International Scholarly Research Notices

International Scholarly Research Notices / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 168698 |

Neil R. Wickramasinghe, Nicholas D. Clement, Ashish Singh, Daniel E. Porter, "Sarcoma Excision and Pattern of Complicating Sensory Neuropathy", International Scholarly Research Notices, vol. 2014, Article ID 168698, 6 pages, 2014.

Sarcoma Excision and Pattern of Complicating Sensory Neuropathy

Academic Editor: A. Goussia
Received04 Feb 2014
Accepted06 Mar 2014
Published24 Mar 2014


A potential complication of sarcoma excision surgery is a sensory neurological dysfunction around the surgical scar. This study utilised both objective and subjective sensation assessment modalities, to evaluate 22 patients after sarcoma surgery, for a sensory deficit. 93% had an objective sensory deficit. Light touch is less likely to be damaged than pinprick sensation, and two-point discrimination is significantly reduced around the scar. Results also show that an increased scar size leads to an increased light touch and pinprick deficit and that two-point discriminatory ability around the scar improves as time after surgery elapses. 91% had a subjective deficit, most likely tingling or pain, and numbness was most probable with lower limb sarcomas. Results also demonstrated that there were no significant relationships between any specific subjective and objective deficits. In conclusion, sensory disturbance after sarcoma surgery is common and debilitating. Efforts to minimize scar length are paramount in the prevention of sensory deficit. Sensation may also recover to an extent; thus, sensory reeducation techniques must become an integral aspect of management plans. Finally to obtain a comprehensive assessment of sensory function, both objective and subjective assessment techniques must be utilised.

1. Introduction

Sarcomas are rare mesenchymal malignancies originating in supportive/connective body tissues including muscle; neural, cartilaginous, vascular, and adipose tissue; and bone [16]. There are approximately 3200 sarcomas diagnosed in the UK each year [7]; they account for 1% of malignant neoplasms in adults and 10% in children [8]. Although sarcomas are infrequent neoplastic manifestations [9], they impact substantially on mortality (50% 5-year survival) [10, 11]. The majority (60%) of sarcomas originate peripherally, 15% affect the head/neck/external trunk, and the remainder are in the retroperitoneal abdomen [12].

In the 1970s, amputation was the cornerstone of sarcoma management. Presently, limb salvage surgery is often preferential [13]; this surgical modification along with contemporary furtherance in imaging, biomedical engineering, and the advent of adjuvant chemotherapy has greatly improved survival [12, 14, 15]. With improved survival rates, complications of sarcoma management afflict all aspects of a patient’s health for longer [16]. A frequently overlooked complication of sarcoma surgery is neurological (specifically sensory) impairment. As many as 73% of patients have developed a new subjective neural impairment after tumour excision, with the majority experiencing a transient mild sensory loss, while some experienced major sensation impairment [17]. Sensory nerve injury has also been documented following other extremity surgeries, such as varicose vein surgery [18, 19] and lower limb arterial surgery [20].

Due to the profound detrimental impact that sensory dysfunction has on patients [21] and the contemporary shift in medicolegal conventions towards a litigation culture [22], it is crucial that patient and clinician are made aware of all aspects of this potential management complication.

The present study utilised objective and subjective sensory measurement tools, to specifically assess the likelihood of a sensation deficit occurring after sarcoma excision surgery, and subsequently quantified and characterized these deficits. The study also aimed to establish any apparent predisposing/precipitating factors in the occurrence of both objective and subjective sensory deficit, with a view to informing future management plans. The study also addressed the question of whether subjective sensory dysfunction correlates to objective sensory dysfunction in individual patients, an important matter with regard to the accurate assessment of a patient’s neuropathy [23].

2. Method

2.1. Recruitment

Over a period of 12 months, 22 patients who had undergone sarcoma excision surgery were identified and recruited, as they attended a sarcoma follow-up clinic, at the Cancer Centre in the Western General Hospital, Edinburgh. There were 13 male patients and 9 female patients, with a mean age of 58 (16–84). There were 9 upper body tumours (defined as occurring superior to the anterior superior iliac spine (ASIS)) and 13 lower body tumours (inferior to ASIS).

