Endoscopic Neurological Surgery David F Jimenez
INDEX
Page numbers followed by f refer to figure.
A
Abscesses 78
Absorbable galeal suture 44
Adson's forceps 141, 143
Alkaline phosphatase 60
Anesthesia
general 54, 73, 81
principles of 26
local 140
regional 140
Anesthetic induction 142
Anesthetic management 140
Antebrachial fascia 143, 144f
Arachnoid cyst 34, 60, 67, 69f, 70f, 153
enlarging midline 110f
surgical procedure 62
treatment options 62
wall 68f, 70f
Arachnoid cystic contents, analysis of 153
Arachnoid knife 135f
Arachnoid membrane 135f
after fenestration of 66f
medial 65f
Arachnoid villi 34
Arachnoidal trabeculations 44f
Arrhythmia 164
Arterial vessel loop 136f, 137f
Arteries 128
Articulated nonpneumatic holders, rigid 20
Autonomic dysfunctions 53
B
Balloon
catheters 24, 25f
rhizotomy 129
Basal veins 68f
Basilar artery 45f
tip 32f
top of 11f
tortuosity 125
Bier block 140
Bimanual microdissection, performing 6
Biopsy
forceps 21, 56f, 119f
types of 22f
intraventricular 88
tumors 115
lesion 119f
less bloody 120f
Bipolar diathermy 115
Bipolar electrode 23f
Bleeding, intraoperative 125
Blood vessels 123f
Blunt probe 43f
Body
of caudate 10f
of frontal horns 9f
of lateral ventricle 12
Bozzini's invention 2
Brain 100f, 104f
cavities 3
lab system 100f, 105
lab's instrument calibration matrix 108f
retractor, small 136f
ribbon 70f
retractor 70f
ventricular system 8
Brainstem 67f, 135
evoked response 138
tumor of 34
Brittle ligaments 146f
Bulging lamina terminalis 120f
Burr hole 76f, 83f, 84f, 134f
anterior 87f
placement
appropriate 124
lateral 32f
single 133f
C
Cannula
distal end of 145f
edges of 146f
Cannulate frontal horn 54
Carpal tunnel 143f, 144f
complete release of 147f
decompressions 6
release 141f
syndrome 140
Catheters, types of 19f
Caudate nucleus
head on
left side 10f
right side 10f
injure head of 81f
Cauterized shrunken capsule 87f
Cavum septum pellucidum 49, 51f, 58f
asymptomatic 50f
cysts, symptomatic midline 49
Cavum vergae
decompression of 58f
enlarged 58f
Cerebellar access 32
Cerebellar artery
posterior inferior 15f
superior 45f
Cerebellar infarct 34
Cerebellopontine angle 129
Cerebellum 67f, 68f
compression of 68f
Cerebral artery
anterior 11f
middle 65f, 66f, 70f
posterior 45f
Cerebrospinal fluid 3, 27, 34, 51, 60, 80, 90, 113, 149
absorption
abnormal 92f
normal 92f
conduits 67
drainage 97
fistula 166
leakage 164
liquorrhea 166
over drainage 90
Charged-coupling devices 6
Choreoathetosis 152
Choroid plexectomies 4
Choroid plexus 10f12f, 15f, 34, 79, 81, 84f86f, 91, 118f, 150, 151
bilateral 40
cauterization 38, 39
cysts 149151, 151f, 159f
epithelium 150
Cochleovestibular nerve compression syndrome 167
Collapsed balloon 44f
Colloid cyst 28, 34, 79, 79f, 80, 80f, 81f, 84f, 87f, 88, 149
at foramen of Monro 84f
column of right fornix 85f
endoscopic management of 87
large 79
resection of 85f
Communicating artery, anterior 11f
Communicating hydrocephalus 35, 96f
Communication system 103
Consciousness, loss of 53
Convexity arachnoid cysts 66
Cook's monopolar electrode 22
Coronal brain section 50f
Coronal magnetic resonance imaging 55f
Corpus callosum 8, 10f, 13
rostrum of 10f
Cranial access 73
Cranial computed tomography 50
Cranial nerve
fifth 136f
IX, lower 136f
Cranial pressure, increased 164
Cranial stabilization 133f
Craniosynostosis 6
Craniotomy 151
Cyst 30, 70f, 123f, 166
after full fulguration of 159f
collapsed walls of 101f
complete resection of 87f
complex intraventricular 105f
contents, after removal of 123f
decompression of 101f, 157f
deep midline 110f, 111f
edges of 158f
fenestration of 100f, 155f
fluid 62
green liquid material inside 123f
interior 161f
intraventricular 149, 154f
laser fenestration of 157f
large 100f
location 60
membranes 150
multiple 111f
recurrence 152
removal 124f
resection, complete 86f
types of 149
Cyst wall 60, 84f, 84f, 123f, 155f, 156f, 160f
fenestration of deep 111f
intervening 111f
laser coagulation of 111f
thick 110f
vessels 160f
Cystic cavity 151
Cytokeratins 149
D
Dandy years 4
Dandy-Walker malformation 34
Deflated balloon 156f
Degenerative spine disease 6
Deliver gold laser energy 25f
Delivering coagulating energy 120f
Desormeaux 2
device 2
endoscope, operation of 3f
