Abstract
Background
Dermatofibrosarcoma Protuberans (DFSP) of the vulva is rare and oncologic surgery with free margins may lead to severe functional damage, requiring multidisciplinary approach regarding resection, margin assessment and reconstruction.
Case Report
Two cases of DFSP in vulva were treated in a single institution. A 28-year-old patient with an incisional biopsy in the vulvar region revealing DFSP underwent a partial vulvectomy with clitoris preservation. Pathological studies revealed free margins and reconstructive surgery was performed. This patient is disease free in a 40 months follow up. The other, a 57-year-old patient was also referred after an incomplete resection of a DFSP in the vulvar region. A 1-cm margim resection followed by Complete Circumferential and Peripheral Deep Margin Assessment (CCPDMA) was performed. Although the upper lateral margin was positive, it was possible to perform another wide local excision with preservation of the clitoris and primary closure.
Conclusion
DFSP of the vulva requires an accurate evaluation of margins, resections following oncological principles and reconstruction. Although being a very challenging lesion that usually implies difficult surgical management, if treated in a multidisciplinary environment, with surgical oncologists, experienced dermatopathologists and reconstructive surgeons can achieve good results. Even in difficult cases that presents with large lesions and compromising challenging areas, a complete oncologic resection can be performed minimizing functional damage for the patient.
Electronic supplementary material
The online version of this article (doi:10.1186/1477-7819-12-399) contains supplementary material, which is available to authorized users.
Keywords: DFSP, Vulva, CCPDMA, Reconstruction, Surgical oncology
Background
Dermatofibrosarcoma protuberans (DFSP) is a rare skin mesenchymal tumor that usually affects the trunk and extremities. Vulvar DFSP is rare, with fewer than 40 cases previously reported in the literature [1, 2]. Surgery has been reported as the main therapeutic option for DFSP treatment. However, there is no consensus on margin assessment protocols. The most frequently used techniques are Mohs surgery, wide local excision (WLE) with 2.0 or 3.0 cm margins and surgery followed by three-dimensional complete circumferential and peripheral deep margin assessment (CCPDMA) [3–6].
The CCPDMA technique consists of excising the tumor with a margin smaller than the traditional 3.0-cm one. The specimen is submitted to conventional histologic processing and margins are completely evaluated by the pathologist. Additional study with immunohistochemistry (IHC) may be useful for margin assessment in some doubtful cases. This technique is associated with a more accurate evaluation of the margins and literature reports rates of recurrence lower than 10% [5, 7].
Another very important aspect of surgery in vulvar DFSP is the clitoris preservation and reconstruction after the lesion is removed, because this directly affects sexuality and quality of life of these patients [8, 9]. Better results are achieved with a multidisciplinary approach. The objective of this study was to present two cases of vulvar DFSP managed by the Skin Cancer and Gynecology Oncology Departments of AC Camargo Cancer Center with minimal functional damage for the patient. This case report was approved for publication by Fundação Antonio Prudente ethics committee.
Case presentation
The first case is a 28-year-old female patient referred to us after an incisional biopsy in the vulvar region revealing DFSP. She presented to us with a 5.0-cm lesion in the mons pubis (Figure 1A). Surgery was indicated, and consisted of a vulvectomy with a local advancement flap as the first approach in order to obtain a 2.0 cm margin from the tumor. Margins were assessed by CCPDMA protocols and they were all free of disease. Therefore, it was possible to avoid clitoris resection.To perform the vulvar reconstruction, a skin expander was placed in the inferior part of the abdominal wall one year after vulvectomy (Figure 1B). Weekly expansion was performed 3 weeks after the procedure and, in the third month, sufficient skin was attained in this area. The expander was taken out and the inferior 2/3 of the flap was split. The skin of the mons pubis was decorticated and the medium and proximal portions of the flap were advanced to protect the pubis bone. The distal portion was incised horizontally on both sides and folded after, in order to reconstruct the labius majoras (Figure 1C and D).This patient has been followed for almost 40 months (Figure 1E). There is no clinical or radiological evidence of recurrence. Regarding the surgery, we considered that a very adequate aesthetic effect was achieved. The patient verbally reported good quality of life, although no quality of life (QOL) questionnaires were applied.The second case is a 57-year-old female patient, also referred to our hospital after an incomplete resection of a DFSP in the vulvar region. She presented to us with a 2.0 cm residual lesion in the right labium major. As the lesion was too close to the clitoris, we performed a 1.0-cm margin instead of the traditional 2.0-cm one, followed by primary closure. The CCPDMA revealed all positive margins except for the upper lateral region of the specimen. The patient was submitted to another WLE of 2.0 cm and subsequent primary closure could be performed once more (Figure 2A). This patient has been followed for 10 months without any aesthetic or functional issue related to the surgery.
