Cavernous Hemangioma of the Third Cranial Nerve

Author:

Itshayek Eyal1,Perez-Sanchez Xicotencatl1,Cohen Jose E.1,Umansky Felix1,Spektor Sergey1

Affiliation:

1. Department of Neurosurgery, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

Abstract

Abstract OBJECTIVE The authors report a rare case of a cavernous hemangioma (CH) involving the third cranial nerve. CLINICAL PRESENTATION A 25-year-old Caucasian woman presented with neuralgic facial pain that responded to pharmacological management. She had no neurological deficit. Magnetic resonance imaging scans revealed a space-occupying lesion in the interpeduncular cistern with no evidence of hemorrhagic event. Preoperative cerebrospinal fluid and blood samples were negative for cytology and tumor markers. INTERVENTION The patient underwent craniotomy and exploration of the interpeduncular cistern. A lesion with the raspberry-like appearance characteristic of a CH was found emerging from between the fibers and completely encircling Cranial Nerve III. The surgeon decided to leave the lesion in place to avoid creation of a new neurological deficit in the young patient. The patient is asymptomatic with a stable radiological picture 18 months after surgery. CONCLUSION CH should be considered as a possible differential diagnosis of extra-axial space-occupying lesions along the course of the cranial nerves. Resection with resulting deficit may not be indicated in patients presenting with normal neurological function. Further research and longer follow-up periods are required to better understand the natural history of CH involving the cranial nerves.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Surgery

Reference10 articles.

1. Surgical management of cavernous malformations involving the cranial nerves;Deshmukh;Neurosurgery,2003

2. Intrinsic hemangiomas of the peripheral nerves, a report of two cases and a review of the literature;Losli;AMA Arch Pathol,1952

3. Cavernous angiomas of the cranial nerves;Matias-Guiu;Report of two cases. J Neurosurg,1990

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