenital and cardiac abnormalities. Presented here we have a 20 year old young man with hypoesthesia and decreased motor function in the right hand. The probl...

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عنوان ژورنال:
journal of cellular and molecular anesthesia

جلد ۲، شماره ۲، صفحات ۶۳-۶۸

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