Conclusion
Regardless being a very rare disease, DFSP in the vulva represents a very challenging situation for the oncologic and plastic surgeons. The resection must follow oncological principles, which sometimes may lead to several aesthetic and functional impacts for the patient due to the difficulty in planning how wide the resection should be [4]. In this context, reconstructive surgery plays a fundamental role in the management of DFSP patients.
There are just few cases of vulvar DFSP reported in the literature. See Table 1 for a summary of previously reported cases of DFSP in the vulva with clinical, treatment and follow-up information. The largest series, from the MD Anderson Cancer Center, reported 13 cases. All of the six cases with positive margins after resection developed tumor recurrence. There was only one relapse between the cases with negative margins after WLE that occurred in a patient showing fibrosarcomatous transformation in the recurrent tumor [1].
Table 1.
Author | Cases | Age, years | Clinical presentation | Size, cm | Initial treatment | Outcome/follow up |
---|---|---|---|---|---|---|
Edelweiss and Malpica [1] | 1 | 36 | Right labium major mass | 5 | Excisional biopsy | LR at 12 months. AWD at 16 months |
Edelweiss and Malpica [1] | 2 | 57 | Right labium major mass | 3 | Excisional biopsy | LR at 60 months, then WLE (2x) until negative margin. NED at 216 months. |
Edelweiss and Malpica [1] | 3 | 69 | Mons pubis mass | 3 | Excisional biopsy + WLE | Dead of other causes at 144 months |
Edelweiss and Malpica [1] | 4 | 48 | Left paraclitoral mass | 1.2 | Excisional biopsy + WLE | LR, then WLE. NED at 144 months. |
Edelweiss and Malpica [1] | 5 | 46 | Right labium major pigmented lesion | 4 | Excisional biopsy + WLE (x2) | NED at 84 months. |
Edelweiss and Malpica [1] | 6 | 76 | Right labium major and crural fold mass | 15 | Excisional biopsy + WLE | LR at 7 months, then WLE with negative margin. At 14 months, metastasis to chest wall. At 18 months, metastasis to hip and thigh. Death of the disease at 34 months. |
Edelweiss and Malpica [1] | 7 | 44 | Left labium major mass | 4 | Excisional biopsy + WLE | NED at 53 months |
Edelweiss and Malpica [1] | 8 | 39 | Right labium major mass | N/A | WLE | LR at 48 months. Then, WLE with positive margin. At 60 months, local recurrence. Then WLE with positive margin. Used Gleevec. NED at 72 months |
Edelweiss and Malpica [1] | 9 | 30 | Right labium major and mons pubis mass | N/A | Excisional biopsy + WLE | LR at 11 months. Then, WLE. AWD at 24 months |
Edelweiss and Malpica [1] | 10 | 23 | Right labium major mass | 4 | Excisional biopsy + WLE | NED at 2 months |
Edelweiss and Malpica [1] | 11 | 30 | Left labium major mass | N/A | Excisional biopsy | LR at 60 months followed by WLE with positive margin. Then, partial vulvectomy with negative margin. NED at 96 months |
Edelweiss and Malpica [1] | 12 | 44 | Right labium major mass | 2.5 | Excisional biopsy + radical vulvectomy | NED at 36 months |
Edelweiss and Malpica [1] | 13 | 58 | Paraclitoral mass extending into vagina | 4.8 | WLE | NED at 3 months |
Soltan [10] | 14 | 83 | Left labium major/minor nodule | 5 | Excisional biopsy | N/A |
