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Acta Ortopedica Brasileira logoLink to Acta Ortopedica Brasileira
. 2018;26(4):244–247. doi: 10.1590/1413-785220182604192681

EXTRA-ABDOMINAL DESMOID TUMOR: ANALYSIS OF 23 CONSECUTIVE CASES IN A SINGLE INSTITUTION

TUMOR DESMOIDE EXTRA-ABDOMINAL: ANÁLISE DE 23 CASOS CONSECUTIVOS EM UMA ÚNICA INSTITUIÇÃO

Juan Pablo Zumárraga 1, Brian Guilherme Monteiro Marta Coimbra 2, Felipe Gonçalves dos Santos 1, André Mathias Baptista 1, Marcelo Tomio Kohara 1, Olavo Pires de Camargo 1,3
PMCID: PMC6131287  PMID: 30210253

ABSTRACT

Objective:

Extra-abdominal desmoid tumor (EDT) is a rare condition, caused by proliferation of fibroblasts. Despite being a benign tumor, it is locally aggressive and has unpredictable clinical behavior. The objective of this study is to present the clinical outcomes of patients with EDT treated surgically between 1995 and 2016.

Methods:

This is a retrospective series of 23 patients with histopathological diagnosis of EDT that underwent surgery at the orthopedic oncology service of our hospital. The information was obtained from the institute's clinical and pathology reports.

Results:

A total of 223 medical records with histopathological reports were evaluated. Only 23 cases of EDT were included in the present study. The mean age was 22.5 years. Twelve (52.2%) patients had the tumor on the lower limbs, seven (30.4%) on the upper limbs and four (17.4%) cases were reported on the back. Five (21.7%) patients had tumors measuring less than 5 cm, while eighteen (78.3%) patients had tumors measuring more than 5 cm. All patients underwent surgery as the definitive treatment in our institute. Twelve (52.2%) cases presented negative margins (NM) and eleven (47.8%) cases had positive margins (PM). Local recurrence (LR) occurred in eleven (47.8%) patients.

Conclusion:

Impairment of the surgical margin was the only prognostic factor found for LR of EDT. Level of Evidence IV, Case Series.

Keywords: Fibromatosis, aggressive; Surgical oncology; Local neoplasm recurrence; Margins of excision; Prognosis

INTRODUCTION

Extra-abdominal desmoid tumors (EDT) are a rare condition caused by the proliferation of fibroblasts. Although the tumor is benign, it is locally aggressive, and its unpredictable clinical behavior leads to disagreement regarding its treatment. 1 , 2 According to the World Health Organization (WHO), EDT is defined as a monoclonal proliferation of fibroblasts that affects deep soft tissues. It is characterized by infiltrative growth and a tendency toward local recurrence (LR). It does not present distant metastasis (DM). 3 EDT can affect any part of the body, but appears more frequently on the limbs and trunk (Figure 1). These tumors are rare, with an incidence of 2-4 cases/1,000,000 individuals in global statistics. Onset ranges from subjects in their 20s to their 70s, with a higher incidence in subjects in their 40s or thereabouts. 4 - 6 The treatment of choice is based on resection surgery with negative margins (NM). Clinical surveillance may be used in duly selected cases where constant outpatient follow-up is maintained. 7 In view of the local characteristics of EDT, resection with NM represents a challenge to the surgeon. The pattern of growth with projections and the impossibility of distinguishing the capsule during the surgical procedure increase the risk of involvement of the surgical margins, which are frequently mentioned in pathology reports. 8 - 11 Therefore adjuvant radiotherapy is a method of choice to avoid LR. When this occurs, it can be isolated or multiple, can acquire a more aggressive biological activity and spread locally. 12 - 14 If resection is not possible, pharmacological treatment may be indicated. Pharmacological options include anti-hormonal agents (e.g. tamoxifen), nonsteroidal anti-inflammatory drugs (e.g. celecoxib), and conventional chemotherapy (CT). 15 , 16 Ultimately, treatment of the disease should be multidisciplinary, focusing on the quality of life and function of the affected patient. 17 The purpose of this research is to present the clinical results obtained in patients with EDT treated at our institution.

Figure 1. MRI: Desmoid tumor in the right gluteal area.