Diabetes insipidus 164
Disposable hook
blade 146f
knife 141
Dissect basal arachnoid membrane 65f
Drowsiness 165
E
Ear 104f
Ectatic vertebral artery 132f, 136f
Electrodes 22
Encephalocele 34
Endodermal
elements 80
origin 149
Endoscope 4, 16
channel of 156f
disposable 18
first 2
holders 20
types of 20
retractor, simpler 28f
smaller 18
trajectory of 31f, 117f
Endoscope-controlled microsurgery 6
Endoscopic approaches 130
Endoscopic carpal tunnel release 140
Endoscopic colloid cyst resection 28f, 83f
Endoscopic cyst fenestration 94, 101f
Endoscopic cystoventriculostomy 62
Endoscopic fenestration 52, 63f, 66f
first 95
Endoscopic instruments 21
Endoscopic investigation 7
Endoscopic management, complications for 125
Endoscopic microvascular decompression 128
clinical presentation 131
patient positioning 132
surgical procedure 132
Endoscopic neuronavigation 103
Endoscopic neurosurgery, complications with 164
Endoscopic prehistory 1
Endoscopic resection of colloid cysts 79
Endoscopic systems 16
large array of 17
Endoscopic techniques 78, 96, 125
Endoscopic technology 5
contemporary 7
Endoscopic third ventriculostomy 6, 34, 37, 38, 165
complications 45
efficacy 36
history of 35
success score 46
Endoscopic tools 166
first 2f
Endoscopic treatment 49, 88
Endoscopic tumor biopsy 116
and resection 113
Endoscopic vascular decompression 129
Endoscopic ventricular
anatomy 8
surgery 15
Endoscopy, image-guided 111f
Endotrac endoscopic instruments 141f
Endotracheal intubation 73
Enterobacter cloaca 98
Ependymal arachnoid cysts 90
Ependymal cyst 149, 152
Epidural
abscess 76f
frontal lesion, right 78f
hematoma 166
lesions 73
Epilepsy 92, 167
focal 150
Epithelial debris 149
Epithelial membrane antigen 149
Excise brain tumors 24
F
Fenestrated arachnoid cyst 71f
Fenestrated wall 156f
Fenestration 70f
into occipital horn 157f
primary 156f
Fevers 97f
Fiber
fascial 143
multiple light 18
optical 19f
optics 5
Fibroglial septa, formation of 93
Fibrous cyst wall 160f
Flexible endoscope 18, 21f, 74f
Floor of fourth ventricle 15f
Fluid attenuation inversion recovery 79f, 80f
Fogarty catheter 66, 156f, 160f, 166
Foramen of magendie, fastigium to 14
Foramen of Monro 8, 10f, 118f
demonstrates, level of 79f
located near 151f
Forcep's cups 21
Forehead incision, superb healing of 119f
Fornices 11f
Fornix 10f, 118f
column of 84f, 86f, 159f
Fossa
cysts, middle 62
middle 67
Fourth ventricle 14
Frame-based stereotactic systems 103
Frazier suction tube 84f
Frazier type suction 83
Frontal arachnoid cyst, large 66f
Frontal epidural lesions, endoscopic management of 73
Frontal horn 8, 29f, 143f
access 27, 28f
demonstrates, right 119f
enlargement of 57f
right 10f, 84f
tip of 118f
Frontal hypointense lesion, right 75f
Frontal lobe syndrome 66f
Fulgirized debris, remove 56f
G
GAAB system 28f
Gadolinium, intravenous injection of 117f
Gait disturbance 150
Gastroenterologists 18
Gastrointestinal tract 3
Gently holds cerebellar hemisphere 136f
Genu of corpus callosum 10f, 41f, 58f, 119f
anterior to 66f
Germ cell tumors 114
Germinoma, biopsy of 120f
Glial cell tumors 114
Glial tumors 114
Gliotic neuropil 152
Glycerol injections 129
Gold laser 24
delivery system 24f
microfiber 70f
Gram-negative organisms 97f
Grasping forceps 22, 123f, 156f
types of 22f
Guyon's canal 142, 143
H
Hamartomas 30
Hand and forearm 143f
Head
enlargement 150
injury 90
of caudate 10f, 41f
in frontal horn 10f
Headache 91, 100, 150
chronic 86
Hearing loss 137
Hematoma 78, 164
intraventricular 34
risk of postoperative 147f
Hemianopia 164
Hemiballismus 152
Hemifacial spasm 167
Hemiparesis 164
Hemorrhage
intraoperative 164
intraventricular 90, 167
severity of 91
Hemostasis, achieving 6
Hopkins’ endoscopes 16
Hopkins’ fiberscope 5
Human central system, unique nature of 16
Hydranencephalic hydrocephalus 40
Hydrocephalic symptoms 150
Hydrocephalus 10f, 28f
acute 53
chronic 35
classification of 34
complex
multiloculated 92f
uniloculated 91, 92f
etiologies of 36
indicative of 121f
loculated 90
longstanding 42f
pathology of 34
treatment of 34
type of 90
Hygroma 164
Hyperdense lesion 121f
Hyperkalemia 165
Hyperphagia 165
Hypertension 164
Hypoglossal trigone 15f
Hyponatremia 165
Hypothalamic autonomic system 49
