AJR 2000; 175:923-925
© American Roentgen Ray Society
Hydatid Cyst of the Temporal Bone
An Exceptional Location
S. Ennouri,
K. Ayadi,
H. Ben Ali and
J. Mnif
Habib Bourguiba Hospital 3029 Sfax, Tunisia
King Khaled Military Hospital Hafr Al Batin 31991, Saudi
Arabia
Habib Bourguiba Hospital 3029 Sfax, Tunisia
Hydatid disease in bone is rare (1-2% of all cases). Most cases have been
observed in adults, with the spine and pelvis being the predominant locations.
We describe an exceptional case of hydatid disease in the temporal bone and
report the CT and MR findings. To our knowledge, only three cases have been
previously reported in the literature and none were documented on MR
imaging.
A 24-year-old man was admitted to the hospital for recurrent left-sided
temporal swelling, progressively increasing over 1 year, with recurrent
left-sided otalgia and vertigo. He had undergone surgery for a similar
swelling in the same area twice, 8 and 3 years earlier. He had also undergone
surgery for a hydatid cyst of the right hepatic lobe 5 years earlier. On
examination, the swelling was painful and firm, measuring 5 x 4 cm. CT
scans obtained before and after injection of contrast material
(Fig. 6A) showed an ill-defined
heterogeneous mass of mixed density that was located in the left petrous bone
and displayed endo- and exocranial extensions. A small left-sided temporal
arachnoid cyst was also observed (Fig.
6A). Fine cuts of the petrous bone
(Fig. 6B) showed left-sided
tympanomastoidal geographic osteolysis with discrete peripheral
osteosclerosis. The tegmen tympani (Fig.
6B) and the ossicular chain were involved by the destructive
process. T1- and T2-weighted MR images obtained before and after gadolinium
administration documented a left-sided temporal extradural multilocular cystic
mass with endo- and exocranial extensions (Figs.
6C and
6D). The wall of the daughter
cyst was thin and regular, and the cuticular membrane showed intense
enhancement. The clinical findings and images were suggestive of a hydatid
cyst in the temporal bone. This diagnosis was subsequently supported by
positive findings at serology for hydatid. At surgery, an extradural
multivesicular hydatid cyst was found and numerous daughter cysts of various
sizes were removed.

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Fig. 6A. 24-year-old man who presented with recurrent left-sided temporal
swelling and recurrent left-sided otalgia and vertigo. On examination,
swelling was painful and firm, measuring 5 x 4 cm. Transverse
contrast-enhanced CT scan shows multiloculated hypodense mass in left temporal
bone and osteolysis of squamous bone.
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Fig. 6B. 24-year-old man who presented with recurrent left-sided temporal
swelling and recurrent left-sided otalgia and vertigo. On examination,
swelling was painful and firm, measuring 5 x 4 cm. Coronal
high-resolution petrous CT scan shows left-sided mastoidotympanic geographic
osteolysis.
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Fig. 6C. 24-year-old man who presented with recurrent left-sided temporal
swelling and recurrent left-sided otalgia and vertigo. On examination,
swelling was painful and firm, measuring 5 x 4 cm. Transverse
T2-weighted MR image shows left-sided temporal multiloculated cystic mass with
multiple daughter cysts and left-sided temporal arachnoid cyst.
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Fig. 6D. 24-year-old man who presented with recurrent left-sided temporal
swelling and recurrent left-sided otalgia and vertigo. On examination,
swelling was painful and firm, measuring 5 x 4 cm. Transverse
contrast-enhanced T1-weighted MR image shows intense contrast enhancement of
cuticular membrane.
|
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This case highlights the imaging pattern of skull hydatid disease. Bone is
usually considered the primary location in most cases without visceral
involvement (75-88%) [1,
2]. Histologically, development
of echinococcus starts in the bone marrow, progresses by diffuse vesicular
proliferation, and spreads by contiguity over the skeleton and the surrounding
structures including soft tissues. Joint locations are rare despite epiphyseal
involvement. Bone echinococcosis most often affects the spine and pelvis,
whereas it rarely involves long bones. Skull locations are uncommon
[2,
3]. In a review of the
literature, we found only three reports that described temporal bone
involvement [4]. Therefore,
imaging features of this lesion are still poorly documented. Conventional
radiography shows a variable-sized ill-delineated osteolysis without
osteosclerosis [2,
3]. CT scans obtained before
and after infusion of contrast material show the multivesicular pattern of the
lesion and reveal its endo- and exocranial extensions
[2,
3].
Our case is the first to be documented on MR imaging. We performed
spin-echo T1- and T2-weighed MR sequences before and after administration of
paramagnetic contrast material. These images allowed identification of the
relationship of the cyst with dura and the temporal lobe and of its endo- and
extracranial extensions. Multiplanar fine cuts clearly illustrated the
multivesicular pattern of the cyst, which displayed regular enhancement in the
cuticular membrane. The imaging features of the lesion are strongly suggestive
of the diagnosis.
The removal of daughter cysts and the cuticular membrane at surgery allowed
confirmation of diagnosis. Excision is often incomplete, thus explaining
frequent recurrences.
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