eISSN: 1509-572x
ISSN: 1641-4640
Folia Neuropathologica
Current issue Archive Manuscripts accepted About the journal Editorial board Journal's reviewers Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
SCImago Journal & Country Rank
vol. 46

Asymptomatic and symptomatic glial cysts of the pineal gland

Anna Taraszewska
Ewa Matyja
Waldemar Koszewski
Artur Zaczyński
Krzysztof Bardanin
Zbigniew Czernicki

Folia Neuropathol 2008; 46 (3): 186-195
Online publish date: 2008/09/19
Article file
- 03taraszewska.pdf  [0.43 MB]
Get citation
JabRef, Mendeley
Papers, Reference Manager, RefWorks, Zotero
Non-neoplastic glial cysts of the pineal gland are relatively common incidental findings in brain MRI [4,12,14,19,33,34,36] or in autopsy studies [10]. Usually they have no clinical implications and remain asymptomatic for years. In analysed series of MRI the occurrence of asymptomatic intrapineal cysts ranged between 0.2% [14] and 10.8% [12] of healthy volunteers and between 1.26% [33] and 4.3% [19] of patients examined for various neurological reasons. Most previous MRI studies revealed pineal cysts with a size of no less than 5 mm in diameter [4,19,36]. With the improved MRI techniques a higher incidence of pineal cysts has been reported including smaller cystic changes, even with measurements of 2 mm [12]. Recently, the use of high-resolution MR imaging demonstrated that 23% of volunteers had pineal cysts with a mean diameter of 4.3 mm (range 2-14 mm) and 13% demonstrated smaller cystic changes with the largest diameter less than 2 mm [34]. The proportion of pineal cysts and pineal small cystic lesions observed by Pu et al. [34] in an MRI study was consistent with previous results of a post-mortem study reported by Hasegawa et al. [10]. These authors found that cysts larger than 2 mm in diameter were seen macroscopically in 34% of pineal glands, whereas microscopically recognizable cystic changes, less than 2 mm in diameter, occurred in 28% of pineal glands.
In contrast to asymptomatic cystic lesions of the pineal gland, symptomatic glial cysts are rare and could require surgical intervention. Enlarged glial cysts with a size of at least 15 mm in diameter are related to clinical syndromes referable to a mass lesion [6,13,22]. The most common symptoms, resulting from compression of the surrounding structures, particularly the quadrigeminal plate and cerebral aqueduct, include headaches of variable intensity, visual and oculomotor disturbances and obstructive hydrocephalus [6,15,25,26,30,41]. Less frequently patients present with ataxia [6,41], motor and sensory impairment [6,15,25,30] or mental and emotional disturbances [15,37]. Sudden death due to a cystic lesion of the pineal gland has also been reported [27,35].
The diagnosis of pineal cyst is usually established by MRI; however, neuroradiological analysis without histological verification does not predict the benign glial nature of the lesion. Often, both clinical and radiological manifestations of symptomatic glial cysts may be indistinguishable from neoplastic pineal cystic lesions [6,8,37]. Therefore, histopathological study is definitive for critical diagnosis, further prognosis and therapy in patients operated on for pineal cystic lesion [5].
Glial cysts of the pineal gland are a relatively rare finding in routine biopsy material [2,5,16]. A cyst with typical morphology can be diagnosed easily, but occasionally the histopathological pattern can be confused with pineal parenchymal or astrocytic tumour, especially if fragmentary surgical specimens are obtained for microscopic examination [5,15]. Klein and Rubinstein [15] indicated that they are histologically most often mistaken for a pineocytoma. In their series of 7 cases of symptomatic glial cysts, referred for histopathological consultation, the initial diagnosis was pineocytoma in 4 cases. Similar observation of frequent misdiagnosis of pineocytoma in cases with glial cysts was obtained by one of the authors (E.M.), reviewing histopathological material from patients operated on in various neurosurgical centres.
In this paper we demonstrate morphological variants of pineal glial cyst that may cause both radiological and histopathological pitfalls. Detailed histopathological features of glial cysts were documented in 2 surgical cases of symptomatic cyst of the pineal gland and in 3 autopsy findings of asymptomatic pineal cysts. Clinical and radiological manifestations of symptomatic glial cysts in presented cases are discussed.
