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AJR 2004; 183:35-37
© American Roentgen Ray Society


Case Report

Hypermetabolism of Elastofibroma Dorsi on PET–CT

Jerome C. Pierce, III1 and Robert Henderson2

1 Department of Radiology, Keck School of Medicine, University of Southern California, LAC + USC Medical Center, 1200 N State St., Rm. 3550, Los Angeles, CA 90033.
2 Department of Radiology, Keck School of Medicine, University of Southern California, University Hospital, 1500 San Pablo St., Los Angeles, CA 90033.

Received September 23, 2003; accepted after revision November 20, 2003.

 
Address correspondence to J. C. Pierce III (jeromecp{at}usc.edu).


Introduction
Top
Introduction
Case Reports
Discussion
References
 
Elastofibromas are benign, slowly growing lesions characteristically located in the subscapular region. Elastofibromas are pseudotumorous lesions characterized by fibroblastic proliferation and accumulation of abnormal elastic fibers [1]. They are relatively common lesions; the prevalence revealed on CT was found to be 2%, and an autopsy series reported an 11–24% prevalence [2]. Most (> 50%) elastofibromas are asymptomatic. The symptomatic cases can present with an enlarging soft-tissue mass as well as with shoulder pain, discomfort, "locking," or "snapping" [3]. Fine-needle aspirates of elastofibromas are notoriously difficult to interpret because of their inherent hypocellularity, and a nonspecific diagnosis of fibromatosis is commonly obtained. A core biopsy is usually needed to establish a specific diagnosis. Symptomatic lesions are treated with surgical excision with relatively favorable results [3, 4].

Elastofibromas have characteristic imaging findings on MRI and CT that allow a definitive diagnosis in most cases. Elastofibromas are typically located in the inferior subscapular region, deep in relation to the rhomboid major, serratus anterior, and latissimus dorsi muscles, and are bilateral in approximately 10% of cases. On CT, an elastofibroma appears as a poorly circumscribed soft-tissue mass with attenuation similar to that of muscle. Strands of lower density (attributed to fat) can be seen within the lesion. On MRI, the lesions show relatively low signal intensity (similar to muscle) on T1- and T2-weighted images. Interlaced fat is seen as strands of high signal intensity within these hypointense lesions [5, 6]. Enhancement after the administration of gadopentetate dimeglumine has been reported [7].

To our knowledge the positron emission tomography (PET) characteristics of elastofibromas have not been previously reported.


Case Reports
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Introduction
Case Reports
Discussion
References
 
In the following two case reports, the PET–CT images were obtained on a Biograph PET–CT scanner (Siemens). Images were obtained 45–60 min after IV injection of 555 MBq of FDG. The patients fasted for 6 hr before the study. Visual and region-of-interest (ROI) analyses were based on 5-mm-thick images. ROIs were used to obtain maximum standardized uptake values for the three lesions of interest.

A 69-year-old man presented with a left shoulder mass and left shoulder discomfort. Unenhanced CT scans of the chest followed by PET–CT hybrid images were obtained.

Unenhanced axial CT scans of the chest revealed a soft-tissue mass in the left inferior subscapular region. The mass was located just deep relative to the serratus anterior muscle, displacing the muscle laterally. The soft-tissue mass was oblong in shape, being longest in the superior–inferior plane. The attenuation of the lesion was similar to that of muscle. On closer inspection, we noted a similar but smaller soft-tissue lesion in a contralateral location.

PET–CT revealed a moderate degree of FDG accumulation within the subscapular masses. The hypermetabolism was more prominent in the left lesion (Fig. 1A, 1B, 1C, 1D). The maximum standardized uptake values for the left and right lesions were 1.88 and 1.52, respectively.



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Fig. 1A. 69-year-old man with left shoulder mass and discomfort. Axial positron emission tomography (PET) image reveals region of FDG accumulation (circled region) in left posterolateral chest. Smaller and less metabolically active lesion (arrow) is noted contralaterally.

 


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Fig. 1B. 69-year-old man with left shoulder mass and discomfort. On fused PET–CT image, area of moderate hypermetabolism (circled region) is noted to correspond to 2 x 5 cm crescent-shaped soft-tissue mass in left subscapular region, just deep in relation to serratus anterior muscle. Smaller lesion (arrow) is present contralaterally.

 


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Fig. 1C. 69-year-old man with left shoulder mass and discomfort. Photomicrograph of pathology section contains mixture of collagen, elastic fibers, and fat globules. (H and E, x160)

 


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Fig. 1D. 69-year-old man with left shoulder mass and discomfort. Photomicrograph of elastic fibers in cross section shows characteristic serrated edges (arrows). (elastic fiber stain, x250)

 

The symptomatic left lesion was surgically excised by an orthopedic surgeon, and pathologic assessment was obtained. On gross examination, the lesion was firm and rubbery. Histologic assessment revealed fibroblastic proliferation with the accumulation of collagen and abnormal elastic fibers. The findings were diagnostic of elastofibroma dorsi (Fig. 1A, 1B, 1C, 1D).

