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Short Communication
16 (
3
); 239-242
doi:
10.4103/JCAS.JCAS_139_21

A Retrospective Study of Re-excised Skin Cancers in a Pathology Center

Faculty of Dentistry, Kurdistan University of Medical Sciences, Sanandaj, Iran
Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Kurdistan University of Medical Sciences, Sanandaj, Iran

Address for correspondence: Dr. Massoumeh Zargaran, Department of Oral and Maxillofacial Pathology, Faculty of Dentistry, Kurdistan University of Medical Sciences, Sanandaj, Iran. E-mail: massoumehzargaran@gmail.com

Licence
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Disclaimer:
This article was originally published by Wolters Kluwer - Medknow and was migrated to Scientific Scholar after the change of Publisher.

Abstract

Abstract

Surgical re-excision is the recommended treatment for the complete removal of incompletely excised skin cancers (SCs), but it may not always lead to this goal. In the present study, the re-excision rate and the presence of residual tumors in re-excised SCs were evaluated. In this retrospective descriptive study, the pathological archives of a hospital center were examined for incompletely excised tumors. Out of the 96 incompletely excised tumors, 19 cases (19.8%) underwent re-excision, of which residual tumors were observed again in 7 cases (36.8%). The highest rate of residual tumor was found in the cheek (66.66%), and the involvement with tumor remnants of both margins combined was greater than the involvement of each of the lateral and deep margins alone. Collecting and reporting of surgical results of re-excised tumors may assist clinicians in determining the patient’s condition and making appropriate decisions to increase the success rate of reoperations.

Keywords

Malignancy
re-excision
skin cancer
surgery

INTRODUCTION

Skin cancers (SCs) are among the most common human malignancies,[1] which for reasons such as progression, tissue destruction, and metastasis should be treated as soon as possible.[12]

Surgical excision is considered as the choice treatment of these cancers.[345] However, the outcome of this method strongly depends on complete removal of the tumor[6] and presence of clear and tumor-free histopathological margins.[7]

Incomplete excision of cancers can be correlated with complications such as recurrence, morbidity, and mortality.[5] Therefore, their re-treatment, preferably with surgery (surgical re-excision), is recommended.[3] This study aimed to evaluate re-excision rate in incompletely excised SCs and the presence of residual tumor in these re-excised samples.

MATERIALS AND METHODS

In this descriptive retrospective study, incompletely excised tumors from our previous study[8] were examined, and of them, a number of re-excised cases were determined. Then, based on histopathology reports and patients’ files, information such as the result of re-excision (with/without residual tumor), type of affected margin, age, sex, tumor location, and clinician specialty was collected.

RESULTS

Out of the 96 incompletely excised tumors, 19 cases (19.8%) were re-excised, of which residual tumors were observed again in 7 cases (36.8%). Clinicopathological characteristics of re-excised samples are presented in general and separately for each sample in Tables 1 and 2, respectively.

Table 1 Characteristics of re-excised skin cancers
Variable Number of re-excised tumors (%) After re-excision
Residual tumor+ Residual tumor−
Type of cancer
 BCC 12 (63.15) 3 (25.00) 9 (75.00)
 SCC 6 (31.57) 4 (66.66) 2 (33.33)
 Melanoma 1 (5.26) 0 (0.00) 1 (100.00)
19 (100.00)
Gender
 Male 10 (52.63) 4 (40.00) 6 (60.00)
 Female 9 (47.36) 3 (33.33) 6 (66.66)
19 (100.00)
Site of re-excised tumor
 Nose 11 (57.89) 3 (27.27) 8 (72.72)
 Cheek 3 (15.78) 2 (66.66) 1 (33.33)
 Ear 1 (5.26) 0 (0.00) 1 (100.00)
 Limbs 4 (21.05) 2 (50.00) 2 (50.00)
19 (100.00)
Involved margin
 Peripheral 5 (26.31) 0 (0.00) 5 (100.00)
 Deep 4 (21.05) 3 (75.00) 1 (25.00)
 Both (peripheral and deep) 10 (52.63) 4 (40.00) 6 (60.00)
19 (100.00)
Specialist
 Otorhinolaryngologist 5 (26.31) 2 (40.00) 3 (60.00)
 Plastic surgeon 9 (47.36) 4 (44.44) 5 (55.55)
 General surgeon 5 (26.31) 1 (20.00) 4 (80.00)

