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1.
Adv Tech Stand Neurosurg ; 45: 359-378, 2022.
Article in English | MEDLINE | ID: mdl-35976457

ABSTRACT

INTRODUCTION: Thoracic disc herniations (TDH) may cause major morbidity. While thoracoscopic microdiscectomy (TMD) is an excellent technique, postoperative band-like pain is an important drawback. MATERIAL AND METHODS: We performed 181 consecutive TMDs (including 39 high-risk cases) with preservation of rib and costovertebral joint (CVJ). We shave a few mm of the rib, drill straight to target, and avoid opening the canal before the TDH is completely free and (in case of giant TDHs) internally debulked, creating initial decompression and limiting epidural venous oozing. Subsequently, we gently mobilize and remove the residual TDH while avoiding leverage. RESULTS: Skin-to-skin time was <90' in 64, 90-120' in 48, >120' in 20, unknown in 10, and 162' mean in 39 high-risk procedures. Blood loss was <100 mL in 76, <250 mL in 48, and 537 mL mean in 39 high-risk procedures. The technique was successfully applied in all (including nine dural repairs) without a single conversion. We observed an increased neurological deficit in two (1.1%) and inadequate decompression in merely one (wrong level). Complications (mainly pulmonary) were few and managed conservatively, except for a segmental artery pseudoaneurysm treated endovascularly. We observed a substantial decrease in acute and chronic postoperative pain. DISCUSSION: The technique is fast, straightforward, minimizes bone resection and blood loss, improves orientation, safely and effectively deals with any TDH, and prevents postoperative band-like pain as the CVJ is preserved. CONCLUSION: We hope this technique will find broader acceptance among a new generation of spine surgeons to benefit patients suffering TDH-related myelopathy or merely intractable pain.


Subject(s)
Intervertebral Disc Displacement , Spinal Cord Diseases , Diskectomy/methods , Humans , Intervertebral Disc Displacement/surgery , Pain/complications , Ribs/surgery , Spinal Cord Diseases/complications , Thoracic Vertebrae/surgery , Treatment Outcome
2.
Acta Neurochir (Wien) ; 159(6): 1163-1166, 2017 06.
Article in English | MEDLINE | ID: mdl-28432520

ABSTRACT

We present a rare fatal complication of an occipital condylar fracture. The patient was initially neurologically intact, but showed secondary clinical deterioration. Imaging revealed extensive extra-axial hemorrhage at the craniocervical junction and an acute obstructive hydrocephalus. MR imaging demonstrated a T2 hyperintens signal in both the lower brainstem and upper cervical spinal cord, likely caused by the extra-axial hemorrhage. As prognosis was estimated infaust, supportive treatment was discontinued and the patient died soon thereafter. This case report illustrates a rare, delayed complication and unexpected death in a patient having sustained an occipital condylar fracture.


Subject(s)
Cervical Atlas/diagnostic imaging , Occipital Bone/diagnostic imaging , Skull Fractures/pathology , Aged , Brain Stem/diagnostic imaging , Brain Stem/pathology , Cervical Atlas/pathology , Fatal Outcome , Female , Humans , Occipital Bone/pathology , Skull Fractures/diagnostic imaging , Skull Fractures/therapy , Tomography, X-Ray Computed/methods
3.
Childs Nerv Syst ; 32(6): 1049-55, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27080093

ABSTRACT

PURPOSE: The purpose of this paper was to study the incidence and clinical significance of fever after intraventricular neuroendoscopic procedures in children. METHODS: We retrospectively assessed all children subjected to an intraventricular neuroendoscopic procedure between 2004 and 2015. Body temperature 6 days postoperatively, symptoms and signs, and eventual cerebrospinal fluid analysis were evaluated. Fever was defined as temperature above 38 °C. RESULTS: Fifty-five children (mean age 4.8 years) had 67 procedures. Forty-three children (47 procedures, 70 %) developed fever, mostly the day of surgery (n = 17; 25 %) or the next day (n = 33; 49 %). All children who were clinically ill (n = 9, including 7 with fever) suffered serious illness, as opposed to none of the children with fever without being clinically ill (n = 36). Fever was unrelated to gender, indication for, and type of procedure and did not influence ETV success rate at 3 months. Children under 1 year less frequently developed fever (p = 0.032). CONCLUSIONS: Fever frequently develops after intraventricular neuroendoscopic procedures in children and follows a rather predictable course, peaking the day of surgery and/or the next day, and rapidly subsiding thereafter. Fever is not a cardinal symptom except when combined with other symptoms in children who are clinically ill (which most of them are not). Close observation avoiding invasive diagnostic tests may suffice for those who are not clinically ill, while extra attention should be paid to those whose temperature rises after day 2 especially when clinically ill, as they likely suffer serious illness. We recommend to closely observe children after any intraventricular neuroendoscopic procedure for at least 5 days.