Hypothalamic walls 32f
medial 42f
Hypothalamus 165
medial 11f
wall of 120f
I
Idiopathic carpal tunnel syndrome
signs of 140
symptoms of 140
Incision 73, 82
small 143f
Inexperienced endoscopist 30
Inflammatory processes 90
Inflated balloon, fully 156f
Infratentorial arachnoid cysts 67
Infundibular recess 41f43f
Intracerebral hemorrhage 167
Intracranial
cysts 6
pressure 27, 41, 62
surgery 90
Intraventricular arachnoid cysts 153
classification 153
Intraventricular cyst
decompression of 156f
large 154f
midline 159f
Intraventricular tumors 6, 113
Ipsilateral frontal horn 64f
Ipsilateral temporal lobe 69f
J
Jannetta's proposal, artistic representation of 128f
Jannetta's surgical procedure 128f
Juxtraventricular region 152
K
Kaplan's cardinal line 142, 142f, 143
Kerrison rongeur 74f
Kocher's point 30, 81
of entrance 54
L
Lamina terminalis 11f, 32f
Laser 23
Left fornix, column of 87f
Lesion
frontal location of 74f
type of 150
LOTTA endoscope 18f
M
Magnetic resonance ventriculography 93
Mammillary body 8, 11f, 32f, 41f, 42f
right 12f
Mayfield clamp 107f
Mayfield cranial fixation clamp 105f
Mayfield head
clamp 133f
holder 41, 105
Meckel's cave 129
Medtronic stealthstation systems 105
Medulla 136f
Mesencephalon 11, 12f
Metastatic germinoma 119f
Microvascular decompression 128, 129, 134, 138, 166
complications 137
Midbrain 11
Middle fossa arachnoid cyst, large right 64f
Minimally invasive neurosurgery 1
Mitaka pneumatic endoscope arm 27f
Monopolar electrodes, types of 23f
Mucicarmine 149
Multiloculated hydrocephalus 90, 91, 93, 94
etiology for 90
physiologically complex 91
simple 91, 92f
Musculature weakness, thenar 140
N
Nausea 100, 150
Needle biopsies 167
Neodymium-doped yttrium-aluminum-garnet 23
laser 23, 24
Neonatal bacterial meningitis 90
Neonatal meningitis 90
Nerve
compression, median 140
palsy 164
transient oculomotor 166
transient trochlear 166
Neural injury 55f
Neural ventricular structures 155f
Neuralgia, relief of 128f
Neuroendoscopic biopsy, intraventricular 113
Neuroendoscopic instruments 113
Neuroendoscopic procedures 35, 109
Neuroendoscopic techniques 96, 161
Neuroendoscopic tools 165
Neuroendoscopy 1, 6, 7, 109111, 115, 125
emerges 3
history of 1
intraoperative image-guided navigation in 103
rebirth of 5
Neuroepithelial cyst 149, 153
Neurologic
complications 165
deficit 152
examination 100
Neurological deficit, permanent 167
Neuromas 140
Neuronavigation 104f
monitor, snapshot of 117f
Neuropen neuroendoscope 19f
Neuropsychiatric disorders 53
Neurosurgical brain tissue procedures 24
Nitze and modern endoscope 3
Nitze's concept 3
Nitze's design 5
Nitze's endoscope 5
Nitze's telescoping design 5
Nitze-Leiter cystoscope, prototype of 3f
Nonabsorbable dermal suture 44
Non-neoplastic masses 114
Nose 104f
Numerous pinocytotic vesicles 153
O
Obstructive hydrocephalus 115
Occipital horn 11f
access 31
and trigone 13
right 14f
Oculomotor nerve, left 42f
OI handypro endoscope 17f
OI system 27f
Ophthalmic ointment, lubricating 73
Optic chiasm 11f, 32f, 41f
posterior aspect of 10f
Optimized visualization, maintaining 6
Ostomy
complete delineation of 56f
of septal leaflet 56f
P
Pacchionian granulations 34
Pain, characterization of 131
Palmaris longus, tendon of 142, 142f
Papilledema 85, 156
Parinaud syndrome 164
Pediatric populations 62
Peel-away cannula 86f
Periodic acid-Schiff stains 149
Petrous bones 135f
canals, enter 135f
Petrus pyramid 134f
Phalen's sign, positive 140
Pineal gland 12f
Pineal parenchymal tumors 114
Pineal recess 12f
Pineal region tumor 114
type of 114
Pineal tumor 34
Pineoblastoma 118
Pituitary adenoma 104
Pneumatic holder 20
Pneumocephalus 125
Pneumoventricolography technique 4
Pons 11f
Poor appetite 100
Populations, adult 62
Posthemorrhagic hydrocephalus 91
Postmeningitic cases 91
Postmeningitic hydrocephalus 40
Potassium-titanyl-phosphate
crystal 23
laser 23
Povidone-iodine scrub 141
Pseudoaneurysm formation 147
Psychiatric
manifestations 152
problems 53
symptoms 79, 152
Puncturing cyst 161
R
Radiosurgery 129
Registered endoscope 108f
Resect colloid cysts 80f
Residual tumor apoplexy, postoperative 125
Respiratory dysfunction 164
Retractable monopolar system 22
Reveals cysts 151
Right ventricular system, communication of 99f
