TY - JOUR
T1 - Giant frontal mucocele complicated by subdural empyema: treatment of a rare association
AU - Visocchi, Massimiliano
AU - Esposito, Giuseppe
AU - Della Pepa, Giuseppe Maria
AU - Doglietto, Francesco
AU - Nucci, Carlotta Ginevra
AU - Fontanella, Marco Maria
AU - Montano, Nicola
PY - 2012
Y1 - 2012
N2 - Giant frontal mucocele (GFM) is an extremely rare cause of frontal lobe syndrome. Subdural empyema (SDE) is an uncommon complication of paranasal sinisutis, for which craniotomy and decompressive craniotomy are the most effective surgical procedures. A 54-year-old man was brought unconscious to the emergency room where recurrent generalized seizures occurred. Heroine abuse, HCV-related hepatitis, prolonged antibiotic therapy for treatment of purulent rhinorrhea, along with recent personality changes were reported. High white blood cell count, pansinusitis, GFM, SDE and cerebritis were documented. The patient underwent bifrontal craniotomy in emergency, extensive drilling of the inner aspect of the frontal bone, surgical toilet of the enlarged frontal sinus and its "cranialization". Prevotella intermedia and Fusobacterium nucleatum were isolated and antibiotic therapy was started intravenously and then continued orally for 3 months. 2 years later the patient has recovered, though minor signs of frontal lobe syndrome persist. To the authors knowledge, this is the first case of GFM with SDE reported in the literature. Although decompressive craniectomy is advocated in extreme conditions, as in this case, "internal decompressive craniectomy", obtained with craniotomy and cranialization of the frontal sinuses, is strongly advocated in cases of SDE associated with megasinuses.
AB - Giant frontal mucocele (GFM) is an extremely rare cause of frontal lobe syndrome. Subdural empyema (SDE) is an uncommon complication of paranasal sinisutis, for which craniotomy and decompressive craniotomy are the most effective surgical procedures. A 54-year-old man was brought unconscious to the emergency room where recurrent generalized seizures occurred. Heroine abuse, HCV-related hepatitis, prolonged antibiotic therapy for treatment of purulent rhinorrhea, along with recent personality changes were reported. High white blood cell count, pansinusitis, GFM, SDE and cerebritis were documented. The patient underwent bifrontal craniotomy in emergency, extensive drilling of the inner aspect of the frontal bone, surgical toilet of the enlarged frontal sinus and its "cranialization". Prevotella intermedia and Fusobacterium nucleatum were isolated and antibiotic therapy was started intravenously and then continued orally for 3 months. 2 years later the patient has recovered, though minor signs of frontal lobe syndrome persist. To the authors knowledge, this is the first case of GFM with SDE reported in the literature. Although decompressive craniectomy is advocated in extreme conditions, as in this case, "internal decompressive craniectomy", obtained with craniotomy and cranialization of the frontal sinuses, is strongly advocated in cases of SDE associated with megasinuses.
KW - Anticonvulsants
KW - Empyema, Subdural
KW - Frontal Lobe
KW - Humans
KW - Imaging, Three-Dimensional
KW - Magnetic Resonance Imaging
KW - Male
KW - Middle Aged
KW - Mucocele
KW - Tomography, X-Ray Computed
KW - Anticonvulsants
KW - Empyema, Subdural
KW - Frontal Lobe
KW - Humans
KW - Imaging, Three-Dimensional
KW - Magnetic Resonance Imaging
KW - Male
KW - Middle Aged
KW - Mucocele
KW - Tomography, X-Ray Computed
UR - http://hdl.handle.net/10807/63534
U2 - 10.1007/s13760-012-0030-4
DO - 10.1007/s13760-012-0030-4
M3 - Article
SN - 0300-9009
VL - 112
SP - 85
EP - 90
JO - Acta Neurologica Belgica
JF - Acta Neurologica Belgica
ER -