Subject(s)
Cerebral Ventricles/surgery , Fever/etiology , Neuroendoscopy/adverse effects , Postoperative Complications/physiopathology , Adolescent , Body Temperature , Child , Child, Preschool , Female , Fever/diagnostic imaging , Humans , Infant , Infant, Newborn , Magnetic Resonance Imaging , Male , Postoperative Complications/diagnostic imaging , Retrospective Studies , Time Factors
5.
Childs Nerv Syst ; 29(7): 1051-8, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23443469

ABSTRACT

BACKGROUND AND PURPOSE: Sprengel's deformity, a rare congenital malformation of the scapula, may be observed in combination with spinal dysraphism. The co-occurrence of these malformations suggests an unknown shared etiology. Therefore, we reviewed the medical records of eight children presenting with both malformations and performed a review of the literature. PATIENTS AND METHODS: Databases from four university medical centers were searched for children presenting between 1992 and 2012 with spinal dysraphism and a Sprengel's deformity. CONCLUSION: The combination of spinal dysraphism and Sprengel's deformity is rare, and is associated with segmentation defects of the spine and ribs. Although the etiology of both spinal dysraphism and Sprengel's deformity remains unclear, all deformities of the spine, ribs, and shoulder might result from a common genetic defect affecting somitogenesis.


Subject(s)
Abnormalities, Multiple/diagnosis , Congenital Abnormalities/diagnosis , Scapula/abnormalities , Shoulder Joint/abnormalities , Spinal Dysraphism/diagnosis , Abnormalities, Multiple/embryology , Child , Child, Preschool , Clubfoot , Congenital Abnormalities/embryology , Female , Hemangioma , Humans , Infant , Infant, Newborn , Magnetic Resonance Imaging , Male , Meningomyelocele , Netherlands , Scapula/embryology , Shoulder/embryology , Shoulder Joint/embryology , Skin Neoplasms , Spinal Dysraphism/embryology , Spine/embryology , Syringomyelia , Tomography, X-Ray Computed
6.
Childs Nerv Syst ; 28(8): 1171-80, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22684477

ABSTRACT

INTRODUCTION: We analyze our preliminary experience using the PoleStar N20 mobile intraoperative MR (iMR) system as an adjunct for pediatric brain tumor resection. METHODS: We analyzed 11 resections in nine children between 1 month and 17 years old. After resection, we acquired iMR scans to detect residual tumor and update neuronavigation. We compared final iMR interpretation by the neurosurgeon with early postoperative MR interpretation by a neuroradiologist. RESULTS: Patient positioning was straightforward, and image quality (T1 7-min 4-mm sequences) sufficient in all cases. In five cases, contrast enhancement suspect for residual tumor was noted on initial postresection iMR images. In one case, a slight discrepancy with postoperative imaging after 3 months was no longer visible after 1 year. No serious perioperative adverse events related to the PoleStar N20 were encountered, except for transient shoulder pain in two. CONCLUSIONS: Using the PoleStar N20 iMR system is technically feasible and safe for both supra- and infratentorial tumor resections in children of all ages. Their small head and shoulders favor positioning in the magnet bore and allow the field of view to cover more than the area of primary interest, e.g., the ventricles in an infratentorial case. Standard surgical equipment may be used without significant limitations. In this series, the use of iMR leads to an increased extent of tumor resection in 45 % of cases. Correlation between iMR and early postoperative MR is excellent, provided image quality is optimal and interpretation is carefully done by someone sufficiently familiar with the system.


Subject(s)
Brain Neoplasms/surgery , Magnetic Resonance Imaging/methods , Monitoring, Intraoperative/methods , Neuronavigation/methods , Neurosurgical Procedures/methods , Adolescent , Child , Child, Preschool , Feasibility Studies , Female , Humans , Infant , Magnetic Resonance Imaging/instrumentation , Male , Medical Oncology/methods , Monitoring, Intraoperative/instrumentation , Neuronavigation/instrumentation , Neurosurgical Procedures/instrumentation , Pediatrics/methods
8.
Surg Neurol Int ; 2: 32, 2011 Mar 23.
Article in English | MEDLINE | ID: mdl-21541200

ABSTRACT

Bringing evidence to practice is a key issue in modern medicine. The key barrier to information searching is time. Clinical decision support systems (CDSS) can improve guideline adherence. Mounting evidence exists that mobile CDSS on handheld computers support physicians in delivering appropriate care to their patients. Subaxial cervical spine injuries account for almost half of spine injuries, and a majority of spinal cord injuries. A valid and reliable classification exists, including evidence-based treatment algorithms. A mobile CDSS on this topic was not yet available. We developed and tested an iPhone application based on the Subaxial Injury Classification (SLIC) and 5 evidence-based treatment algorithms for the surgical approach to subaxial cervical spine injuries. The application can be downloaded for free. Users are cordially invited to provide feedback in order to direct further development and evaluation of CDSS for traumatic lesions of the spinal column.