BCC = basal cell carcinoma, SCC = squamous cell carcinoma

Table 2 Characteristics of re-excised skin cancers separately for each sample
No. Gender Age, years Cancer type Site of tumor Involved margin After re-excision Physician specialty
Residual tumor+/−
1 Male 68 BCC Nose Both + (deep margin) Otorhinolaryngologist
2 Male 86 BCC Cheek Deep + Plastic surgeon
3 Male 65 SCC Cheek Deep + Plastic surgeon
4 Male 71 BCC Cheek Both Otorhinolaryngologist
5 Male 87 SCC limbs Peripheral Plastic surgeon
6 Male 74 BCC Nose Deep General surgeon
7 Male 63 SCC Limbs Both + (deep margin) Plastic surgeon
8 Male 84 Melanoma Limbs Both Plastic surgeon
9 Male 80 BCC Nose Deep General surgeon
10 Male 60 BCC Nose Peripheral General surgeon
11 Female 74 BCC Nose Peripheral Plastic surgeon
12 Female 79 BCC Ear Both Plastic surgeon
13 Female 82 SCC Nose Both Plastic surgeon
14 Female 70 SCC Limbs Both + (deep margin) General surgeon
15 Female 67 BCC Nose Deep + Otorhinolaryngologist
16 Female 81 BCC Nose Both General surgeon
17 Female 69 SCC Nose Both + ( both margin) Plastic surgeon
18 Female 58 BCC Nose Both Otorhinolaryngologist
19 Female 73 BCC Nose Peripheral Otorhinolaryngologist

BCC = basal cell carcinoma, SCC = squamous cell carcinoma

DISCUSSION

For incompletely excised SCs, re-excision of the lesion is preferably recommended to minimize the risk of recurrence,[4] which is considered the worst surgical complication.[2] Published data on re-excision of SCs are scarce and have been briefly supplied in a small number of studies. In this study, re-excision rate and presence of residual tumor in re-excised samples were investigated.

In the present study, 19.8% of the incompletely excised tumors underwent re-excision, which is almost similar to that reported by Codazzi et al.[9] (18.14%). Comparing different studies, the rate of re-excised tumors has been found to vary from 1.9% to 100%.[14,610,11] This difference between studies can be due to the following reasons:

  • (I)

    Different biological behaviors of SCs, due to which in some tumors such as basal cell carcinoma (BCC), failure to completely remove the lesion does not necessarily correlate with recurrence. The reason for this can be the destruction of residual tumor by the cicatrization process[2] and the theory of disappearing tumor cells as part of the second stage of the wound-healing process (inflammatory phase). So not enough tumor cells are left to survive. Therefore, in some cases, close monitoring of the patient is recommended and reoperated in the case of recurrence. However, this procedure is dangerous for some other tumors, such as invasive squamous cell carcinoma (SCC) which can metastasize to regional lymph nodes and then to distant sites.[4]

  • (II)

    Failure to perform reoperation in the same center under study and then referring it to another center either at the request of the patient or due to the uncertainty of the clinician about the availability of the necessary facilities for repair and reconstruction of tissue defects caused by re-excision.

  • (III)

    Lack of knowledge, sufficient experience, and practical skills required for the proper management of patients in need of re-excision.

  • (IV)

    Patient’s unwillingness for re-excision, which can be either due to inefficient follow-up systems and failure of the healthcare system in making the patient aware of a present problem or due to the patient’s unpleasant experience with previous surgery and/or high surgical treatment costs.

Meanwhile, performing re-excision is an individual’s choice, taking into account the patient’s age and general condition.

In histopathological report of re-excised tumors, 36.8% had a residual tumor, which is similar to the result of Patel et al.[10] (36%). This rate is relatively high in previous studies.[13,79] For example, Spyropoulou et al.[4] reported residual tumor in 100% of the cases.

In most studies, including ours, the presence of residual tumor may be due to not using Mohs micrographic surgery. In this technique, all removed margins are histopathologically examined to ensure the absence of tumor cells, whereas further incision is made only where the tumor remains until complete resection.[12] Non-application of this method in the present study with respect to the more invasive tendency of SCC to subclinical infiltration is probably the reason for the higher rate of residual tumor in this malignancy compared with BCC.

