- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
International Journal of Endocrinology
Volume 2012 (2012), Article ID 958732, 8 pages
Diagnostic Significance of Intracystic Nodules on MRI in Rathke’s Cleft Cyst
1Department of Neurosurgery, Fuzhou General Hospital, Fuzong Clinical College, Fujian Medical University, 156 Xihuanbei Road, Fuzhou 350025, China
2Department of Pathology, Fuzhou General Hospital, Fuzong Clinical College, Fujian Medical University, 156 Xihuanbei Road, Fuzhou 350025, China
Received 15 June 2012; Revised 9 August 2012; Accepted 13 August 2012
Academic Editor: Barry Posner
Copyright © 2012 Shou-sen Wang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background and Purpose. To explore strategies for the diagnosis and treatment of Rathke’s cleft cyst (RCC). Methods. The medical records of 24 patients with sellar RCC were retrospectively reviewed. Two patients had concomitant pituitary adenoma, 2 underwent transcranial surgery, and 22 underwent transsphenoidal surgery. The clinical features, especially the findings of intracystic nodules on MRI, were evaluated and compared with the pathological findings. Results. Preoperatively, only 2 patients were diagnosed with RCC or suspected RCC. Pre- and postoperative MRI images revealed 10 intracystic nodules in 9 (37.5%) patients. Two nodules had bull's eyelike changes. The signal intensity of the intracystic nodules varied on T1- and T2-weighted images. Not all nodules on T2-weighted images were visualized. Postoperative MRI revealed recurrence or residual lesion in 5 patients; none had new symptoms and a second surgery was not required. Conclusions. Identifying intracystic nodules is important in patients with sellar cystic lesions. Bull’s eyelike change in an intracystic nodule on MRI, which is reported here for the first time, potentially might have value for confirming the diagnosis.
Rathke’s cleft cyst (RCC) is a benign, epithelium-lined intrasellar cyst. It is believed to originate from remnants of Rathke’s pouch, and its initial site is located in the middle lobe of the pituitary gland. The clinical manifestations of RCC are characterized by headache, hypopituitarism, visual disorder, and diabetes insipidus. Imaging examinations usually indicate a lesion located in the sellar or suprasellar region. Rathke’s cleft cyst is found in 12–33% of routine autopsies [1, 2]. Some RCCs grow progressively over time [1, 3], but few patients with RCCs have obvious clinical symptoms. However, rupture of a RCC may cause severe symptoms [4–7], and RCC is prone to recurrence to a certain extent following surgery . In some patients, RCCs remain stable during long-term followup, whereas some RCCs may undergo reduction after treatment with glucocorticoid . In several cases, RCCs have resolved spontaneously .
Although several clinical studies on RCC have been conducted, the precise source and natural history of RCC are still poorly understood. The features of RCCs on imaging are still not clearly defined, and thus many patients are misdiagnosed before surgery. In addition, indications for surgery are controversial, as are specific operative procedures that are used. Even with modern imaging techniques, it can be difficult to distinguish RCCs from other types of cystic sellar lesions such as cystic pituitary adenoma and craniopharyngioma . It may be somewhat easier to differentiate RCCs from craniopharyngiomas than from intracellular arachnoid cysts because craniopharyngiomas are more associated with psychiatric symptoms and calcifications or solid components on imaging . It has also been reported that single-shot fast spin-echo diffusion-weighted MR imaging is of value for differentiating RCCs from craniopharyngiomas and hemorrhagic components of pituitary adenomas, but not from cystic components of pituitary adenoma . Making a preoperative diagnosis is important because various types of cystic sellar lesions are treated differently. Often the minimally invasive transsphenoidal endoscopic approach is used for symptomatic RCC.
Obtaining an accurate preoperative diagnosis, determining the proper surgical indications, and selecting the optimal surgical methods continue to be the major concerns of neurosurgeons. In the present study, the medical records of 24 patients with sellar RCC in the past 7 years were retrospectively reviewed, and the findings on imaging and pathological examinations were compared with the aim of proposing improved diagnostic approach and treatment strategy for RCC.
2.1. General Information
A total of 24 patients (6 male and 18 female) with RCC treated at our hospital from January 2005 to August 2011 were included. The average age was 40 years (range: 20–62 years). Patients were excluded if they underwent surgery not performed by the first author or received conservative therapy. All patients were followed up by face-to-face interview or telephone. The follow-up period ranged from 4 weeks to 6.5 years (median of 25 months).