Material and Methods
A histopathological study was performed on surgical specimens obtained from 2 cases of symptomatic pineal cysts and on 3 cystic pineal glands taken at random from non-selected autopsy cases. Formalin-fixed material was routinely processed for paraffin and the sections were stained with haematoxylin and eosin (H&E). Immunohistochemical staining was performed with primary antibodies against glial fibrillar acidic protein (GFAP), neurofilament proteins (NFP) and synaptophysin, using the streptavidin-biotin-peroxidase complex method (all reagents provided from Dako).
Report of cases
Biopsy cases 1-2
Case 1. An 18-year-old girl presented with a history of severe headache not responding to medical treatment. Headache was accompanied by nausea and vertigo and for 2 months by syncope. The symptoms began after contusion of the brain that she had undergone in a road accident 2 years ago. Since then she had been treated with Lamitrin because of suspicion of epilepsy. At admission, neurological examination and routine laboratory tests were normal. MRI of the brain revealed a round cyst measuring 14 mm in diameter in the pineal gland region (Fig. 1A). The cyst compressed and modulated the quadrigeminal plate without signs of cerebral aqueduct obstruction. Size of the ventricular system was normal. Preoperative diagnosis was pineal cyst. Total resection of the cyst was accomplished by occipital-transtentorial approach. Postoperatively, the patient experienced
a gradually resolving Parinaud’s symptom, not present before surgery. Frequency and intensity of headache were significantly diminished. In the control MRI obtained 6 months after cyst resection the deformation of the quadrigeminal plate was partially reduced (Fig. 1B).
The patient was free of severe headache.
For the histopathological study small fragments of the cyst wall were obtained. Microscopically, the cyst wall consisted of layers of dense fibrillar gliotic tissue, containing Rosenthal fibres and a narrow zone of pineal parenchyma (Fig. 2A-B). Some segments of the cyst wall disclosed ependymal cells lining the inner glial layer (Fig. 2C). The external surface of the wall was covered by a thin band of connective tissue. Immunostains showed strong reactivity of GFAP in glial layers (Fig. 3A) and in dispersed interstitial astrocytes within pineal parenchyma, whereas the pineocytes were immunopositive for NFP and synaptophysin (Fig. 3B).
Case 2. A 17-year-old boy suffered for months severe headache with insomnia and occasional vertigo. The first MRI examination of the brain, obtained
6 months ago, demonstrated a cystic mass of irregular outline in the region of the pineal gland, with dimensions of 14×16×11 mm. The lesion showed inhomogeneous contrast enhancement and suggested tumour of the pineal gland. At admission, MR imaging showed the same appearance of the lesion as previously (Fig. 4). Neurological examination and laboratory tests, including tests for alpha-fetoprotein, CEA and HCG, were normal. The lesion was totally resected by the infratentorial supracerebellar approach. Postoperative course was uneventful, but headache symptoms were maintained.
Histopathological study of surgical specimens revealed multilocular cysts surrounded by bands of fibrous glial tissue (Fig. 5A) or directly by pineal parenchyma. The cyst cavities demonstrated variable dimensions and protein fluid content in some smaller ones. Rosenthal fibres within glial tissue and deposits of calcification within pineal parenchyma were observed (Fig. 5B). In immunohistochemistry, the layers of glial tissue showed strong reactivity for GFAP (Fig. 6A), whereas pineal parenchyma was stained with synaptophysin and NFP (Fig. 6B).
Autopsy cases 3-5
Case 3. A 69-year-old man, without history of disease, died suddenly because of rupture of the aorta aneurysm. Autopsy study of the brain revealed
a round tumour of 13 mm in diameter, which was loosely attached with leptomeninges of the brain stem and resembled meningioma. On cross-section it was greyish and cystic. Microscopic examination of the tumour revealed a cystic body of the pineal gland, with a large cyst of 7 mm in diameter surrounded by a vast layer of fibrous glial tissue (Fig. 7A). In the adjacent pineal parenchyma numerous interstitial astrocytes and small areas of fibrillar gliosis with Rosenthal fibres were seen (Fig. 7B). The diagnosis was glial cyst of the pineal gland.
Case 4. A 34-year-old woman died because of post-alcoholic hepatic insufficiency.
At autopsy study, the brain was macroscopically unchanged. The pineal gland with size of 8 mm in diameter was multicystic in appearance on crosssection. Microscopically, there were several areas of gliotic tissue, exhibiting signs of cystic degeneration and formation of small cavities in the centre of some ones within the pineal parenchyma (Fig. 8A-B). Lobular arrangement of pineal cells was seen.
