Jugular foramen tumors: diagnosis and treatment

Neurosurgical Focus - Tập 17 Số 2 - Trang 31-40 - 2004
Ricardo Ramina1, João J. Maniglia, Yvens Barbosa Fernandes, Jorge Rizzato Paschoal, Leopoldo Nizan Pfeilsticker, Maurício Coelho Neto, Guilherme Borges
1Neurosurgery Department of Instituto de Neurologia de Curitiba, Brazil. [email protected]

Tóm tắt

Object Jugular foramen tumors are rare skull base lesions that present diagnostic and complex management problems. The purpose of this study was to evaluate a series of patients with jugular foramen tumors who were surgically treated in the past 16 years, and to analyze the surgical technique, complications, and outcomes. Methods The authors retrospectively studied 102 patients with jugular foramen tumors treated between January 1987 and May 2004. All patients underwent surgery with a multidisciplinary method combining neurosurgical and ear, nose, and throat techniques. Preoperative embolization was performed for paragangliomas and other highly vascularized lesions. To avoid postoperative cerebrospinal fluid (CSF) leakage and to improve cosmetic results, the surgical defect was reconstructed with specially developed vascularized flaps (temporalis fascia, cervical fascia, sternocleidomastoid muscle, and temporalis muscle). A saphenous graft bypass was used in two patients with tumor infiltrating the internal carotid artery (ICA). Facial nerve reconstruction was performed with grafts of the great auricular nerve or with 12th/seventh cranial nerve anastomosis. Residual malignant and invasive tumors were irradiated after partial removal. The most common tumor was paraganglioma (58 cases), followed by schwannomas (17 cases) and meningiomas (10 cases). Complete excision was possible in 45 patients (77.5%) with paragangliomas and in all patients with schwannomas. The most frequent and also the most dangerous surgical complication was lower cranial nerve deficit. This deficit occurred in 10 patients (10%), but it was transient in four cases. Postoperative facial and cochlear nerve paralysis occurred in eight patients (8%); spontaneous recovery occurred in three of them. In the remaining five patients the facial nerve was reconstructed using great auricular nerve grafts (three cases), sural nerve graft (one case), and hypoglossal/facial nerve anastomosis (one case). Four patients (4%) experienced postoperative CSF leakage, and four (4.2%) died after surgery. Two of them died of aspiration pneumonia complicated with septicemia. Of the remaining two, one died of pulmonary embolism and the other of cerebral hypoxia caused by a large cervical hematoma that led to tracheal deviation. Conclusions Paragangliomas are the most common tumors of the jugular foramen region. Surgical management of jugular foramen tumors is complex and difficult. Radical removal of benign jugular foramen tumors is the treatment of choice, may be curative, and is achieved with low mortality and morbidity rates. Larger lesions can be radically excised in one surgical procedure by using a multidisciplinary approach. Reconstruction of the skull base with vascularized myofascial flaps reduces postoperative CSF leaks. Postoperative lower cranial nerves deficits are the most dangerous complication.

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Tài liệu tham khảo

10.1288/00005537-196206000-00006

10.1016/0090-3019(87)90224-2

10.3171/jns.2002.97.6.1356

Ariyan S, 1990, Brown, 512

10.3171/jns.1995.83.5.0903

Bikhazi PH, 1999, Am J Otol, 20, 639

10.1097/00013414-200403000-00004

Brackmann DE, 1972, Trans Am Acad Ophthalmol Otolaryngol, 76, 1423

10.1288/00005537-198503000-00008

10.1097/00006123-200003000-00007

10.1097/00006534-200105000-00003

10.1227/00006123-199409000-00024

10.1002/1097-0142(19840615)53:12<2635::AID-CNCR2820531211>3.0.CO;2-9

Fisch U, 1982, Ann Otol Rhinol Laryngol, 91, 474, 10.1177/000348948209100502

10.1097/00005537-199804000-00003

10.1288/00005537-199408000-00001

Guild SR, 1941, Anat Rec, 79, 28

Gulya AJ, 1993, Laryngoscope, 103, 7, 10.1288/00005537-199307000-00009

10.1097/00005537-199612000-00007

Jackson CG, 1982, Otolaryngol Clin North Am, 15, 897, 10.1016/S0030-6665(20)32125-3

10.1016/0007-1226(87)90188-3

10.1097/00006123-199707000-00030

Kempe LG, 1982, WB Saunders, 3285

10.1016/0360-3016(80)90317-X

10.1288/00005537-198711000-00016

Lalwani AK, 1993, Am J Otol, 14, 398

Lang J, 1989, Springer-Verlag, 59

10.1002/1097-0142(19920401)69:7<1813::AID-CNCR2820690725>3.0.CO;2-P

10.1002/1097-0142(194905)2:3<447::AID-CNCR2820020309>3.0.CO;2-E

Molony TB, 1992, Otolaryngol Head Neck Surg, 106, 128, 10.1177/019459989210600202

10.1288/00005537-198912000-00007

Mustoe TA, 1995, Clin Plast Surg, 22, 543, 10.1016/S0094-1298(20)30996-2

10.1097/00006534-199612000-00005

Netterville JL, 1993, Laryngoscope, 103, 55, 10.1002/lary.1993.103.s60.55

10.1086/313732

Robertson JT, 1990, WB Saunders, 3654

Rosenwasser H, 1945, Arch Otolaryng, 41, 64, 10.1001/archotol.1945.00680030087006

10.1288/00005537-195206000-00009

10.1097/00013414-199609000-00002

10.1097/00006123-200104000-00029

10.1227/00006123-199202000-00015

10.1097/00006123-199106000-00016

10.1288/00005537-197506000-00016

10.1002/hed.2880120405

10.1288/00005537-198106000-00019

10.1016/S0140-6736(89)91908-9

10.1007/BF01405504

Zak FG, 1954, N Y State J Med, 54, 1153