2.2. Surgery

Sarcoma excision surgery was performed by a consultant orthopaedic surgeon; 20 patients underwent limb-salvage surgery, and 2 had above-knee amputations.

2.3. Questionnaire

The questionnaire formed the subjective evaluation of sensory function [24]. Having gained written consent, patients were asked to complete a questionnaire about sensation changes following surgery. The questionnaire asked about tumour location and subsequent surgical scar. Patients were then asked whether they had experienced any sensory neurological symptoms (specifically sensation loss, tingling, or numbness) before/after their surgery and whether these symptoms had spread to other parts of the body. Patients were also asked whether, excluding postoperative pain, they had ever experienced pain around their scar, and if so, they were asked to rate this on a pain scale [25, 26] and identify whether any analgesics had been taken. Finally, patients were asked whether any of their symptoms after surgery had caused them inconvenience or resulted in a reduction of limb function.

2.4. Tests of Sensory Nerve Function

The objective evaluation comprised three tests of sensory nerve function. Prior to conducting the tests, scar length was measured in millimeters.

The first test assessed light touch (LT). A cotton wool ball was dabbed on the patient’s skin around the scar, while the patient was blindfolded, and the patient was asked to respond verbally to each touch they felt [27]. The same location on the contralateral (unoperated) side of the body was also assessed as the control.

The second test assessed superficial pain. A neurotip (neurological tool to assess pinprick (PP)) was touched on the patient’s skin around the scar (at the same points the cotton wool was dabbed), while the patient was blindfolded, and the patient was asked to respond verbally to each touch they felt [27]. The contralateral side of the body was tested in the same way as in test one for use as a control.

For both tests the cotton wool/neurotip was placed 0.5 cm from the scar and at the same positions along the scar; if sensation was absent at a point, the stimulus was moved a further 0.5 cm perpendicular to the scar, and sensation was tested at this point. This was repeated until the point that sensation was present. Thus the boundaries of the areas with absent sensation could be marked on a diagrammatic representation of the patient’s scar, and utilizing the measurement of scar length and the knowledge of how many points were tested along the scar’s length, the LT/PP area deficit could be calculated. The third test assessed two-point discrimination. A pair of blunt-ended calipers was placed on the patient’s skin at several positions around the area of the scar, while the patient was blindfolded. Both points of the calipers were applied until the first sign of blanching, and the patient was asked whether one/two points were felt; the minimum separation at which both points were felt was recorded [27, 28]. The same points on the contralateral side of the body were tested for use as a control. The average minimum separation was then calculated for both ipsilateral and contralateral sides, and the difference between the two values was used to calculate a two-point discrimination percentage deficit.

2.5. Data Collection and Statistics

The NHS Lothian TRAK system was utilized to obtain the following additional information: tumour volume, tumour grade, operative anaesthetic, and adjuvant radiotherapy.

Baseline characteristics of study patients were summarized with frequencies and percentages for categorical variables and as mean and standard deviation for continuous variables. Normality of data was checked using Shapiro-Wilk and Kolmogorov-Smirnov tests. The demographic and clinical characteristics of patients were evaluated using bivariate analysis. The significance of categorical variables was assessed using the Chi-squared tests or two-sided Fisher’s exact tests (where less than five cases occurred in a cell). The significance of continuous variables was assessed using Student’s -test or Mann-Whitney (MWU) test for continuous nonparametric data. Significance was set at , and two-tailed values were reported throughout.

3. Results

3.1. Objective Sensory Deficit

86% of patients had some deficit in LT, PP, or both around the scar compared to the unaffected contralateral side of the body. 59% had deficit in LT sensation, with a mean area deficit of 12.99 cm2. 73% had deficit in PP sensation, with a mean area deficit of 14.28 cm2. 93% had a decreased discriminatory ability in the affected limb compared with the contralateral side of the body. Utilising a Wilcoxon’s test, the difference in two-point discrimination between the scar side and contralateral side was shown to be statistically significant (, ) (Figure 1).

