This article has Open Peer Review reports available.
Surgical resection of unilateral thalamic tumors in adults: approaches and outcomes
© Cao et al. 2015
Received: 11 February 2015
Accepted: 31 October 2015
Published: 7 November 2015
The thalamic tumors were less common in adults and this study aimed to determine the clinical features, surgical approaches, and outcomes of adult thalamic tumors, which have not been well-described in the literature.
We reviewed the clinical presentation, surgical approach, perioperative mortality and morbidity, and outcomes of 111 operated patients (71 males, 40 females; mean age at presentation, 33.4 ± 13.2 years) with unilateral thalamic tumor.
The most common clinical presentations were increased intracranial pressure (65 %) and motor deficits (40 %). Five surgical approaches were used depending on tumor location; the most common was the transparieto-occipital approach (47.7 %). According to peri- and post-operative magnetic resonance imaging findings, the tumors were totally resected in 29 cases (26.1 %), subtotally resected in 54 cases (48.6 %), and partially resected in 21 cases (18.9 %). Five patients died during the perioperative period (4.5 %, 5/111). The most common morbidity was motor deficits (21.7 %, 23/106). According to histological findings, there were 50 high-grade and 61 low-grade tumors. Median survival of patients with low- and high-grade tumors were 40 and 12 months, respectively (mean follow-up, 37.3 months). Survival was significantly longer in cases of total or subtotal resection (median, 28 months) compared to partial resection or biopsy (median, 12 months). Survival was poorer in adults than in previous reported pediatrics.
Surgical treatment of adult thalamic tumors must be individualized according to tumor location. Low-grade tumors and total/subtotal resection seem to be predictors of better surgical outcomes. Nevertheless, the outcome of adult patients were still worse than pediatric patients.
KeywordsAdult Thalamic tumor Unilateral Surgical approach Clinical result
Thalamic tumors are rare, comprising 5 % of all brain tumors, and can occur in all age groups, but are more common in children than in adults [1, 2]. In the past, the outcome of thalamic tumors was generally poor because they are deep-seated and surrounded by vital structures, such as the internal capsule and subthalamus, and the risks of postoperative morbidity and mortality were high [3, 4]. However, recent improvements in neuroimaging and surgical techniques have made surgical resection of thalamic tumors feasible in children and have reduced the morbidity and mortality rates associated with this approach [2, 5–9]. For unilateral thalamic tumors, many studies have reported that surgical resection can improve survival of patients with low morbidity and mortality, so they recommend that surgical resection should be performed in combination with adjunct therapies, such as radiotherapy and chemotherapy, based on the histological characteristics of the tumors [10–12].
Thalamic tumors have received much less attention in adults than in pediatric patients. Moreover, the clinical characteristics, operative indications, postoperative morbidity and mortality rates, prognosis, and outcome of unilateral thalamic tumors in adults may differ from those of pediatric patients. It has been reported that thalamic tumors can be resected via several different approaches, although the indications for surgery are not well-described for adults. Correspondingly, the characteristics, treatment approach, and prognosis for unilateral thalamic tumors in adults need to be better defined. To the best of our knowledge, the present series of 111 adults with unilateral thalamic tumors is the largest to be reviewed, and both indications for surgery and clinical results were examined.
This retrospective medical record review was performed in accordance with tenants of the Declaration of Helsinki. All patients gave informed consent and the study protocol was approved by the Ethical Review Board of Beijing Tiantan Hospital. Operated cases involving adult patients (>18 years old) with unilateral thalamic lesions who presented to the Capital Medical University Beijing Tiantan Hospital for the first time between 2003 and 2010 were retrospectively reviewed (n = 111). Tumors arising from adjacent structures (basal ganglia, optic pathways, hypothalamus, ventricle, brainstem, and pineal region) and involving the thalamic region were excluded. With regret, the “only observed” patients were not included.
