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242
11 Ultrasound Examination After Breast Surgery
fl uid, which spreads as an anechoic layer sur­rounding the implant on an extent, increases the risk of pericapsular fi brosis and capsular con­tracture and demands surgical care. US often reveals cysts, local lymphatic edema with skin thickening, and the increase in echodensity of tissues.
The character of tissues, which form a postop­erative scar (collagen fi bers, quaggy connective tissue, fi brosis); the expression of edema; and
aseptic in fl ammation in fl uence the diversity of US picture of postoperative area.
US sometimes detects no signs of a scar. However, in many cases, it reveals the following signs: areas of structural deformation; fi elds of decreased and/or increased echodensity of irreg­ular echostructure; linear (sometimes irregular) shape, sometimes with acoustic shadows, avas­cular in CDI, PDI, and 3DPD; and mixed color pattern with US elastography.

Recurrent Breast Cancer

1 2
Early detection of the recurrences of malignant tumors is a principal problem of modern oncol­ogy. The incidence of breast carcinoma recur­rence after radical resection or radical mastectomy ranges from 2.8 % to 71 %. Even in the cases without metastases in regional lymph nodes, its incidence reaches 25–30 %.
Despite the advances in treatment of patients with breast carcinoma, 40–50 % of women exhibit cancer dissemination in fi ve years’ term after radical treatment. The fl ow of the disease does not necessarily depend on the stage of the tumor. Different types of preoperative therapy can in fl uence both the duration of healthy period and the location of metastases (Goldhirsch et al. 1994 ; Goldhirsch et al. 2001 ) . The ef fi cacy of treatment of cancer recurrence and metastases depends on the one hand on their site and the degree of local extension and, on the other, on the methods of treatment of the primary tumor.
The basic prognostic criteria that character­ize biological properties of a tumor are the type, histological structure, and clinical stage of the malignant process. Diffuse type of carcinoma has 10–16 times worse prognosis than the nodu­lar type. Scirrhous structure exhibits 2–3 times worse prognosis than the glandular. When the process is generalized, these prognostic features appear insigni fi cant. Localization, the duration of disease, and the rate of tumor growth are relative prognostic tests in breast carcinoma.
Results of numerous studies underline high risk of recurrence of breast carcinoma in young women, especially with breast- conserving
operations. According to Fowble ( 1997 ) , local recurrence appeared in 40 % of patients younger than 35 years and only in 13 % of patients above 50 years during 4.5 years of follow-up. Local recurrence results in the dissemination of tumoral process in 20–40 % of cases.
The risk of cancer recurrence is higher in the fi rst 5 years. Nevertheless, it exists within 15–20 years after surgery.
Some clinical features in fl uence the rate of recurrences of breast carcinoma. The incidence of local recurrences corresponds with the size of primary tumor and its local extension. Lobular breast carcinoma is quite often associated with local recurrence. It may be the consequence of high incidence of multicentric growth, frequent bilateral location, clinically latent affection of lymph nodes, and positive edge of resection in greater number of cases. Meanwhile, some ret­rospective studies did not reveal any signi fi cant difference in long-term results after different types of surgeries in patients with invasive lobu­lar carcinoma.
Multicentric growth of breast tumor is associ­ated with increased incidence of recurrence. Many studies demonstrated that the rate of local recurrence increases in patients with metastases in lymph nodes correlates with their number.
Routine US is an affordable method of early detection of the recurrence of breast carcinoma and its regional and remote metastases ( Solbiati and Rissato 1995 ; Zabolotskaya and Zabolotsky 1997 ; Sinyukova and Sholokhov 2010 ; Sencha et al. 2011 ) . Complex use of standard and new
A.N. Sencha et al., Breast Ultrasound, DOI 10.1007/978-3-642-36502-7_12, © Springer-Verlag Berlin Heidelberg 2013
243
244
12 Recurrent Breast Cancer
US technologies permits to supervise the ef fi cacy of treatment (Sinyukova and Sholokhov 2010 ; Evseeva et al. 2011 ) .
However, interpretation of US images is dif fi cult. It especially concerns the examination of the patients operated for breast cancer or after radiation therapy. The dif fi culties arise due to fre­quent fi brosis within the breast and anterior tho­racic wall. It signi fi cantly complicates early detection and differential diagnosis of carcinoma recurrence in the region of primary surgery.
