29.12.2021 Views

Diagnostic ultrasound ( PDFDrive )

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

1664 PART V Pediatric Sonography

efective in 95% of children. 49 If head tilt persists, muscle release

or tenotomy is performed to prevent development of signiicant

craniofacial asymmetry and scoliosis. 5

Masses

Pilomatricoma

Pilomatricomas (previously called “pilomatrixomas”) are benign

neoplasms arising from the hair follicles. 198 hey are the second

most frequently resected mass in the head and neck in children,

ater lymph nodes. 198 However, pilomatricomas are infrequently

imaged because diagnosis is oten made clinically. Imaging is

oten requested when the clinician is unfamiliar with the diagnosis

or the lesion is in the preauricular region and needs to be excluded

from an intraparotid mass or branchial apparatus remnant. 198,199

hese lesions typically occur in the head and neck in children

younger than 10 years, with a smaller peak occurring in the

sixth and seventh decades. 199 Multiple pilomatricomas can be

seen in the setting of Gardner syndrome, myotonic dystrophy,

Steinert disease, Turner syndrome, and sarcoidosis. 199 Clinically,

the lesions are irm nodules attached to the skin and are freely

mobile over the subcutaneous tissues. On ultrasound, these lesions

are frequently well-deined, hypoechoic lesions with mild internal

heterogeneous echogenicity, speckled or chunky internal calciications,

and hypoechoic rim. he lesions may have internal vascularity

demonstrated by spectral Doppler (Fig. 48.60). Rarely, when

the lesion has ruptured, the mass has an irregular heterogeneous

sonographic appearance, indistinguishable from other subcutaneous

lesions. 200,201 here may be some perilesional hypoechogenicity,

which is found to correlate with perilesional inlammation. 202

Complete surgical resection is curative.

Congenital Infantile Myoibromatosis

Congenital infantile myoibromatosis, although rare, is the most

common ibrous tumor in the neonate and infant. he cause is

unknown, although some familial cases have been reported. 203,204

Histologically, these lesions are composed of well-circumscribed

nodules of plump spindle-shaped cells with staining characteristics

intermediate between smooth muscle cells and ibroblasts. Oten,

there is central necrosis with focal calciications. 203 hese masses

can occur in the skin, muscle, bone, or viscera or intracranially.

203,205,206 Infantile myoibromatosis lesions almost exclusively

afect infants and young children, with 88% occurring before 2

years of age. 203 Over half of the lesions are identiied in the

neonatal period, and some cases are diagnosed prenatally. 203,207

he World Health Organization (WHO) classiies congenital

infantile myoibromatosis into three types: the solitary type, also

called “infantile myoibroma”; the multicentric form without

visceral involvement; and the multicentric form with visceral

involvement. 203,206 he solitary infantile myoibroma is more

common in males (69%) and frequently occurs in the head,

neck, and trunk. he multicentric form is more common in

females (63%). he solitary form of infantile myoibromatosis

and the multicentric form without visceral involvement generally

have a good prognosis, and recurrence is rare. Surgical excision

is the treatment of choice when feasible; chemotherapy is used

in inoperable cases. Some cases may show spontaneous

regression. 203

On ultrasound, the lesions oten show a lobulated heterogeneous

appearance with central anechoic and hyperechoic

structures (Fig. 48.61). hick septations may separate the

anechoic regions. he lesions are typically hypovascular. 205

CT and MRI are useful in assessment of disease extent and

bone and sot tissue involvement and to screen for additional

lesions.

Other, less common ibrous lesions that can occur in the head

and neck include nodular fasciitis and inlammatory myoibroblastic

tumor. hese lesions have a nonspeciic sot tissue mass

imaging appearance and require additional imaging and biopsy

for deinitive diagnosis.

Malignant Neoplasms

Malignant neoplasms of the head and neck represent 12% of all

childhood cancers. Lymphomas and sarcomas encompass 50%

A

B

FIG. 48.60 Pilomatricoma. Seven-year-old girl with right scalp bump for 4 months. (A) Gray-scale ultrasound image shows a well demarcated

heterogeneous hypoechoic lesion with internal echogenic foci. (B) Color Doppler image shows presence of internal vascularity within the lesion.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!