Clinical and imaging data
Clinical data, including age at presentation, duration and type of symptoms, treatment received, extent of resection, symptom improvement, and status at the end of the follow-up period, were recorded. All patients underwent magnetic resonance imaging (MRI) before treatment and during the follow-up period. Special attention was given to the tumor epicenter, its extension to adjacent structures, and the extent of tumor removal. The tumor volume was calculated using the following formula: axial *coronal *sagittal/2 (referring to the largest diameters), as described by Kramm .
Based on the location of the tumor in the thalamus and surrounding structures, transfrontal, transcallosal, transtemporal, subtemporal, and transparieto-occipital approaches were used. In addition, stereotactic biopsy was performed when the patients were too weak to undergo craniotomy. Neuronavigation or ultrasonography was applied intraoperatively to position the transcortical point and define the tumor margins. Intraoperative electrophysiology was used to identify sensorimotor pathways in 46 cases since 2007. High-grade tumors were treated by additional adjunctive radiotherapy or chemotherapy. The extent of resection was defined as partial (<90 %), subtotal (>90 %), or total based on both postoperative imaging (evaluated by three experienced radiologists at our institute) and intraoperative evaluations (evaluated by the operator). The quality of life of each patient before and after surgery was evaluated using the Karnofsky performance status (KPS) score.
Tumor diagnoses were reviewed by three experienced neuropathologists at our institute according to the WHO 2007 classification standards for central nervous system tumors .
Of the 111 patients of this series, 86 underwent follow-up monitoring after surgery. Correlations were made using univariate analysis according to the Kaplan–Meier method. The threshold for statistical significance was a p-value of ≤ 0.05.
Clinical features for 111 adults with unilateral thalamic tumors
No. of patients (%)
All patients underwent MRI before surgery. Special attention was given to the volume and location of each tumor. The mean tumor volume was 38.4 ± 28.9 cm  (range, 4–140 cm ). Tumors were also divided into two major groups based on their location in the MR images. Tumors with an epicenter in the thalamic region were in one group, while tumors arising from the junction of the thalamus and cerebral peduncle—with most of their mass being in the thalamic region—were included in the second group. In the first group (n = 84), the tumor epicenter was located in the anterior thalamic nuclei (n = 20), the lateral nuclei (n = 7), the medial nuclei (n = 18), or the pulvinar (n = 39). In this group, the tumors also extended in the anterior or superior direction towards the front horn of the lateral ventricle (n = 14), medially toward the third ventricle (n = 11), laterally toward the adjacent lobe or gyrus (n = 7), and posteriorly toward the parietal and temporal lobes (n = 29). In the second group (n = 27), the tumors originated from the thalamus and extended to the midbrain.
Extent of resection based on the anatomic location of the 111 adult unilateral thalamic tumors
No. cases n (%)
Extent of resection
Median KPS score (range)
20 (18 %)
7 (6.3 %)
18 (16.2 %)
39 (35.1 %)
Junction of thalamus and cerebral peduncle
27 (24.3 %)
Perioperative morbidity and mortality
Postoperative clinical features of 106 adults with unilateral thalamic tumors
Change of myodynamic muscle strength level
No. of patients (%)
Perioperative hydrocephalus was encountered before and after surgical resection. In 42 cases where hydrocephalus was identified preoperatively, four patients underwent ventriculo-peritoneal (VP) shunt placement surgery at another hospital for treatment of severe ICP symptoms. In 28 of the remaining 38 cases, the hydrocephalus improved without VP shunt placement after tumor resection. In the other 10 cases, the hydrocephalus did not improve and eventually a VP shunt was required. After tumor resection, ventricle enlargement was observed in six patients that did not exhibit preoperative hydrocephalus, including five patients who required a VP shunt and one patient who underwent placement of an external ventricular drain.