Case 5. A 66-year-old man died because of circulatory insufficiency. At autopsy study old postapoplectic foci were found in the brain. The pineal gland with diameter of 9 mm was multicystic in cross-section with the central cyst measuring 4 mm in the largest dimension. Microscopically there were multilocular cysts, in parts surrounded by glial fibrillar layers (Fig. 9A)
or directly by bands of pineal parenchyma, separating smaller cavities (Fig. 9B). Pineal parenchyma showed lobular architecture and obvious interstitial gliosis.
Glial cysts without known clinical implications may exist in 23% [34] to about 40% of the human pineal gland in adults [10], but the natural history of cyst development and the risk of its subsequent enlargement and clinical manifestation are not well understood [1].
Generally, it is assumed that mechanisms responsible for pineal glial cyst formation include dysontogenic and degenerative phenomena [6,11,23]. The pineal gland develops by the proliferation of walls of the third ventricle diverticulum in the diencephalic roof. A remnant of the pineal diverticulum or distension of its obliterated portion has been postulated as a possible source of pineal cysts [36,39]. Particularly, this mechanism could be taken into consideration in glial cysts exhibiting ependymal cell lining, like the cyst in the reported case 1. However, ependymal lining was not present in case 2 or in the asymptomatic cysts from autopsy cases, in which degenerative origin of pineal cyst formation could be suggested. In these cases the cysts of variable dimensions were surrounded either by fibrous glial tissue or directly by pineal parenchyma, containing an admixture of prominent interstitial gliosis. It has been stated that degeneration of pineal parenchyma leads to increased astrocytic proliferation, in particular to hyperplasia of interstitial astroglial fibres [11]. However, no specific causes have been correlated with these abnormalities. Morphological studies of pineal glands have evidenced focal gliosis or gliotic plaques with central cystic degeneration in patients who died from various diseases at different ages [31,40]. Pineal cysts adjacent to gliotic plaques were also demonstrated in newborns and young infants at autopsy study, suggesting that many of them may evolve from necrotic and hemorrhagic changes found in the fetal pineal glands [17].
The processes causing an asymptomatic pineal cyst to become symptomatic are unclear and occur infrequently [1]. Follow-up MR imaging of the asymptomatic cysts demonstrated that their size remained stable after months or years [1,4,9,34,37]. In individual patients the cysts exhibited enlargement [1,6] or involution [1,37], but small changes in their size were not associated with specific clinical symptoms [1].
A relationship between size of the cyst and appearance of the symptoms is generally postulated [2,23], but in many cases it may be irrelevant. Overlapping dimensions of the asymptomatic and symptomatic cysts, especially within the range of the cyst diameter from 10 to 20 mm, have frequently been observed [25]. Symptomatic cysts vary in size from 7 mm to 4.5 cm in diameter [7,15], whereas asymptomatic cysts are usually less than 10 mm in diameter [19] but sometimes reach dimensions of 20 to 22 mm [1,33]. In rare instances, relatively small cysts with diameter of 12 to 14 mm are known to cause sudden death due to intracystic bleeding and acute hydrocephalus [27,35]. Therefore, the appearance of clinical symptoms has been attributed to factors determining the rapid enlargement of a pineal cyst, such as intracystic bleeding [6,8,15,24,29], rapid coalescences of pre-existing smaller cavities [6,37], increase of the fluid pressure gradient between the third ventricle and cyst cavity [3] or direct inflow of CSF to the pineal cyst due to communication of the cyst with the third ventricle [13].
In our patient 1 contusion of the brain could be appreciated as the factor initiating enlargement of the pineal cyst, presumably via the mechanism of increased pressure of CSF within the third ventricle [3]. No evidence of recent or previous haemorrhage was found in our cases.
In this report both surgically treated patients presented with severe headaches. Moreover, a rare clinical presentation of syncope was noted in patient 2. In previous cases “pineal syncope” has been related to anterior-inferior movement of the cyst with subsequent aqueductal occlusion [41] or flexion at the waist [22].
Headaches are the most common and frequently the only symptom of pineal cysts in children [20] and in adults [6,25,26,39]. Several factors might be responsible for headaches, including disturbances of the CSF flow through the cerebral aqueduct [20], obstructive hydrocephalus and raised intracranial pressure [15,26], compression on the Galen vein and venous congestion [37]. On the other hand, in patients with otherwise normal neurological exam, the real relation between headache and the presence of a pineal cyst is not well established [32]. Pineal cysts prevail in women [4,7,9,34] and symptomatic cysts are most frequent in young women, at the age with also the highest frequency of migraine headache, suggesting the hypothesis of cyst formation dependent on hormonal influences in such condition as in the period of puberty or pregnancy [6,15,29,36,41].