9.
Minim Invasive Neurosurg ; 53(4): 198-202, 2010 Aug.
Article in English | MEDLINE | ID: mdl-21132613

ABSTRACT

BACKGROUND: The purpose of this study is to demonstrate the added value of intraoperative MRI in treating secondary empty sella syndrome. CASE REPORT: We describe the case of a 66-year-old woman who was diagnosed with a prolactinoma stage IIIb. During treatment with cabergoline she presented with a secondary empty sella syndrome resulting in visual symptoms. We performed intraoperative MRI-guided packing of the secondary empty sella. We explain why this is useful in surgical treatment of secondary empty sella syndrome. CONCLUSION: Intraoperative MRI helps to achieve adequate sellar packing while avoiding insufficient packing as well as overpacking.


Subject(s)
Empty Sella Syndrome/pathology , Empty Sella Syndrome/surgery , Ergolines/adverse effects , Pituitary Neoplasms/drug therapy , Prolactinoma/drug therapy , Aged , Cabergoline , Empty Sella Syndrome/chemically induced , Ergolines/therapeutic use , Female , Humans , Magnetic Resonance Imaging , Treatment Outcome , Visual Fields/drug effects
10.
Pediatr Neurosurg ; 45(4): 281-90, 2009.
Article in English | MEDLINE | ID: mdl-19690444

ABSTRACT

Intraspinal dermoid and epidermoid tumors are two histopathological subtypes of cutaneous inclusion tumors of the spine. This classification is based on obsolete embryological knowledge. In fact, according to current embryology, both tumor types consist of ectodermal derivatives. Therefore, we hypothesized that dermoid and epidermoid tumors do not differ in clinical practice. To explore this hypothesis, we studied the clinical, radiological and intraoperative findings of 18 patients, and related these findings to the histopathological characteristics of the tumor. No differences were found between dermoid and epidermoid tumors regarding clinical presentation, radiological examination and outcome, while intraoperative diagnosis by the surgeon correlated with the histopathological diagnosis in only 8 of 18 cases. Therefore, the histopathological difference between intraspinal dermoid and epidermoid tumors is not important in clinical practice and should be avoided. A new nomenclature is proposed in which both tumor types are referred to as 'spinal cutaneous inclusion tumors'.


Subject(s)
Dermoid Cyst/diagnosis , Dermoid Cyst/surgery , Epidermal Cyst/diagnosis , Epidermal Cyst/surgery , Spinal Neoplasms/diagnosis , Spinal Neoplasms/surgery , Adult , Child , Child, Preschool , Cohort Studies , Female , Follow-Up Studies , Humans , Infant , Male , Middle Aged , Retrospective Studies
11.
Childs Nerv Syst ; 25(2): 191-7, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18618125

ABSTRACT

OBJECTS: In this study, a disjunction anomaly mimicking the spinal congenital dermal sinus (DS) is described. This anomaly is referred to as the dermal-sinus-like stalk. Dissimilarities between a true dermal sinus and a dermal-sinus-like stalk are discussed. CLINICAL MATERIAL: Three cases in which a spinal congenital dermal sinus was suspected are presented. A similar anatomical configuration, different from that of a dermal sinus, was found. All cases presented with a skin-covered dimple from which a solid tract was seen continuing intramedullary in two cases and intraspinally in one case. None of the patients presented with signs of infection or an associated dermoid-epidermoid tumor. Clinical, radiological, and surgical findings are discussed. A hypothesis is made on the pathological genesis of this malformation. CONCLUSION: A dermal-sinus-like stalk is a malformation similar to a spinal congenital dermal sinus but is not associated with DS-related complications. Despite important clinical, radiological, surgical, and histopathological differences, it is difficult to distinguish this malformation from a true DS based on clinical and radiological examination alone. Therefore, surgical intervention, at the time of diagnosis, is recommended in all cases.


Subject(s)
Spina Bifida Occulta/diagnosis , Spinal Cord Diseases/diagnosis , Diagnosis, Differential , Dura Mater/pathology , Humans , Infant, Newborn , Magnetic Resonance Imaging/methods , Spina Bifida Occulta/surgery , Spinal Cord Diseases/surgery , Spinal Dysraphism/pathology , Spinal Dysraphism/surgery , Treatment Outcome
12.
Acta Neurochir (Wien) ; 150(4): 403-5, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18278574

ABSTRACT

A 20 year old male patient who had been successfully treated for epilepsy with vagus nerve stimulation (VNS) for 7 years (50% seizure frequency reduction), had experienced multiple episodes of severe hoarseness, throat pain and impaired breathing during physical exercise. As malfunctioning of the pulse generator was suspected, it was decided to replace the device. During surgery, the pulse generator was found to have broken in two, due to an unstable connection between the battery subunit and the connector subunit. With a new pulse generator seizure frequency reduction was restored. No side effects occurred.