Agress et al. [11] | 15 | 56 | Left labium major | N/A | Excisional biopsy | LR, then WLE |
Bock et al. [12] | 16 | 52 | Right mons pruritus | 8 | Excisional biopsy | LR, then WLE |
Barnhill et al. [13] | 17 | 42 | Right vulva lateral to clitoris nodule | 1 | Excisional biopsy | LR, then WLE and hemivulvectomy |
Leake et al. [14] | 18 | 37 | Left mons and labium major nodule | 6.2 | Excisional biopsy | LR, then wide radical excision |
Leake et al. [14] | 19 | 59 | Right labium major nodule | 5 | Excisional biopsy | LR, then partial radical vulvectomy |
Panidis et al. [15] | 20 | 30 | Right labium major nodule | 2 | WLE | LR, then radical vulvectomy |
Aartsen and Albus-Lutter [16] | 21 | 50 | N/A | 1.2 | Radical vulvectomy | N/A |
Karlen et al. [17] | 22 | 36 | Left labium major irritated lump | 5 | WLE | N/A |
Nirenberg et al. [18] | 23 | 41 | Left labium major lump | 8 | WLE | N/A |
Alverez-Canas [19] | 24 | 58 | Left labium major mass | 3.2 | WLE | N/A |
Soergel et al. [20] | 25 | 47 | Left vulva mass + lung metastasis | 3 | Partial radical vulvectomy + chemotherapy | LR, then WLE + radiotherapy |
Ghorbani et al. [21] | 26 | 47 | Left paraclitoral area | N/A | Hemivulvectomy | LR, then wide radical excision |
Ghorbani et al. [21] | 27 | 44 | Left labium major mass | 4 | Wide radical excision | N/A |
Ghorbani et al. [21] | 28 | 66 | Mons mass | 1.5 | WLE | N/A |
Ghorbani et al. [21] | 29 | 36 | Right labium mass | 5 | Excsional biopsy | N/A |
Moodley and Moodley [22] | 30 | 39 | Left labium major mass | 12 | WLE | N/A |
Vanni et al. [23] | 31 | 39 | Inferior vulva/perineum mass | 6 | WLE | N/A |
Kholova et al. [24] | 32 | 31 | Left labium major recurrent nodule | 1.5 | Excisional biopsy | LR, then WLE + radiotherapy |
Ohlinger et al. [25] | 33 | 36 | Left vulva nodule | 2.8 | Excisional biopsy | LR, then WLE |
Hancox et al. [26] | 34 | 55 | Right labium major mass | 8 | MMS | NED |
Hammonds and Hendi [6] | 35 | 59 | Right labium major mass | 4 | MMS | NED |
Doufekas et al. [3] | 36 | 39 | Left labium major nodule | N/A | Incisional biopsy | MMS with primary closure. NED at 3 years |
Zizi-Sermpetzoglou et al. [27] | 37 | 66 | Mons pubis | N/A | WLE | NED |
N/A, not available; WLE, wide local excision; MMS, Mohs micrographic surgery; LR, local recurrence; AWD, alive with disease; AWOD, alive without disease; NED, no evidence of disease).
Based on this paper, the role of an adequate assessment of margins in these cases can be assumed. In our service, the protocol is to submit the specimen to conventional histologic processing with complete evaluation of the margins by CCPDMA by the pathologist, and IHC study whenever necessary [2, 5]. The morphologic and molecular pathologic findings of vulvar DFSP are quite similar to DFSP in other sites, including the frequent finding of the fusion between collagen type I alpha 1 gene (COL1A1) on chromosome 17 and the platelet-derived growth factor B-chain (PDGFB) gene on chromosome 22 [23, 28].
There is also scarce literature on reconstructive options in vulvar DFSP. There are two recent reports on Mohs surgery for vulvar DFSP, and both were submitted to primary closure [3, 6]. No data related to clitoris preservation or major vulvar reconstructions have been found.
