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AJR 2001; 177:1313-1318
© American Roentgen Ray Society


Original Report

Perineural Cysts Presenting as Complex Adnexal Cystic Masses on Transvaginal Sonography

Mark J. McClure1,2, Mostafa Atri1, Masoom A. Haider3 and John Murphy1

1 Department of Medical Imaging, Sunnybrook & Women's Health Science Centre, 2075 Bayview Ave., Ontario, M4N 3M5 Canada.
2 Present address: Department of Radiology, Craigavon Area Hospital, 68 Lurgan Rd., Portadown Craigavon, BT63 5QQ Northern Ireland.
3 Department of Medical Imaging, Mount Sinai Hospital and University Health Network, 600 University Ave., Toronto, Ontario, M5G 1X5 Canada.

Received September 20, 2000; accepted after revision June 25, 2001.

 
Address correspondence to M. J. McClure.


Abstract
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
OBJECTIVE. This study describes the sonographic features of sacral perineural cysts that initially presented as adnexal complex cystic masses on transvaginal sonography.

CONCLUSION. Perineural cysts may have a complex cystic appearance, including septation and internal debris, on transvaginal sonography. The extraovarian, extraperitoneal, and posterior location on real-time sonography are suggestive features.


Introduction
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Transvaginal sonography is a frequently performed examination for the evaluation of adnexal masses. Sonography confirms the location of these masses in relation to the ovary, the cystic or solid nature of such lesions, and further characterizes complexity such as wall thickening or nodulation, septation, internal debris, and vascularity. Causes of complex adnexal cysts include ovarian cystic benign and malignant tumors, functional ovarian masses, endometriomas, and extraovarian lesions such as fallopian tube related masses, paraovarian cysts, abscesses, hematomas, and lymph nodes. With extraovarian lesions, the ovaries should be identified as separate structures.

Identification of perineural cysts is more frequent with the increasing use of MR imaging of the pelvis and lumbosacral spine [1,2,3]. The MR signal characteristics and multiplanar capability readily show the cystic nature of these lesions and their origin from the sacral foramina. We describe transvaginal sonographic features of this condition with CT and MR correlation.


Materials and Methods
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
This series consists of five women (age range, 28-44 years; mean age, 39.6 years) presenting with adnexal complex cystic masses identified on transvaginal sonography over one year. Patients were referred for investigation of pelvic pain (n = 4), dysmenorrhea (n = 2), dyspareunia (n = 1), and perineal pain (n = 1). All patients (n = 5) were examined by transvaginal sonography followed by MR imaging (pelvis, n = 4; lumbosacral spine, n = 1). Two patients also underwent a CT examination before MR imaging. MR imaging was performed for further assessment of these lesions because of its known role in further characterizing and localizing nonspecific adnexal masses seen on transvaginal sonography [4, 5]. We used MR imaging to document the final diagnosis in these cases.

Sonographic images were obtained with an HDI 5000 scanner (Advanced Technology Laboratories, Bothwell, WA). Transabdominal sonography using curved array transducers with a frequency of 3 or 5 MHz was performed on all patients (n = 5), followed by transvaginal sonography with a transducer frequency range of 4 to 8 MHz. The examinations included assessment of gray-scale and color Doppler sonography in all five patients. Contrast-enhanced helical CT was performed on a HiSpeed Advantage scanner (General Electric Medical Systems, Milwaukee, WI), with a slice collimation of 8 mm performed after administration of 150 mL of iodinated IV contrast material at 3 mL/sec. Pelvic MR imaging (n = 4) was performed with a 1.5-T GE scanner (Horizon LX; General Electric Medical Systems) using a torso coil. Four patients underwent axial T1-weighted spin-echo sequences (TR/TE, 650/10; slice thickness, 8 mm) and axial and coronal T2-weighted fast spin-echo sequences (6200/100; slice thickness, 4 mm). A contrast-enhanced T1-weighted spoiled gradient-echo sequence (6.1/1.4; slice thickness, 5 mm) was also performed on two of the four patients after a bolus IV injection of 0.1 mmol/kg of gadolinium dimeglumine (Magnevist; Berlex Canada, Montreal, Canada). Lumbosacral spine MR imaging using a phased-array surface coil was performed on one patient. Sagittal T1-weighted spin-echo sequence (360/20; slice thickness, 3 mm) and sagittal and oblique coronal T2-weighted fast spin-echo sequences (4000/80; slice thickness, 3 mm) were performed.