A Spearman’s test was performed to determine the relationship between scar length and objective sensory dysfunction. Both LT and PP deficits were significantly positively correlated with the size of the scar ( and , resp.) (Figures 2 and 3).

We then investigated whether the objective sensory deficit showed any improvement over time. Spearman’s test was performed to determine the relationship between months since operation and two-point discrimination percentage deficit; there was a negative correlation (−0.664), which was statistically significant (). Figure 4 shows the relationship.

Two-point discrimination deficit decreases as time elapses after sarcoma surgery (i.e., the difference in two-point discrimination between the operated side and contralateral side of the body decreases over time after surgery).

3.2. Subjective Sensory Deficit

91% of patients had some subjective deficit around the scar compared with the contralateral side. 36% had sensation loss, 55% had numbness, and 59% had tingling. 59% felt pain around the scar (mean severity was 4.3/10). 59% felt their sensory symptoms had inconvenienced them and/or affected limb function.

There was a significant relationship between tumour location and numbness, as shown by Fisher’s test (). 22% of upper body tumours occurred with numbness, whereas 77% of lower body tumours occurred with numbness. The relationship is shown in Figure 5.

Mean tumour volume also differed with location; upper body tumours had a mean volume of 470.5 cm2, whereas lower body tumours had a mean volume of 402.7 cm2. Tumour grade also differed with location; 100% of upper body tumours were high grade, whereas 73% of lower body tumours were high grade.

3.3. Do Subjective Deficits Relate to Objective Deficits?

We tested whether any aspect of a subjective deficit was significantly related to any aspect of objective deficit. There were no significant relationships between any subjective or objective sensation deficits.

4. Discussion

86% had some LT/PP deficit. Interestingly, the deficits in LT and PP were similar but not congruent. More patients had a PP deficit and the mean area of PP deficit was larger. This lack of congruence may arise as LT sensation and PP sensation are conveyed via different sensory pathways. Pacinian/Meissner corpuscles mediate LT [29], whereas PP is mediated by A-fibre nociceptors [30]. Our results suggest that the PP pathway is more likely to be damaged via sarcoma surgery. However another plausible explanation is that both LT and PP pathways are damaged to similar extent, but the LT pathway is more resilient; indeed LT receptors have been shown to function in an atrophied state for lengthy periods [29]. Identification of these resilient features of LT receptors may be valuable in the future for understanding and managing peripheral neuropathies.

Results show that 93% had significantly decreased discriminatory ability in the affected limb, indicating that sarcoma surgery disrupts tactile discrimination. This finding is corroborated by a study observing median nerve function after injury, which also reported a tactile discrimination loss [31].

Although two-point discrimination is an extremely popular/practical test, some studies highlight procedural flaws [32]. Studies show discriminatory ability diminishes with age [33]; however, the current study shows a nonsignificant relationship between patient age and discriminatory deficit. Patient concentration has also been shown to influence results [34]. Another study showed that test repetition could improve discriminatory ability [35]. This phenomenon may have affected our results, as the contralateral (unaffected) limb was always tested second, and hence the improved discrimination could be partially due to repetition. Future improved methodology would remove this confounding factor via randomising testing order.

Results show that as scar length increases LT/PP deficit increases. Results also show that patients with no inconvenience had a smaller mean scar length (183 mm) than patients with inconvenience (258 mm), although this was nonsignificant. Other studies have described an increased frequency of complications with larger scars such as increased healing times [36], psychological issues [37], and poorer cosmetic results [38]. It may therefore be worthwhile to surgically minimize scar length, without compromising tumour excision. Indeed other surgical forms are focusing on reducing scar length to improve outcome, for example, in haemangioma removal [39] and abdominoplasty [40].

