ABSTRACT
BACKGROUND: Ventriculoperitoneal (VP) shunts are commonly used for managing hydrocephalus, with mechanical dysfunction being the most common cause of complications that require revision. A VP shunt placed using a real-time three-dimensional (3D) robotic C-arm navigation system may have better outcomes and fewer complications. METHODS: In this technical note, we introduced the workflow of the use of the real-time 3D robotic C-arm navigation system for ventriculoperitoneal shunting. CONCLUSION: The real-time 3D robotic C-arm can provide a more precise approach to the target. Furthermore, this technique may lower the risk of complications and increase the success rate of shunt placements.
Subject(s)
Hydrocephalus , Imaging, Three-Dimensional , Robotic Surgical Procedures , Ventriculoperitoneal Shunt , Ventriculoperitoneal Shunt/methods , Ventriculoperitoneal Shunt/instrumentation , Humans , Hydrocephalus/surgery , Robotic Surgical Procedures/methods , Robotic Surgical Procedures/instrumentation , Imaging, Three-Dimensional/methods , Surgery, Computer-Assisted/methodsABSTRACT
BACKGROUND: Failed back surgery syndrome (FBSS) is a general term for persistent postoperative back pain with or without accompanying radicular pain. FBSS may present as chronic facet joint pain. METHODS: We introduced full endoscopic lumbar rhizotomy for patients suffering from facet joint pain due to FBSS. Facet joint block was introduced into the facet joint to determine whether pain improved after the injection. CONCLUSION: With full endoscopic lumbar rhizotomy, the surgeon can identify the regions involved more clearly and directly. Although it is an invasive procedure, it provides a more effective and safe treatment for patients with FBSS-related facet joint pain.
Subject(s)
Bone Diseases , Failed Back Surgery Syndrome , Low Back Pain , Zygapophyseal Joint , Arthralgia/surgery , Bone Diseases/surgery , Failed Back Surgery Syndrome/surgery , Humans , Low Back Pain/surgery , Lumbar Vertebrae/surgery , Rhizotomy/methods , Zygapophyseal Joint/diagnostic imaging , Zygapophyseal Joint/surgeryABSTRACT
Vascular injury is one of the potential complications of percutaneous transpedicular screws fixation. Carefully review the vascular anatomy preoperatively is important. Once unexpected low blood pressure or anemia occurs, vascular injury should be taken into consideration.
Subject(s)
Aneurysm, False , Pedicle Screws , Spinal Fusion , Vascular System Injuries , Humans , Bone Screws/adverse effects , Aneurysm, False/diagnostic imaging , Aneurysm, False/etiology , Vascular System Injuries/diagnostic imaging , Vascular System Injuries/etiology , Treatment Outcome , Arteries , Hematoma/diagnostic imaging , Hematoma/etiology , Lumbar Vertebrae/surgeryABSTRACT
BACKGROUND: In terms of melanoma, recent advances have been made in target therapies and immune checkpoint inhibitors, but durable remission is rare. Ganoderma immunomodulatory proteins (GMI) induce a cytotoxic effect in cancer cells via autophagy. However, the role of GMI in melanoma is not clear. PURPOSE: The aims of this study are to investigate the inhibiting effects of GMI combined with chidamide on survival and metastases of melanoma cells via integrin-related signaling pathway and to propose strategies for combining GMI and chidamide using animal model. METHODS: Cell viability was measured by cell CCK-8. The activities of apoptosis- and migration-related proteins were detected on Western blot. Flow cytometry was used to analyze cell cycle distribution and sub-G1 fraction in treated melanoma cells. To evaluate the activity of combination GMI and chidamide treatment, an in vivo anti-tumor metastasis study was performed. RESULTS: GMI combined with chidamide additively induced apoptosis. GMI inhibited the expressions of Integrin α5, αV, ß1, and ß3. The level of p-FAK was inhibited by GMI. Combination treatment of GMI and chidamide decreased survivin and increased cleaved caspase-7 and LC3 II/I. Integrin-αV overexpression activated p-FAK pathways in A375.S2 cells. GMI significantly inhibited cell growth and migration of A375.S2 cells on wound healing assay. In vivo, GMI combined with chidamide suppressed distal tumor metastasis. CONCLUSION: GMI inhibits the migration and growth of melanoma cells via integrin-related signaling pathway. GMI and chidamide induces apoptosis. In vivo, GMI and chidamide additively reduce distant metastases. GMI and chidamide are potential immunotherapeutic adjuvant for metastatic melanoma.