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1.
Neurosurg Focus ; 56(5): E8, 2024 May.
Article in English | MEDLINE | ID: mdl-38691866

ABSTRACT

OBJECTIVE: Skull base chordomas are rare, locally osseo-destructive lesions that present unique surgical challenges due to their involvement of critical neurovascular and bony structures at the craniovertebral junction (CVJ). Radical cytoreductive surgery improves survival but also carries significant morbidity, including the potential for occipitocervical (OC) destabilization requiring instrumented fusion. The published experience on OC fusion after CVJ chordoma resection is limited, and the anatomical predictors of OC instability in this context remain unclear. METHODS: PubMed and Embase were systematically searched according to the PRISMA guidelines for studies describing skull base chordoma resection and OC fusion. The search strategy was predefined in the authors' PROSPERO protocol (CRD42024496158). RESULTS: The systematic review identified 11 surgical case series describing 209 skull base chordoma patients and 116 (55.5%) who underwent OC instrumented fusion. Most patients underwent lateral approaches (n = 82) for chordoma resection, followed by midline (n = 48) and combined (n = 6) approaches. OC fusion was most often performed as a second-stage procedure (n = 53), followed by single-stage resection and fusion (n = 38). The degree of occipital condyle resection associated with OC fusion was described in 9 studies: total unilateral condylectomy reliably predicted OC fusion regardless of surgical approach. After lateral transcranial approaches, 4 studies cited at least 50%-70% unilateral condylectomy as necessitating OC fusion. After midline approaches-most frequently the endoscopic endonasal approach (EEA)-at least 75% unilateral condylectomy (or 50% bilateral condylectomy) led to OC fusion. Additionally, resection of the medial atlantoaxial joint elements (the C1 anterior arch and tip of the dens), usually via EEA, reliably necessitated OC fusion. Two illustrative cases are subsequently presented, further exemplifying how the extent of CVJ bony elements removed via EEA to achieve complete chordoma resection predicts the need for OC fusion. CONCLUSIONS: Unilateral total condylectomy, 50% bilateral condylectomy, and resection of the medial atlantoaxial joint elements were the most frequently described independent predictors of OC fusion in skull base chordoma resection. Additionally, consistent with the occipital condyle harboring a significantly thicker joint capsule at its posterolateral aspect, an anterior midline approach seems to tolerate a greater degree of condylar resection (75%) than a lateral transcranial approach (50%-70%) prior to generating OC instability.


Subject(s)
Cervical Vertebrae , Chordoma , Occipital Bone , Skull Base Neoplasms , Spinal Fusion , Humans , Chordoma/surgery , Chordoma/diagnostic imaging , Skull Base Neoplasms/surgery , Skull Base Neoplasms/diagnostic imaging , Occipital Bone/surgery , Occipital Bone/diagnostic imaging , Spinal Fusion/methods , Cervical Vertebrae/surgery , Cervical Vertebrae/diagnostic imaging , Female , Atlanto-Occipital Joint/surgery , Atlanto-Occipital Joint/diagnostic imaging , Male , Adult , Middle Aged
2.
Neurosurg Rev ; 47(1): 189, 2024 Apr 25.
Article in English | MEDLINE | ID: mdl-38658425

ABSTRACT

BACKGROUND: Pial arteriovenous fistulas (pAVFs) are rare vascular malformations characterized by high-flow arteriovenous shunting involving a cortical arterial supply directly connecting to venous drainage without an intermediate nidus. Dural arteriovenous fistulas (dAVFs) can infrequently involve additional pial feeders which can introduce higher flow shunting and increase the associated treatment risk. In the posterior fossa, arteriovenous fistula (AVF) angioarchitecture tends to be particularly complex, involving either multiple arterial feeders-sometimes from both dural and pial origins-or small caliber vessels that are difficult to catheterize and tend to be intimately involved with functionally critical brainstem or upper cervical cord structures. Given their rarity, published experience on microsurgical or endovascular treatment strategies for posterior fossa pAVFs and dAVFs with pial supply remains limited. METHODS: Retrospective chart review from 2019-2023 at a high-volume center identified six adult patients with posterior fossa pAVFs that were unable to be fully treated endovascularly and required microsurgical disconnection. These cases are individually presented with a technical emphasis and supported by comprehensive angiographic and intraoperative images. RESULTS: One vermian (Case 1), three cerebellopontine angle (Cases 2-4) and two craniovertebral junction (Cases 5-6) posterior fossa pAVFs or dAVFs with pial supply are presented. Three cases involved mixed dural and pial arterial supply (Cases 1, 4, and 6), and one case involved a concomitant microAVM (Case 2). Endovascular embolization was attempted in four cases (Cases 1-4): The small caliber and tortuosity of the main arterial feeder prevented catheterization in two cases (Cases 1 and 3). Partial embolization was achieved in Cases 2 and 4. In Cases 5 and 6, involvement of the lateral spinal artery or anterior spinal artery created a prohibitive risk for endovascular embolization, and surgical clip ligation was pursued as primary management. In all cases, microsurgical disconnection resulted in complete fistula obliteration without evidence of recurrence on follow-up imaging (mean follow-up 27.1 months). Two patients experienced persistent post-treatment sensory deficits without significant functional limitation. CONCLUSIONS: This illustrative case series highlights the technical difficulties and anatomical limitations of endovascular management for posterior fossa pAVFs and dAVFs with pial supply and emphasizes the relative safety and utility of microsurgical disconnection in this context. A combined approach involving partial preoperative embolization-when the angioarchitecture is permissive-can potentially decrease surgical morbidity. Larger studies are warranted to better define the role for multimodal intervention and to assess associated long-term AVF obliteration rates in the setting of pial arterial involvement.