2.2. Imaging Examinations
MRI was performed on all patients utilizing the following 2 systems and parameters: (1) GE Signa 1.5T MR system—routine MRI head coil using fast spin-echo (FSE) or spin-echo (SE) pulse sequences. Coronal and sagittal T1-weighted images and coronal and axial T2-weighted images were obtained. At the same time, enhanced three-dimensional scanning was also performed using GD-DTPA (0.1 mmol/kg) as the contrast agent. For coronal and sagittal images, slice thickness: 3 mm, slice interval: 3 mm; for axial images, slice thickness: 6 mm, slice interval: 7.5 mm; Parameters: T1WI: tr500 ms, TE15 ms, matrix: , field of view: mm; T2WI: TR4200 ms, TE98 ms, matrix: , field of view: mm, 2 excitations. (2) Siemens Magnetom Trio Tim 3.0 T MRI system—axial thickness: 5 mm; slice interval: 6.5 mm; coronal and sagittal thickness: 2.5 mm; slice interval: 2.75 mm. Parameters: T2WI: coronal and axial images: TR/TE 3000 ms/83–98 ms; field of view: mm; matrix: ; 2 excitations. T1WI: coronal and axial images: TR/TE 400–500 ms/8 ms; field of view: mm; matrix: ; 3 excitations. Enhanced three-dimensional scanning: contrast agent: GD-DTPA at 0.1 mmol/kg.
2.3. Surgical Methods
All patients underwent surgery due to mass effect of a space-occupying lesion. Additional reasons for performing surgery were headache that could not be explained by other etiologies, decreased visual acuity or increased visual field defect, and endocrine dysfunction. Craniotomy was performed via the pterion approach in 2 patients, and via the unilateral nasal-nasal septum-sphenoid sinus (transsphenoidal) approach in the remaining 22 patients. In transcranial surgery, the RCC contents were suctioned and most or all of the cyst wall was resected. In transsphenoidal surgery, following incision of sellar dura mater, RCC was located beneath the dura mater, and the cystic fluid was removed by suction before resecting the cyst wall. In cases where normal pituitary gland was located beneath the dura mater, the RCC was usually light yellow, yellow, or grey-white and could be either softened or hardened. The pituitary gland would be incised and the lesion removed after the cystic region was reached. The tissues surrounding the cyst were collected for pathological examination. After surgery, the sellar floor was opened to assure smooth drainage.
2.4. Endocrine Examination
Preoperative and postoperative endocrinological lab tests were conducted, including tests for adrenocorticotropic hormone (ACTH), growth hormone (GH), thyroid-stimulating hormone (TSH), testosterone, cortisol, estradiol, prolactin, and follicle-stimulating hormone/luteinizing hormone (FSH/LH).
2.5. Histopathological Examination
Surgical specimens were diagnosed as RCC via routine pathological examination. Tissues were routinely embedded in paraffin and cut into sections which were stained with hematoxylin and eosin (H&E).
Only 2 of the 24 patients were diagnosed with RCC or suspected RCC before surgery, and 2 were diagnosed with sellar cystic occupying lesions. In the remaining patients, tumor or pituitary adenoma was suspected in the preoperative diagnosis.
3.1. Imaging Findings
The imaging findings are presented in Table 1. According to the images and surgical findings, the mean maximal cyst size was 14.5 mm in diameter (range: 7.0–30.0 mm). Cyst size appeared to be related to blurry vision; for lesion size > 15 mm, there was a greater incidence of decreased visual acuity and increased visual field defect, and for cyst size ≤ 15 mm, visual acuity appeared to be unaffected but visual field defect was noted without central involvement. A slightly lateral location was observed for the RCC in 2 patients and in the remaining patients, RCCs were located in the midline of the pituitary fossa. Evident intracystic nodules were found in 8 patients (Figures 1, 2, and 3) and a suspected nodule in one patient. In all, 10 intracystic nodules were identified by MRI in 9 patients, and the nodules had homogenous intensity without enhancement. One patient (case 17) had 2 nodules within the RCC. Two nodules had bull’s eyelike changes (cases 10 and 19) (Table 2). In the 9 patients with intracystic nodules, puncturing of the sellar dura mater during transsphenoidal surgery led to the flow of thin mucous fluid. After opening the sellar floor and pituitary tissue layer, both thin and thick mucous fluid, and semisolid or solid jellylike tissues were present, but blood supply was absent. Because the thin fluid flowed out immediately during the operation, the tissues could not be comprehensively observed. Thus, the location of intracystic nodules could not be accurately verified during surgery. Observations of sagittal MRI images revealed a cyst anterior to the adenohypophysis in one patient, anterosuperior to the adenohypophysis in 2, posterior to the adenohypophysis in 15, surrounded by the pituitary in 4 patients (Figure 4) and located between the pituitary and tumor in 2 patients. Morphologically, the majority of cysts were round or oval, and the minorities were snowman-like, spindle-like, pancake-shaped or boot-shaped (Table 1). In several patients, the cysts presented characteristic waists.