Figure 1

MATERIALS AND METHODS

The study was approved by the Institutional Review Board of HCFMUSP under number 1174. It is a cross-sectional retrospective study in which 23 medical records of patients diagnosed with EDT by the IOT-HC-FMUSP Orthopedic Oncology Group covering the period from 1995 to 2016 were used. We reviewed 223 medical records, 200 of which were excluded due to lack of data. All patients included in this study received surgical treatment. Age, sex, laterality, date of diagnosis, tumor size, type of surgery and postoperative outpatient follow-up were acquired from the medical records (Table 1). The histological diagnosis was made by the pathologists of the institute. The patients’ characteristics were described using absolute and relative frequencies, and their age was also described using mean and standard deviation. 18 The mean disease-free survival with the respective intervals was estimated with 95% confidence according to characteristics of interest. The mean times were estimated when it was not possible to estimate the median time using the Kaplan-Meier estimator, 19 and times were compared between the categories of characteristics using log-rank tests. 19 The hazard ratios (HR) of LR-free time were estimated between the categories with the respective 95% confidence intervals using bivariate Cox regression models. 19 The tests were conducted with a significance level of 5%.

Table 1. Description of patient demographics.

Variable Frequency %
Sex
Female 12 52.2
Male 11 47.8
Age *
≤20 years 10 45.5
>20 years 12 54.5
Mean (SD) 22.5 (11.9)
Tumor Site
Lower Limb 12 52.2
Upper Limb 7 30.4
Back 4 17.4
Laterality *
Right 10 47.6
Left 11 52.4
Margin
Negative 12 52.2
Positive 11 47.8
Tumor Size
<5 cm 5 21.7
≥5 cm 18 78.3
Recurrence
No 12 52.2
Yes 11 47.8
Total 23 100

RESULTS

A total of 223 medical records with pathology reports were reviewed for this study. Only 23 cases of EDT were included in the present study. The mean age was 22.5 years. Twelve patients were female (52.2%) and eleven male (47.8%). The left side was affected most often with 11 (52.4%) cases, while there were 10 right-sided cases (47.6%) and two cases involving the midline back. Twelve (52.2%) cases were located in the lower limbs, seven (30.4%) cases in the upper limbs, and four (17.4%) cases were located on the back. Regarding tumor size, five (21.7%) cases measured <5cm and 18 (78.3%) cases measured size >5cm. All patients received surgical treatment as definitive therapy at the institute. The surgery of choice for all patients was surgical resection with NM. The histopathology reports listed twelve (52.2%) cases with NM and eleven (47.8%) cases with PM. LR occurred in eleven (47.8%) patients. Only the surgical margins influenced the disease-free survival of patients with EDT (Figure 2). Patients with PM presented a 90-fold higher risk of LR when compared to patients with NM (p <0.001) (Table 2).

Figure 2. Kaplan-Meier plot of local recurrence according to margin.

Figure 2

Table 2. Mean disease-free survival according to the information resulting from comparative tests.

Variable Median Time (months) CI (95%) Recurrence Total % HR CI (95%) p
Lower Upper Lower Upper
Sex 0.24
Female 96 34.3 157.7 7 12 58.3 1
Male* 170.7 98.1 243.3 3 11 27.3 0.43 0.11 1.69
Age 0.7
≤20 years 98 20.9 175.1 5 10 50 1
>20 years 96 35.7 156.3 5 12 41.7 0.78 0.22 2.75
Tumor Site 0.058
Lower Limb 63 31.7 94.3 7 12 58.3 1
Upper Limb * 183.3 107.8 258.7 2 7 28.6 0.11 0.01 0.91
Back 69 # # 1 4 25 0.86 0.1 7.25
Laterality 0.344
Right 96 # # 3 10 30 1
Left 98 24.4 171.6 6 11 54.5 1.94 0.48 7.84
Margin <0.001
Negative 252 # # 0 12 0 1
Positive 61 17.6 104.4 10 11 90.9 88.34 0.5 15498.91
Tumor Size 0.789
<5 cm 98 52.8 143.2 3 5 60 1
≥5 cm 96 39.4 152.6 7 18 38.9 1.21 0.31 4.72
Total 98 58 138 10 23 43.5
*

Mean recurrence-free survival.

#

Cannot be estimated.

