BACKGROUND Intracranial hydatid disease constitutes 1%-2% of all cases
of hydatid disease. Multiple, infected, extradural, parasellar hydati
d cysts in a patient constitutes an extremely rave presentation. CASE
REPORT This 21-year-old man presented with a progressive left supracla
vicular swelling of 3 years duration and raised intracranial pressure
of 6 months duration with a past history of left-sided chronic suppura
tive otitis media that had resolved with antibiotics. On neurologic ex
amination, he had bilateral deferioration of vision with optic atrophy
; right temporal field defect; left III, IV, VI, V1, and V2 cranial ne
rves palsy and left ear conductive deafness. The patient's E.S.R was r
aised. His computed tomography (CT) scan showed a hypodense, lobulated
lesion in the middle cranial fossa with a hypodense, nonenhancing rim
, septations, and focal calcification without perifocal edema. A purul
ent fluid was aspirated from the left supraclavicular swelling, which
did not reveal any organism sw on staining and culture. Aspiration of
the left temporal swelling showed whitish watery fluid, the cytology o
f which revealed an infected hydatid cyst. Excision of the left tempor
al extradural, hydatid cysts was done, except the portion of the capsu
le adherent to the dura, and albendazole was started. One month later,
the supraclavicular hydatid cysts were removed. Six months later, a l
eft mastoidectomy was performed for chronic suppurative otitis media.
A repeat CT scan showed complete resolution of the hydatid cysts. Ther
e was no recurrence at 1 year follow-up. CONCLUSIONS A rare case of mu
ltiple infected extradural hydatid cysts of the parasellar region is r
eported. The unusual CT picture of a hypodense lobulated mass with sep
tations and a hyperdense rim is presented. The difficulties in its com
plete excision and successful management with long-term albendazole th
erapy are discussed. (C) 1997 by Elsevier Science Inc.