Atrophic dermatofibrosarcoma protuberans: report of a case demonstrated by detecting COL1A1-PDGFB rearrangement
© Qiao et al.; licensee BioMed Central Ltd. 2012
Received: 28 August 2012
Accepted: 22 November 2012
Published: 30 November 2012
Dermatofibrosarcoma protuberans is a locally aggressive mesenchymal neoplasm. It usually presents as an indurated plaque that protrudes above the surface of the skin. Some patients have clinically persistent plaques that might be atrophic. The atrophic variant of dermatofibrosarcoma protuberans may be confused with some common skin diseases with atrophic appearance. We reported a 40-year-old woman who had a 10-year history of an atrophic dermatofibrosarcoma protuberans. Molecular analysis showed a fusion between COL1A1 exon 31 to exon 2 of PDGFB. The lesion was totally excised, with negative margins of the resection demonstrated by CD34 immunostaining. To our knowledge, this is the second case of atrophic dermatofibrosarcoma protuberans confirmed by detection of COL1A1-PDGFB fusion gene. This appears to be the first report of a fusion between COL1A1 exon 31 to exon 2 of PDGFB in atrophic dermatofibrosarcoma protuberans.
The virtual slides for this article can be found here:http://www.diagnosticpathology.diagnomx.eu/vs/1249657688795311
KeywordsDermatofibrosarcoma protuberans COL1A1-PDGFB CD34 Atrophic Sarcoma
Dermatofibrosarcoma protuberans is a locally aggressive mesenchymal neoplasm. The lesions of this tumor usually present as indurated plaques that protrude above the surface of the skin[1, 2]. The atrophic variant is a rare form of the tumor[3–5]. Translocation of t(17;22)(q22;q13) is the cytogenetic features of dermatofibrosarcoma protuberans. As a consequence of this chromosomal rearrangement, fusion of the collagen type I α 1 (COL1A1) gene on 17q, with the platelet-derived growth factor β-chain (PDGFB) gene on 22q, is detected. The fusion gene has been detected in several unusual variants of dermatofibrosarcoma protuberans (pigmented variant, giant cell fibroblastoma, and granular variant)[1, 6]. The fusion gene has been detected only in one case of atrophic variant of dermatofibrosarcoma protuberans. Here we report a case of atrophic dermatofibrosarcoma protuberans confirmed by detection of the COL1A1-PDGFB fusion gene. The gene fusion between COL1A1 exon 31 to exon 2 of PDGFB observed in our patient is firstly reported in atrophic dermatofibrosarcoma protuberans.
Dermatofibrosarcoma protuberans is a locally aggressive mesenchymal neoplasm with an intermediate grade and a high rate of local recurrence[1, 6]. The incidence has been reported between 0.8–5.0 cases per 1 million persons per year. Men and women are equally affected. Dermatofibrosarcoma protuberans most commonly occurs in adults between the ages of 20 and 50, and are most commonly located on the trunk and the proximal extremities[1, 2].
Dermatofibrosarcoma protuberans usually appears as an indurated, exophytic, asymptomatic, flesh-to-red/brown plaque that protrude above the surface of the skin. These characteristic lesions are usually not difficult to diagnose clinically. However, the often slow clinical evolution of dermatofibrosarcoma protuberans is typified by an initial plaque stage and a later nodular stage. Some patients have clinically persistent plaques that might be atrophic, as in our patient. These atrophic plaques are believed to represent early lesions in the course of dermatofibrosarcoma protuberans[8, 9], and have rarely been reported and characterized in detail. Given the typical ‘protuberant’ morphology, the diagnosis of atrophic lesions of dermatofibrosarcoma protuberans is frequently delayed[5, 8].
The atrophic variant of this tumor is often clinically confused with common conditions characterized by atrophy or sclerosis, such as morphea, atrophic scar, morpheaform basal cell carcinoma, lipoatrophy, idiopathic atrophoderma, anetoderma, atrophic dermatofibroma, neurofibroma, resolving panniculitis, steroid atrophy, and medallion-like dermal dendrocyte hamartoma[3–5, 8, 10, 11].
Histopathologically, dermatofibrosarcoma protuberans tumor cells are composed of densely packed, monomorphous spindle cells arranged in a storiform or whorled pattern, frequently infiltrating into subcutis and extending laterally into the surrounding dermis. It may also involve the fascia, muscle and bone. Cells of this tumor typically exhibit low mitotic activity. There are some variants of dermatofibrosarcoma protuberans, including pigmented variant (Bednar tumor), congenital variant, giant cell fibroblastoma, atrophic variant, and fibrosarcomatous variant. The former four variant typically behave similarly to the classic type. However, the fibrosarcomatous variant is more aggressive, with a high propensity for metastasis[1, 6].