Rigid endoscope 16, 27f
GAAB system 17f
Rigid rod-lens system 7
Rod-lens system 5, 16
S
Scalp incision 26
Schizophrenia 152
Scissors 22
types of 23f
Seizure 53, 166
disorder, chronic 167
Self-focusing optical lens 5
Selfoc lens 5
technology 6
Semirigid holders 20
Sensory
branches, superficial 143
rhizotomy, partial 129
Septal vein 83, 86f, 118f, 159f
Septated hydrocephalus 91
Septum pellucidotomies 28
Septum pellucidum 10f, 49, 86f, 87f
absence of 11f
cyst of 50, 53
leaflets of 49f
Shunt
implantation 37
infection 90
treatment 37
Shunt-related infection 93
Silica glass 18
Skin incision 73
Skull base endoscopy 6
Spine 104f
Spongioblastic cells, differentiation of 152
Stereotaxy 103
Striae terminalis 15f
Stryker's mask 108f
Stryker's system 108f
Subcortical nuclei 93
Subdural hematoma 166
Subdural hygroma 166
Subtemporal transtentorial route 128
Sulcus, median 15f
Suprasellar arachnoid cysts 28
Supratentorial cerebral parenchyma 152
Surgical procedure 40
burr hole and dural opening 41
patient positioning 41
preoperative preparation 40
ventricular access 41
Surgically complex multiloculated hydrocephalus 91
Sylvius, aqueduct of 12f, 123f
Symptomatic arachnoid cysts, treatment of 67
Syndrome of inappropriate antidiuretic hormone secretion 164
Synovial elevator 141, 144f
T
Tamponade bleeding 25f
Tectal tumor 34
Teflon pledget 136f
Tela choroidea, superior layer of 11
Temporal arachnoid cyst 65f
Temporal branches, primary 70f
Temporal fossa, middle 70f
Temporal gyrus, middle 33, 33f
Temporal horn 13, 15f
access 33
Temporal lobe 70f
adjacent 60
inferior 69f
Temporal ventricular horns 121f
Tenotomy scissors 141
pair of 144f
Thalamic tubercle, anterior 10f, 41f, 42f
Thalamostriate vein 41f, 42f, 118f
on right side 11f
Thalamus 10f, 11f
left 12f
Thicker inner wall, remove 123f
Third ventricle 12f, 123f
anterior 8, 10f, 30f, 41f, 161f
floor of anterior 11f
posterior 10, 11f, 123f
wall of 12f
structures, posterior 31f
Third ventricular access
anterior 30
posterior 29
Third ventricular cyst 123f
Third ventricular floor 43f
Third ventriculostomy 30f, 34, 118f
complications 45
Throat 104f
Tinel's sign, positive 140
Transverse carpal ligament 140, 143f, 145f147f
cutting 146f
Trigeminal cranial nerve 136f
Trigeminal nerve 135f, 136, 136f, 137f
decompressing 128f
left 133f
Trigeminal neuralgia 128, 128f, 131, 167
left-sided 136f
Trochlear nerve palsy 137
Tuber cinereum 11f, 41f
Tumor 30, 128
biopsy 21, 166
dissemination 125
highly vascularized 115
larger 115
medial wall of 120f
originating 114
posterior 125
recurrence, evidence of 85
U
Ulnar nerve decompressions 7
Under focal pressure 57f
Uniloculated hydrocephalus, simple 91, 91f
V
Vagal trigone 15f
Vein 128
of Galen 68f
Venous
hemorrhage 166
structure 135f
Venous/arterial hemorrhage 164
Ventricular anatomy, anatomy of 14
Ventricular catheter 160f
tip of 19f
Ventricular collapse 125
Ventricular compartmentalization 91
Ventricular dilation, acute 154f
Ventricular neuroendoscopy 113
Ventricular septations 91
Ventricular system 8, 161f
approaches to 26
left 80f
posterior lateral 11f
right 95f
tumor of 113
Ventriculofibroscope 6
Ventriculogram, intraoperative 95f
Ventriculoscopy 113
Ventriculostomy
location of 43f
patent third 45f
technique 42
Vertebral artery 136f
Vessel loop 137f
Viscous center 79
Vomiting 100, 150
W
Washboard 143, 146
Wireless soft-touch pointer for registration 105f
Wound infection 164
Y
Yttrium aluminum garnet laser 159f, 160f
fiber 119f, 120f, 123f, 159f
Z
Zygomatic arch 62
×
Chapter Notes

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History of NeuroendoscopyCHAPTER 1

David N Garza,
David F Jimenez
 
INTRODUCTION
Knowing historical facts relating to a specific area, provides the reader with a better understanding and appreciation for the efforts undertaken by previous pioneers. In this introductory chapter, we wish to provide the reader with a glimpse to the past of Neuroendoscopy and how the discipline evolved. Key technical advances made by a few and courageous clinicians/surgeons and their disciples have led to our current state of affairs where we can provide our patients with minimally invasive, safe and successful surgical options.