Histopathological findings, adjuvant treatment, and survival analysis
Histological classification of adult unilateral thalamic gliomas of the present cohort (n = 111)
No. of cases (%)
88 (80 %)
5 (5 %)
12 (11 %)
3 (3 %)
1 (1 %)
2 (2 %)
Comparison of the present series with other published series of thalamic tumors
No. pediatric patients
No. adult patients
Postoperative improvement in preexisting motor deficits
Median survival rate (months)
5-year overall survival
High- grade tumors
Low- grade tumors
Albright AL, 
Puget S, 
Kramm CM, 
Sai Kiran NA, 
Baroncini M, 
Bilgniner B, 
The indications and complications of different surgical approaches to thalamic tumors
Anterior transcallosal approach
① The epicenter was located in the anterior thalamus with/without anterior extension to the fontal horn of the lateral ventricle or callosum;
The approach is limited laterally by stretching of the pericallosal artery; some cases suffered from transient mental disorders or memory deficits
② The epicenter was located in the medial thalamic region with/without extension into the third ventricle
The epicenter was located in the anterior thalamus and extended too much laterally (over 2 centimeters from the lateral broader to the middle line)
High risk of postoperative seizures
① The epicenter of the tumor was located in the lateral thalamic region with/without lateral extension to the basal ganglia, adjacent lobes, or the gyrus, or extending beneath the temporal cortex;
Visual field defects due to injury to the optic radiation and language disturbances on the dominant side
② Tumors arising from the junction of the thalamus and the cerebral peduncle and extended to the thalamic and peduncle to a similar extent
The epicenter of the tumor was located in the lateral thalamic region with lateral extension to the basal ganglia
High risk in internal capsule injuries
① Tumors located in the pulvinar with posterior extension toward adjacent structures;
High risk in cortical draining veins and temporal lobe injuries when elevating the temporal lobe
② Tumors arising from the junction of the thalamus and the cerebral peduncle with most of their mass located in the thalamic region
Tumors arising from the junction of the thalamus and the cerebral peduncle occupied the cisterna ambiens and extended inferiorly to the infratentorial area
Visual field and memory deficits, due to injury to adjacent optic radiation of the crus fornicis covering the thalamus
Posterior transcallosal approach
Pulvinar tumors that are primarily located medially (within 1 centimeter from the lateral broader to the middle line)
High risk in optic radiation injuries
Multivariate Cox regression analysis was performed to identify variables that independently affected survival (e.g., extent of tumor resection, tumor volume, age, duration of symptoms, preoperative KPS score, histological findings). The results showed that the extent of tumor resection (total/subtotal resection compared with partial resection/biopsy, p = 0.005), preoperative KPS score (KPS score ≥ 70 compared with < 70, p = 0.003) and histological results (high-grade vs. low-grade tumors, p = 0.01) were correlated with patient survival.
A total of 111 operated cases of adult unilateral thalamic tumors were reviewed. Similar to the symptoms described for children affected by thalamic tumors, such adult patients usually present with increased ICP and motor deficits [5, 10]. The tumor often has a mass effect and can lead to hydrocephalus when located in the medial or posterior thalamus, thereby resulting in greater ICP. When the tumor is located in the anterior or lateral thalamus, motor and sensory deficits are usually observed. In contrast, other symptoms, such as seizures, hemianopia, speech disorders, and tremors, are uncommon .
Various surgical approaches have been described for the resection of thalamic tumors, including transfrontal, transcallosal, transtemporal, subtemporal, and transparieto-occipital [7, 10, 15]. However, the indications for these approaches have not been clearly described. In the present series, the surgical approach was determined according to tumor location (summarized in Fig. 4 and Table 6). The anterior transcallosal approach was used for anteriorly located thalamic tumors that extended toward the lateral ventricle. However, access through the transcallosal approach is limited laterally by stretching of the pericallosal artery. If the tumor extended too laterally, then the transfrontal approach was preferred, although the latter approach is associated with a high risk of postoperative seizures. Moreover, if the ventricle was not enlarged, then access to the ventricle was difficult without the help of neuronavigation or intraoperative ultrasonography.
