Natural evolution of desmoplastic fibroblastoma on magnetic resonance imaging: a case report
© Kamata et al; licensee BioMed Central Ltd. 2011
Received: 19 September 2009
Accepted: 7 April 2011
Published: 7 April 2011
Desmoplastic fibroblastoma (collagenous fibroma) is a recently described tumor thought to arise predominantly from subcutaneous tissue or skeletal muscle. The natural evolution of this tumor on magnetic resonance imaging has never been described, to the best of our knowledge. We herein report a case of desmoplastic fibroblastoma arising in the thigh and show the longitudinal magnetic resonance imaging findings.
A 60-year-old Japanese man presented with swelling of the medial side of his right thigh, and he complained of nighttime pain and slight tenderness. Magnetic resonance imaging demonstrated a 4 × 4 cm mass in the right thigh. Open biopsy was performed. The mass was diagnosed histologically as a benign fibrous tumor, and we maintained follow-up without surgical therapy. After one year, magnetic resonance imaging showed an increase in tumor size to 4 × 5 cm, but the histologic findings were the same as those obtained one year earlier. Resection was performed with narrow surgical margins. Pathologic diagnosis was desmoplastic fibroblastoma. Two years after surgery, the patient is free from pain and shows no signs or symptoms of recurrence.
The natural evolution of desmoplastic fibroblastoma is characterized by no changes in patterns on magnetic resonance imaging despite increasing size. This finding is clinically helpful for distinguishing desmoplastic fibroblastoma with increasing pain from the desmoid tumor.
In 1995, Evans  first described desmoplastic fibroblastoma, a unique fibrous soft tissue tumor comprising spindle-shaped to stellate fibroblastic cells sparsely distributed in a dense fibrous background. This tumor, alternatively called collagenous fibroma, was clinically and morphologically distinct, as well as completely benign in previously reported series. Details of magnetic resonance imaging (MRI) findings for this tumor have been described for three cases [3, 4], but the natural evolution of this tumor has never been described. Here, we present the natural evolution of this tumor on MRI.
A 60-year-old Japanese man presented with swelling of the medial side of his right thigh and complained of night pain and slight tenderness. Palpation disclosed a hard, well-circumscribed, mobile tumor. Otherwise healthy, he had no history of trauma to the thigh. The results of routine laboratory studies were normal.
At the most recent follow-up examination two years after surgery, the patient was free from pain and showed no signs or symptoms of recurrence.
Evans  used the designation desmoplastic fibroblastoma when he described seven patients having masses with distinct morphologic characteristics. Subsequently, Nielsen et al. reported seven other cases and proposed that the tumor be renamed collagenous fibroma, arguing that desmoplastic fibroblastoma misleads the reader into believing that the lesion consists of immature tumor cells inducing a desmoplastic response in host tissues.
These neoplasms typically occur in the fifth or sixth decades of life and occur two and a half times more often in men than women. Clinically, desmoplastic fibroblastoma presents as a firm, mobile, slowly growing mass located in subcutaneous tissue or near the deep aspect of skeletal muscles. Common locations include the arm, shoulder, posterior neck and upper back [1–8]. Few previous reports have described tumors arising in the thigh [1, 2, 6, 8]. In the present patient, the tumor appeared to arise from the fascia of the thigh muscles. Such tumors located in the intermuscular space have not been described. The mass is usually painless; however, our patient complained of pain, as have those in some previous reports [3, 5, 6]. In our case, location of the tumor adjacent to Hunter's canal may have contributed to pain by compressing the saphenous nerve in the canal.
Previous authors recommended treatment of desmoplastic fibroblastoma by total surgical excision. No tumor recurrence during follow-up has been reported, including the present case.
On MRI, T1-weighted images of the mass depicted a mixture of low SI and isointensity. With T2-weighting, the mass showed scattered high-SI areas within a zone of low SI. Contrast T1-weighted images demonstrated inhomogeneous enhancement after contrast administration, and nonenhanced areas corresponding to regions showing low SI on noncontrast T1-weighted images. The size of the tumor increased over the course of one year, but the MRI findings of the tumor showed no changes.
Several reports have described the MRI appearance of this tumor, but in only three cases have MRI findings been described in detail [3, 4], and those findings have varied. T1-weighted findings were described as having diverse SI, low SI compared with muscle, scattered isointense areas , and isointense areas with scattered areas of low and high SI . T2-weighted findings also have varied among cases, including high-SI areas with small low-SI areas  and low-SI areas with small high-SI areas . Postcontrast T1-weighted images have only been described in two cases. They showed enhanced areas within areas of low SI, and enhanced areas showed strong enhancement in one case, with inhomogeneous enhancement seen in the other case [3, 4].
In previous reports, the relationship between MRI findings and histologic findings has been described. On T2-weighted images, low-SI areas correspond to abundant collagen fibers [3, 4, 9], and high-SI areas showing marked enhancement on contrast T1-images correspond to those histologically consisting of fibroblasts and loose collagen fibers . On T1-weighted images, low-SI areas represent areas with low cellularity and abundant collagen fibers .
These reports indicate that MRI findings vary among and within individual tumors because of the variable cellularity.
Evans  suggested that the most significant differential diagnostic consideration was desmoid tumor because it may have similar cytologic features and is often locally aggressive.
On the other hand, Marco et al. reported that desmoplastic fibroblastoma is a myofibroblastic lesion ultrastructurally demonstrating the presence of fibronexus junctions; markers of myofibroblastic differentiation, typically present on the cytoplasmic membrane of the cells, while desmoid tumor is fibroblastic. This ultrastructural finding is important in the differential diagnosis between desmoplastic fibroma and desmoid tumor.