Histopathologically, dermatofibrosarcoma protuberans should be differentiated from other cutaneous spindle cell tumors, including dermatofibroma, fibrosarcoma, malignant fibrohistocytoma, atypical fibroxanthoma, desmoplastic melanoma, keloid, Kaposi sarcoma, and solitary fibrous tumor[1, 12, 13]. Immunostains are helpful to differentiate dermatofibrosarcoma protuberans from other fibrohistiocytic neoplasms. Typically, cells of dermatofibrosarcoma protuberans are diffusely labeled with CD34 and are negative for factor XIIIa[1, 5], distinguishing it from analogous neoplasms. The converse is true for most cases of dermatofibroma. Dermatofibrosarcoma protuberans is negative for CD68, allowing differentiation from atypical fibroxanthoma and malignant fibrohistocytoma, and is also typically negative for S100, helping distinguish it from desmoplastic melanoma.
Solitary fibrous tumor also consists of bland spindle cells but the tumor is well circumscribed. Similar to that in dermatofibrosarcoma protuberans, solitary fibrous tumor commonly labeled with CD34 and vimentin. However spindle cells in solitary fibrous tumor also express CD99 and bcl-2, which are negative for dermatofibrosarcoma protuberans.
Kaposi sarcoma is a vascular tumor with low-grade malignant potential. The tumor often composed of spindle cells, with slit-like vascular channels containing erythrocytes. The spindle cells not only express CD34 but also are immunoreactive for CD31 and human herpes virus 8.
Medallion-like dermal dendrocyte hamartoma is a newly described and rare entity. This tumor is benign. However, it shows morphologic, histological, and immunohistochemistrial overlap with atrophic dermatofibrosarcoma protuberans[15, 16]. The lesions of medallion-like dermal dendrocyte hamartoma are round, solitary, well-demarcated, oval or triangular erythematous and atrophic plaques of several centimetres in diameter[15, 16]. They are histologically characterized by a spindle cell proliferation in the dermis and in the subcutaneous fat. Furthermore, immunochemical staining for CD34 and factor XIIIa is usually positive in the hamartoma. Molecular testing is an important tool to differentiate these lesions from atrophic dermatofibrosarcoma protuberans, as there is not known rearrangements associated with hamartoma[15–17].
Nearly all dermatofibrosarcoma protuberans carry a t(17;22)(q22;q13) chromosomal translocation, which fuses the COL1A1 gene on chromosome 17 to PDGFB on chromosome 22, and result in a chimeric COL1A1-PDGFB protein. The translocation can be identified by fluorescence in situ hybridization, or RT-PCR, and confirmed by sequencing of the chimeric COL1A1/PDGFB. Llombart et al. reported the first case of atrophic dermatofibrosarcoma protuberans that was confirmed by COL1A1-PDGFB fusion gene detection. To our knowledge, this is the second case of atrophic dermatofibrosarcoma protuberans whose diagnosis was confirmed by detection of the fusion gene. COL1A1 encodes the α-chains of type 1 collagen, and PDGFB codes for the β-chain of platelet-derived growth factor. The latter is a potent mitogen that acts on a variety of cells. After gene fusion of COL1A and PDGFB, the inhibitory regulatory element of PDGFB is replaced by COL1A1, which allows for producing high levels of the chimeric COL1A1-PDGFB mRNA. PDGFB is cleaved from the COL1A1-PDFGB protein and the cleaved PDGFB turns to stimulate cells in an autocrine fashion, leading to malignant transformation. Fusion of COL1A1 exon 31 to exon 2 of PDGFB, as seen in our patient, was not reported previously in atrophic dermatofibrosarcoma protuberans. However, it has been postulated that the different types of fusion between COL1A1 and PDGFB are not related with the clinical or histological features[7, 19].
The standard treatment of the sarcoma is local excision with wide margins. Mohs surgery allows complete examination of the margins while sparing the maximum amount of healthy tissue[20–23]. Surgical treatment, however, is not always possible. Imatinib mesylate, targeting platelet-derived growth factor receptor beta, has clinical potential in dermatofibrosarcoma protuberans. It has been demonstrated that imatinib mesylate inhibits the tyrosine kinase activity of PDGF-BB and causes apoptosis of the dermatofibrosarcoma protuberans cells[24, 25]. Clinical trials demonstrated that imatinib has profound antitumor effects in advanced dermatofibrosarcoma protuberans harboring t(17;22) (q22;q13)[25–28].
In conclusion, we report a case of atrophic dermatofibrosarcoma protuberans, which clinically masquerades as various atrophic cutaneous disorders. This variant is believed to represent an early stage of this lesion. This entity can be differentiated from other clinically similar lesions by histology, immunohistochemistry, and molecular genetics.
Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Collagen type I α 1
Platelet-derived growth factor β-chain.
- Dimitropoulos VA: Dermatofibrosarcoma protuberans. Dermatol Ther. 2008, 21: 428-432. 10.1111/j.1529-8019.2008.00242.x.View ArticlePubMed
- Kampshoff JL, Cogbill TH: Unusual skin tumors: Merkel cell carcinoma, eccrine carcinoma, glomus tumors, and dermatofibrosarcoma protuberans. Surg Clin North Am. 2009, 89: 727-738. 10.1016/j.suc.2009.02.005.View ArticlePubMed
- Sinovich V, Hollowood K, Burge S: Atrophic dermatofibrosarcoma protuberans. Australas J Dermatol. 2005, 46: 114-117. 10.1111/j.1440-0960.2005.00156.x.View ArticlePubMed
- Sheehan DJ, Madkan V, Strickling WA, Peterson CM: Atrophic dermatofibrosarcoma protuberans: a case report and reappraisal of the literature. Cutis. 2004, 74: 237-242.PubMed
- Young CR, Albertini MJ: Atrophic dermatofibrosarcoma protuberans: case report, review, and proposed molecular mechanisms. J Am Acad Dermatol. 2003, 49: 761-764. 10.1067/S0190-9622(03)00793-X.View ArticlePubMed
- Bogucki B, Neuhaus I, Hurst EA: Dermatofibrosarcoma protuberans: a review of the literature. Dermatol Surg. 2012, 10.1111/j.1524-4725.2011.02292.x.
- Llombart B, Sanmartin O, Requena C, Monteagudo C, Botella-Estrada R, Nagore E, Serra C, Alfaro A, Pellin A, Llombart-Bosch A, et al.: Atrophic dermatofibrosarcoma protuberans with the fusion gene COL1A1-PDGFB. J Eur Acad Dermatol Venereol. 2008, 22: 371-374. 10.1111/j.1468-3083.2007.02327.x.View ArticlePubMed
- Hanabusa M, Kamo R, Harada T, Ishii M: Dermatofibrosarcoma protuberans with atrophic appearance at early stage of the tumor. J Dermatol. 2007, 34: 336-339. 10.1111/j.1346-8138.2007.00283.x.View ArticlePubMed
- Martin L, Piette F, Blanc P, Mortier L, Avril MF, Delaunay MM, Dreno B, Granel F, Mantoux F, Aubin F, et al.: Clinical variants of the preprotuberant stage of dermatofibrosarcoma protuberans. Br J Dermatol. 2005, 153: 932-936. 10.1111/j.1365-2133.2005.06823.x.View ArticlePubMed
- Fujimoto M, Kikuchi K, Okochi H, Furue M: Atrophic dermatofibrosarcoma protuberans: a case report and review of the literature. Dermatology. 1998, 196: 422-424. 10.1159/000017936.View ArticlePubMed
- Wu JK, Malik MM, Egan CA: Atrophic dermatofibrosarcoma protuberans: an uncommon and misleading variant. Australas J Dermatol. 2004, 45: 175-177. 10.1111/j.1440-0960.2004.00083.x.View ArticlePubMed
- Grayson W, Pantanowitz L: Histological variants of cutaneous Kaposi sarcoma. Diagn Pathol. 2008, 3: 31-10.1186/1746-1596-3-31.PubMed CentralView ArticlePubMed
- Martorell M, Perez-Valles A, Gozalbo F, Garcia-Garcia JA, Gutierrez J, Gaona J: Solitary fibrous tumor of the thigh with epithelioid features: a case report. Diagn Pathol. 2007, 2: 19-10.1186/1746-1596-2-19.PubMed CentralView ArticlePubMed
- Hollmig ST, Sachdev R, Cockerell CJ, Posten W, Chiang M, Kim J: Spindle cell neoplasms encountered in dermatologic surgery: a review. Dermatol Surg. 2012, 38: 825-850. 10.1111/j.1524-4725.2012.02296.x.View ArticlePubMed
- Rodriguez-Jurado R, Palacios C, Duran-McKinster C, Mercadillo P, Orozco-Covarrubias L, Saez-de-Ocariz Mdel M, Ruiz-Maldonado R: Medallion-like dermal dendrocyte hamartoma: a new clinically and histopathologically distinct lesion. J Am Acad Dermatol. 2004, 51: 359-363. 10.1016/j.jaad.2003.11.070.View ArticlePubMed
- Marque M, Bessis D, Pedeutour F, Viseux V, Guillot B, Fraitag-Spinner S: Medallion-like dermal dendrocyte hamartoma: the main diagnostic pitfall is congenital atrophic dermatofibrosarcoma. Br J Dermatol. 2009, 160: 190-193. 10.1111/j.1365-2133.2008.08896.x.View ArticlePubMed