Skin expansions are often used to reconstruct burned areas or breasts after a mastectomy or to hide scars [29]. Although there is no strong evidence in the literature to supports its use in skin tumors, we believe that it can be safely used since the tumor resection is not delayed because of the use of the expansion. Also, in our case we have had a very rigorous assessment of the pathological margins to ensure that the resection was complete. Moreover, the patient was kept for over a year in clinical follow up before starting the expansion.
Our first case illustrates an example of a major vulvar reconstruction using skin expansion followed by a skin and fat tissue flap. Although it has been done in only one patient, the clinical outcome suggests this can be a feasible option in such cases. Both our patients were submitted to clitoris-sparing surgery, which was only possible due to the utilization of the CCPDMA protocol by our Pathology Department.
We conclude that vulvar DFSP, although a very challenging lesion that usually implies difficult surgical management, if treated in a multidisciplinary environment with surgical oncologists, experienced pathologists and reconstructive surgeons, can achieve good results. And even in difficult cases that present with large lesions and compromising challenging areas, a complete oncologicresection can be performed, minimizing functional damage for the patient.
Acknowledgement
We acknowledge A.C. Camargo Cancer Center for institutional support.
Abbreviations
- DFSP
dermatofibrosarcoma protuberans
- WLE
wide local excision
- CCPDMA
3-dimensional complete circumferential and peripheral deep margin assessment
- IHC
immunohistochemistry
- COL1A1
collagen type I alpha 1
- PGDF
Platelet-derived growth factor B-chain.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
The Skin Cancer Department staff (EB, ERB, WRC, MC, ASM, JPDN) was involved in the diagnosis, management and post-operative recovery of the patients. The Gynecology Oncology Department staff (GB) was also involved with the operative proceedings in both cases. The Pathology department (MPM, IWC, CALP) was responsible for the CCPDMA and pathological reports in both cases. All authors have contributed with the literature review and with the preparation of this manuscript. All authors read and approved the final manuscript.
Contributor Information
Eduardo Bertolli, Email: ebertolli@hotmail.com.
Eduard Renè Bretchbuhl, Email: dr.erb@uol.com.br.
William Ricardo Camarço, Email: wrcamarco@msn.com.
Mariane Campagnari, Email: maricampa@hotmail.com.
André Sapata Molina, Email: drandremolina@gmail.com.
Glauco Baiocchi, Email: glbaiocchi@yahoo.com.br.
Mariana Petaccia de Macedo, Email: maripetaccia@gmail.com.
Clovis Antonio Lopes Pinto, Email: coipinto@uol.com.br.
Isabela Werneck da Cunha, Email: iwerneck@ig.com.br.
João Pedreira Duprat Neto, Email: Joao.duprat@accamargo.org.
References
- 1.Edelweiss M, Malpica A. Dermatofibrosarcoma protuberans of the vulva: a clinicopathologic and immunohistochemical study of 13 cases. Am J Surg Pathol. 2010;34:393–400. doi: 10.1097/PAS.0b013e3181cf7fc1. [DOI] [PubMed] [Google Scholar]
- 2.Molina AS. Dermatofibrossarcoma protuberans: Análise dos marcadores de proliferação celular, invasividade e apoptose. Estudo da fusão de col-1α1/pdgf-β por fish e correlação com a recidiva. MSc thesis. 2011. [Google Scholar]