If the tumor extends beneath the temporal cortex, a trans-temporal middle gyrus approach is a better choice. A cortical incision between T1 and T2 is recommended to reduce the risk of vessel injury. The risk of internal capsule injuries is lower than with the transinsular approach. For lateral thalamic tumors that extend beneath the insular cortex, a pterional transsylvian transinsular approach seems to be the best option . However, the success of this approach depends on the experience of the neurosurgeon, but yet is also associated with a high risk of internal capsule injuries.
In the case of thalamic tumors that extended medially to the third ventricle, a transcallosal approach was often chosen. If the tumor extended beneath the floor of the lateral ventricle, the floor (top of thalamus) can be incised to access the tumor directly without dissection of the crus fornicis. If the tumor did not reach the lateral ventricle floor, then the third ventricle was accessed via a natural fissure using a transcallosal interfomiceal-transforaminal approach, which allowed cortical incision and crus fornicis injuries to be avoided. Moreover, memory deficits were not found to correlate with this surgical approach, consistent with the results of a previous report .
The posterior-interhemispheric-transcallosal approach has been proposed for pulvinar tumors that are primarily located medially . However, this approach cannot be used for laterally extended tumors on account of callosum stretching. For pulvinar tumors that extended posteriorly, the transparieto-occipital transventricular approach was used. However, this approach is associated with visual field and memory deficits due to injury to adjacent optic radiation of the crus fornicis covering the thalamus.
For tumors arising from the junction of the thalamus and cerebral peduncle that are mostly located in the thalamic region, use of a transparieto-occipital approach to remove the thalamic part of the tumor is advocated. Afterwards, the inferior part that slightly extends to the cerebral peduncle can be exposed and subsequently removed. If the tumor occupies the cisterna ambiens and extends inferiorly to the infratentorial area, the tumor can be exposed by elevating the temporal lobe and making a tentorial incision via a subtemporal approach. If the thalamic part is almost equal to the infratentorial part, a transtemporal approach is appropriate for exposure of both parts.
In our group, the extent of total and subtotal resection was less when the tumor infiltrated the cerebral peduncles. Sometimes, it may be impossible to determine the tumor margin adjacent to the cerebral peduncle. Frameless stereotactic guidance or intraoperative ultrasonography guidance was helpful to evaluate the margins in this series. However, the risk of peduncle injury remained high, as even with these techniques, errors in distance calculation are possible. In our group, two patients were comatose and died postoperatively due to intraoperative peduncle injury. Therefore, for cases in which it is difficult to intraoperatively resect the tumor totally or subtotally, partial resection or biopsy may be a better choice, in agreement with a previous report .
Intraoperative neuronavigation or ultrasonography guidance is very important for the surgical treatment of thalamic tumors, as these techniques provide the shortest route to the tumor, sufficiently depict the tumor margins, and allow for a postresection assessment of any obvious residue. Diffusion tensor imaging can be used to reveal the corticospinal tract and to determine how the tumor can be resected maximally without inducing corticospinal tract injury . A disadvantage of neuronavigation is that it results in tissue shift after resection or cerebrospinal fluid (CSF) release. However, using ultrasonography guidance, the tumor margin can be monitored intraoperatively without tissue shift and residues can be assessed after resection.
In the present series, five patients died during the perioperative period, all of whom had high-grade tumors. Two of the five patients were comatose with cerebral peduncle injuries. Three of the five patients died as a result of uncontrolled cerebral swelling followed by disruption of blood supply and infarct formation. This mortality rate was higher than that for series with smaller sample sizes (e.g., < 40 patients), but was consistent with, or better than, previously reported series with larger sample sizes (e.g., > 40 patients) (Table 5). Motor, sensory, and visual deficits were observed in cases where the tumors had compressed adjacent structures, especially the posterior limb of the internal capsule. After decompression, function was found to improve. Motor and sensory deficits were the most common morbidities. About half of the patients had transient hemiparesis, which may have been caused by postoperative cerebral swelling that influenced the posterior limbs of the internal capsule. Sensory deficits were due to central thalamic radiation injuries and visual field deficits were caused by visual radiation. Aphasic problems can be caused by pulvinar injuries, as the pulvinar is the site of neuronal projection to the language centers . The high rate of postoperative sensorimotor and visual deficits may be due to the cerebral swelling or heat injury caused by bipolar coagulation. Moreover, the unavailability of intraoperative electrophysiology in the early stage was also another factor impacting postoperative functional deficits.
