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AJR 2004; 182:1081-1083
© American Roentgen Ray Society


Case Report

Breast MRI for Cancer Detection in a Patient with Diabetic Mastopathy

Helena A. Gabriel1, Chun Feng, Ellen B. Mendelson and Stefanie Benjamin

1 All authors: Department of Radiology, Northwestern University Medical School, 676 North St. Clair St., Ste. 800, Chicago, IL 60611.

Received June 30, 2003; accepted after revision August 22, 2003.

 
Address correspondence to H. A. Gabriel (hgabriel{at}nmff.org).


Introduction
Top
Introduction
Case Report
Discussion
References
 
First described by Soler and Khardori in 1984 [1], diabetic mastopathy refers to the formation of palpable fibrous nodules and asymmetries in the breasts of women with long-standing type 1 diabetes mellitus. It can simulate a malignancy and poses a diagnostic challenge. Conversely, patients with this condition may also develop breast carcinomas hidden within areas of dense fibrotic breast tissue. We report a case of inflammatory breast carcinoma in a patient with insulin-dependent diabetic mastopathy to illustrate the usefulness of MRI in evaluating possible malignant lesions and differentiating diabetic fibrosis from malignancy.


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 40-year-old woman who had insulin-dependent diabetes mellitus since childhood presented to the breast specialist with questionable thickening in the upper outer left breast. Physical examination by the breast surgeon showed bilateral areas of nodularity. No discrete mass was perceived, and no skin or nipple changes were present. Mammography at the time of initial presentation consisted of routine and tangential compression images, which showed only asymmetric density in the left breast superiorly and laterally (Fig. 1A) with no discrete masses, suspicious calcifications, or any other evidence of malignancy in either breast. Sonography, performed using a 12-5–MHz linear array transducer (Philips Medical Systems), showed areas of posterior acoustic shadowing in the upper outer left quadrant (Fig. 1B), with no masses seen on orthogonal images. The sonographic examination was interpreted as compatible with diabetic fibrosis, a probably benign assessment, and the patient was then advised to follow up with clinical breast examination and a short-interval imaging study in 6 months.



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Fig. 1A. 40-year-old woman with diabetic mastopathy. Bilateral mediolateral oblique mammograms show dense fibroglandular tissue with minimally increased density in superior aspect of left breast (arrow).

 


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Fig. 1B. 40-year-old woman with diabetic mastopathy. Sonogram of questionable palpable thickening of upper outer left quadrant shows nonspecific areas of shadowing, thought to be related to diabetic mastopathy. No cysts or solid masses are seen.

 

Within 3 months, the patient returned with increased left-sided thickening and breast tenderness in the upper outer quadrant. Physical examination by the same breast surgeon now corroborated a thickening in the upper left breast with no axillary, supraclavicular, or cervical lymphadenopathy.

Because of the additional symptoms, confusing clinical scenario, equivocal mammographic and sonographic findings just 3 months earlier, and mammographic limitation imposed by breast density, MRI (1.5-T Sonata scanner, Siemens) of the breast was performed, seeking any focal areas that might represent a malignant process. The attempt was to distinguish possible malignancy from diabetic mastopathy by examining lesion morphology and enhancement kinetics. We performed the following pulse sequences of our routine protocol: T1-weighted MRI in the axial plane; STIR imaging in the axial, coronal, and sagittal planes; and dynamic 3D T1-weighted gradient-echo MRI preceding and after the IV administration of gadopentetate dimeglumine (Magnevist [0.1 mg/kg], Berlex Laboratories). Four contrast-enhanced sequences were performed. Postprocessing manipulation included subtraction images and multiplanar reconstruction in the axial plane and maximum-intensity-projection images. The images were also reviewed on a 3D workstation.

The STIR images showed asymmetric high signal within the left breast and in the skin, suggestive of edema. After contrast enhancement, a dominant, 2.1 x 2.3 x 1.8 cm, lobulated mass in the upper outer quadrant was seen. The mass showed intense heterogeneous enhancement with enhancing septa. The rapid rise and early washout of contrast material generated a suspicious time–signal intensity enhancement curve. Additional small enhancing foci were seen throughout the left breast, with suspicious enhancement curves. The left breast was also marked by diffuse reticular enhancement suggestive of infiltrative tumor. Skin thickening was seen especially within the inferior portion of the left breast, with small nodular enhancing subcutaneous foci, raising suspicion of inflammatory breast cancer (Figs. 1C, 1D, 1E, 1F).



