Endoscopic Endonasal Transsphenoidal Approach



Fig. 2.1
Anatomical images of endoscopic exploration of the right nostril and identification of the nasal landmarks. (a) The inferior portion of the right nostril. (b) The middle turbinate. (c) The sphenoethmoid recess. (d) The sphenoid sinus mucosa after the opening of its anterior wall. IT inferior turbinate, MT middle turbinate, SER sphenoethmoid recess, NS nasal septum, Co choana, SO sphenoid ostium, ST superior turbinate, SP sphenoid prow, SM sphenoid mucosa, * branches of the nasopalatine artery



Hence, at the level of the sphenoethmoid recess, the nasal septum is detached from the prow of the anterior wall of the sphenoid bone; this latter is opened circumferentially and thus far the endoscope enters into the sphenoid cavity, often divided by one or more septa. The degree of pneumatization of the sphenoid bone is an important factor for the identification of the bony protuberances and depressions inside it. Depending on the degree of its pneumatization, a series of protuberances and depressions molded on its posterior and lateral walls can be identified. The sellar floor is at the center, the sphenoid planum is above, and the clival indentation is below; lateral to the sellar floor, the bony prominences of the intracavernous carotid artery and the optic nerve can be observed. Between them, the lateral optocarotid recess lies; it is molded by the pneumatization of the optic strut of the anterior clinoid process. The intracranial aspect of the upper border of the lateral optocarotid recess is covered by a thickening of the dura and periosteum that forms the distal dural ring, which separates the optic nerve from the clinoidal segment of the internal carotid artery (ICA). The inferior border of the lateral optocarotid recess also presents a thickening of the dura and periosteum, which forms the proximal dural ring, which separates the intra-cavernous portion of carotid artery from the clinoidal segment. The lateral aspect of tuberculum sellae represents the point where the bony prominences of the carotid artery and the optic nerve join medially (medial optocarotid recess). This recess is less evident than the lateral one; rather it represents the lateral limit to be opened to unlock the suprasellar area (Fig. 2.2).

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Fig. 2.2
Exposure of the sphenoid sinus after opening of its anterior wall and identification of the anatomical landmark. (a) Panoramic endoscopic view of the sphenoid sinus. (b) Bone removal of the sellar floor, the tuberculum sellae, and the posterior portion of the planum sphenoidale. C clivus, SF sellar floor, PS planum sphenoidale, CPs bony protuberance covering the parasellar tract of the intracavernous internal carotid artery, CPc bony protuberance covering the paraclival tract of the intracavernous internal carotid artery, OP bony protuberance covering the optic nerve, OCR opticocarotid recess, * sphenoid septum remnant. DMp dura mater of the planum sphenoidale, DMs sellar dura mater

The sella turcica is limited superiorly by the diaphragma sellae, a fold of dura with a central opening through which is pierced by the pituitary stalk and its blood supply. The diaphragma sellae separates the anterior lobe of the pituitary gland from the optic chiasm and the suprasellar cistern. The intercavernous sinus (anterior and posterior) lies in the anterior and posterior borders of the diaphragma sellae. Additional small venous sinuses in the base of the pituitary fossa drain into the intercavernous sinuses [53].