 
ENDOSCOPIC PREHISTORY
Endoscopy has existed, albeit in a crude form, since the time of the ancient Egyptians around 1550 BC.1 Their practice of transnasal excerebration involved the use of hook-shaped rods that helped them peer inside the human nasal cavity and extract cerebral components during mummification. This technique has been postulated by some to be the earliest example of minimally invasive neurosurgery.2 The approach used by the ancient Egyptians (as depicted by Herodotus in his book Histories) is surprisingly similar to modern-day transphenoidal surgery.1
The next phase of endoscopic evolution deals with the development of speculum technology. The Talmud, which dates back to 1300 BC, contains a description of a speculum precursor that was used to examine Jewish women in order to determine their eligibility to participate in sexual intercourse.2 Specula were also used by physicians like Hippocrates between 460 BC and 370 BC.3 Excavations conducted in Dion, a village located in northern Greece, uncovered bronze instruments that bear a resemblance to the specula used by modern physicians. The instruments from Dion date back to approximately 200 BC; tools of similar construction from around 70 AD have also been recovered from the ruins of Pompei (Fig. 1).
Speculum implementation was advanced by Albukasim of Cordoba (936–1013 AD), an Arabian physician who used reflected ambient light during his examinations to aid visibility.3 In 1585, Giulio Cesare Aranzi improved on this technique by using closed tubes and mirrors to reflect ambient light into the nasal cavity.3 This eventually paved the way for the “Godfather” of modern endoscopy, Philipp Bozzini (1773–1809), whose “Lichtleiter” or “light guide” used a candle as an external light source along with a set of reflective mirrors on one end of the device and various examining tubes that could be fitted to the opposite end.2
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Fig. 1: Ancient Greek specula recovered from the ruins of Pompei, dated around 70 AD.Source: Reprinted with permission from Elsevier. Abd-El-Barr MM, Cohen AR. The origin and evolution of neuroendoscopy. Childs Nerv Syst. 2013;29:727-37.
2
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Fig. 2: One of the first endoscopic tools: Philipp Bozzini's “Lichtleiter” or light guide, 1805.Source: Reprinted with permission from Elsevier. Edmonson JM. History of the instruments for gastrointestinal endoscopy. Gastrointest Endosc. 1991;37:S27-56.
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Fig. 3: Illustration depicting Antonin Desormeaux's endoscope. The kerosene lamp at bottom of device burned alcohol and turpentine to fuel illumination.
 
THE FIRST ENDOSCOPES
Bozzini was hopeful that his endoscopic device (Fig. 2) could be used to visualize body cavities, but he encountered some resistance in the process of trying to legitimize his invention. Although many ecclesiastical prohibitions banning the exploration of human anatomy had been lifted since the Renaissance, the church's influence was still not totally withdrawn from the activities of the scientific community. Church officials halted the progress of Bozzini's invention during its second round of testing when they withheld their approval for the Lichtleiter to be used on live patients.2 Because of petty rivalries already in place, the device was ridiculed by the Alert Faculty of the University of Vienna and subsequently rejected.2 Bozzini's work was not appreciated in its time, but his three part design principle of a light source, reflective mirrors, and an investigative eye piece remains a staple guide for the construction of endoscopic technology even within our modern age.
Despite the widespread opposition against Bozzini's invention, there were two individuals who followed his model and tried to improve his work: Pierre Salomon Segalas and John D Fisher. Their endoscopic instruments resembled the Lichtleiter through the incorporation of a light source, a reflective surface, and a graduated series of tubular specula.4 Fisher added a double convex lens to sharpen and enlarge the image produced by his endoscope while Segalas modified his scope to visualize bladder stones and then crush them with a lithotrite.4 Segalas is also noteworthy because his guidance informed the work of the individual responsible for the next major innovative leap in endoscopic design: French urologist Antonin Desormeaux.4
Desormeaux is credited with several “firsts” in endoscopic history. In 1853, he designed a scope with a kerosene lamp that burned alcohol and turpentine (Figs. 3 and 4) coupled with a 45° mirror that could reflect that lamp's light into different parts of the body.3,5 Some scholars consider this cystoscope (an endoscope used specifically for visualizing the urinary bladder through the urethra) to be the first proper endoscope.6 Desormeaux used this instrument to remove a papilloma from a patient's urethra, which was recognized as the first recorded therapeutic use of an endoscope.6 He is also credited as being the first person to use the term “l'endoscopie” (endoscopy).3
The problem with Desormeaux's device was that while it produced better illumination, the heat emitted from the lamp's galvanized platinum wires was so intense that it could easily burn a patient. German dental surgeon Julius Bruck was able to alleviate this problem, in part, when he designed a glass cooling system that diminished heat emission with a stream of water surrounding the platinum filament.33
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Fig. 4: Illustration depicting the operation of Desormeaux's endoscope.
zoom view
Fig. 5: A prototype of the Nitze-Leiter cystoscope, 1877.Source: Reprinted with permission from Elsevier. Herr HW. Max Nitze, the cystoscope and urology. J Urol. 2006;176:1313-6.