- 3.Doufekas K, Duncan TJ, Williamson KM, Varma S, Nunns D. Mohs micrographic surgery for dermatofibrosarcoma protuberans of the vulva. Obstet Gynecol Int. 2009;2009:1–2. doi: 10.1155/2009/547672. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Farma JM, Ammori JB, Zager JS, Marzban SS, Bui MM, Bichakjian CK, Johnson TM, Lowe L, Sabel MS, Wong SL, Douglas Letson G, Messina JL, Cimmino VM, Sondak VK. Dermatofibrosarcoma protuberans: how wide should we resect? Ann Surg Oncol. 2010;17:2112–2118. doi: 10.1245/s10434-010-1046-8. [DOI] [PubMed] [Google Scholar]
- 5.Häfner HM, Moehrle M, Eder S, Trilling B, Röcken M, Breuninger H. 3D Histological evaluation of surgery in dermatofibrosarcoma protuberans and malignant fibrous histiocytoma: Differences in growth patterns and outcome. Eur J Surg Oncol. 2008;34:680–686. doi: 10.1016/j.ejso.2007.07.004. [DOI] [PubMed] [Google Scholar]
- 6.Hammonds LM, Hendi A. Dermatofibrosarcoma protuberans of the vulva treated using mohs micrographic surgery. Dermatol Surg. 2010;36:558–563. doi: 10.1111/j.1524-4725.2010.01493.x. [DOI] [PubMed] [Google Scholar]
- 7.Bertolli E, Campagnari M, Molina AS, Macedo MP, Pinto CA, Cunha IW, Duprat Neto JP. Int Wound J. 2013. Artificial dermis (Matriderm®) followed by skin graft as an option in dermatofibrosarcoma protuberans with complete circumferential and peripheral deep margin assessment. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Chan JK, Sugiyama V, Tajalli TR, Pham H, Gu M, Rutgers J, Monk BJ. Conservative clitoral preservation surgery in the treatment of vulvar squamous cell carcinoma. Gynecol Oncol. 2004;95:152–156. doi: 10.1016/j.ygyno.2004.07.004. [DOI] [PubMed] [Google Scholar]
- 9.Forner DM, Dakhil R, Lampe B. Can clitoris-conserving surgery for early vulvar cancer improve the outcome in terms of quality of life and sexual sensation? Eur J Obstet Gynecol Reprod Biol. 2013;171:150–153. doi: 10.1016/j.ejogrb.2013.08.028. [DOI] [PubMed] [Google Scholar]
- 10.Soltan MH. Dermatofibrosarcoma protuberans of the vulva. Br J Obstet Gynaecol. 1981;88:203–205. doi: 10.1111/j.1471-0528.1981.tb00968.x. [DOI] [PubMed] [Google Scholar]
- 11.Agress R, Figge DC, Tamimi H, Greer B. Dermatofibrosarcoma protuberans of the vulva. Gynecol Oncol. 1983;16:288–291. doi: 10.1016/0090-8258(83)90104-X. [DOI] [PubMed] [Google Scholar]
- 12.Bock JE, Andreasson B, Thorn A, Holck S. Dermatofibrosarcoma protuberans of the vulva. Gynecol Oncol. 1985;20:129–135. doi: 10.1016/0090-8258(85)90133-7. [DOI] [PubMed] [Google Scholar]
- 13.Barnhill DR, Boling R, Nobles W, Crooks L, Burke T. Vulvar dermatofibrosarcoma protuberans. Gynecol Oncol. 1988;30:149–152. doi: 10.1016/0090-8258(88)90059-5. [DOI] [PubMed] [Google Scholar]
- 14.Leake JF, Buscema J, Cho KR, Currie JL. Dermatofibrosarcoma protuberans of the vulva. Gynecol Oncol. 1991;41:245–249. doi: 10.1016/0090-8258(91)90317-X. [DOI] [PubMed] [Google Scholar]
- 15.Panidis D, Rousso D, Achparaki A, Georgiadis H, Vlassis G. Recurrence of dermatofibrosarcoma protuberans of the vulva. A clinical, histological, and ultrastructural study. Eur J Gynaecol Oncol. 1993;14:182–186. [PubMed] [Google Scholar]