DISCUSSION

The literature presents an extensive list of publications on EDT. Most of the published studies are retrospective series and case reports. 2 , 6 This study was no exception: we analyzed 23 consecutive cases over 16 years. We did not find many studies addressing EDT in our field. The mean age in our study was 22.5 years, which coincides with that described in the literature. 7 , 9 In bibliographical terms, EDT predominates slightly in female subjects. 1 In this study we also observed female predominance (52.2%). Published studies indicate that EDT occurs mainly in the abdomen. 14 , 15 , 20 This data cannot be compared as the study was conducted at an orthopedic institute. Therefore, we found widespread wide predominance of limb involvement, with a rate of 82.6%. As defined in the literature, the mean preoperative size ranges between 8 and 12 cm. 21 In our study the size varied a great deal, yet most cases involved tumors >5 cm, a fact similar to the published data. We also reported a PM rate of 47.8%. This data is not commonly reported in numerical values in the literature. One of the few studies with this data reported a rate of 42.5%. 22 Again, this finding is similar to that of our research. The main complication of EDT is LR, with rates ranging between 40 and 60%. 17 , 21 , 23 Our study found a LR rate of 47.8%, again coinciding with the literature. The mean patient follow-up time was 98 months. Finally, we report that surgical margin impairment is directly related to the decrease in disease-free survival of the patient presenting with this tumor.

CONCLUSIONS

Surgical margin impairment was the only prognostic factor found for EDT LR.

Footnotes

Work conducted at the Instituto de Ortopedia e Traumatologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, SP, Brazil.