It is unclear whether or not Bruck was able to implement his design in a clinical setting, but his cooling system as well as the placement of his light source were both significant contributions to the field.2 The notion to place a light source inside the human body was particularly important because all sources of light used for endoscopic visualization up to that point in time had been external.
 
NITZE AND THE MODERN ENDOSCOPE
German physician Maximilian Nitze also recognized the limitations created by external light sources. He wanted to incorporate Bruck's ingenious lighting system into a prospective design, but felt that the endoscope's small field of view still posed a problem for the operator. He supposedly got the inspiration for a solution to this problem while cleaning the eyepiece of his microscope. When he looked out through the lens, Nitze realized that he could see through it clear across to a neighboring church; this observation led him to incorporate a telescoping system into his design in order to obtain a wider field of view.2 Nitze's concept was a major step in endoscope evolution because it finally afforded the device magnification, a quality all previous systems lacked up to that point because they were simply tubes that directed light down to their distal tips.7
In 1879, Nitze collaborated with Austrian engineer Josef Leiter to produce a cystoscope that used Bruck's water-cooled platinum filament lamp at its distal end along with a series of telescoping optical lenses set inside a metal tube that would relay an image down the scope.2,3 Although it was the first endoscope to combine all these crucial elements (Fig. 5), the device was still burdened by insufficient illumination, cumbersome usage, and expensive operation costs.6 Eight years after Thomas Edison's incandescent light bulb became commercially available, Nitze incorporated it into the distal end of his cystoscope, which made the instrument much more manageable and gained the physician widespread acclaim in the process.2
 
NEUROENDOSCOPY EMERGES
Before the 19th century, there were several obstacles in place that hindered the successful application of endoscopy to the field of neurosurgery. For example, compared to the gastrointestinal tract the brain is a much darker organ; it cannot be illuminated sufficiently by ambient sources of light.8 Another difficulty was that early anatomists had a flawed understanding of neurophysiology that perpetuated misconceptions about cerebrospinal fluid (CSF) and the structure of the brain's cavities.8 But 4by the 20th century, substantial work had been done that mapped out the ventricular and subarachnoid spaces and, thanks to Nitze's contributions, physicians were finally equipped with the tools they needed to explore those dark corridors.
Endoscopes were finally used for neurosurgical purposes in 1910, when American urologist Victor L’Espinasse introduced a cystoscope into the lateral ventricle and bilaterally fulgurated the choroid plexus of two infants suffering from hydrocephalus.9 One patient died postoperatively and the second lived for 5 years before passing.10 L’Espinasse himself did not seem to think much of the endeavor. He presented his work at a local meeting, but never formally published it.2 He later wrote the operation off as a sort of novelty, describing the procedure to his daughter, Victoire (also a physician), as “an intern's stunt”.10 Still, in spite of this modest assessment, the long-term impact made by his experimental foray into neurosurgery should not be understated. Readers should not gloss over the fact that the first person to perform neuroendoscopic surgery was not a neurosurgeon, but a young urologist with an unprecedented idea. His example can serve us as a reminder about the importance of innovation and inter-discipline dialogue.
 
THE DANDY YEARS
Although L’Espinasse deserves credit for being the first person to perform neuroendoscopic surgery, the acknowledged father of modern neuroendoscopy is Walter E Dandy, who used the endoscope in his study and treatment of hydrocephalus. Dandy determined that communicating hydrocephalus could be alleviated by extirpating the choroid plexus. Doing so would reduce the production of CSF, which was out of balance due to an obstruction in the subarachnoid space.11 In 1918, he published a manuscript describing this extirpation.11 It was a somewhat crude procedure that required a nasal dilator to keep the cortex open and necessitated that he drain the patient's entire volume of CSF before removing the choroid plexus.2 The operation left three out of four patients dead within 1 month of treatment; the fourth survived and showed no signs of hydrocephalus 10 months after surgery.2
In 1922, Dandy tried to incorporate a cystoscope into these choroid plexectomies.12 Unfortunately, he was unable to complete the operations without assistance from his nasal dilator and forceps.8 Though these initial attempts were not successful, Dandy was steadfast in his efforts. During the same year, he published the first endoscopic observations of the ventricles and coined the term “ventriculoscopy”.9 Dandy was enthusiastic about refining his approach, but admitted that the images created by his ventriculoscope did not surpass in quality those produced by the more routine pneumoventricolography technique.9 He reluctantly concluded that neuroendoscopy had little to offer brain surgery that could not be achieved through conventional means.8
Elsewhere, while Dandy struggled to find a space for neuroendoscopy, progress was being made by his contemporaries. In 1923, William Mixter published the first report describing an endoscopic third ventriculostomy in a patient with noncommunicating hydrocephalus.13 During the same year, Fay and Grant reported the first black and white photos taken of a child's dilated ventricles, which they took using a cystoscope affixed with a camera.9,13 In 1936, John Scarff performed an endoscopic plexectomy using a new version of the ventriculoscope made of a tube with an inner stylet connected to irrigation channels that maintained constant intraventricular pressure; this prevented the ventricular collapse that might have contributed to Dandy's poor initial results.9
In spite of his skepticism, Dandy did not completely abandon the prospect of endoscopy playing a larger role in neurosurgery. He turned to Howard Kelly (the renowned father of cystoscopy) for design advice and personally directed engineers from the Wappler Electric Co. in order to construct a better ventriculoscope.8 He also took notice of the advancements made by his peers. In 1934, Tracey J Putnam adapted a urethroscope for endoscopic electrocautery and introduced endoscopic choroid plexus coagulation, a procedure that could successfully obliterate the choroid plexus without the need for resection.8 The operation was different from Dandy's because the CSF was not completely evacuated from both ventricles before cauterization of the choroid plexus took place.14 Dandy eventually adopted this coagulation technique when performing his own endoscopic choroid plexectomies; he also used a probe similar to Putnam's that could be threaded through the scope.8
By 1945, despite the progress he had made, Dandy ultimately considered the endoscope's neurosurgical application to be restricted to young children with ventricular tumors or older patients with tumors that had accidentally disclosed during choroid plexectomies.8 5Because he was a prominent surgeon who played such a huge role in pioneering the technique, Dandy's criticism of neuroendoscopy might have contributed to the 20-year period of stagnation that followed.8 The lack of endorsement was not the only factor, of course. Ventricular CSF shunt surgery and microsurgery both minimized the need for neuroendoscopy to be further explored in the coming generation.