It is assumed that asymptomatic cysts do not require treatment or follow-up study by MRI but a close clinical observation with indispensable neuroradiological control should be recommended [1,34].
In cases of symptomatic pineal cyst a common problem arises in interpretation of clinical and neuroimaging findings predicting indications or contraindications for surgical procedures. Although it is still debated whether patients with symptomatic cysts should be followed or treated surgically, there is agreement that surgical intervention should be undertaken in patients presenting hydrocephalus, progression of neurological symptoms or enlargement of the cyst [20,25,26,37,38]. The observation of Mandera et al. [20] indicated that symptomatic pineal cysts in children should be followed up for many years and surgical treatment should be recommended only in a minority of cases.
Special importance for management prediction is preoperative discrimination of neoplastic cystic lesion from a non-neoplastic glial cyst. On MRI, the benign pineal cyst is typically rounded, unilocular, isointense or slightly hyperintense in relation to the CSF signal on T1-weighted and FLAIR images, with the wall thickness no more than 2 mm [5,7,8,15,19,37]. In contrast to usually unilocular, round or oval homogeneous cysts, a heterogeneous appearance of multilocular or multiseptate cysts with irregular enhancement often does not permit discrimination of benign and neoplastic cysts [5,8,19,28]. Especially, small cystic pineocytoma and glial pineal cysts showed similar MRI signal characteristics [5]. Nodular contrast enhancement and irregularities of the cyst wall, suggestive of pineocytoma, have been described in some glial cysts [8,28]. Also in our patient 2, the MRI examination resulted in no conclusive diagnosis of multilocular cystic lesion in the pineal gland region.
The importance of histopathological verification of such lesions for further prognosis and therapeutic concepts in operated patients was stressed by Engel et al. [5]. In their series of 13 patients with MRI diagnosis of pineal cysts histological diagnosis revealed 4 glial cysts, 6 pineocytomas, one low-grade astrocytoma, one arachnoid cyst and a teratoma.
When dealing with histopathological examination of pineal cystic lesions, special attention must be paid to obtaining adequate surgical specimens, permitting one to distinguish a glial cyst from pineal parenchymal or low-grade astrocytic neoplasms [2,5,25]. Sometimes, histological diagnosis of a glial cyst may cause serious problems, especially when fragmentary biopsy specimens lack the representative glial and pineal components of the cyst wall. Gross specimens regaining cystic shape by floating it intact and cutting perpendicular sections through the cyst wall should minimize the chance of misdiagnosis [2].
Typically, the cyst wall consists of three layers, namely glial, pineal and collagenous [5,6,15,22,25,28]. Small fragments of the cyst wall, comprising dense gliotic tissue with numerous Rosenthal fibres, might be confused with pilocytic astrocytoma. However, gliosis in the pineal glial cyst differs from pilocytic astrocytoma by lack of cellular heterogeneity and paucicellular, uniformly dense fibrillar feature [18,23]. Difficulties in the interpretation of reactive gliosis, containing Rosenthal fibres, have been noted also in other conditions such as the cyst wall of haemangioblastoma [21].
Histologically, pineal cysts are most often mistaken for a pineocytoma [5,6,15]. The features distinguishing pineal cysts from pineocytoma include presence of an external fibrous capsule, normal pineocytes arranged in lobules with interstitial reactive fibrillary gliosis, absence of pineocytomatous rosettes, and lack of the proliferation index with MIB-1 staining [2,15,18].
In this report, case 1 presented both radiological and histopathological features typical for pineal glial cyst; thus the diagnosis did not present any difficulties. In case 2, the diagnostic difficulties in MRI are rather characteristic for multiseptate cysts, which could also cause some problems in histopathological discrimination. Histologically, the cyst in case 2 was most similar to pineal cystic lesions observed in autopsy cases. There were many cavities of various sizes within areas of gliotic tissue or directly within the pineal parenchyma. Typical ependymal lining was not present. Parenchymal pineal cells were arranged in lobules with an admixture of interstitial glia, calcified deposits and interlobular connective tissue. In accordance with previous reports, it may be concluded that independently of pathophysiological aspects of pineal glial cysts, histopathological findings in asymptomatic and symptomatic cysts are essentially the same.