Details of imaging studies of desmoid tumors have been well documented in previous reports [11–13], and the margins of the tumor are mostly ill defined. However, some MRI findings of desmoid tumor are similar to those of desmoplastic fibroblastoma [11, 12]. Several reports have described desmoid tumors as resulting in pain , and Agrawal et al. reported an increasing desmoid tumor with pain. When desmoplastic fibroblastoma increases with pain, such as in our case, the tumor needs to be distinguished from desmoid tumor.
The natural evolution of desmoid tumor has been documented , but that of desmoplastic fibroblastoma has not been previously reported. Vandevenne et al. described the MRI findings of the natural evolution of desmoid tumors. Desmoid tumors showing high SI on T2-weighted images tend to increase in size. Subsequently, they show an increase in areas of low SI on T2-weighted images. Finally, they acquire an overall low SI both on T1- and T2-weighted images and decrease in size. In contrast, the MRI findings of desmoplastic fibroblastoma in our case showed an increase in tumor size, with the same pattern: mainly low SI on T1-weighted images. The follow-up period of one year and the two sets of MRIs may not be sufficient to understand the true behavior of slow-growing tumors, such as desmoplastic fibroblastoma. Clinically, however, changes in MRI findings provide important information in distinguishing between aggressive and slow-growing tumors.
This case study has described the MRI findings of desmoplastic fibroblastoma in relation to its natural evolution. The natural evolution of desmoplastic fibroblastoma is characterized by no change in patterns on MRI despite increasing size. This finding is clinically helpful for distinguishing desmoplastic fibroblastoma with increasing pain from desmoid tumor.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
- Evans HL: Desmoplastic fibroblastoma. A report of seven cases. Am J Surg Pathol. 1995, 19: 1077-1081. 10.1097/00000478-199509000-00012.View ArticlePubMedGoogle Scholar
- Nielsen GP, O'Connell JX, Dickersin GR, Rosenberg AE: Collagenous fibroma (desmoplastic fibroblastoma): a report of seven cases. Mod Pathol. 1996, 9: 781-785.PubMedGoogle Scholar
- Ogose A, Hotta T, Emura I, Higuchi T, Kusano N, Saito H: Collagenous fibroma of the arm: a report of two cases. Skeletal Radiol. 2000, 29: 417-420. 10.1007/s002560000223.View ArticlePubMedGoogle Scholar
- Shuto R, Kiyosue H, Hori Y, Miyake H, Kawano K, Mori H: CT and MR imaging of desmoplastic fibroblastoma. Eur Radiol. 2002, 12: 2474-2476.View ArticlePubMedGoogle Scholar
- Beggs I, Salter DS, Dorfman HD: Synovial desmoplastic fibroblastoma of hip joint with bone erosion. Skeletal Radiol. 1999, 28: 402-406. 10.1007/s002560050537.View ArticlePubMedGoogle Scholar
- Hasegawa T, Shimoda T, Hirohashi S, Hizawa K, Sano T: Collagenous fibroma (desmoplastic fibroblastoma): report of four cases and review of the literature. Arch Pathol Lab Med. 1998, 122: 455-460.PubMedGoogle Scholar
- Miettinen M, Fetsch JF: Collagenous fibroma (desmoplastic fibroblastoma): a clinicopathologic analysis of 63 cases of a distinctive soft tissue lesion with stellate-shaped fibroblasts. Hum Pathol. 1998, 29: 676-682. 10.1016/S0046-8177(98)90275-1.View ArticlePubMedGoogle Scholar
- Sciot R, Samson I, van den Berghe H, Van Damme B, Dal Cin P: Collagenous fibroma (desmoplastic fibroblastoma): genetic link with fibroma of tendon sheath?. Mod Pathol. 1999, 12: 565-568.PubMedGoogle Scholar
- Dinauer PA, Brixey CJ, Moncur JT, Fanburg-Smith JC, Murphey MD: Pathologic and MR imaging features of benign fibrous soft-tissue tumors in adults. Radiographics. 2007, 27: 173-187. 10.1148/rg.271065065.View ArticlePubMedGoogle Scholar
- Alberghini M, Pasquinelli G, Zanella L, Bacchini P, Bertoni F: Desmoplastic fibroblastoma: a light and ultrastructural description of two cases. Ultrastruct Pathol. 2004, 28: 149-157. 10.1080/01913120490475761.View ArticlePubMedGoogle Scholar
- Hartman TE, Berquist TH, Fetsch JF: MR imaging of extraabdominal desmoids: differentiation from other neoplasms. AJR Am J Roentgenol. 1992, 158: 581-585.View ArticlePubMedGoogle Scholar
- Papagelopoulos PJ, Mavrogenis AF, Mitsiokapa EA, Papaparaskeva KT, Galanis EC, Soucacos PN: Current trends in the management of extra-abdominal desmoid tumours. World J Surg Oncol. 2006, 3: 4-21.Google Scholar
- Vandevenne JE, De Schepper AM, De Beuckeleer L, Van Marck E, Aparisi F, Bloem JL, Erkorkmaz Z, Brijs S: New concepts in understanding evolution of desmoid tumors: MR imaging of 30 lesions. Eur Radiol. 1997, 7: 1013-1019. 10.1007/s003300050243.View ArticlePubMedGoogle Scholar
- Rock MG, Pritchard DJ, Reiman HM, Soule EH, Brewster RC: Extra-abdominal desmoid tumors. J Bone Joint Surg Am. 1984, 66: 1369-1374.PubMedGoogle Scholar
- Agrawal PS, Jagtap SM, Mitra SR: Extra-abdominal desmoid tumour of the leg. Singapore Med J. 2008, 49: e6-e7.PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.