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Fig. 1C. 40-year-old woman with diabetic mastopathy. STIR axial MR image (TR/TE, 5,700/72) shows marked asymmetry in appearance of breasts. Left breast has diffusely increased signal within parenchyma and skin, suggesting diffuse breast edema and skin thickening (arrow).

 


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Fig. 1D. 40-year-old woman with diabetic mastopathy. Dynamic sagittal T1-weighted 3D gradient-echo MR image obtained after contrast enhancement reveals lobulated 2.4 x 1.9 cm mass in upper outer left quadrant. This mass has heterogeneous contrast agent uptake with enhancing septa in spiculated configuration (arrowhead) and enhancing thin peripheral rim.

 


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Fig. 1E. 40-year-old woman with diabetic mastopathy. Subtraction sagittal T1-weighted 3D gradient-echo MR image again shows dominant mass (arrowhead) and other diffuse reticular areas of enhancement and nodularity (straight arrows), suggesting diffuse tumor infiltration. Note skin enhancement (curved arrow), suggesting dermal lymphatic invasion.

 


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Fig. 1F. 40-year-old woman with diabetic mastopathy. Graph of MRI time–signal intensity curves from MR image with mean enhancement plotted on y-axis against time on x-axis shows distinctive enhancement kinetics of mass. Curve of dominant lobulated mass shows washout of contrast agent, which is suspicious for malignancy.

 

After the suspicious mass was identified on MRI, sonography was again performed to locate the lesion so that sonographic guidance could be used for biopsy. A hypoechoic mass was observed in the 2-o'clock position of the left breast; its size and location were consistent with the dominant mass seen on MRI. Areas of shadowing were seen throughout the left breast, with small irregular hypoechoic lesions posterior to the nipple. As seen on MRI, the skin of the lower left breast was thickened, measuring 0.6 cm, and edema was present. Repeated mammography showed further increase in left breast density compared with that in the previous study.

Sonographically guided core biopsy of the mass was performed using a 14-gauge core biopsy needle with a 22-mm throw. A skin punch biopsy in an area of skin thickening was also performed. Histopathology of the core biopsy specimen revealed poorly differentiated grade 3 infiltrating ductal carcinoma and ductal carcinoma in situ. Dermal lymphatic invasion was present in the skin-punch biopsy, signifying inflammatory carcinoma.

The patient was treated with chemotherapy for inflammatory breast carcinoma and underwent repeated MRI, which showed marked reduction in the size of the mass in the upper outer quadrant and significant resolution of abnormal enhancement, although small enhancing foci were seen within the breast. Mastectomy was performed after four cycles of chemotherapy, and histopathology of the specimen revealed areas of fibrosis consistent with diabetic mastopathy and residual infiltrating poorly differentiated ductal carcinoma, grade 3 of three, in four quadrants, as scattered nests and single cells, with nodules of infiltrating carcinoma. Focal residual ductal carcinoma in situ was also present. Three of eight axillary lymph nodes harbored metastatic carcinoma.


Discussion
Top
Introduction
Case Report
Discussion
References
 
Associated with long-standing type 1 (insulin-dependent) diabetes mellitus, diabetic mastopathy is an unusual fibroinflammatory breast lesion that often presents in premenopausal women and is associated with other multiple microvascular complications. The cause of diabetic mastopathy is unknown but is thought to be related to an autoimmune reaction to diabetogenic abnormal matrix accumulation [2]. Histologically, diabetic mastopathy consists of focal, dense, keloid-like areas of fibrosis, which show B cell–predominant lymphocytic lobulitis, ductitis, and vasculitis [3, 4]. Our patient had both the clinical and histopathologic features of diabetic mastopathy.

The differentiation of mastopathy from cancer is imperative but difficult both at clinical examination and by conventional imaging. In our patient, the mammographic and sonographic studies were difficult to interpret and equivocal at best because of the dense tissue and posterior acoustic shadowing from the diabetic mastopathy [5]. In contrast, MRI was helpful in differentiating the similar-appearing benign and malignant processes and confirming malignancy.