Results also showed negative correlations between months since operation and two-point discrimination/LT/PP deficits; however only the relationship between two-point discrimination and months since operation was significant. An explanation is that there is a recovery of sensory function over time (tolerance to sensory dysfunction, although a recognized phenomenon [41], is not a plausible explanation, as sensation deficit was objectively measured). Recovery was also reported in a study on schwannomas, where 73.2% developed a new neurological deficit after enucleation, but at final follow-up 70% had no deficit [17]. Recovery of neurological function has also occurred after peripheral nerve injury [29, 42]. Another study, where sensory recovery occurred, emphasizes the role that injury mechanism, age, and sensory reeducation have [43]. The possibility of sensation recovery demands that sensory reeducation be a mandatory component of the management strategy for those with deficits after sarcoma surgery.

91% had some form of subjective sensory deficit; in another study 73.2% had a new subjective neurological deficit following tumour surgery [17]. In both studies the subjective sensory characteristic of tingling was most common. Results showed that numbness was significantly more likely in lower body than upper body tumours. An explanatory theory is that lower body tumours are larger and more often high grade at presentation (both characteristics are linked with more complications [4447]). Our study could not confirm either of these points. Upper body tumours had a larger mean volume (however, volume data was only obtained for 2 upper body tumours); and 100% of upper body tumours were high grade, whereas only 73% of lower body tumours were high grade. A plausible explanation for our results is that, due to the greater density of sensory receptors in the upper body [48], a surgical excision would damage a smaller proportion of receptors (although actually a larger total number) in the upper body; therefore, less sensory dysfunction occurs.

Evaluating sensation deficit is fundamental in many neurological examinations, and numerous objective and subjective methods exist; but should objective/subjective modalities be utilised together to confer a more comprehensive insight into sensory function? Our results show that there were no significant relationships between subjective and objective deficits, indicating that these modalities cover different aspects of sensory dysfunction. There was, however, a smaller mean LT deficit in patients with no sensation loss (5.8 cm2) than in patients with sensation loss (10.89 cm2), indicating some overlap in assessment tools. These results validate findings by other researchers that although objective sensation tests are a useful tool to evaluate sensory dysfunction, they only partially replicate the complex perception of sensation [49], and hence they must be utilised in conjunction with subjective tools, in order to thoroughly understand a patient’s sensory deficit.

5. Conclusion

We have demonstrated that sensory neuropathy is a relatively common complication of sarcoma excision surgery. Our results indicate that as scar size increases, sensation deficit also increases; therefore, efforts to minimise the length of scar during sarcoma excision surgery are important. Our results demonstrate that the sensory neuropathy improves as time after sarcoma surgery elapses; therefore, there could be an element of sensation recovery. It is therefore important that sensory reeducation techniques be considered as part of the postoperative management plans in these patients. Finally our results showed that there were no significant relationships between any objective and subjective deficits; therefore, when assessing sensation deficits after sarcoma surgery it would be pertinent to use both objective and subjective assessment techniques.

Conflict of Interests

The authors have no competing interests to declare.