Cerebral swelling was one reason for the postoperative increase in ICP, which can usually be reversed using medical therapy or cranial decompression. Another cause of increased ICP was postoperative hydrocephalus. In this series, hydrocephalus was treated by tumor resection in 74 % of patients, as CSF drainage can be re-established after tumor resection. In six patients, the CSF pathway was still obstructed postoperatively as a result of cerebral swelling or gliosis surrounding the aqueduct or interventricular foramen of Monro, requiring CSF diversion. Therefore, in our experience, preoperative shunting of thalamic tumors are not necessary due to the potential for neurological degradation or subsequent shunt blockade. Similar findings were published by Gole .
The outcomes of the thalamic tumors examined in this series were found to correlate with the histopathological results and the median survival period for patients with low-grade tumors was longer than that for patients with high-grade tumors, consistent with previous reports [2, 5, 7, 21]. The overall survival of low-grade tumors in adults is reportedly lower than that in children, perhaps due to the lower degree of neuroplasticity in adults compared to children . For patients with high-grade tumors, the overall survival period was 12 months, similar to that observed for children. Patients who underwent total or subtotal resection also achieved a better survival rate than those who underwent partial resection or biopsy. This finding is consistent with the results of other studies, which found that maximal safe resection of thalamic tumors is feasible and generally results in a better outcome [10, 19, 22, 23]. These findings support a surgical approach for management of these tumors and imply that extended tumor resection can improve prognosis.
Deep-seated thalamic tumors, especially in adults, are a challenge for many neurosurgeons. Based on the findings from the present series, surgical removal appears to be an appropriate treatment for thalamic tumors in adults. Moreover, the appropriate surgical approach should be determined based on the location of the tumor and its relationship with surrounding structures. The extent of tumor resection and histological classification are also two very important factors to consider when determining the prognosis of patients with thalamic tumors. Nevertheless, further studies will be necessary to improve the poor outcomes of adults with thalamic tumors.
This work was supported by National Health Industry Research Funds for Public Welfare Projects (201402008) and the National High Technology Research and Development Program of China (863 Program) (2014AA020610). Thank Xuran Li for drawing the diagram in this paper.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Cheek WR, Taveras JM. Thalamic tumors. J Neurosurg. 1966;24:505–13.View ArticlePubMedGoogle Scholar
- Cuccia V, Monges J. Thalamic tumors in children. Childs Nerv Syst. 1997;13:514–21.View ArticlePubMedGoogle Scholar
- Albright AL, Sclabassi RJ. Use of the Cavitron ultrasonic surgical aspirator and evoked potentials for the treatment of thalamic and brain stem tumors in children. Neurosurgery. 1985;17:564–8.View ArticlePubMedGoogle Scholar
- Tovi D, Schisano G, Lilieqvist B. Primary tumors of the region of the thalamus. J Neurosurg. 1961;18:730–40.View ArticlePubMedGoogle Scholar