 
THE DECLINE AND REBIRTH OF NEUROENDOSCOPY
In 1951, Nulsen and Spitz described a treatment for hydrocephalus using ventricular shunt placement.6 Because it was easier to perform and had lower associated mortality rates than other available techniques, shunting quickly became popular.12 In the 1960s, the emergence of microneurosurgery also played a role in neuroendoscopy's decline because the microscope provided surgeons with everything the endoscope seemed to lack: high magnification, adequate illumination, and the ability to work in deep structures with little damage to the surrounding tissue.2 While interest in neuroendoscopy waned during this era, there were several technological advancements taking place that helped set the stage for the field's resurgence in the 1970s. These included the development of fiber optics, the rod-lens system, SELFOC (self-focusing) lenses, and charged-coupling devices (CCDs). Many of these advancements can actually be connected to a single individual: British optical physicist Harold Hopkins. It is primarily because of his contributions that the endoscope became a viable surgical tool after so many years of dormancy.
 
FIBER OPTICS
In 1951, Hopkins was at a dinner party seated next to a gastroenterologist who complained about the shortcomings of endoscopic technology.2 Most scopes available at the time followed Nitze's design, which used a series of lenses housed in an air-filled tube. This system engendered several problems for the operator, including color distortion, poor illumination, excessive heat, cumbersome size, and rigidity.7 While working with research student Narinder Kapany, Hopkins utilized coherent bundles of glass fibers to create the fiberscope, a flexible device with a shaft that could be bent and still conduct an image from one end to the other.3,7 The glass fibers also permitted the transmission of light without excessive heat.12
Although Hopkins was the person who successfully manifested them into a practical tool, some of the concepts that made up his fiber optic technology had already been described by previous researchers. For example, Heinrich Lamm demonstrated that light could be conducted through a bundle of glass fibers in 1932.7 Daniel Colladon and Jacques Babinet demonstrated the earliest light conductors in the 1840s.13
 
ROD-LENS SYSTEM
Although the advancements produced by Hopkins’ fiberscope were helpful, the device was still lacking, particularly when it came to image quality and light transmittance. In 1959, Hopkins was approached by James G Gow, a urologist who wanted to take photographs of the inside of the bladder in order to develop cancer therapies.3 He needed the current cystoscope improved so that it could provide superior illumination. This prompted Hopkins to develop the rod-lens system, which replaced the large gaps of air in between a series of small lenses that were found in Nitze's endoscope with large glass rods in between a series of small air spaces.3 This new design allowed those spaces of air to act as a series of thin lenses, which resulted in an all-around superior experience for the user.