In all patients, the postoperative diagnosis of RCC was based on the intraoperative findings. In 2 patients with concomitant pituitary adenoma, resection of the pituitary adenoma was performed. In case 7, the RCC was located at the apex of the tumor cavity, which was separated by a thin and uneven transparent membrane; the RCC was not removed directly. In case 24, both the RCC and pituitary adenoma were completely removed. In the remaining patients, the intracystic contents were completely removed.
After surgery, transient diabetes insipidus was present in about 50% of patients and it continued for 3 days to 2 weeks. Diabetes insipidus in 3 patients that lasted for one month resolved spontaneously. In case 13, the patient already had diabetes insipidus for several years and postoperative urinary volume returned to the normal level. In the 8 patients with visual impairment before surgery, eyesight was improved after surgery. Postoperative visual acuity improved by a mean of 0.35 (range: 0.1–0.6). Among 17 patients with pre-operative headache, 8 had improvement and only had mild headache postoperatively; among 9 patients who had pre-operative dizziness, 4 had improvement and only had mild dizziness postoperatively.
Following surgery, patients were reexamined with MRI and no recurrence was noted in 21 of them.
4.1. New Features of Intracystic Nodules of RCC and Their Significance
In the present study, the MRI findings of 24 patients were reviewed and 9 patients (37.5%) had intracystic nodules. Most of the nodules had homogenous intensity without enhancement on MRI. Intracystic nodules have been investigated in several studies and are regarded to have diagnostic value [10, 11, 14]. We found that 2 intracystic nodules were characterized by bull’s eyelike changes. This is the first time that bull’s eye-like changes are reported in sellar intracystic nodules. The bull’s eye-like changes might be specific for RCC and provide valuable information for confirming the diagnosis, although it cannot be ruled out that these changes might also occur in other sellar masses. Further research is needed to determine whether the bull’s eye-like changes are specific to RCCs. The mechanism underlying the formation of bull’s eye-like changes is still unclear, and further research is required for understanding how these changes occur.
Several nodules were only clearly present on T1-weighted images and 2 nodules with different intensities were found within a single cyst. These features have also never been reported before. In our study, we also observed that the intensity of intracystic nodules varied on T1- and T2-weighted images. These cysts on T1-weighted images could have lower intensity than cystic fluid, and not all cysts could be visualized on T2-weighted images. These findings are not consistent with previous reports, which found that the cysts were hyperintense on T1-weighted images and hypointense on T2-weighted images, and always could be clearly identified on T2-weighted images [10, 11, 14].
A minor fraction of cysts can demonstrate ring enhancement. Billeci et al.  observed ring-enhancement in 2 of 14 RCC patients. In our study, 4 patients had ring enhancement (cases 4, 16, 17, and 19). Some researchers have proposed that ring enhancement on MRI was related to squamous metaplasia, inflammation, and deposition of hemosiderin or cholesterol crystals . Other researchers have also speculated that this enhancement was caused by the thin pituitary tissues surrounding the RCC [1, 16], which is consistent with our findings. Of note, pituitary abscess and RCC have extremely similar ring enhancement and patients with these lesions also present with fever and inflammatory response, and have abscess-like cystic fluid. However, inflammatory granulation tissue should surround the cystic fluid in pituitary abscess, which may also demonstrate changes related to sphenoid sinusitis on imaging examinations.
In some studies, researchers have speculated that the cystic fluid of RCC was mainly composed of proteins and cholesterol, although the cholesterol content was extremely low [3, 10, 16]. In the present study, MRI revealed that the intensity of intracystic nodules varied. The viscosity and texture of intracystic contents also varied as demonstrated by the surgical findings. Hematoxylin and eosin staining of RCC samples revealed that the cystic fluid contained proteins of different sizes and had a red/blue staining pattern. These findings imply that the appearance of intracystic nodules may be related to the concentration of mucins and have multiple proteins.