- Ducharme EE, Baribault KE, Husain S, Engler DE: Medallion-like dermal dendrocyte hamartoma in a 36-year-old male. J Am Acad Dermatol. 2008, 59: 169-172. 10.1016/j.jaad.2008.03.003.View ArticlePubMed
- Patel KU, Szabo SS, Hernandez VS, Prieto VG, Abruzzo LV, Lazar AJ, Lopez-Terrada D: Dermatofibrosarcoma protuberans COL1A1-PDGFB fusion is identified in virtually all dermatofibrosarcoma protuberans cases when investigated by newly developed multiplex reverse transcription polymerase chain reaction and fluorescence in situ hybridization assays. Hum Pathol. 2008, 39: 184-193. 10.1016/j.humpath.2007.06.009.View ArticlePubMed
- Maire G, Fraitag S, Galmiche L, Keslair F, Ebran N, Terrier-Lacombe MJ, de Prost Y, Pedeutour F: A clinical, histologic, and molecular study of 9 cases of congenital dermatofibrosarcoma protuberans. Arch Dermatol. 2007, 143: 203-210. 10.1001/archderm.143.2.203.View ArticlePubMed
- Lemm D, Mugge LO, Mentzel T, Hoffken K: Current treatment options in dermatofibrosarcoma protuberans. J Cancer Res Clin Oncol. 2009, 135: 653-665. 10.1007/s00432-009-0550-3.View ArticlePubMed
- Paradisi A, Abeni D, Rusciani A, Cigna E, Wolter M, Scuderi N, Rusciani L, Kaufmann R, Podda M: Dermatofibrosarcoma protuberans: wide local excision vs. Mohs micrographic surgery. Cancer Treat Rev. 2008, 34: 728-736. 10.1016/j.ctrv.2008.06.002.View ArticlePubMed
- Galimberti G, Montano AP, Kowalczuk A, Ferrario D, Galimberti R: Outcomes in 11 patients with dermatofibrosarcoma protuberans treated with Mohs micrographic surgery. Int J Dermatol. 2012, 51: 89-93. 10.1111/j.1365-4632.2010.04721.x.View ArticlePubMed
- Tan WP, Barlow RJ, Robson A, Kurwa HA, McKenna J, Mallipeddi R: Dermatofibrosarcoma protuberans: 35 patients treated with Mohs micrographic surgery using paraffin sections. Br J Dermatol. 2011, 164: 363-366. 10.1111/j.1365-2133.2010.10095.x.View ArticlePubMed
- McArthur GA, Demetri GD, van Oosterom A, Heinrich MC, Debiec-Rychter M, Corless CL, Nikolova Z, Dimitrijevic S, Fletcher JA: Molecular and clinical analysis of locally advanced dermatofibrosarcoma protuberans treated with imatinib: imatinib target exploration consortium study B2225. J Clin Oncol. 2005, 23: 866-873. 10.1200/JCO.2005.07.088.View ArticlePubMed
- Rutkowski P, Wozniak A, Switaj T: Advances in molecular characterization and targeted therapy in dermatofibrosarcoma protuberans. Sarcoma. 2011, 2011: 959132-PubMed CentralView ArticlePubMed
- Rubin BP, Schuetze SM, Eary JF, Norwood TH, Mirza S, Conrad EU, Bruckner JD: Molecular targeting of platelet-derived growth factor B by imatinib mesylate in a patient with metastatic dermatofibrosarcoma protuberans. J Clin Oncol. 2002, 20: 3586-3591. 10.1200/JCO.2002.01.027.View ArticlePubMed
- Rutkowski P, Debiec-Rychter M, Nowecki Z, Michej W, Symonides M, Ptaszynski K, Ruka W: Treatment of advanced dermatofibrosarcoma protuberans with imatinib mesylate with or without surgical resection. J Eur Acad Dermatol Venereol. 2011, 25: 264-270. 10.1111/j.1468-3083.2010.03774.x.View ArticlePubMed
- Rutkowski P, Van Glabbeke M, Rankin CJ, Ruka W, Rubin BP, Debiec-Rychter M, Lazar A, Gelderblom H, Sciot R, Lopez-Terrada D, et al.: Imatinib mesylate in advanced dermatofibrosarcoma protuberans: pooled analysis of two phase II clinical trials. J Clin Oncol. 2010, 28: 1772-1779. 10.1200/JCO.2009.25.7899.PubMed CentralView ArticlePubMed
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.