Results
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Normal-appearing ovaries were identified as separate structures in all patients (Fig. 1A,1B,1C). All cystic masses (n = 8) were identified posteriorly in relation to the ovaries and located anteriorly to the sacrum (Figs. 1A,1B,1C,2A,2B,3A,3B,4A,4B,4C,5A,5B,5C). Three cases were bilateral (Figs. 1A,1B,1C, 4A,4B,4C, and 5A,5B,5C) and two were unilateral (Figs. 2A,2B and 3A,3B). The lesions were multilocular (n = 7, three bilateral and one unilateral left-sided) and unilocular (n = 1, unilateral left-sided). The number of locules per lesion ranged from one to seven (mean, 4.5). The largest locule size ranged from 21 to 33 mm (mean, 26 mm). Wall thickness was uniformly thin (<2 mm) in all cysts, with no mural nodularity identified. Septa were identified in three patients (Figs. 2A,2B,3A,3B,4A,4B,4C) and were uniformly thin (<2 mm), with no septal nodularity. All patients contained internal debris in at least one locule, which was floating (n = 4), layered (n = 4), and heterogenous (n = 1). Color Doppler sonography revealed no vascularity in any lesion.



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Fig. 1A. 42-year-old woman with perineal pain and bowel disturbance. Sagittal transvaginal sonogram of right adnexa shows complex cystic mass (white arrows) containing heterogenous internal debris. Mass is clearly separate from right ovary (RO) and posteriorly located anterior to sacrum (black arrow). Multiocular cystic lesion was also identified in left adnexa (not shown).

 


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Fig. 1B. 42-year-old woman with perineal pain and bowel disturbance. Transverse transvaginal sonogram of right adnexa shows absence of detectable blood flow on color Doppler sonography. Some internal debris is seen layered dependently with change in patient's position.

 


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Fig. 1C. 42-year-old woman with perineal pain and bowel disturbance. Axial T2-weighted MR image shows bilateral hyperintense multilocular cysts (arrows). Note uniformly thin walls and absence of septa. Heterogenous signal intensity of right-sided lesions correlates with heterogenous debris seen on transvaginal sonography.

 


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Fig. 2A. 43-year-old woman with left lower quadrant pain and dysmenorrhea. Sagittal transvaginal sonogram of left adnexa shows complex cystic mass containing thin (<2 mm) septation (curved arrow) and fine internal floating debris with dependent layering (white straight arrow). Lesion is posteriorly located on sacrum (black arrow).

 


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Fig. 2B. 43-year-old woman with left lower quadrant pain and dysmenorrhea. Axial T2-weighted MR image shows hyperintense fluid in unilocular cyst that contains layering internal debris (arrow).

 


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Fig. 3A. 28-year-old woman with persistent pelvic pain, dysmenorrhea, and dyspareunia. Transverse transvaginal sonogram of left adnexa shows complex cyst containing several thin (<2 mm) septa (curved arrow), with some floating and layered internal debris (straight solid arrow) located posteriorly adjacent to sacrum (open arrow).

 


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Fig. 3B. 28-year-old woman with persistent pelvic pain, dysmenorrhea, and dyspareunia. Axial T2-weighted MR image shows multilocular left-sided cysts. Location of these cysts abutting left piriformis muscle (P) may help explain initial consideration of piriformis muscle hematoma in differential diagnosis based on transvaginal sonographic appearance.

 


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Fig. 4A. 41-year-woman with 2-month history of pelvic pain. Sagittal transvaginal sonogram of right adnexa shows complex multilocular cystic mass containing few thin (<2 mm) septations (curved arrow) and floating and layered internal debris (white arrow). Lesions are located posteriorly on sacrum (black arrow). Note presence of free fluid (FF).

 


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Fig. 4B. 41-year-woman with 2-month history of pelvic pain. Contrast-enhanced CT image reveals bilateral hypodense (<10 H) lesions (arrows).

 


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Fig. 4C. 41-year-woman with 2-month history of pelvic pain. Coronal T2-weighted MR image shows origin of cysts from sacral foramina bilaterally (arrows).

 


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Fig. 5A. 44-year-old woman with lower abdominal pain. Transverse transvaginal sonogram of left adnexa shows complex tubular-shaped cystic lesion (small white dots) containing internal floating (white arrow) and layered (asterisk) echogenic debris. Dorsal location is evident by sacrum (black arrow).

 


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Fig. 5B. 44-year-old woman with lower abdominal pain. Contrast-enhanced CT image shows bilateral hypodense (<10 H) lesions (arrows).

 


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Fig. 5C. 44-year-old woman with lower abdominal pain. Sagittal T2-weighted MR image shows connection of cystic masses with sacral foramina (asterisk).