- Albright AL. Feasibility and advisability of resections of thalamic tumors in pediatric patients. J Neurosurg (Pediatrics). 2004;100:468–47.View ArticleGoogle Scholar
- Souweidane MM, Hoffman HJ. Current treatment of thalamic gliomas in children. J Neurooncol. 1996;28:157–66.View ArticlePubMedGoogle Scholar
- Ozek MM, Ture U. Surgical approach to thalamic tumors. Childs Nerv Syst. 2002;18:450–6.View ArticlePubMedGoogle Scholar
- Bernstein M, Hoffman HJ, Halliday WC, Hendrick EB, Humphreys RP. Thalamic tumors in children. Long-term follow-up and treatment guidelines. J Neurosurg. 1984;61:649–56.View ArticlePubMedGoogle Scholar
- Beks JW, Bouma GJ, Journee HL. Tumours of the thalamic region. A retrospective study of 27 cases. Acta Neurochir. 1987;85:125–7.View ArticlePubMedGoogle Scholar
- Puget S, Crimmins DW, Garnett MR. Thalamic tumors in children: a reappraisal. J Neurosurg. 2007;106:354–62.PubMedGoogle Scholar
- Lizarraga KJ, Gorgulho A, Lee SP, Rauscher G, Selch MT, DeSalles AA. Stereotactic radiation therapy for progressive residual pilocytic astrocytomas. J Neurooncol. 2012;109:129–35.View ArticlePubMedGoogle Scholar
- Moshel YA, Link MJ, Kelly PJ. Stereotactic volumetric resection of thalamic pilocytic astrocytomas. Neurosurgery. 2007;61:66–75.View ArticlePubMedGoogle Scholar
- Kramm CM, Butenhoff S, Rausche U, Warmuth-Metz M, Kortmann RD, Pietsch T. Thalamic high-grade gliomas in children: a distinct clinical subset? Neuro Oncol. 2011;13:680–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Louis DN, Ohgaki H, Wiestler OD, Cavenee WK, Burger PC, Jouvet A. The 2007 WHO classification of tumours of the central nervous system. Acta Neuropathol. 2007;114:97–109.View ArticlePubMedPubMed CentralGoogle Scholar
- Sai Kiran NA, Thakar S, Dadlani R, Mohan D, Furtado SV, Ghosal N. Surgical management of thalamic gliomas: case selection, technical considerations, and review of literature. Neurosurg Rev. 2013;36:383–93.View ArticlePubMedGoogle Scholar
- Yasargil MG. Microneurosurgery (vol 4B). Stuttgart: Thieme; 1996. p. 291–304.Google Scholar
- Winkler PA, Ilmberger J, Krishnan KG, Reulen HJ. Transcallosal interforniceal-transforaminal approach for removing lesions occupying the third ventricular space: clinical and neuropsychological results. Neurosurgery. 2000;46:879–88.PubMedGoogle Scholar
- Broadway SJ, Ogg RJ, Scoggins MA, Sanford R, Patay Z, Boop FA. Surgical management of tumors producing the thalamopeduncular syndrome of childhood. J Neurosurg Pediatr. 2001;7:589–95.View ArticleGoogle Scholar
- Steiger HJ, Götz C, Schmid-Elsaesser R, Stummer W. Thalamic astrocytomas: surgical anatomy and results of a pilot series using maximum microsurgical removal. Acta Neurochir (Wien). 2000;142:1327–36.View ArticleGoogle Scholar
- Goel A. Preoperative shunts in thalamic tumors. Neuro India. 2000;48:347–50.Google Scholar
- Baroncini M, Vinchon M, Minéo JF, Pichon F, Francke JP, Dhellemmes P. Surgical resection of thalamic tumors in children: approaches and clinical results. Childs Nerv Syst. 2007;23:753–60.View ArticlePubMedGoogle Scholar
- Pathy S, Jayalakshmi S, Chander S, Singh R, Julka PK, Rath GK. Prognostic factors influencing the outcome of thalamic glioma. Neurol India. 2002;50:37–40.PubMedGoogle Scholar
- Kelly PJ. Stereotactic biopsy and resection of thalamic astrocytomas. Neurosurgery. 1989;25:185–94.View ArticlePubMedGoogle Scholar
- Bilginer B, Narin F, Isikay I, Oguz KK, Söylemezoglu F, Akalan N. Thalamic tumors in children. Childs Nerv Syst. 2014;30:1493–8.View ArticlePubMedGoogle Scholar