Subject(s)
Central Nervous System Vascular Malformations , Pia Mater , Humans , Male , Female , Middle Aged , Central Nervous System Vascular Malformations/surgery , Aged , Pia Mater/blood supply , Pia Mater/surgery , Retrospective Studies , Adult , Arteriovenous Fistula/surgery , Cranial Fossa, Posterior/surgery , Neurosurgical Procedures/methods , Embolization, Therapeutic/methods , Intracranial Arteriovenous Malformations/surgery
4.
Muscle Nerve ; 44(6): 873-6, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22102456

ABSTRACT

INTRODUCTION: In this study we sought to evaluate the reproducibility of sensory nerve conduction studies (NCS) using ultrasound-guided needle positioning (USNP). METHODS: Orthodromic NCS of the sural nerve using needle electrodes with USNP as well as surface electrodes were conducted twice in 20 healthy volunteers. RESULTS: The mean sensory nerve action potential (SNAP) amplitude in the initial examination was 39.5 µV using needle electrodes with USNP, and 12.5 µV using surface electrodes (P < 0.0001). The mean SNAP amplitude in the follow-up examination was 39.2 µV using needle electrodes with USNP, and 12.4 µV using surface electrodes (P < 0.0001). The mean intraindividual change in SNAP amplitude (test-retest) was 21.2% using needle electrodes with USNP, and 24.8% using surface electrodes (P = 0.6). CONCLUSIONS: Sensory NCS of the sural nerve using needle electrodes with USNP have reliable test-retest reproducibility and yield greater SNAP amplitudes than sensory NCS using surface electrodes.


Subject(s)
Neural Conduction/physiology , Sural Nerve/diagnostic imaging , Ultrasonography, Interventional/standards , Action Potentials/physiology , Adult , Electrodes/standards , Female , Humans , Male , Reproducibility of Results , Sensory Receptor Cells/diagnostic imaging , Ultrasonography, Interventional/methods , Young Adult
5.
Biomaterials ; 28(16): 2677-86, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17321590

ABSTRACT

Osteogenic agents, such as bone morphogenetic protein-2 (BMP-2), can stimulate the degradation as well as the formation of bone. Hence, they could impair the osteoconductivity of functionalized implant surfaces. We assessed the effects of BMP-2 and its mode of delivery on the osteoconductivity of dental implants with either a naked titanium surface or a calcium-phosphate-coated one. The naked titanium surface bore adsorbed BMP-2, whilst the coated one bore incorporated, adsorbed, or incorporated and adsorbed BMP-2. The implants were inserted into the maxillae of adult miniature pigs. The volume of bone deposited within a defined "osteoconductive" (peri-implant) space, and bone coverage of the implant surface delimiting this space, were estimated morphometrically 1-3 weeks later. After 3 weeks, the volume of bone deposited within the osteoconductive space was highest for coated and uncoated implants bearing no BMP-2, followed by coated implants bearing incorporated BMP-2; it was lowest for coated implants bearing only adsorbed BMP-2. Bone-interface coverage was highest for coated implants bearing no BMP-2, followed by coated implants bearing either incorporated, or incorporated and adsorbed BMP-2; it was lowest for uncoated implants bearing adsorbed BMP-2. Hence, the osteoconductivity of implant surfaces can be significantly modulated by BMP-2 and its mode of delivery.


Subject(s)
Bone Morphogenetic Proteins/pharmacology , Bone Regeneration/physiology , Dental Implants , Osseointegration/physiology , Transforming Growth Factor beta/pharmacology , Animals , Bone Morphogenetic Protein 2 , Bone Morphogenetic Proteins/administration & dosage , Bone Morphogenetic Proteins/metabolism , Calcium Phosphates/metabolism , Coated Materials, Biocompatible/chemistry , Coated Materials, Biocompatible/metabolism , Dental Implantation, Endosseous , Implants, Experimental , Materials Testing , Surface Properties , Swine , Titanium/metabolism , Transforming Growth Factor beta/administration & dosage , Transforming Growth Factor beta/metabolism
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