  1. C. A. S. Arndt and W. M. Crist, “Common musculoskeletal tumors of childhood and adolescence,” The New England Journal of Medicine, vol. 341, no. 5, pp. 342–352, 1999. View at: Publisher Site | Google Scholar
  2. A. Ferrari, G. Bisogno, A. Macaluso et al., “Soft-tissue sarcomas in children and adolescents with neurofibromatosis type 1,” Cancer, vol. 109, no. 7, pp. 1406–1412, 2007. View at: Publisher Site | Google Scholar
  3. K. Almefty, S. Pravdenkova, B. O. Colli, O. Al-Mefty, and M. Gokden, “Chordoma and chondrosarcoma: similar, but quite different, skull base tumors,” Cancer, vol. 110, no. 11, pp. 2457–2467, 2007. View at: Publisher Site | Google Scholar
  4. A. Carneiro, P.-O. Bendahl, J. Engellau et al., “A prognostic model for soft tissue sarcoma of the extremities and trunk wall based on size, vascular invasion, necrosis, and growth pattern,” Cancer, vol. 117, no. 6, pp. 1279–1287, 2011. View at: Publisher Site | Google Scholar
  5. J. Golledge, C. Fisher, and P. H. Rhys-Evans, “Head and neck liposarcoma,” Cancer, vol. 76, no. 6, pp. 1051–1058, 1995. View at: Google Scholar
  6. V. O. Lewis, “What's new in musculoskeletal oncology,” Journal of Bone and Joint Surgery A, vol. 91, no. 6, pp. 1546–1556, 2009. View at: Publisher Site | Google Scholar
  7. U. K. Sarcoma, “What is sarcoma?” View at: Google Scholar
  8. B. Brockstein, “Management of sarcomas of the head and neck,” Current Oncology Reports, vol. 6, no. 4, pp. 321–327, 2004. View at: Google Scholar
  9. A. Jemal, R. Siegel, J. Xu, and E. Ward, “Cancer statistics, 2010,” CA: Cancer Journal for Clinicians, vol. 60, no. 5, pp. 277–300, 2010. View at: Publisher Site | Google Scholar
  10. A. Bleyer, M. Montello, T. Budd, and S. Saxman, “National survival trends of young adults with sarcoma: lack of progress is associated with lack of clinical trial participation,” Cancer, vol. 103, no. 9, pp. 1891–1897, 2005. View at: Publisher Site | Google Scholar
  12. B. Kasper, A. D. Ho, and G. Egerer, “Is there an indication for high-dose chemotherapy in the treatment of bone and soft-tissue sarcoma?” Oncology, vol. 68, no. 2-3, pp. 115–121, 2005. View at: Publisher Site | Google Scholar
  13. R. J. Grimer, “Surgical options for children with osteosarcoma,” The Lancet Oncology, vol. 6, no. 2, pp. 85–92, 2005. View at: Publisher Site | Google Scholar
  14. S. S. Bielack, B. Kempf-Bielack, G. Delling et al., “Prognostic factors in high-grade osteosarcoma of the extremities or trunk: an analysis of 1,702 patients treated on neoadjuvant cooperative osteosarcoma study group protocols,” Journal of Clinical Oncology, vol. 20, no. 3, pp. 776–790, 2002. View at: Publisher Site | Google Scholar
  15. R. M. Wilkins, J. W. Cullen, L. Odom et al., “Superior survival in treatment of primary nonmetastatic pediatric osteosarcoma of the extremity,” Annals of Surgical Oncology, vol. 10, no. 5, pp. 498–507, 2003. View at: Publisher Site | Google Scholar
  16. R. Dozor, “The biopyschosocial model,” Journal of Family Practice, vol. 31, no. 4, p. 353, 1990. View at: Google Scholar
  17. M. J. Park, K. N. Seo, and H. J. Kang, “Neurological deficit after surgical enucleation of schwannomas of the upper limb,” Journal of Bone and Joint Surgery B, vol. 91, no. 11, pp. 1482–1486, 2009. View at: Publisher Site | Google Scholar
  18. R. C. Sam, S. H. Silverman, and A. W. Bradbury, “Nerve injuries and varicose vein surgery,” European Journal of Vascular and Endovascular Surgery, vol. 27, no. 2, pp. 113–120, 2004. View at: Publisher Site | Google Scholar