Nishioka et al.  reported that intracystic nodules were identified in 16 of 37 patients (43.2%), Byun et al.  identified intracystic nodules in 10 of 13 patients (76.9%), and Binning et al.  observed intracystic nodules in 9 of 20 patients (45.0%). The incidence of intracystic nodules was relatively high in these studies. In our study, while a lower incidence of 37.5% is reported, it is worth noting that intracystic nodules were not even observed in some studies [1, 15–17]. Intracystic nodules with nonenhancement and homogenous intensity could be used to differentiate RCC from other cystic lesions in the sellar region. Therefore, more attention should be paid to the presence of intracystic nodules in clinical practice.
Distinguishing among RCC, craniopharyngioma, and cystic lesions remains a challenging diagnostic problem . To address this issue, Shin et al.  used clinical, biochemical, and radiographic features to identify distinctive characteristics. Patients with craniopharyngioma had significantly more psychiatric symptoms than patients with RCC or arachnoid cyst, and significantly fewer patients with arachnoid cyst had two or more impaired pituitary axes than patients with RCC or craniopharyngioma. On CT scan, a significantly higher percentage of patients with craniopharyngioma had calcification detected than patients with RCC or arachnoid cyst.
4.2. Determination of Surgical Indications Based on the Therapeutic Efficacy
The goal of surgical intervention is to remove the intracystic contents and eliminate the source of space-occupying lesions and pituitary inflammation. The cyst wall is also partially resected for pathological examination for diagnostic confirmation. Opening of the sellar floor is beneficial for the drainage of cystic fluid. Some researchers have proposed that early surgical intervention is necessary for RCC patients in order to prevent the aggravation of pituitary function [1, 18]. The inflammatory response in the pituitary tissues surrounding the cyst is not found in pituitary adenoma and has become an intrinsic indicator for active surgical intervention in symptomatic RCC. Other researchers have recommended that surgery is required even when the symptoms are mild . Of note, protecting endocrine function should be more important than resection of the RCC. Attempting to remove as much cyst wall as possible may compromise pituitary function and even worsen diabetes insipidus. We believe that while the intracystic contents should be completely removed, biopsy or partial resection of the cyst wall should also be simultaneously performed. Aggressive resection of the cyst wall is not recommended, and this has also been noted in other studies . We would rather perform surgery following recurrence, instead of performing radical resection of the cyst wall that may lead to compromised endocrine function. For patients with recurrent RCC, the indications of surgery should be based on the clinical manifestations (especially new symptoms). Mere findings on MRI are not indications for surgery. In the present study, patients with recurrence did not undergo a second surgery because the growth of recurrent RCC stopped without developing new symptoms. Finding typical cystic contents during surgery is helpful for the surgical diagnosis, and observing typical cystic epithelial cells on histological examination is not necessary for diagnostic confirmation. It is important to note that surgery is associated with risk of damaging the pituitary tissues, especially when the RCC is located behind the adenohypophysis.
This study had several limitations. First, it is a retrospective case series. Second, the sample size of 24 patients was small. Third, the length of followup, which ranged from 4 weeks to 6.5 years, was less than optimal. Finally, it can be extremely difficult, if not impossible, to distinguish RCC from cystic craniopharyngioma in many cases unless sufficient lesional epithelium is removed for detailed histologic examination. In 6 patients (cases 1, 4, 11, 12, 15, and 16), adequate specimen for detailed histologic examination was not obtained.
We made several unique observations. The most notable was that intracystic nodules in RCC can have bull’s eye-like changes; these changes might be specific to RCC. In addition, 2 nodules with different intensities were found within a single RCC. Also, we found that, for the first time, that some nodules are only clearly present on T1-weighted images, while being difficult to distinguish on T2-weighted images. These findings should be helpful in diagnosing RCC preoperatively, which is an important goal because different types of sellar cysts require different forms of treatment.
Conflict of Interests
The authors declare no conflict of interests exists in this study.
- D. Billeci, E. Marton, M. Tripodi, E. Orvieto, and P. Longatti, “Symptomatic Rathke's cleft cysts: a radiological, surgical and pathological review,” Pituitary, vol. 7, no. 3, pp. 131–137, 2004.
- Y. Miyajima, H. Oka, S. Utsuki, K. Kondo, K. Sato, and K. Fujii, “Symptomatic Rathke's cleft cyst with cavernous sinus syndrome—case report,” Neurologia Medico-Chirurgica, vol. 47, no. 12, pp. 576–578, 2007.
- C. C. Chuang, Y. L. Chen, S. M. Jung, and P. C. Pai, “A giant retroclival Rathke's cleft cyst,” Journal of Clinical Neuroscience, vol. 17, no. 9, pp. 1189–1191, 2010.