Local recurrence of breast carcinoma in the region of radical resection or mastectomy usually exhibits the following US features (Sencha et al. 2011 ) (Fig.
12.1 ):
Solid lesion • Size of 1–2 cm • Decreased echodensity • Homogeneous structure • Irregular or roundish shape • Rough borders • Indistinct contours
Fig. 12.1 Status after
radical breast resection. Recurrent breast carcinoma. Sonograms. Grayscale US, PDI, multislice view, and US elastography
24512 Recurrent Breast Cancer
Fig. 12.1 (continued)
246
12 Recurrent Breast Cancer
Fig. 12.1 (continued)
24712 Recurrent Breast Cancer
Fig. 12.1 (continued)
248
Fig. 12.2 Status after
mammoplasty. Recurrent breast carcinoma. Grayscale US
12 Recurrent Breast Cancer
Intranodular blood fl ow pattern in CDI, PDI, • and3DPD Intensive hard (blue) staining with US • elastography
The recurrences of breast carcinoma after radical mastectomy arise more often in postoper­ative scar. Alternatively, recurrence after breast­conserving surgery is usually not connected to the scar ( Vtorushin 2012 ). Recurrence appears often out of postoperative scar in the cases of expressed in fl ammatory in fi ltration of the stroma of primary neoplasm. According to Sinyukova and Sholokhov ( 2010 ) , the recurrence in patients after radical mastectomy located in 78 % of cases
in subcutaneous fat and in 18 % in the muscular layer of anterior thoracic wall in the region of pri­mary surgery. Only 57 % of patients had recur­rent tumor in the depth of postoperative scar. The recurrences, which arose in the region of radical resection, located within the postoperative scar in 66 % of cases and in the breast tissue in 32 % (Sinyukova and Sholokhov 2010 ) .
US differentiation of recurrent breast tumors and other lesions in the presence of implants or gel fragments requires special attention. Shumakova et al. ( 2011 ) reported the incidence of breast car­cinoma in 1.1 % and fi broadenoma in 3.5 % of patients with silicone implants (Fig. 12.2 ).
24912 Recurrent Breast Cancer
Any surgical intervention may be accompanied by oleogranuloma or adipose necrosis in late postoperative term (3–6 months and later after surgery). They arise as a reaction to the injury during the operation. According to Sinyukova and Sholokhov ( 2010 ) , lipogranulomas constitute 21 % of all lesions in the region of surgery.
Lipogranuloma can be detected along the postoperative scars as a lesion of various echoden­sity (an-, hypo-, or hyperechoic) and size (more
often smaller than 10 mm) of roundish shape with clear margins, homogeneous (or impure) echo­structure, and avascular with CDI, PDI, and 3DPD (Fig.
12.3 ).
It is often accompanied with acoustic shad­ows, especially in cases of calci fi cations, which are characteristic for lipogranulomas. Surrounding tissues are usually intact or exhibit the signs of lymphostasis. Adipose necrosis and lipogranu­loma are dif fi cult to differentiae from recurrent
Fig. 12.3 Status after
radical breast resection. Lipogranuloma. Sonograms. Gray scale, PDI, 3D, and US elastography
250
12 Recurrent Breast Cancer
Fig. 12.3 (continued)
Fig. 12.4 Status after radical
breast resection. Granuloma ( arrows ). Sonograms. Gray scale and CDI
25112 Recurrent Breast Cancer
breast carcinoma. Recurrent tumors of small sizes can have the same echodensity, echostruc­ture, shape, contours, and vascularity.
Local fi brosis is characterized with decreased echodensity (100 %) and layered structure (93 %) and lipogranuloma with average or mixed echodensity (29 and 45 % accordingly), heteroge­neous structure (97 %), small calci fi ed incorpora­tions (68 %), “egg shell” calci fi cation (32 %), and
fl uid component (29 %) (Figs. 12.4 and 12.5 ). Acoustic shadows can be observed signi fi cantly more often in patients with lipogranulomas (87 %) than in recurrent tumors (2 %). Posterior enhancement of US does not depend on the type of the mentioned lesions. Lipogranulomas, local fi brosis, and cystic lesions are usually avascular, while recurrent breast carcinoma is vascularized in CDI, PDI, and 3DPD in 83 % of cases.