AJR Teaching File: Facial Mass in a Child
Annette C. Douglas-Akinwande1,
Chewarat Wirojtananugoon1 and
Eyas M. Hattab2
1 Department of Radiology, Indiana University School of Medicine, 550 N
University Blvd., Rm. 0279, Indianapolis, IN 46202.
2 Department of Pathology and Laboratory Medicine, Indiana University School of
Medicine, Indianapolis, IN.

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Fig. 1A —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall.
Soft-tissue window setting of head CT scan shows well-circumscribed mass that
is isodense to muscle.
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Fig. 1B —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall. Axial
unenhanced CT image obtained with bone window setting shows erosion of right
mandibular ramus and right temporal bone.
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Fig. 1C —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall. Axial
unenhanced T1-weighted image shows hypo- to isointense, well-circumscribed
mass in right masticator space.
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Fig. 1D —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall. Coronal
T2-weighted image shows mixed-signal (isointense to hyperintense) lesion in
right masticator space.
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Fig. 1E —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall. Coronal
contrast-enhanced fat-saturated T1-weighted image shows homogeneous
enhancement and extension of mass into right infratemporal fossa.
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Fig. 1F —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall. H and
E–stained sections show low cellular lesion characterized by
intersecting broad bands of spindle cells in variably collagenous stroma.
Tumor consists of bland spindle-shaped cells (proliferating fibroblasts).
Mitotic activity and necrosis are absent. Abundant collagen was present on
trichrome preparation. Reticulum stain showed minimal amount of reticulin.
Immuno staining for Ki-67 showed low proliferative activity (< 1% nuclear
staining).
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Fig. 1G —3-year-old girl with medical history of shunted
hydrocephalus, seizures, and cranial reconstruction for cranial synostosis at
7 months of age who presented to emergency department after a fall. H and
E–stained sections show low cellular lesion characterized by
intersecting broad bands of spindle cells in variably collagenous stroma.
Tumor consists of bland spindle-shaped cells (proliferating fibroblasts).
Mitotic activity and necrosis are absent. Abundant collagen was present on
trichrome preparation. Reticulum stain showed minimal amount of reticulin.
Immuno staining for Ki-67 showed low proliferative activity (< 1% nuclear
staining).
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Copyright © 2008 by the American Roentgen Ray Society.