- C. M. Dancer, M. L. Woods, R. D. Henderson, T. Robertson, M. Mungomery, and A. Allworth, “Mollaret's meningitis and pituitary failure associated with a Rathke's cleft cyst,” Internal Medicine Journal, vol. 38, no. 7, pp. 609–611, 2008.
- H. Nishioka, J. Haraoka, H. Izawa, and Y. Ikeda, “Headaches associated with Rathke's cleft cyst,” Headache, vol. 46, no. 10, pp. 1580–1586, 2006.
- J. Schittenhelm, R. Beschorner, T. Psaras et al., “Rathke's cleft cyst rupture as potential initial event of a secondary perifocal lymphocytic hypophysitis: proposal of an unusual pathogenetic event and review of the literature,” Neurosurgical Review, vol. 31, no. 2, pp. 157–163, 2008.
- E. Sonnet, N. Roudaut, P. Mériot, G. Besson, and V. Kerlan, “Hypophysitis associated with a ruptured Rathke's cleft cyst in a woman, during pregnancy,” Journal of Endocrinological Investigation, vol. 29, no. 4, pp. 353–357, 2006.
- D. M. S. Raper and M. Besser, “Clinical features, management and recurrence of symptomatic Rathke's cleft cyst,” Journal of Clinical Neuroscience, vol. 16, no. 3, pp. 385–389, 2009.
- H. Maruyama, Y. Iwasaki, M. Tsugita et al., “Rathke's cleft cyst with short-term size changes in response to glucocorticoid replacement,” Endocrine Journal, vol. 55, no. 2, pp. 425–428, 2008.
- W. M. Byun, O. L. Kim, and D. S. Kim, “MR imaging findings of Rathke's cleft cysts: significance of intracystic nodules,” American Journal of Neuroradiology, vol. 21, no. 3, pp. 485–488, 2000.
- M. J. Binning, O. N. Gottfried, A. G. Osborn, and W. T. Couldwell, “Rathke cleft cyst intracystic nodule: a characteristic magnetic resonance imaging finding,” Journal of Neurosurgery, vol. 103, no. 5, pp. 837–840, 2005.
- J. L. Shin, S. L. Asa, L. J. Woodhouse, H. S. Smyth, and S. Ezzat, “Cystic lesions of the pituitary: clinicopathological features distinguishing craniopharyngioma, Rathke's cleft cyst, and arachnoid cyst,” Journal of Clinical Endocrinology and Metabolism, vol. 84, no. 11, pp. 3972–3982, 1999.
- N. Kunii, T. Abe, M. Kawamo, D. Tanioka, H. Izumiyama, and T. Moritani, “Rathke's cleft cysts: differentiation from other cystic lesions in the pituitary fossa by use of single-shot fast spin-echo diffusion-weighted MR imaging,” Acta Neurochirurgica, vol. 149, no. 8, pp. 759–769, 2007.
- H. Nishioka, J. Haraoka, H. Izawa, and Y. Ikeda, “Magnetic resonance imaging, clinical manifestations, and management of Rathke's cleft cyst,” Clinical Endocrinology, vol. 64, no. 2, pp. 184–188, 2006.
- S. H. Choi, B. J. Kwon, D. G. Na, J. H. Kim, M. H. Han, and K. H. Chang, “Pituitary adenoma, craniopharyngioma, and Rathke cleft cyst involving both intrasellar and suprasellar regions: differentiation using MRI,” Clinical Radiology, vol. 62, no. 5, pp. 453–462, 2007.
- L. Wen, L. B. Hu, X. Y. Feng et al., “Rathke's cleft cyst: clinicopathological and MRI findings in 22 patients,” Clinical Radiology, vol. 65, no. 1, pp. 47–55, 2010.
- F. Komatsu, H. Tsugu, M. Komatsu et al., “Clinicopathological characteristics in patients presenting with acute onset of symptoms caused by Rathke's cleft cysts,” Acta Neurochirurgica, vol. 152, no. 10, pp. 1673–1678, 2010.
- G. Frank, V. Sciarretta, D. Mazzatenta, G. Farneti, G. C. Modugno, and E. Pasquini, “Transsphenoidal endoscopic approach in the treatment of Rathke's cleft cyst,” Neurosurgery, vol. 56, no. 1, pp. 124–128, 2005.
- B. Sade, S. Albrecht, P. Assimakopoulos, J. L. Vézina, and G. Mohr, “Management of Rathke's cleft cysts,” Surgical Neurology, vol. 63, no. 5, pp. 459–466, 2005.