  19. C. Morrison and M. C. Dalsing, “Signs and symptoms of saphenous nerve injury after greater saphenous vein stripping: prevalence, severity, and relevance for modern practice,” Journal of Vascular Surgery, vol. 38, no. 5, pp. 886–890, 2003. View at: Publisher Site | Google Scholar
  20. M. R. Moawad, Y. A. Masannat, A. Alhamdani, and C. P. Gibbons, “Nerve injury in lower limb vascular surgery,” Surgeon, vol. 6, no. 1, pp. 32–35, 2008. View at: Google Scholar
  21. J. R. Mendell and Z. Sahenk, “Painful sensory neuropathy,” The New England Journal of Medicine, vol. 348, no. 13, pp. 1243–1255, 2003. View at: Google Scholar
  22. A. Atrey, C. M. Gupte, and S. A. Corbett, “Review of successful litigation against english health trusts in the treatment of adults with orthopaedic pathology: clinical governance lessons learned,” Journal of Bone and Joint Surgery A, vol. 92, no. 18, pp. e36.1–e36.6, 2010. View at: Publisher Site | Google Scholar
  23. R. P. Calfee, P. R. Manske, R. H. Gelberman, M. O. van Steyn, J. Steffen, and C. A. Goldfarb, “Clinical assessment of the ulnar nerve at the elbow: reliability of instability testing and the association of hypermobility with clinical symptoms,” Journal of Bone and Joint Surgery A, vol. 92, no. 17, pp. 2801–2808, 2010. View at: Publisher Site | Google Scholar
  24. L. J. Poort, J. W. van Neck, and K. G. H. van der Wal, “Sensory testing of inferior alveolar nerve injuries: a review of methods used in prospective studies,” Journal of Oral and Maxillofacial Surgery, vol. 67, no. 2, pp. 292–300, 2009. View at: Publisher Site | Google Scholar
  25. J. B. Wade, D. D. Price, R. M. Hamer, S. M. Schwartz, and R. P. Hart, “An emotional component analysis of chronic pain,” Pain, vol. 40, no. 3, pp. 303–310, 1990. View at: Publisher Site | Google Scholar
  26. D. D. Price, F. M. Bush, S. Long, and S. W. Harkins, “A comparison of pain measurement characteristics of mechanical visual analogue and simple numerical rating scales,” Pain, vol. 56, no. 2, pp. 217–226, 1994. View at: Publisher Site | Google Scholar
  27. J. Macleod, G. Douglas, F. Nicol, and C. Robertson, Macleod's Clinical Examination, Churchill Livingstone, 12th edition.
  28. J. Bell-Krotoski, S. Weinstein, and C. Weinstein, “Testing sensibility, including touch-pressure, two-point discrimination, point localization, and vibration,” Journal of Hand Therapy, vol. 6, no. 2, pp. 114–123, 1993. View at: Google Scholar
  29. M. G. Burnett and E. L. Zager, “Pathophysiology of peripheral nerve injury: a brief review,” Neurosurg Focus, vol. 16, no. 5, article E1, 2004. View at: Google Scholar
  30. W. Magerl, P. N. Fuchs, R. A. Meyer, and R.-D. Treede, “Roles of capsaicin-insensitive nociceptors in cutaneous pain and secondary hyperalgesia,” Brain, vol. 124, no. 9, pp. 1754–1764, 2001. View at: Google Scholar
  31. T. Hansson and T. Brismar, “Loss of sensory discrimination after median nerve injury and activation in the primary somatosensory cortex on functional magnetic resonance imaging,” Journal of Neurosurgery, vol. 99, no. 1, pp. 100–105, 2003. View at: Google Scholar
  32. R. W. Van Boven and K. O. Johnson, “The limit of tactile spatial resolution in humans: grating orientation discrimination at the lip, tongue, and finger,” Neurology, vol. 44, no. 12, pp. 2361–2366, 1994. View at: Google Scholar
  33. G. Lundborg and B. Rosén, “The two-point discrimination test: time for a re-appraisal?” Journal of Hand Surgery, vol. 29, no. 5, pp. 418–422, 2004. View at: Publisher Site | Google Scholar