If the surgeon wants to explore the cavernous sinus, the bone that covers the intracavernous carotid artery (carotid protuberance) must be removed in order for both the medial and lateral compartments of the cavernous sinus to be exposed [15]. The space between the ICA and the pituitary gland varies depending on the anatomy of both structures. The medial wall may consist of tenacious connective tissue or may be fenestrated, incomplete, or inexistent, offering little or no anatomical resistance against tumor invasion. Surgical access to the medial and posterior wall of the cavernous sinus is possible by elevating or retracting the pituitary gland medially and by retracting the C4 (intracavernous segment) or C4–C5 bend of the ICA, laterally [21, 56]. The carotid artery itself is located in the major portion of the cavernous sinus so that the entire cavernous sinus will be disclosed only when the carotid artery is mobilized medially. Upon opening of the medial wall, the posterior and upper parts of the cavernous sinus are entered. The inferior hypophyseal artery is identified inferolaterally to the pituitary gland, arising from the meningohypophyseal trunk together with the dorsal meningeal and tentorial artery. Anteriorly to it, the inferolateral trunk, with its collaterals to the cavernous sinus cranial nerves, is detected, branching off the lateral aspect of the ICA; its origin can be seen by medial dislocation of the intracavernous segment of the ICA. Inferior hypophyseal artery divides into a medial and a lateral branch, which anastomose with the corresponding vessels of the opposite side, forming an arterial ring around the hypophysis [16, 28, 54] (Figs. 2.3, 2.4, and 2.5). The inferolateral trunk supplies all the cavernous sinus nerves, with the exception of the proximal segment of the VI cranial nerve, which receives blood from the tentorial artery. The oculomotor and trochlear nerves can be visualized from the sella through the C-shaped portion of the intracavernous sinus ICA. The oculomotor nerve enters the cavernous sinus under the posterior clinoid and then runs along the middle of the C-shaped ICA to enter into the cavernous sinus apex. At the apex, it runs along the inferior margin of the optic strut triangle until it reaches the superior orbital fissure. The trochlear nerve runs parallel and just inferior to the oculomotor nerve. When the ICA is displaced medially, the oculomotor nerve, the trochlear nerve, and the proximal and distal dural ring can be seen. The ophthalmic division of the trigeminal nerve runs obliquely in a rostral and anterior direction toward the cavernous sinus apex reaching the oculomotor and trochlear nerves at the superior orbital fissure. The abducens nerve passes through Dorello’s canal approximately 5–10 mm inferior to the sellar floor at the medial aspect of the ICA and a few millimeters below the sellar floor at the lateral aspect of the ICA. The abducens nerve heads toward the orbital apex running inferiorly to the medial aspect of the ophthalmic branch of the trigeminal nerve [21, 31, 33, 34, 43] (Fig. 2.3).

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Fig. 2.3
Exploration of the cavernous sinus and medialization of the internal carotid artery. ICA internal carotid artery, III third oculomotor nerve, IV trochlear nerve, VI abducens nerve, V1 ophthalmic branch of trigeminal nerve, V2 maxillary branch of the trigeminal nerve, * inferolateral trunk (artery of the inferior cavernous sinus)


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Fig. 2.4
Endoscopic endonasal view of the neurovascular structures localized above the pituitary gland. CH chiasm, PS pituitary stalk, ON optic nerve, A2, post communicating anterior cerebral artery, * superior hypophyseal artery (sha)


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Fig. 2.5
Endoscopic endonasal view of the pituitary gland and surrounding neurovascular structures. CH chiasm, PS pituitary stalk, Pg pituitary gland, ON optic nerve, PCoA posterior communicating artery, III third cranial nerve, * superior hypophyseal artery

The exposure of the suprasellar region requires a more anterior trajectory: the posterior ethmoid cells and the anterior wall of the sphenoid sinus have to be widely removed. Above the sella, the angle formed by the convergence of the sphenoid planum with the sellar floor corresponds to the tuberculum sellae. This structure named after the classic Latin word “tuber,” which etymologically means “small swelling, pimple, protuberance,” appears to fit such a description when observed from above via a transcranial route, but it does not as seen from below through an endoscopic endonasal corridor. As a matter of fact, through direct visualization via an endoscopic endonasal approach, it has recently renamed “suprasellar notch” (SSN), that means “angular or V-shaped cut indentation” [29]. Indeed, in the majority of cases, the inferior point of view coincides with a sort of indentation between the superior aspect of the sella turcica and the declining part of the planum sphenoidale. Moving anteriorly, we can recognize the sphenoid planum, laterally delimited by the protuberances of the optic nerves. At this point, the bone of the suprasellar notch and the planum sphenoidale can be removed 1.5–2 cm in a posteroanterior direction and laterally up to the optic protuberances. The sellar and suprasellar dura are then opened to permit the exploration of the neurovascular structures localized above the diaphragma sellae. In the suprachiasmatic region, the chiasmatic and the lamina terminalis cisterns with relative contents are accessible. The anterior margin of the chiasm and the medial portion of the optic nerves, the anterior cerebral arteries, the anterior communicating artery, and the recurrent Heubner arteries, together with the gyri recti of the frontal lobes, can be identified. In the subchiasmatic space, the pituitary stalk is at the center of the field below the chiasm, with the superior hypophyseal artery and its perforating branches, supplying the inferior surface of the chiasm and the optic nerves. The superior aspect of the pituitary gland and the dorsum sellae are also visible. The superior hypophyseal arteries supply the optic chiasm, the floor of the hypothalamus, and the median eminence.