An 83-year-old woman with a history of breast cancer presented to the PET center for metastatic workup, and PET–CT hybrid images were obtained.

PET–CT images of the 83-year-old woman revealed a poorly circumscribed, oblong, subscapular, soft-tissue mass located between the inferior tip of the scapula and the chest wall. The mass was similar in attenuation to muscle, with strands of lower density interspersed within the lesion. The location and the CT appearance of the lesion were characteristic of elastofibroma dorsi. On the PET portion of the study, a moderate degree of FDG radiotracer accumulation was noted in the mass (Fig. 2A, 2B). The calculated maximum standardized uptake value was 1.98.



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Fig. 2A. 83-year-old woman with history of breast cancer. Axial positron emission tomography (PET) image reveals focus of FDG accumulation (circled region) in right posterolateral chest. Intense intrathoracic uptake is seen in myocardium.

 


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Fig. 2B. 83-year-old woman with history of breast cancer. Fused PET–CT image shows area of hypermetabolism (arrow) corresponding to soft-tissue mass in right subscapular region between inferior scapula and chest wall. Note left breast implant.

 

Biopsy of the lesion was not performed because the lesion was asymptomatic and the imaging features as well as the location of the mass were thought to be diagnostic of elastofibroma dorsi.


Discussion
Top
Introduction
Case Reports
Discussion
References
 
Elastofibromas are relatively common lesions that are frequently overlooked clinically and radiologically. The first objective of this report is to familiarize the reader with the CT and MRI appearances of this condition. The second objective is to present two cases of elastofibroma dorsi that show hypermetabolism on FDG PET, which has not been previously described. In both cases, the diagnosis of elastofibroma dorsi was made on the basis of the typical subscapular location of the lesions and the characteristic CT appearance (poorly circumscribed soft tissue with attenuation similar to that of muscle). A lack of awareness of the CT characteristics of elastofibromas could have resulted in erroneous interpretation of the PET portion of these studies; the FDG hypermetabolism may have been attributed in a nonspecific manner to an inflammatory or neoplastic process.

In the 69-year-old man, the diagnosis of elastofibroma dorsi was not made on the initial CT of the chest. This led to further evaluation with PET–CT. The recognition of the characteristic imaging features of elastofibroma dorsi on the CT portion of this study enabled a preoperative diagnosis to be made. This was important because the presumptive diagnosis of elastofibroma dorsi affected surgical planning, and a wide surgical margin was not required. The lesion was removed because of symptomatology referable to the left shoulder. The patient's postoperative course was uneventful.

In the 83-year-old woman with a history of breast cancer, recognition of the classic CT features of elastofibroma dorsi was particularly important. Attributing the FDG hypermetabolism to metastatic disease would have caused unnecessary patient anxiety and may have led to an unnecessary surgical procedure or biopsy. In addition, the medical treatment of breast cancer patients with metastatic disease is different from that of patients in remission. Patients with metastatic disease are typically treated with hormonal or chemotherapy [8].

As the number of PET and PET–CT hybrid images obtained increases, more benign lesions with the potential for hypermetabolism are likely to be discovered. The two cases presented in this report show the potential for FDG hypermetabolism in elastofibromas. Knowledge of the typical location of elastofibromas and recognition of their characteristic CT appearance are helpful when encountering a hypermetabolic subscapular mass on PET–CT images.


References
Top
Introduction
Case Reports
Discussion
References
 

  1. Nagira K, Yamamoto T, Akisue T, et al. Scrape and fine-needle aspiration cytology of elastofibroma. Anticancer Res2002; 22:3561 –3567[Medline]
  2. Brandser EA, Goree JC, El-Khoury GY. Elastofibroma dorsi: prevalence in an elderly patient population as revealed by CT. AJR 1998;171:977 –980[Abstract/Free Full Text]
  3. Majo J, Gracia I, Doncel A, Valera M, Nunez A, Guix M. Elastofibroma dorsi as a cause of shoulder pain or snapping scapula. Clin Orthop2001; 388:200 –204
  4. Vastamaki M. Elastofibroma scapulae. Clin Orthop 2001;392:404 –408
  5. Naylor MF, Nascimento AG, Sherrick AD, McLeod RA. Elastofibroma dorsi: radiologic findings in 12 patients. AJR1996; 167:683 –687[Abstract/Free Full Text]
  6. Kransdorf MJ, Meis JM, Montgomery E. Elastofibroma: MR and CT appearances with radiologic-pathologic correlation. AJR 1992;159:575 –579[Abstract/Free Full Text]
  7. Schick S, Zembsch A, Gahleitner A, et al. Atypical appearance of elastofibroma dorsi on MRI: case reports and review of the literature. J Comput Assist Tomogr2000; 24:288 –292[Medline]
  8. Cha CH, Kennedy GD, Niederhuber JE. Metastatic breast cancer. Surg Clin North Am1999; 79:1117 –1143[Medline]

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