1. Barboriak DP, Lee L, Provenzale JM. Serial MR imaging of pineal cysts: implications for natural history and follow-up. AJR Am
J Roentgenol 2001; 176: 737-743.
2. Burger PC, Scheithauer BW (eds.). Atlas of Tumor Pathology. Tumors of the Central Nervous System. AFIP, Washington 1994; pp. 233-236
3. Di Chirico A, Di Rocco F, Velardi F. Spontaneous regression of
a symptomatic pineal cyst after endoscopic third-ventriculostomy. Childs Nerv Syst 2001; 17: 42-46.
4. Di Costanzo A, Tedeschi G, Di Salle F, Golia F, Morrone R, Bonavita V. Pineal cysts: an incidental MRI finding? J Neurol Neurosurg Psychiatry 1993; 56: 207-208.
5. Engel U, Gottschalk S, Niehaus L, Lehmann R, May C, Vogel S, Janisch W. Cystic lesions of the pineal region – MRI and pathology. Neuroradiology 2000; 42: 399-402.
6. Fain JS, Tomlinson FH, Scheithauer BW, Parisi JE, Fletcher GP, Kelly PJ, Miller GM. Symptomatic glial cysts of the pineal gland. J Neurosurg 1994; 80: 454-460.
7. Fetell MR, Bruce JN, Burke AM, Cross DT, Torres RA, Powers JM, Stein BM. Non-neoplastic pineal cysts. Neurology 1991; 41: 1034-1040.
8. Fleege MA, Miller GM, Fletcher GP, Fain JS, Scheithauer BW. Benign glial cysts of the pineal gland: unusual imaging characteristics with histologic correlation. Am J Neuroradiol 1994; 15: 161-166.
9. Golzarian J, Balériaux D, Bank WO, Matos C, Flament-Durand J. Pineal cyst: normal or pathological? Neuroradiology 1993; 35: 251-253.
10. Hasegawa A, Ohtsubo K, Mori W. Pineal gland in old age: quantitative and qualitative morphological study of 168 human autopsy cases. Brain Res 1987; 409: 343-349.
11. Haymaker W, Liss L, Vogel SF, Johnson Jr. JE, Adams RD, Scharenberg K. The pineal gland. In: Haymaker W, Adams RD (eds.). Histology and Histopathology of the Nervous System. ChC Thomas, Springfield, Ill, 1982; vol. 2; pp. 1801-2023.
12. Jinkins JR, Xiong L, Reiter RJ. The midline pineal "eye": MR and CT characteristics of the pineal gland with and without benign cyst formation. J Pineal Res 1995; 19: 64-71.
13. Kang HS, Kim DG, Han DH. Large glial cyst of the pineal gland:
a possible growth mechanism. J Neurosurg 1987; 88: 138-140.
14. Katzman GL, Dagher AP, Patronas NJ. Incidental findings on brain magnetic resonance imaging from 1000 asymptomatic volunteers. JAMA 1999; 282: 36-39.
15. Klein P, Rubinstein LJ. Benign symptomatic glial cysts of the pineal gland: a report of seven cases and a review of the literature. J Neurol Neurosurg Psychiatry 1989; 52: 991-995.
16. Kumar P, Tatke M, Sharma A, Singh D. Histological analysis of lesions of the pineal region: a retrospective study of 12 years. Pathol Res Pract 2006; 202: 85-92.
17. Laure-Kamionowska M, Maœliñska D, Derêgowski K, Czichos E, Raczkowska B. Morphology of pineal glands in human fetuses and infants with brain lesions. Folia Neuropathol 2003; 41: 209-215.
18. Louis DN, Reifenberger G, Brat DJ, Ellison DW. Tumours: introduction and neuroepithelial tumours. In: Love S, Louis DN, Ellison DW (eds.). Greenfield’s Neuropathology. Edward Arnold 2008; pp. 1942-1943.
19. Mamourian AC, Towfighi J. Pineal cysts: M.R. imaging. AJNR 1986; 7: 1081-1086.
20. Mandera M, Marcol W, Bierzyñska-Macyszyn G, Kluczewska E. Pineal cysts In childhood. Childs Nerv Syst 2003; 19: 750-755.
21. Matyja E, Grajkowska W, Taraszewska A, Marchel A, Bojarski P, Nauman P. Advanced reactive astrogliosis associated with hemangioblastoma versuss astroglial-vascular neoplasm (“angioglioma”). Folia Neuropathol 2007; 45: 120-125.