2.3 Neuroimaging


Magnetic resonance imaging (MRI) has replaced other techniques for the morphological study of the sellar region, because of the elevated tissue contrast and multiplanar capability. A complete MR protocol should include, at least, T1- and T2-weighted images and T1-weighted post-contrast (gadolinium) images, in the three orthogonal planes at max 3 mm sections. Complementary sequences, i.e., MR angiography, are also useful, especially upon the suspicion of a possible vascular nature of sellar lesion. Computed tomography (CT) should be used only in selected cases, to provide further details whether calcified components of the lesion are present, to achieve an accurate definition of the bony boundaries at presurgical planning of the approach, mainly sphenoid sinus septations. At the presurgical planning, CT remains the diagnostic imaging study of choice in patients who are unable to undergo an MR study. The purposes of the neuroradiologic study of pituitary adenomas are: to identify the lesion,; to define the spatial relationships of the lesion (presurgical planning), to monitor the medical treatment, and to clear the entity of the lesion (postsurgical follow-up) [2].

Pituitary microadenomas comprise lesions measuring 10 mm or less. They are the most common intrasellar neoplasms. The neuroradiologic diagnosis of microadenomas is drawn on the presence of indirect and direct findings. The indirect findings that should lead to diagnosis of microadenoma are: the lateral dislocation of the pituitary stalk and the alteration of the pituitary gland (upward convexity) or of the sellar floor (depression, slope, angulation). The stalk is usually found dislocated controlaterally off the tumor, but there have been reports describing homolateral stalk dislocation; as well it can be absent in contrast to tumor presence. The direct findings reveal proper MRI features of pituitary macroadenomas; they can be identified as rounded or ovular, sometimes flattened intrasellar lesions, and hypointense on T1-weighted images compared to the unaffected anterior pituitary gland (Fig. 2.6). Microadenomas can also exhibit hyperintensity on the T1-weighted images, due to the hemorrhage of a part or of whole lesion. At the T2-weighted images, pituitary microadenomas present a variety of aspects, according to the line of endocrine activity. T2 hyperintensity could be found in 80 % of prolactin-secreting microadenomas, while iso- or hypointensity is disclosed in ca 70 % of growth hormone-secreting microadenomas. The use of intravenous contrast medium injection becomes mandatory to further refine the diagnosis; upon half-dose gadolinium (0.05 mmol/kg) injection, most of microadenomas enhance less rapidly than the normal pituitary gland, appearing as hypointense areas. Late scans, 30–40 min after the injection, can sometimes show a late enhancement of the adenoma. Sometimes, in patients harboring a small lesion—particularly in case of Cushing disease—difficult to detect, specific dynamic techniques are performed to rule out diagnosis. This technique consists of repeated scans of the gland immediately upon intravenous injection of contrast medium, so that the progressive enhancement of the stalk and then of the gland is observed. The early phases of the acquisition demonstrate lesions that are not identifiable on conventional contrast-enhanced studies. In presence of clinical signs and symptoms of a functioning adenoma, with no lesion detected at the MRI, the inferior petrosal sinuses could be run to evaluate the hormonal output of the pituitary gland. This is most commonly performed in patients with Cushing’s syndrome, because the corticotropin-secreting tumors may be extremely small and difficult to visualize [52].