- 16.Aartsen EJ, Albus-Lutter CE. Vulvar sarcoma: clinical implications. Eur J Obstet Gynecol Reprod Biol. 1994;56:181–189. doi: 10.1016/0028-2243(94)90168-6. [DOI] [PubMed] [Google Scholar]
- 17.Karlen JR, Johnson K, Kashkari S. Dermatofibrosarcoma protuberans of the vulva. A case report. J Reprod Med. 1996;41:267–269. [PubMed] [Google Scholar]
- 18.Nirenberg A, Ostör AG, Slavin J, Riley CB, Rome RM. Primary vulvar sarcomas. Int J Gynecol Pathol. 1995;14:55–62. doi: 10.1097/00004347-199501000-00010. [DOI] [PubMed] [Google Scholar]
- 19.Alverez-Cañas MC, Mayorga M, Fernandez F, Val-Bernal JF, Moral E, Leon C, Erasun F, Lerma D. Dermatofibrosarcoma protuberans of the vulva: clinico-pathological, immunohistochemical and flow cytometric study of a case. Acta Obstet Gynecol Scand. 1996;75:82–85. doi: 10.3109/00016349609033292. [DOI] [PubMed] [Google Scholar]
- 20.Soergel TM, Doering DL, O’connor D. Metastatic dermatofibrosarcoma protuberans of the vulva. Gynecol Oncol. 1998;71:320–324. doi: 10.1006/gyno.1998.5173. [DOI] [PubMed] [Google Scholar]
- 21.Ghorbani RP, Malpica A, Ayala AG. Dermatofibrosarcoma protuberans of the vulva: clinicopathologic and immunohistochemical analysis of four cases, one with fibrosarcomatous change, and review of the literature. Int J Gynecol Pathol. 1999;18:366–373. doi: 10.1097/00004347-199910000-00012. [DOI] [PubMed] [Google Scholar]
- 22.Moodley M, Moodley J. Dermatofibrosarcoma protuberans of the vulva: a case report and review of the literature. Gynecol Oncol. 2000;78:74–75. doi: 10.1006/gyno.2000.5821. [DOI] [PubMed] [Google Scholar]
- 23.Vanni R, Faa G, Dettori T, Melis GB, Dumanski JP, O’Brien KP. A case of dermatofibrosarcoma protuberans of the vulva with a COL1A1/PDGFB fusion identical to a case of giant cell fibroblastoma. Virchows Arch. 2000;437:95–100. doi: 10.1007/s004280000184. [DOI] [PubMed] [Google Scholar]
- 24.Kholová I, Ryska A, Dedic K. Composite tumor consisting of dermatofibrosarcoma protuberans and giant cell fibroblastoma associated with intratumoral endometriosis. Report of a case. Pathol Res Pract. 2001;197:263–267. doi: 10.1078/0344-0338-00045. [DOI] [PubMed] [Google Scholar]
- 25.Ohlinger R, Kühl A, Schwesinger G, Bock P, Lorenz G, Köhler G. Dermatofibrosarcoma protuberans of the vulva. Acta Obstet Gynecol Scand. 2004;83:685–686. doi: 10.1111/j.0001-6349.2004.0226b.x. [DOI] [PubMed] [Google Scholar]
- 26.Hancox JG, Kelley B, Greenway HT., Jr Treatment of dermatofibroma sarcoma protuberans using modified Mohs micrographic surgery: no recurrences and smaller defects. Dermatol Surg. 2008;34:780–784. doi: 10.1111/j.1524-4725.2008.34146.x. [DOI] [PubMed] [Google Scholar]
- 27.Zizi-Sermpetzoglou A, Savvaidou V, Fournogerakis S, Moustou E, Konstantidelli M, Vlachakos N. Dermatofibrosarcoma protuberans of the mons pubis. Eur J Gynaecol Oncol. 2012;33:537–539. [PubMed] [Google Scholar]
- 28.Gökden N, Dehner LP, Zhu X, Pfeifer JD. Dermatofibrosarcoma protuberans of the vulva and groin: detection of COL1A1-PDGFB fusion transcripts by RT-PCR. J Cutan Pathol. 2003;30:190–195. doi: 10.1034/j.1600-0560.2003.00037.x. [DOI] [PubMed] [Google Scholar]
- 29.Pamplona DC, Weber HI, Leta FR. Optimization of the use of skin expanders. Skin Res Technol. 2014;20:463–472. doi: 10.1111/srt.12141. [DOI] [PubMed] [Google Scholar]