Subject(s)
Electric Stimulation Therapy/instrumentation , Epilepsies, Myoclonic/therapy , Equipment Failure , Vagus Nerve/physiopathology , Adult , Device Removal , Electric Impedance , Epilepsies, Myoclonic/physiopathology , Humans , Male , Martial Arts/injuries , Prosthesis Design , Thoracic Injuries/complications , Wounds, Nonpenetrating/complications
13.
Childs Nerv Syst ; 23(2): 151-5, 2007 Feb.
Article in English | MEDLINE | ID: mdl-16964518

ABSTRACT

OBJECTIVES: In infants less than 1 year of age, the value of endoscopic third ventriculostomy (ETV) is controversial. It is believed to cause more morbidity and to have higher failure rates. We analyzed our data enlarging the reported pool of ETV outcome in infants less than 1 year of age. MATERIALS AND METHODS: We performed 12 ETVs in ten patients younger than 1 year of age. All patients had predominant supratentorial hydrocephalus. We defined ETV success as a shunt-free follow-up of at least 12 months, however, allowing re-ETV. CONCLUSION: ETV should be considered as initial treatment and carries low morbidity in these infants. As the immune system rapidly matures, postponing shunt implantation for several months or even weeks would make an ETV procedure worthwhile. On the other hand, as success probability rapidly increases 4 months after birth, re-ETV should always be considered first.


Subject(s)
Endoscopes , Hydrocephalus/pathology , Hydrocephalus/surgery , Third Ventricle/surgery , Ventriculostomy/methods , Age Factors , Female , Humans , Infant , Infant, Newborn , Male , Treatment Outcome
14.
Childs Nerv Syst ; 22(10): 1307-15, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16708253

ABSTRACT

OBJECT: Cases of infected dermal sinus are scarce and detailed surgical anatomical descriptions are hardly found in literature. The clinical, radiological, and surgical findings in four cases of an infected dermal sinus located at the lower spine are presented to elucidate the pathological anatomical configuration. CLINICAL MATERIAL: The first case showed two dermal sinuses with a parallel course extra- and intradurally, ending in a confluence of cavities connected to the conus. In this case, as well as in the fourth case, the signs and symptoms were those of meningitis. The second case presented with meningitis and a subdural empyema, while the third case presented with an intradermoid-intramedullary abscess at the junction between the DS and the conus. This child probably showed signs and symptoms of conus involvement as early as during pregnancy. CONCLUSION: The anatomy of the nervous elements in this congenital anomaly is heavily disturbed, more particularly in case of infection, due to extensive arachnoidal scarring. The latter renders dissection laborious and recognition of anatomical details difficult, resulting in complete excision of a dermal sinus in less than half of the cases. Despite their variability in presentation, most cases of an infected dermal sinus show similar characteristic features.


Subject(s)
Spina Bifida Occulta/pathology , Spina Bifida Occulta/surgery , Spine/pathology , Spine/surgery , Female , Humans , Infant , Magnetic Resonance Imaging/methods , Male
15.
Childs Nerv Syst ; 21(12): 1020-4, 2005 Dec.
Article in English | MEDLINE | ID: mdl-15864598

ABSTRACT

METHODS: A patient is described in which a complete osteofibrotic dorsally implanted septum was found in combination with a split cord malformation in a single dural tube. This case cannot be explained using the widely used theory as proposed by Pang et al. [Pang D, Dias MS, Ahab-Barmada M (1992) Split cord malformation, part I: A unified theory of embryogenesis for double spinal cord malformations. Neurosurgery 31:451-480] but must be regarded as a combination of type I and II split cord malformation. RESULTS: The authors state that all types of split cord malformation can be reduced to a single derailment during development, with various degrees of severity. CONCLUSIONS: The configuration of the malformation is determined by the way the median parts of the mesoderm come to development. Type I and II split cord malformation are not distinct entities.


Subject(s)
Spina Bifida Occulta/diagnosis , Spinal Cord Diseases/diagnosis , Spinal Cord/abnormalities , Adolescent , Female , Humans , Magnetic Resonance Imaging/methods , Neurosurgical Procedures/methods , Spina Bifida Occulta/surgery , Spinal Cord/pathology , Spinal Cord Diseases/surgery , Tomography Scanners, X-Ray Computed
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