REFERENCES

  • 1.van Broekhoven DL, Deroose JP, Bonvalot S, Gronchi A, Grünhagen DJ, Eggermont AM, et al. Isolated limb perfusion using tumour necrosis factor and melphalan in patients with advanced aggressive fibromatosis. Br J Surg. 2014;101(13):1674–1680. doi: 10.1002/bjs.9659. [DOI] [PubMed] [Google Scholar]
  • 2.Houdek MT, Rose PS, Kakar S. Desmoid tumors of the upper extremity. J Hand Surg Am. 2014;39(9):1761–1765. doi: 10.1016/j.jhsa.2014.06.015. [DOI] [PubMed] [Google Scholar]
  • 3.Eastley N, Aujla R, Silk R, Richards CJ, McCulloch TA, Esler CP, et al. Extraabdominal desmoid fibromatosis--a sarcoma unit review of practice, long term recurrence rates and survival. Eur J Surg Oncol. 2014;40(9):1125–1130. doi: 10.1016/j.ejso.2014.02.226. [DOI] [PubMed] [Google Scholar]
  • 4.Hori A, Murata S, Kono M, Maeda M, Sueyoshi S, Seki A, et al. [Effect of transarterial chemoembolization for recurrent desmoid tumor - a case report.] Gan To Kagaku Ryoho. 2013;40(9):1259–1262. [PubMed] [Google Scholar]
  • 5.Prodinger PM, Rechl H, Keller M, Pilge H, Salzmann M, von Eisenhart-Rothe R, et al. Surgical resection and radiation therapy of desmoid tumours of the extremities: results of a supra-regional tumour centre. Int Orthop. 2013;37(10):1987–1993. doi: 10.1007/s00264-013-1942-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Maher J, Smith DA, Parker WL. Desmoid tumor of the hand: a case report. Ann Plast Surg. 2014;73(4):390–392. doi: 10.1097/SAP.0b013e31827f4dea. [DOI] [PubMed] [Google Scholar]
  • 7.Oweis Y, Lucas DR, Brandon CJ, Girish G, Jacobson JA, Fessell DP. Extra-abdominal desmoid tumor with osseous involvement. Skeletal Radiol. 2012;41(4):483–487. doi: 10.1007/s00256-011-1336-7. [DOI] [PubMed] [Google Scholar]
  • 8.Stollwerck PL, Namdar T, Bartscher T, Lange T, Stang FH, Kujath P, et al. A rare desmoid tumor of the shoulder--excision, implantation of brachytherapy applicators and wound closure by pedicle musculus latissimus dorsi flap. Ger Med Sci. 2011;9 doi: 10.3205/000127. Doc04. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Sciallis GF, Sciallis AP. Becker nevus with an underlying desmoid tumor: a case report and review including Mayo Clinic's experience. Arch Dermatol. 2010;146(12):1408–1412. doi: 10.1001/archdermatol.2010.369. [DOI] [PubMed] [Google Scholar]
  • 10.Solanki NS, Macfarlane PL, Marshall NJ. Images for surgeons. An extra-abdominal desmoid tumour in a young woman. ANZ J Surg. 2010;80(10):743–744. doi: 10.1111/j.1445-2197.2010.05459.x. [DOI] [PubMed] [Google Scholar]
  • 11.Jakowski JD, Mayerson J, Wakely PE., Jr Fine-needle aspiration biopsy of the distal extremities: a study of 141 cases. Am J Clin Pathol. 2010;133(2):224–231. doi: 10.1309/AJCPBWJP3CG6JZKA. [DOI] [PubMed] [Google Scholar]
  • 12.Couto-Gonzalez I, Brea-Garcia B, Taboada-Suárez A, González-Álvarez E. Aggressive Dupuytren's diathesis in a young woman. BMJ Case Rep. 2010;2010 doi: 10.1136/bcr.12.2009.2592. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Gallucci GL, Boretto JG, De Carli P. Desmoid tumor of the forearm. Reconstructive surgery and functional result. Chir Main. 2009;28(5):326–329. doi: 10.1016/j.main.2009.08.001. [DOI] [PubMed] [Google Scholar]
  • 14.Shido Y, Nishida Y, Nakashima H, Katagiri H, Sugiura H, Yamada Y, et al. Surgical treatment for local control of extremity and trunk desmoid tumors. Arch Orthop Trauma Surg. 2009;129(7):929–933. doi: 10.1007/s00402-008-0750-3. [DOI] [PubMed] [Google Scholar]
  • 15.Altmann S, Lenz-Scharf O, Schneider W. [Therapeutic options for aggressive fibromatosis] Handchir Mikrochir Plast Chir. 2008;40(2):88–93. doi: 10.1055/s-2007-965738. [DOI] [PubMed] [Google Scholar]
  • 16.Engelhardt TO, Jeschke J, Piza-Katzer H. [About the self-reported quality of life after amputation of the hand in patients with upper extremity tumors] Handchir Mikrochir Plast Chir. 2008;40(1):23–30. doi: 10.1055/s-2007-989452. [DOI] [PubMed] [Google Scholar]
  • 17.Ozger H, Eralp L, Toker B, Agaoglu F, Dizdar Y. [Evaluation of prognostic factors affecting recurrences and disease-free survival in extra-abdominal desmoid tumors] Acta Orthop Traumatol Turc. 2007;41(4):291–294. [PubMed] [Google Scholar]
  • 18.Kirkwood BR, Sterne JA. Essential medical statistics. 2nd ed. Massachusetts: Blackwell Science; 2006. [Google Scholar]
  • 19.Kleinbaum DG. Survival analysis: a self-learning text. New York: Springer; 1996. [Google Scholar]
  • 20.Sakamaki Y, Kido T, Yasukawa M, Fujiwara T, Kuwae K, Maeda M. Wide resection of the upper right hemithorax combined with amputation of the right arm for a recurrent desmoid tumor. Jpn J Thorac Cardiovasc Surg. 2006;54(8):338–341. doi: 10.1007/s11748-006-0003-8. [DOI] [PubMed] [Google Scholar]
  • 21.Ballo MT, Zagars GK, Pollack A, Pisters PW, Pollack RA. Desmoid tumor: prognostic factors and outcome after surgery, radiation therapy, or combined surgery and radiation therapy. J Clin Oncol. 1999;17(1):158–167. doi: 10.1200/JCO.1999.17.1.158. [DOI] [PubMed] [Google Scholar]
  • 22.Duggal A, Dickinson IC, Sommerville S, Gallie P. The management of extra-abdominal desmoid tumours. Int Orthop. 2004;28(4):252–256. doi: 10.1007/s00264-004-0571-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Wang YF, Guo W, Sun KK, Yang RL, Tang XD, Ji T, et al. Postoperative recurrence of desmoid tumors: clinical and pathological perspectives. World J Surg Oncol. 2015;13:26–26. doi: 10.1186/s12957-015-0450-8. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Acta Ortopedica Brasileira are provided here courtesy of Department of Orthopedics and Traumatology, Faculdade de Medicina da Universidade de São Paulo

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