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Fig. 2.6
Microadenoma. (af) Coronal T1-weighted dynamic images during contrast medium injection. Presence of a small hypointense area within the right lateral part of the gland, better demonstrated during the early phases of the dynamic scan (bd), not identifiable in the delayed acquisition (f)

On the other side, pituitary macroadenomas are bigger intrasellar masses, usually extending out of the sella. The aim of the neuroradiologic study is to clarify the origin side of the lesion (pituitary or not), its consistency (firm, cystic, necrotic, or hemorrhagic), and its relationships with anatomical surrounding structures. From these data an accurate differential diagnosis can be reached [11]. MRI typically demonstrates a mass arising from the pituitary fossa, completely filling the sella, which appears remodeled and enlarged. The normal pituitary tissue is compressed: after contrast medium injection, the normal gland appears as a strongly enhancing tissue, representing the pseudocapsula of the adenoma, usually posteriorly and/or on one side, between the tumor and the cavernous sinus. The posterior lobe and pituitary stalk appear more hyperintense as compressed and or displaced.

Pituitary macroadenomas may appear as homogeneous, soft-tissue masses, with variable signal intensity, often similar to gray matter. At the T2-weighted images, areas of inhomogeneous signal can be identified, because many macroadenomas harbor cystic, necrotic, or hemorrhagic components (Figs. 2.7 and 2.8). The adenoma may appear predominantly cystic, showing a typical hyperintense signal on the T1- and T2-weighted images (Fig. 2.9). Hemorrhage occurs in about 20 % of pituitary macroadenomas, revealed by spontaneous hypersignal intensity on the T1-weighted images. A fluid-fluid level can sometimes be seen within the hemorrhage, due to blood cell membranes remnants and hemoglobin residues. The clinical syndrome known as “pituitary apoplexy,” representing hemorrhage into a pituitary adenoma, can be defected also on CT as hyperdense material in the pituitary fossa and possibly in the suprasellar cistern, within the lesion. MRI could differentiate various stages of the hemorrhage evolution. Small linear or curved spots, caused by hemosiderin deposits, can sometimes be found after intratumoral hemorrhage on the T2-weighted images. Concerning the consistency of the lesion, the T2-weighted scans are more helpful in providing relevant details: hyperintense lesions could be presumed as cystic, while hypointense ones as firmer. Additional data can be obtained by the diffusion-weighted imaging (DWI).

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Fig. 2.7
Macroadenoma. (a) Sagittal T1-weighted image; (b) coronal T2-weighted image; (cd) sagittal and coronal T1-weighted images after contrast medium injection. Presence of an intra- and suprasellar lesion, laterally displacing the axis and the left cavernous sinus


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Fig. 2.8
Macroadenoma. (a) Sagittal T1-weighted image; (b) coronal T2-weighted image; (cd) sagittal and coronal T1-weighted images after contrast medium injection. Presence of a large intra- and suprasellar lesion, clearly infiltrating the left cavernous sinus


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Fig. 2.9
Macroadenoma. (a) Sagittal T1-weighted image; (b) coronal T2-weighted image; (cd) sagittal and coronal T1-weighted images after contrast medium injection. Presence of a very large intra- and suprasellar lesion with a prevalent, non-enhancing colliquative component

The use of contrast medium injection helps in defining the structure of the lesion, homogeneous or inhomogeneous, and the degree of its vascularization. After contrast medium, the tumor enhances moderately at early stage and retains this signal feature at later delayed scans.

The extension of the macroadenoma and its relationships with the surrounding structures constitute key-points of the neuroradiologic diagnosis. The tumor usually extends upward, to impinge and/or compress the optic chiasm, remaining subdiaphragmatic or breaching the diaphragma sellae with a typical “figure-eight” appearance, compressing the floor of third ventricle and sometimes the foramen of Monro. The adenoma can also extend downward, into the sphenoidal sinus, or laterally toward the cavernous sinus. Whether the cavernous sinus is compressed or invaded is of crucial importance for the neurosurgeon; this radiological diagnosis can be very difficult because the medial wall of the sinus is often thin and not directly visualized. The cavernous sinus invasion can be excluded in presence of normal pituitary tissue lying between the tumor and the sinus. In case of massive involvement of the cavernous sinus, complete encircling of the intra-cavernous internal carotid artery (ICA) tumor is visible and only tumor signal features are identified in this area. Prolactin or growth hormone-secreting adenomas are more often found to enter the cavernous sinus as compared to nonsecreting tumors [44]. A grading system with a high predictive value for the identification of true cavernous sinus invasion has been proposed by Knosp et al., in 1993 [44] (Fig. 2.10).

