Yonsei Med J.  2007 Aug;48(4):704-710. 10.3349/ymj.2007.48.4.704.

Congenital Cavernous Sinus Cystic Teratoma

• Shim KW
• Kim DS
• Choi JU
• Kim SH

• KMID: 2158179
• DOI: http://doi.org/10.3349/ymj.2007.48.4.704

Abstract

Teratomas represent 0.5% of all intracranial tumors. These benign tumors contain tissue representative of the three germinal layers. Most teratomas are midline tumors located predominantly in the sellar and pineal regions. The presence of a teratoma in the cavernous sinus is very rare. Congenital teratomas are also rare, especially those of a cystic nature. To our knowledge, this would be the first case report of a congenital, rapidly growing cystic teratoma within the cavernous sinus. A three-month-old boy presented with a past medical history of easy irritability and poor oral intake. A magnetic resonance image (MRI) scan of the head disclosed a large expanding cystic tumor filling the right cavernous sinus and extending into the pterygopalatine fossa through the foramen rotundum. These scans also demonstrated a small area of mixed signal intensity, the result of the different tissue types conforming to the tumor. Heterogeneous enhancement was seen after the infusion of contrast medium. However, this was a cystic tumor with a large cystic portion. Thus, a presumptive diagnosis of cystic glioma was made. With the use of a right frontotemporal approach, extradural dissection of the tumor was performed. The lesion entirely occupied the cavernous sinus, medially displacing the Gasserian ganglion and trigeminal branches (predominantly V1 and V2). The lesion was composed of different tissues, including fat, muscle and mature, brain-like tissue. The tumor was completely removed, and the pathological report confirmed the diagnosis of a mature teratoma. There was no evidence of recurrence. Despite the location of the lesion in the cavernous sinus, total removal can be achieved with the use of standard microsurgical techniques.

Keyword

Benign tumors; cavernous sinus; pathology; surgery; teratoma

MeSH Terms

Cavernous Sinus/*pathology
Humans
Infant
Magnetic Resonance Imaging
Male
Paranasal Sinus Neoplasms/*congenital/*diagnosis/surgery
Teratoma/*congenital/*diagnosis
Tomography, X-Ray Computed

Figure

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  Fig. 1 A preoperative brain CT scan at birth shows a mass lesion in the right cavernous sinus and pterygopalatine fossa. (A) A brain CT without contrast enhancement shows a faint mass lesion in the right cavernous sinus. (B) A brain CT with contrast enhancement shows a more precise mass lesion in the right cavernous sinus.

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  Fig. 2 Preoperative brain MRI shows a large cyst and solid tumor within the right cavernous sinus filling the middle cranial fossa and pushing the temporal lobe superiorly. (A) A T1-weighted axial image shows the solid component of the tumor anteromedially. (B) The lateral wall of the cavernous sinus was pushed superomedially by the mass. The superior portion of the cavernous sinus and right cavernous portion of the carotid artery were pushed medially. (C) A T1-weighted sagittal image shows a cystic mass in the pterygopalatine fossa.

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  Fig. 3 The operation was performed through a right frontotemporal craniotomy. The tumor consisted mainly of a cystic portion as well as a relatively small solid portion within the cavernous sinus. After aspiration of fluid from the cystic cavity, the dura was incised in a curvilinear fashion (A) The tumor was pulled from the pterygopalatine fossa through the foramen rotundum (B, ★). The tumor in the pterygopalatine fossa was easily removed through the foramen rotundum because it was cystic and not adhered to adjacent structures.

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  Fig. 4 (A) A postoperative MRI scan (T1-weighted axial and coronal image with Gadolinium enhancement), which was taken 48 hours after the operation, shows complete tumor removal. (B) A postoperative brain MRI scan shows total tumor removal.

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  Fig. 5 (A) A low-power view shows brain tissue with cystic changes. (B) Architecturally, malformed brain tissue is noted. (C) A high-power view shows neurons with laminar distortion, along with multifocal calcification.

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  Fig. 6 (A and B) A multilocular cystic area with lining epithelium is noted. (C) Scattered glands resembling salivary glands and (D) adipose and muscle tissue are seen.

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