  34. R. Birch, Surgical Disorders of the Peripheral Nerves, Springer, New York, NY, USA, 2nd edition.
  35. J. C. Craig and K. O. Johnson, “The two-point threshold: not a measure of tactile spatial resolution,” Current Directions in Psychological Science, vol. 9, no. 1, pp. 29–32, 2000. View at: Google Scholar
  36. Y.-H. Kim, K.-S. Sohn, and J.-S. Kim, “Short-term results of primary total knee Arthroplasties Performed with a Mini-Incision or a Standard Incision,” Journal of Arthroplasty, vol. 21, no. 5, pp. 712–718, 2006. View at: Publisher Site | Google Scholar
  37. L. D. Dorr, D. Thomas, W. T. Long, P. B. Polatin, and L. E. Sirianni, “Psychologic reasons for patients preferring minimally invasive total hip arthroplasty,” Clinical Orthopaedics and Related Research, no. 458, pp. 94–100, 2007. View at: Publisher Site | Google Scholar
  38. V. S. Tung, B. Buchberg, H. Masoomi et al., “No visible scar (NVIS) colectomy: A new approach to minimal access surgery to the colon,” Surgical Innovation, vol. 18, no. 1, pp. 79–85, 2011. View at: Publisher Site | Google Scholar
  39. J. B. Mulliken, G. F. Rogers, and J. J. Marler, “Circular excision of hemangioma and purse-string closure: the smallest possible scar,” Plastic and Reconstructive Surgery, vol. 109, no. 5, pp. 1544–1554, 2002. View at: Google Scholar
  40. A. Momeni, N. Torio-Padron, H. Bannasch, J. Borges, and G. B. Stark, “A new method for reducing postoperative complications and scar length in abdominoplasty,” Plastic and Reconstructive Surgery, vol. 121, no. 4, pp. 227e–228e, 2008. View at: Publisher Site | Google Scholar
  41. K. M. Woodrow, G. D. Friedman, A. B. Siegelaub, and M. F. Collen, “Pain tolerance: differences according to age, sex and race,” Psychosomatic Medicine, vol. 34, no. 6, pp. 548–556, 1972. View at: Google Scholar
  42. M. D. Robinson and S. Shannon, “Rehabilitation of peripheral nerve injuries,” Physical Medicine and Rehabilitation Clinics of North America, vol. 13, no. 1, pp. 109–135, 2002. View at: Publisher Site | Google Scholar
  43. A. L. Dellon, “Sensory recovery in replanted digits and transplanted toes: a review,” Journal of reconstructive microsurgery, vol. 2, no. 2, pp. 123–129, 1986. View at: Google Scholar
  44. C. Collin, J. Godbold, S. Hajdu, and M. Brennan, “Localized extremity soft tissue sarcoma: an analysis of factors affecting survival,” Journal of Clinical Oncology, vol. 5, no. 4, pp. 601–612, 1987. View at: Google Scholar
  45. C. F. Collin, C. Friedrich, J. Godbold, S. Hajdu, and M. F. Brennan, “Prognostic factors for local recurrence and survival in patients with localized extremity soft-tissue sarcoma,” Seminars in Surgical Oncology, vol. 4, no. 1, pp. 30–37, 1988. View at: Google Scholar
  46. R. J. Geer, J. Woodruff, E. S. Casper, and M. F. Brennan, “Management of small soft-tissue sarcoma of the extremity in adults,” Archives of Surgery, vol. 127, no. 11, pp. 1285–1289, 1992. View at: Google Scholar
  47. C. M. Pezzi, M. S. Rawlings Jr., J. J. Esgro, R. E. Pollock, and M. M. Romsdahl, “Prognostic factors in 227 patients with malignant fibrous histiocytoma,” Cancer, vol. 69, no. 8, pp. 2098–2103, 1992. View at: Google Scholar
  48. D. Kenshalo, The Skin Senses, Charles Thomas, Springfield, Ill, USA, 3rd edition, 1968.
  49. M. Curatolo, S. Petersen-Felix, and L. Arendt-Nielsen, “Assessment of regional analgesia in clinical practice and research,” British Medical Bulletin, vol. 71, pp. 61–76, 2004. View at: Publisher Site | Google Scholar

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