The conduction of light in an endoscope is a function of the refractory index of the conducting medium.7 In the case of Nitze's telescoping design, that medium was air. Hopkins realized that glass has a refractory index that is 1.5 times greater than air. By exchanging glass for air and air for glass, the system's refractory index increased, which significantly expanded the scope's field of vision and light gathering capacity.7 This adjustment also reduced the diameter of the endoscope, which made it less invasive for patients.3 The rod-lens system was a crucial innovation in design that made the endoscope so much more effective. It still forms the basis of the rigid endoscopes that are currently used today.2
 
SELFOC LENS
In 1966, Hopkins collaborated with German optical instrument manufacturer Karl Storz to design a rigid endoscope that used a new type of lens: the self-focusing optical (SELFOC) lens.3 While conventional lenses have a uniform refractive index, the SELFOC lenses contain a gradient index glass with a variable refractive index that changes according to the radial dimension of the lens.12 6Conventional endoscopes used during this time period required the meticulous placement of relay and field lenses to construct an image. The SELFOC lens technology essentially eliminated the need for relay lenses while creating a wider field of vision and preserving light conduction.12 Surgeons were able to operate without making large incisions and could peer into body cavities with more clarity than ever before. This refined endoscope was made commercially available in 1967 and marked the technological beginning of modern neuroendoscopy as we know it today.3
 
CHARGED-COUPLING DEVICES
Charged-coupling devices are solid-state devices that are capable of converting optical data and light signals into electrical impulses and digital data.3,12 They were invented by Willard Boyle and George Smith in 1969 in order to address the question of how to incorporate video camera technology into endoscopic operations.3 CCDs decreased the size of endoscopic systems and improved the quality of their transmitted images by conducting them over to high-resolution screens.3
 
NEUROENDOSCOPY: YESTERDAY, TODAY, AND TOMORROW
In the 1970s, after decades of disinterest, neurosurgeons started to reconsider endoscopy's role as a surgical tool. This resurgence can be attributed to several factors. Other specialties had already demonstrated the benefits of minimally invasive surgery (shorter convalescence period, lower morbidity rates, and greater patient satisfaction).15 Endoscopic tools had become smaller and more efficient. They were easier to use and provided superior imaging than their predecessors. Perhaps the main reason why neurosurgeons revisited endoscopy was because of the complications related to CSF shunting, such as shunt malfunction, infection, migraines, and overdrainage.12 Shunt failure was (and still is) an especially dangerous risk for patients in developing countries because those individuals might live far away from facilities that could repair a faulty shunt.2 Endoscopic third ventriculostomy is often preferable to shunt surgery because it offers a more physiological solution to the problem posed by hydrocephalus: it allows the ventricular CSF to drain directly into the subarachnoid space.12
In 1973, Takanori Fukushima introduced the first flexible neuroendoscope (the “ventriculofibroscope”), which was used to explore treatments related to intraventricular tumor biopsy, cyst fenestration, and hydrocephalus.9,15 However, it was not until 1994 that Jones and colleagues described an endoscopic third ventriculostomy procedure that had a 61% success rate in treating hydrocephalus.12 Since that time, endoscopic third ventriculostomy and choroid plexus cauterization have both become popular treatment options for hydrocephalus. Their success recovered neuroendoscopy's once-damaged reputation and suggested to curious neurosurgeons the possibility that this approach could be applied to other areas of surgical interest as well.
Neuroendoscopy is currently being used to treat many other kinds of disorders, including skull base tumors, intraventricular tumors, intracranial cysts, degenerative spine disease, and craniosynostosis.12 However, some of these applications offer unique obstacles that must be addressed before the field can progress any further. Some of the challenges associated with intraventricular surgery include operating within a fluid medium, achieving hemostasis, performing bimanual microdissection, and maintaining optimized visualization.13 The development of direct endoscopic visualization (endoscope-controlled microsurgery) will likely facilitate bimanual microdissection and assist in the maintenance of hemostasis for intraventricular lesions.13 Improvements made to endoscopic instrument design, such as the development of a miniaturized endoscopic ultrasonic aspirator, should also enable surgeons to resect lesions with more accuracy and safety.13
Skull base endoscopy is a much younger field than intraventricular endoscopy. While intraventricular investigation rebooted in the 1970s and 1980s, a routine endoscopic approach to skull base pathology was not firmly established until almost 20 years later.13 Challenges endemic to endoscopic skull base surgery have included demarcating surgical boundaries that are limited by critical neurovascular structures, maintaining hemostasis, losing binocular vision, and developing sufficient skull base reconstruction techniques.13 Much work has been done to address these limitations so that safe access along a wide arc of the midline skull base from the frontal sinuses to the odontoid process is now attainable.13
One of the main reasons why endoscopy is so appealing is because it is minimally invasive. This attribute has been particularly beneficial to peripheral nerve applications, such as carpal tunnel decompressions.13 Carpal tunnel decompression took off in the late 1980s and is 7now the operation of choice for many surgeons because of its excellent success rates and low complication rates.13 Endoscopic approaches have been considered for other peripheral nerve surgeries as well, including ulnar nerve decompressions.13
In the future, flexible endoscopes and wireless camera technology could reduce our dependence on the rigid rod-lens system.13 Robotic endoscopic devices might provide more sophisticated panoramic and circumferential views of the ventricular system and three-dimensional endoscopic technology could potentially compensate for the loss of binocular vision currently associated with contemporary endoscopic technology.13 Robot-assisted systems might equip surgeons with the ability to perform techniques that could not otherwise be executed in confined spaces like the ventricular system or the paranasal sinus, but one major limitation of such surgery would be the loss of haptic feedback that normally exists during standard procedures.13 That problem could potentially be overcome, but only with sufficient advancement in haptic sensor and pressure generator technology.
Endoscopic investigation began centuries ago, with vague conceptions and primitive instruments. The field persisted thanks to the tenacity and ingenuity of innovators from various specialties, but its progress was still slow. A practical, reliable endoscope did not emerge until only recently, within the last 60 years. The incorporation of endoscopic technique into routine neurosurgery took time to establish because the first operations that used it were fraught with so much danger and technical difficulty.
After its associated technology improved, neuroendoscopy finally started to build up its reputation. It is no longer merely a feasible technique; in many cases it is the preferred treatment option. Some consider its comprehension to be an absolute necessity for neurosurgeons and suggest that it will soon become the standard of care by which many of today's procedures are performed.16 Although neuroendoscopy has flourished since the time of its humble origins, with the right technological advancements bolstering it there is still much room left for it to grow, both in terms of general efficacy and surgical application.
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