 

The initial differential diagnostic considerations, based on the sonographic features, included endometrioma (n = 3), tubo-ovarian abscess (n = 1), internal iliac lymphadenopathy (n = 1), hydrosalpinx (n = 1), piriformis muscle hematoma (n = 1), and ectopic pregnancy (n = 1). The patient with the largest lesion (Fig. 1A,1B,1C), and who complained of perineal pain, was undergoing treatment for anal fissures and irritable bowel syndrome that were thought to contribute to her symptoms. One patient (Fig. 2A,2B) had laparoscopic confirmation of extraovarian endometriosis and transvaginal sonography of the previous year for comparison, which remained unchanged. A hematoma was considered in one patient, given the location to the ipsilateral piriformis muscle (Fig. 3A,3B). In another patient, the adnexal cystic mass was associated with free pelvic fluid (Fig. 4A), and ectopic pregnancy was considered. A subsequent test for pregnancy was negative.

CT (n = 2) (Figs. 4A,4B,4C and 5A,5B,5C) showed the lesions to be of uniform water attenuation (<10 H), located anterior to the sacrum, and with widened sacral foramina. MR imaging (n = 5) confirmed the presence of perineural cysts, and multiplanar acquisition helped to show ventral herniation through the sacral foramina and connection with the thecal sac. All perineural cysts were of high signal intensity on T2-weighted sequences and of low signal intensity on T1-weighted sequences. A heterogeneous high signal intensity on T2-weighted sequences in some lesions (Fig. 1C) correlated with the internal debris seen on transvaginal sonography (Fig. 1A). No wall or septal thickening was seen in any lesion, and no enhancement of the wall was present on CT or MR imaging.


Discussion
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Abstract
Introduction
Materials and Methods
Results
Discussion
References
 
Perineural cysts are relatively common. Tarlov [6] originally described five cases in 1938 as incidental findings during autopsies of 30 adults. More recently, Paulsen et al. [3] reported 23 cases of perineural cysts in 500 sequential lumbosacral MR examinations. Usually, the perineural cysts are located in the lower lumbar and sacral spinal canal and may extend through adjacent foramina with associated bony erosion [7]. It is unusual to identify these lesions in the pelvis by ventral extension through the anterior sacral foramina. To our knowledge, we report the first series in the radiology literature on sacral perineural cysts presenting as adnexal complex cystic masses on transvaginal sonography.

In two patients, extraovarian endometrioma was considered in the differential diagnosis on sonographic appearance, with a history of surgically confirmed endometriosis in one patient. The third patient was unusual in that her cystic mass appeared to be located in the left piriformis muscle, with associated muscular pressure atrophy. On real-time examination, these masses appeared to be fixed to the pelvic side wall, as indicated by lack of movement during breathing. The differential diagnosis included a muscle hematoma. Atrophy of muscle associated with pressure from a perineural cyst is evident on MR imaging (Fig. 3B), is previously unreported, and may be a causative factor in producing pain. The fourth patient showed bilateral cystic adnexal lesions, and although tubo-ovarian abscess and endometrioma were considered, the free fluid suggested the possibility of ectopic pregnancy. In the fifth patient, the unusual tubular configuration of the lesions suggested hydrosalpinx or internal iliac lymphadenopathy.

The cause of perineural cysts remains uncertain. Tarlov [8] proposed that they were related to trauma, with hemorrhage causing impedance of venous drainage and subsequent rupture. Others believe they are of congenital origin [9]. The cyst cavity is anatomically located between the perineurium (nerve root arachnoid covering) and the endoneurium (pial layer) and communicates with the subarachnoid space [10]. The cyst wall usually contains nerve fibers. Tarlov [10] described the pathologic finding of frequent multilocularity of lesions in surgically resected cases. The sonographic multilocularity of the lesions that we describe correlates well with this finding. The presence of internal septa on transvaginal sonography and MR imaging, internal debris on transvaginal sonography, and corresponding heterogeneous T2-weighted MR signal may represent the presence of blood or cells and might support the traumatic etiology proposed by Tarlov [8]. We propose that a further possible cause for pain may be the stretching of nerve fibers contained in the cyst wall. Alternatively, superimposed bleeding may be the cause of pain in an otherwise asymptomatic cyst.

On the basis of the sonographic features of these five patients, we believe that perineural cysts should be considered in the presence of an extraovarian adnexal cystic mass that is posteriorly located and does not move with breathing. The most common extraovarian adnexal cystic masses are hydrosalpinges and paraovarian cysts. Although these lesions could be fixed as a result of the associated adhesions, they are often mobile because of their intraperitoneal location. Most hydrosalpinges are more elongated and tubular than those in the cases we have described. Although an endometriotic cyst with adhesion is a possibility, extraovarian endometriosis is rarely cystic and, in general, does not reach large proportions.