In our patient, the MR image depicted masses and enhancement that had both suspicious morphologic features and contrast kinetics [6, 7]. The dominant mass had lobulated margins with enhancing septa and a time–signal intensity curve that showed rapid uptake and washout of contrast material, all worrisome features. Reticular enhancement was also seen, consistent with diffuse malignancy, and dermal invasion was suggested by the nodular enhancement of the skin. In this case, breast MRI was the one technique to reveal a highly suspicious lesion requiring biopsy. MRI enhancement kinetics and postprocessing image subtraction techniques helped to differentiate the benign diabetic mastopathy and breast cancer and to depict the wide extent of disease in this patient, thus aiding in staging the cancer. MRI also showed the diffuse nature of the patient's inflammatory carcinoma, represented by the reticular breast and skin enhancement.

The patient underwent adjuvant chemotherapy with repeated MRI, which showed a strong response to the therapy, although MRI findings of residual disease were present. The MRI examination underestimated the amount of disease found in the mastectomy specimen; this phenomenon has been previously reported in patients who exhibit a strong response to chemotherapy [8].

Recently, a case report described the use of MRI in a patient with diabetic mastopathy, in whom a focal area of asymmetry had continuous enhancement [9]. The authors concluded, however, that MRI may not be useful in differentiating diabetic mastopathy from breast cancer. In their patient, MRI showed a benign type of enhancement, potentially differentiating the two. In our patient, MRI was extremely helpful in detecting the malignancy and was the best technique for diagnosing the tumor and assessing its extent. Thus, MRI may have an important application in evaluating breast abnormalities in exactly this patient population, in which mammography and sonography are limited by breast density and cancer-mimicking breast lesions. More studies need to be performed, however, to evaluate the utility of breast MRI in diabetic mastopathy.

In conclusion, this case emphasizes the diagnostic ambiguity of breast cancer in patients with diabetic mastopathy, which is a confusing clinicopathologic and radiographic entity that can confound the detection of breast carcinoma in affected patients. The value of breast MRI lies in its ability to detect possible malignant lesions in highly dense breast tissue. When used in combination with conventional breast imaging techniques, breast MRI can be an effective aid in the diagnostic evaluation of suspected breast malignancy in patients with diabetic mastopathy.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Soler NG, Khardori R. Fibrous disease of the breast, thyroiditis and cheiroarthropathy in type I diabetes mellitus. Lancet 1984;1:193 –195[Medline]
  2. Camuto PM, Zetrenne E, Ponn T. Diabetic mastopathy: a report of 5 cases and a review of the literature. Arch Surg2000; 135:1190 –1193[Abstract/Free Full Text]
  3. Logan WW, Hoffman NY. Diabetic fibrous breast disease. Radiology1989; 172:667 –670[Abstract/Free Full Text]
  4. Tomaszewski JE, Brooks JSJ, Hicks D, Livolsi VA. Diabetic mastopathy: a distinctive clinicopathologic entity. Hum Pathol 1992;23:780 –786[Medline]
  5. Garstin WIH, Kaufman Z, Michell MJ, Baum M. Fibrous mastopathy in insulin dependent diabetes. Clin Radiol1991; 44:89 –91[Medline]
  6. Kuhl CK, Mielcareck P, Klaschik S, et al. Dynamic breast MR imaging: are signal time course data useful for differential diagnosis of enhancing lesions? Radiology1999; 211:101 –110[Abstract/Free Full Text]
  7. Daniel BL, Yen YF, Glover GH, et al. Breast disease: dynamic spiral MR imaging. Radiology1998; 209:499 –509[Abstract/Free Full Text]
  8. Rieber A, Brambs HJ, Gabelmann A, Heilmann V, Kreienberg R, Kuhn T. Breast MRI for monitoring response of primary breast cancer to neo-adjuvant chemotherapy. Eur Radiol2002; 12:1711 –1719[Medline]
  9. Sakuhara Y, Shinozaki T, Hozumi Y, Ogura S, Omoto K, Furuse M. MR imaging of diabetic mastopathy. AJR2002; 179:1201 –1203[Free Full Text]

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