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Kimura disease:
diagnostic imaging findings and surgical treatment.
J Craniofac Surg. 2007 Sep;18 (5):1062-7.
We have
encountered 11 cases of Kimura disease, comprising 10 males and 1
female. The ages at presentation ranged from 16 to 48 years, with a
mean of 31.5 years. The sites of the subcutaneous masses were
bilateral posterior auricular regions in two cases, frontal region
in two cases, temporal region in two cases, head region in one case,
parotid region in two cases, parotid and temporal regions in one
case, and left earlobe in one case. The interval from onset to
surgery ranged from 1 to 10 years, with a mean of 4.7 years.For
diagnostic imaging, a combination of magnetic resonance imaging (MRI)
and ultrasonography had a high diagnostic value. MRI depicted
abnormalities at sites in contact with bone, such as posterior
auricular regions, and sites with abundant soft tissue, such as
parotid and cheek regions. Diffuse atrophy of subcutaneous fat was
observed at the sites of the masses. On ultrasonography, the
interior of lymph nodes was homogeneous and hyperechoic, whereas the
periphery was hyperechoic, and blood vessels entering lymph nodes
were clearly depicted.Surgery was performed in all cases.
Postoperative adjuvant radiotherapy was conducted in one patient and
radiotherapy and steroid therapy in one other patient. There were
two relapses, and both were excised by repeated surgery. Surgical
excision of the subcutaneous mass in Kimura disease has the
advantages that the treatment period is short and precise
histopathologic diagnosis can be obtained.
Kimura's disease:
case report and review of the literature.J
Thorac Imaging. 2005 Nov;20(4):298-300.
Kimura's
disease is a rare, chronic inflammatory disease characterized by
subcutaneous nodules in the head and neck regions associated with
regional cervical lymphadenopathy. Following its recognition as a
pathologic entity, numerous reports have been published detailing
the pathogenesis, radiologic manifestations, and treatment
modalities. An extensive review of the literature did not reveal any
cases of diffuse thoraco-abdominal lymphadenopathy described in
relation to Kimura's disease. Hence, the interest in the case
discussed here. |