The five patients we describe are interesting in that they presented initially with lower abdominal and pelvic pain. To our knowledge, no previous reports exist in the literature of pelvic adnexal perineural cysts causing pain. It is uncertain if the pain described by these patients was in fact related to the presence of the perineural cysts. One patient had histologically proven endometriosis and another patient had a long history of irritable bowel syndrome. These conditions certainly could play a role in their symptomatology. The other three patients had no relevant medical history and a relatively short duration of symptoms. It is unlikely that the cysts we describe caused pain by pressure on adjacent structures or local nerve stretching as a result of the short duration of symptoms and absence of low back pain, sciatica, or urinary disturbance. Hemorrhage into an otherwise asymptomatic cyst is possible based on the sonographic evidence. Raza et al. [11] reported a case of bilateral adnexal perineural cysts that were discovered during a routine sonogram in a patient experiencing no pain. In a retrospective series by Paulsen et al. [3], five of 23 patients with perineural cysts experienced low back pain that they attributed to presence of the cyst, but these cysts were all located in the more typical dorsal sacral location.

Current treatment options for symptomatic perineural cysts involve extensive surgery with sacral laminectomy and cyst excision [10] or, more recently, microsurgical cyst fenestration and imbrication [12]. Paulsen et al. [3] described a method of CT-guided percutaneous cyst aspiration in five women with painful radiculopathy, but cyst fluid reaccumulated in four of the five patients. The authors advocated this method for attaining a pain-free interval in symptomatic patients. On the basis of our experience with transvaginal sonography of perineural cysts, transvaginal sonographically guided aspiration of symptomatic cysts could offer an alternative technique that would be simple, quick, and safe to perform. The proximity of the needle-guide to the cyst and the real-time imaging would offer advantages, although further studies would be required to further evaluate these procedures.

Limitations of our study are the relatively small sample size and the lack of pathologic correlation. A possible bias in the study group is the complex nature of the masses that lead to further appropriate investigation. It is conceivable that perineural cysts could present as simple adnexal cysts on transvaginal sonography. On the basis of the MR imaging experience and data, we believe that the adnexal cystic appearance of perineural cysts will be more commonly recognized in the future, and the appearance could potentially be less complicated than described in this series.

In conclusion, if an adnexal extraovarian cystic mass is identified on transvaginal sonography, unilateral or bilateral, the differential diagnosis should include perineural cyst, especially if the posterior extraperitoneal location of the mass is suggested on realtime sonography. This finding is important because the correct diagnosis is often reassuring for the patient and may prevent unnecessary surgery.


References
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
 

  1. Willinsky RA, Grosman H, Cooper PW, Kassel EE, Fazl M. The radiology of sacral cysts. Can Assoc Radiol J 1988;39:21 -25[Medline]
  2. Araki Y, Tsukaguchi I, Ishida T, et al. MRI of symptomatic sacral perineural cysts. Radiat Med 1992;10:250 -252[Medline]
  3. Paulsen RD, Call GA, Murtagh FR. Prevalence and percutaneous drainage of cysts of the sacral nerve root sheath (Tarlov cysts). AJNR 1994;15:293 -297[Abstract]
  4. Komatsu T, Konishi I, Mandai M, et al. Adnexal masses: transvaginal US and gadolinium-enhanced MR Imaging assessment of intratumoral structure. Radiology 1996;198:109 -115[Abstract/Free Full Text]
  5. Hricak H, Chen M, Coakley FV, et al. Complex adnexal masses: detection and characterization with MR imaging-multivariate analysis. Radiology 2000;214:39 -46[Abstract/Free Full Text]
  6. Tarlov IM. Perineural cyst of the spinal nerve roots. Arch Neurol Psychiatry 1938;40:1067 -1074
  7. Truwit CL. Harle TS. Case report 524. Skeletal Radiol 1989;18:75 -77[Medline]
  8. Tarlov IM. Sacral nerve-root cysts: pathogenesis and clinical significance. J Nerv Ment Dis 1953;117:156 -157
  9. Fortuna A, La Torre E, Ciappetta P. Arachnoid diverticula: a unitary approach to spinal cysts communicating with the subarachnoid space. Acta Neurochir 1977;39:259 -268[Medline]
  10. Tarlov IM. Spinal perineurial and meningeal cysts. J Neurol Neurosurg Psychiatry 1970;33:833 -843[Medline]
  11. Raza S, Klapholz H, Benacerraf BR. Tarlov cysts: A cause of bilateral adnexal masses on pelvic sonography. J Ultrasound Med 1994;13:803 -805[Medline]
  12. Mummaneni PV, Pitts LH, McCormack BM, Corroo JM, Weinstein PR. Microsurgical treatment of symptomatic sacral Tarlov cysts. Neurosurgery 2000;47:74 -78[Medline]

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