In addition, severe surgical outcomes such as significant cosmetic and functional defects or disfigured scars in the involved areas, especially in the visible areas, can also affect the outcome of surgical re-excision.

According to our findings, the residual tumor rate was 66.66% in the cheek, 50% in the limbs, and 27.27% in the nose. In the study of Griffiths et al.,[7] the residual tumor rate was found to be 40% in the cheek, 36% in the nose, and 32% in limbs, whereas Spyropoulou et al.[4] found it to be 83.3% in the cheek, 52.94% in the nose, and 75% in the ears. Similar to Griffiths et al.[7] and Spyropoulou et al.,[4] the highest frequency of residual tumor was observed in the cheek (probably due to using narrower margins for cosmetic, functional, and/or preserving underlay facial nerve reasons), but unlike the latter study,[4] we found the residual tumor rate to be zero in re-excised cancers of ears (75% vs. 0.0%).

The most re-excised margins were both margins followed by lateral margin and deep margin of lesions alone, whereas in the study of Griffiths et al.[7] and Masud et al.,[3] it was found to be in the order of lateral margin, deep margin, and both margins, respectively.

In this study, in agreement with Masud et al.,[3] although in disagreement with Griffiths et al.,[7] the highest frequency of residual tumor was observed in the deep margin of re-excised tumors. In contrast, in the study of Pua et al.,[5] the margin of all re-excised cases was free of tumor cells.

CONCLUSION

Given the limitations of this descriptive study, further research with larger sample size and involving other study designs (e.g., prospective and analytical studies), focussing on finding the factors influencing the success of SCs re-excision, is suggested. Collecting and reporting of surgical results of re-excised tumors may help clinicians enhance the success rate of reoperations.

Financial support and sponsorship

This work was supported by Kurdistan University of Medical Sciences (grant number: 1398.165) and approved by the Ethics Committee of Kurdistan University of Medical Sciences (IR.MUK.REC.1398.165).

Conflicts of interest

The authors declare no conflicts of interest

References

  1. , , , , , . Incomplete excision of squamous cell carcinoma of the skin: A prospective observational study. Plast Reconstr Surg. 2007;120:910-6.
    [Google Scholar]
  2. , , , , . Positive margins in basal cell carcinoma: Relationship to clinical features and recurrence risk. A retrospective study of 248 patients. J Eur Acad Dermatol Venereol. 2003;17:167-70.
    [Google Scholar]
  3. , , , , . Basal cell carcinomata: Risk factors for incomplete excision and results of re-excision. J Plast Reconstr Aesthet Surg. 2016;69:652-6.
    [Google Scholar]
  4. , , , , , , . Cutaneous squamous cell carcinoma with incomplete margins demonstrate higher tumour grade on re-excision. J Eur Acad Dermatol Venereol. 2020;34:1478-81.
    [Google Scholar]
  5. , , , . Evaluation of the treatment of non-melanoma skin cancers by surgical excision. Australas J Dermatol. 2009;50:171-5.
    [Google Scholar]
  6. , , , , , , . Incomplete excision of basal cell carcinoma: A prospective multicentre audit. Br J Plast Surg. 2002;55:616-22.
    [Google Scholar]
  7. , , , . Basal cell carcinoma histological clearance margins: An analysis of 1539 conventionally excised tumours. Wider still and deeper? J Plast Reconstr Aesthet Surg. 2007;60:41-7.
    [Google Scholar]
  8. , , . Frequency of and risk factors for incomplete surgical margins of cutaneous cancers: A retrospective study. J Dermatolog Treat. 2021;20:1-4.
    [Google Scholar]
  9. , , , , , , . Positive compared with negative margins in a single-centre retrospective study on 3957 consecutive excisions of basal cell carcinomas. Associated risk factors and preferred surgical management. J Plast Surg Hand Surg. 2014;48:38-43.
    [Google Scholar]
  10. , , , . Incomplete removal of basal cell carcinoma: What is the value of further surgery? Oral Maxillofac Surg. 2013;17:115-8.
    [Google Scholar]
  11. , , , , , . Risk factors predicting positive margins at primary wide local excision of cutaneous melanoma. Dermatol Surg. 2016;42:646-52.
    [Google Scholar]
  12. , , . Surgical margins in the treatment of nonmelanoma skin cancer and Mohs micrographic surgery. Curr Surg. 2005;62:518-26.
    [Google Scholar]
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