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162
Fig. 7.9 (continued)
7 Differential Diagnosis of Breast Diseases
Posterior echo enhancement • Easy deformation and painlessness with • compression Avascularity with CDI, PDI, and 3DPD • Absence of color pattern within the lesion • with US elastography
Up to 95 % of breast cysts have no solid com­ponent on the capsule (Korzhenkova 2004 ) . Such cysts are characterized as simple (typical) and uncomplicated. There are also breast microcysts (with the size of 1–2 mm), macrocysts (simple
and multilocular), individual, and multiple (Trufanov et al. 2009 ) .
Breast cysts in some cases may not exhibit such a characteristic symptom as posterior echo enhancement. This happens more often in small cysts, the cysts surrounded by dense structures, near to the thorax, or in cysts with expressed fi brous capsule (Zabolotskaya 2006 ) .
Atypical cysts may be sometimes observed among fl uid breast lesions ( Sergeeva and Sotskova 2009 ) . They confer long-existing,
1637.2 Non-tumoral Diseases
Fig. 7.10 Simple breast cyst. Sonograms. Gray scale, CDI, PDI, panoramic scan, 3DPD, and US elastography
164
Fig. 7.10 (continued)
7 Differential Diagnosis of Breast Diseases
1657.2 Non-tumoral Diseases
Fig. 7.10 (continued)
166
7 Differential Diagnosis of Breast Diseases
Fig. 7.10 (continued)
Fig. 7.11 Complex breast
cyst. Grayscale US
1677.2 Non-tumoral Diseases
recurrent cysts and cysts with in fl ammation (Zabolotskaya 2006 ) .
US features of atypical cysts are listed below
(Fig. 7.11 ):
Thick cystic walls • Contents with inclusions • Solid component with different types of • vascularization
Atypical US images of cysts in up to 2 % of cases can be the result of intracavitary growth originating from the cystic wall (Korzhenkova
2004 ) . Seventy- fi ve percent of them are papil­lomas of benign nature. Twenty percent of intra­cystic breast lesions are associated with papillary cancer (Fig. 7.12 ). All kinds of growth con- nected with cystic wall, especially if vascular­ized, demand US-guided biopsy with cytology and are indicated for sector resection with urgent histology.
Complex breast US permits easy cyst detec­tion, characterization of their contents, wall structure, and vascularity with the accuracy of
168
Fig. 7.12 Cystadenocarcinoma
of the breast. Grayscale US
7 Differential Diagnosis of Breast Diseases
95–100 % (Shevchenko 1997 , Sergeeva 2010 ) .
Atheroma is a retention cyst of the sebaceous gland located in the benign skin and subdermal tissues, which occurs by increased sweating of the sebaceous gland, occlusion of its duct, and form­ing of a capsule around the fatty content. It accounts for 0.2 % of all breast lesions (Rozhkova 1993 ) . Atheroma is clinically represented with a dense formation with clear contours, painless, and welded to the skin. Atheromas quite often in fl ame and abscess. Local edema, hyperemia, morbidity, and fl uctuation can be revealed in these cases.
Atheroma exhibits the following US features
(Fig.
7.13 ):
Hypoechoic or anechoic lesion • Closely adjacent to the skin with scission of • skin layers Accurately boarded • Avascular with CDI, PDI, and 3DPD • Without color pattern with US elastography • Complex diagnosis and differentiation of
breast lesions with careful analysis of obtained US data and assessment of the effect of antibacte­rial and anti-in fl ammatory treatment often help to rule out malignant process.
1697.2 Non-tumoral Diseases
Fig. 7.13 Atheroma. Sonograms. Gray scale, 3DPD, and US elastography
170
7 Differential Diagnosis of Breast Diseases
Fig. 7.13 (continued)

Age-Related Changes in Breast Structure: Breast Ultrasound in Children and Adolescents

8
Breasts have special US features in various ages. Mammary glands start their development at the sixth week of embryogenesis. In a 5-month embryo, mammary sprouts begin to ramify into a small number of ductules. They also develop a lumen with an opening to the skin, marked by the forma­tion of the nipple sheath. Further development of mammary glands is irregular. A signi fi cant num­ber of newborn (both girls and boys) has enlarge­ment and in fi ltration of mammary glands at the fi rst week of life due to physiological mastopathy. They are detected with US as masses of oblong shape with normal echodensity without differen­tiation of structural elements. Super fi cial and deep leaves of fascia, which “embrace” the gland, can be clearly identi fi ed. The average dimensions of the gland are 1.5 × 0.6 × 1.4 cm. This status usually does not demand any treatment as in most cases it spontaneously regresses within 2–3 weeks.
Two periods in childhood, at the ages of 4 and 9, exhibit an increase in the number of glandular structures. Normally, distinct breast enlargement occurs at the age of 11–13 years. In some cases, the enlargement of mammary glands in girls of 5–7 years or 7–9 years may be observed in the absence of the clinical and laboratory data of pre­cocious puberty. It is regarded as isolated prema­ture thelarche. The dimensions and structure of the breast in these girls do not differ from those of the newborn with physiological mastopathy. Beginning with 10–11 years, the mammary glands start to develop more intensively. Stromal component often develops signi fi cantly faster than the glandular tissue.
The greatest activity of mammogenesis is registered with activation of growth and develop­ment of a female organism at the age from 11 to 25 years. The fi rst wave of breast development comes at 12–14 years; the second, 2–3 years later; and then 5–7 years later. It is noticed that if the second wave is absent, the degree of mam­mary gland development appears very low.
In puberty, fi brous and adipose stroma start to develop earlier than glandular tissue. It confers two types: supporting stroma and periglandular stroma. Breast enlargement in girls of 11–13 years (prior to menarche) is accompanied with signi fi cant changes in its structure. US reveals layers of low echodensity of 0.1–0.3 cm thick, which alternate with thin layers of high echoden­sity (Fig. 8.1 ).
The layers of low echodensity merge in sub­areolar area and form a region of irregular shape. Therefore, US fails to differentiate glandular tis­sue from periglandular stroma in most cases. The expression of periglandular stroma corresponds to the development of glandular tissue.
In puberty, at 12–16 years of age, the breasts continue to develop glandular tissue. The morpho­logical feature of mammary glands in girls of 14–16 years is the formation of new structures – tubular lobules. Breasts in girls of this age after menarche exhibit “reticular” structure with US. Transverse scanning demonstrates areas of decreased echoden­sity of 0.1 cm (small-cell type), 0.2 cm (middle-cell type), or 0.3 cm (large-cell type) in size surrounded with layers of high echodensity. Longitudinal scan­ning of these areas reveals their elongated shape.
A.N. Sencha et al., Breast Ultrasound, DOI 10.1007/978-3-642-36502-7_8, © Springer-Verlag Berlin Heidelberg 2013
171