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Fig. 2.10
Macroadenoma. (a) Coronal T1-weighted image; (b) coronal T2-weighted image; (cd) coronal and sagittal T1-weighted images after contrast medium injection. Presence of a large intra- and suprasellar lesion, clearly infiltrating the left cavernous sinus and the sphenoid sinus

The neuroradiology techniques play also an important role in evaluating the effects of the medical therapy for functioning adenomas [51].

In case of PRL-secreting adenomas, dopamine agonists can reduce the size of lesions since the 10th day of treatment and could last for several years. The shrinkage of macroadenomas caused by the medical treatment can determine the downward displacement of the optic tracts and chiasm although this usually doesn’t produce symptoms. Within macroadenomas focal areas of necrosis or cysts, revealed by hypointense signal on T1-wieghted and hyperintense signal on T2-weighted images and an increasing T2 signal intensity, can occur. Hemorrhage within prolactinomas has also been observed.

It is worth reminding that, when an EEA is planned for the removal of pituitary adenoma, MRI and CT ease presurgical planning, giving details in regard to the bony boundaries of the approach, the anatomy of the nasal and paranasal sinuses, and eventual variations.

Thin-slice axial and coronal CT scans allow a detailed overview of major nasal cavities and bony structures, which are anatomical landmarks of the endoscopic route (nasal turbinates, uncinate processes, sphenoid ostium, etc.) and of the sinusal structures (symmetry and aeration of the sphenoid sinus and the relationships of the sphenoid septa with the sellar floor and carotid canal).

Finally, when MRI is adopted to diagnose any complication of surgery or to define eventual residual tumor or recurrence, the usual postoperative distortion of sellar anatomy should not be underestimated. Indeed, in the first 1 or 2 weeks following transsphenoidal resection, a sizeable “mass” may still be present; the surgical cavity is often filled with packing material (gelatin foam, autologous fat), soaked with blood and secretions, which slowly dissolves along following 2 or 3 months. The slow reduction of the “mass” in the surgical cavity, despite significant or complete removal of the tumor, reflects the reabsorption time of the reconstruction material or may represent peritumoral scars preserving the cavity from collapsing. Therefore, MRI examination should be required after 2 or 3 months after surgery (Fig. 2.11), after these changes have regressed. If fat or muscle grafts are used to reconstruct the sellar cavity, their reabsorption requires more time: that is, the fat may exhibit a hyperintense signal up to 2 or 3 years after surgery [55, 59].

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Fig. 2.11
Postoperative changes. (a) Sagittal T1-weighted image; (b) coronal T2-weighted image; (c) coronal T1-weighted image after contrast medium injection. The sellar cavity is completed filled by cerebrospinal fluid (“empty sella”), with downward retraction of the axis and the optic chiasm


2.4 Surgical Technique


Since the endoscopic transsphenoidal technique has been introduced during the 1990s, several variations of this procedure (endonasal, transnasal, single or binostril, with or without the use of the microscope, etc.) have been used worldwide for the removal of pituitary adenomas and of other variety of sellar lesions [3, 13, 32, 38, 48]. In this section we will describe the binostril procedure we currently adopt for the removal of the pituitary adenomas.

The patient is positioned supine with the trunk elevated 10° and the head turned 10° toward the surgeon seated in a horse-hole headrest.

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May 26, 2017 | Posted by in NEUROSURGERY | Comments Off on Endoscopic Endonasal Transsphenoidal Approach

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