22. Maurer PK, Ecklund J, Parisi J, Ondra S. Symptomatic pineal cyst: case report. Neurosurgery 1990; 27: 451-453.
23. McLendon RE, Tien RD. Tumors and tumor-like lesions of maldevelopmental origin. In: Binger DD, McLendon RE, Bruner JM (eds.). Russell & Rubinstein’s Pathology of Tumors of the Nervous System. Arnold, London 1998; pp. 350-352.
24. McNeely PD, Howes WJ, Mehta V. Pineal apoplexy: is it a facilitator for the development of pineal cysts? Can J Neurol Sci 2003; 30: 67-71.
25. Mena H, Armonda RA, Ribas JL, Ondra SL, Rushing EJ. Nonneoplastic pineal cysts: a clinicopathologic study of twenty-one cases. Ann Diagn Pathol 1997; 1: 11-18.
26. Michielsen G, Benoit Y, Baert E, Meire F, Caemaert J. Symptomatic pineal cysts: clinical manifestations and management. Acta Neurochir (Wien) 2002; 144: 233-242.
27. Milroy CM, Smith CL. Sudden death due to a glial cyst of the pineal gland. J Clin Pathol 1996; 49: 267-269.
28. Miyatake S, Kikuchi H, Yamasaki T, Terashima T, Asahi M, Asato R,
Higuchi K, Nakashima Y. Glial cyst of the pineal gland with characteristic computed tomography, magnetic resonance imaging, and pathological findings: report of two cases. Surg Neurol 1992; 37: 293-299.
29. Musolino A, Cambria S, Rizzo G, Cambria M. Symptomatic cysts of the pineal gland: stereotactic diagnosis and treatment of two cases and review of the literature. Neurosurgery 1993; 32: 315-320.
30. Oeckler R, Feiden W. Benign symptomatic lesions of the pineal gland. Report of seven cases treated surgically. Acta Neurochir (Wien) 1991; 108: 40-44.
31. Papasozomenos SCh. Glial fibrillary acidic (GRA) protein-containing cells in the human pineal gland. J Neuropatol Exp Neurol 1983; 42: 391-407.
32. Peres MF, Zukerman E, Porto PP, Brandt RA. Headaches and pineal cyst: a (more than) coincidental relationship? Hedache 2004; 44: 926-930.
33. Petitcolin V, Garcier JM, Mohammedi R, Ravel A, Mofid R, Viallet JF,
Vanneuville G, Boyer L. Prevalence and morphology of pineal cysts discovered at pituitary MRI: review of 1844 examinations. J Radiol 2002; 83: 141-145.
34. Pu Y, Mahankali S, Hou J, Li J, Lancaster JL, Gao J-H, Appelbaum DE, Fox PT. High Prevalence of Pineal Cysts in Healthy Adults Demonstrated by High-Resolution, Noncontrast Brain MR Imaging. Am
J Neuroradiol 2007; 28: 1706-1709.
35. Richardson JK, Hirsch CS. Sudden, unexpected death due to pineal apoplexy. Am J Forensic Med Pathol 1986; 7: 64-68.
36. Sawamura Y, Ikeda J, Ozawa M, Minoshima Y, Saito H, Abe H. Magnetic resonance images reveal a high incidence of asymptomatic pineal cysts in young women. Neurosurgery 1995; 37: 11-15.
37. Tamaki N, Shirataki K, Lin TK, Masumura M, Katayama S, Matsumoto S. Cysts of the pineal gland. A new clinical entity to be distinguished from tumors of the pineal region. Childs Nerv Syst 1989; 5: 172-176.
38. Tartara F, Regolo P, Terreni MR, Giovanelli M. Glial cyst of the pineal gland: case report and considerations about surgical management. J Neurosurg Sci 2000; 44: 89-93.
39. Vaquero J, Martinez R, Escandon J, Bravo G. Symptomatic glial cysts of the pineal gland. Surg Neurol 1988; 30: 468-470.
40. Vuia O. The pineal gland and Rosenthal fibers. Appl Neurophysiol 1975; 38: 47-55.
41. Wisoff JH, Epstein F. Surgical management of symptomatic pineal cysts. J Neurosurg 1992; 77: 896-900.
Copyright: © 2008 Mossakowski Medical Research Centre Polish Academy of Sciences and the Polish Association of Neuropathologists. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2021 Termedia Sp. z o.o. All rights reserved.
Developed by Bentus.