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284

M. Rubenzik et al.

 

 

Table 23.2 Leiomyosarcomas treated by MMS

 

Number of

Number of

References

cases

recurrences

Iacobucci et al. [24]

1

0

Brown et al. [26]

1

0

Davidson et al. [27]

1

0

Bernstein and Roenigk [21]

2

0

Huether et al. [28]

7

1

Humphreys et al. [29]

3

1

Vujevich et al. [25]

1

0

Total

16

2 (12.5%)

 

 

 

serial sectioning using a “bread-loafing” technique provides a very limited examination of the surgical margins, and false negative histologic reporting may contribute to the high recurrence rate of LMS with conventional excision. Wide excisional margins may also lead to greater tissue destruction resulting in profound functional, cosmetic, psychological, and social consequences [25]. Mohs micrographic surgery theoretically provides complete peripheral and deep margin evaluation, which prevents both inadequate and excessive tissue removal. While there are only 16 documented cases of LMS treated by Mohs micrographic surgery, only 2 cases have recurred (Table 23.2) [21, 24–29]. The aggregate recurrence rate of 12.5% for Mohs micrographic surgery compares favorably to that reported for wide excision.

MMS also has the advantage of tissue sparing when compared with the wide excision. The large LMS on the shin was excised using MMS. Sparing of the tibial nerve was possible in this particular case using Mohs surgery to assess the deep margins rather than a deep en bloc resection. Limiting the defect size while obtaining clear margins can significantly reduce postoperative morbidity especially on areas of the body such as the leg characterized by delayed wound healing. Although preliminary studies show the benefits of MMS for LMS, additional cases and longer follow-up periods are required to establish its efficacy.

Cryotherapy may be an alternative for patients unable to undergo surgery. Montes et al. described two elderly patients that were treated with cryosurgery for LMS of the scalp [30]. Treatments were done with tissue temperature 40–50°C for a period of 5 min and repeated treatment every 2 weeks for a total of three to six treatments. Neither patient showed evidence of recurrence 2 years after treatment. Adjuvant radiation or chemotherapy has no proven benefit for superficial LMS [31–33].

Patients diagnosed with subcutaneous LMS should receive a chest radiograph because of the potential for lung metastasis. Close clinical follow-up for a minimum of 5 years is recommended, as tumors usually recur within 1–5 years of initial surgery [10, 32].

Summary: Conclusion

The overall cure rate of leiomyosarcoma treated by Mohs micrographic surgery is 87% which compares favorably to wide excision and offers the advantage of tissue sparing. Immunosuppression may promote aggressive tumor behavior. Deeply invasive tumors may result in cutaneous or distant metastases regardless of the method of excision.

23.5 Conclusion

LMS is a rare spindle cell tumor of smooth muscle derivation that may originate in the skin or deeper soft tissue. Because of the locally aggressive nature and propensity for recurrence, Mohs micrographic surgery may result in superior local control of superficial LMS.

References

1. Rouhani P, Fletcher CD, Devesa SS, Toro JR. Cutaneous soft tissue sarcoma incidence patterns in the U.S.: an analysis of 12,114 cases. Cancer. 2008;113(3):616–27.

2. Annest NM, Grekin SJ, Stone MS, Messingham MJ. Cutaneous leiomyosarcoma: a tumor of the head and neck. Dermatol Surg. 2007;33(5):628–33.

3.Holst VA, Junkins-Hopkins JM, Elenitsas R. Cutaneous smooth muscle neoplasms: clinical features, histologic find-

ings, and treatment options. J Am Acad Dermatol. 2002; 46(4):477–90; quiz 491–474.

4. Altinok G, Dogan AI, Aydin SO, Gedikoglu G. Primary leiomyosarcomas of the skin. Scand J Plast Reconstr Surg Hand Surg. 2002;36(1):56–9.

5. De Giorgi V, Sestini S, Massi D, Papi F, Alfaioli B, Lotti T. Superficial cutaneous leiomyosarcoma: a rare, misleading tumor. Am J Clin Dermatol. 2008;9(3):185–7.

6. Massi D, Franchi A, Alos L, et al. Primary cutaneous leiomyosarcoma: clinicopathological analysis of 36 cases. Histopathology. 2010;56(2):251–62.

7. Ragsdale BD. Tumors with fatty, muscular, osseous, and/or cartilaginous differentiation. In: Elder DE, Elenitsas R, Johnson BL, Murphy GF, Xu X, editors. LEVER’S histopathology of

23 Leiomyosarcoma

285

 

 

the skin. 10th ed. Philadelphia: Lippincott Williams & Wilkins; 2004. p. 781–2.

8. Pijpe J, Broers GH, Plaat BE, et al. The relation between histological, tumor-biological and clinical parameters in deep and superficial leiomyosarcoma and leiomyoma. Sarcoma. 2002;6(3):105–10.

9. Miettinen M, Fetsch JF. Evaluation of biological potential of smooth muscle tumours. Histopathology. 2006;48(1): 97–105.

10.Porter CJ, Januszkiewicz JS. Cutaneous leiomyosarcoma. Plast Reconstr Surg. 2002;109(3):964–7.

11. Brown FM, Fletcher CD. Problems in grading soft tissue sarcomas. Am J Clin Pathol. 2000;114(Suppl):S82–9.

12.Dahl I, Angervall L. Cutaneous and subcutaneous leiomyosarcoma. A clinicopathologic study of 47 patients. Pathol Eur. 1974;9(4):307–15.

13. Fields JP, Helwig EB. Leiomyosarcoma of the skin and subcutaneous tissue. Cancer. 1981;47(1):156–69.

14.Wascher RA, Lee MY. Recurrent cutaneous leiomyosarcoma. Cancer. 1992;70(2):490–2.

15. Oliver GF, Reiman HM, Gonchoroff NJ, Muller SA, Umbert IJ. Cutaneous and subcutaneous leiomyosarcoma: a clinicopathological review of 14 cases with reference to antidesmin staining and nuclear DNA patterns studied by flow cytometry. Br J Dermatol. 1991;124(3):252–7.

16. Svarvar C, Bohling T, Berlin O, et al. Clinical course of nonvisceral soft tissue leiomyosarcoma in 225 patients from the Scandinavian Sarcoma Group. Cancer. 2007;109(2): 282–91.

17. Tsujimoto M, Aozasa K, Ueda T, Morimura Y, Komatsubara Y, Doi T. Multivariate analysis for histologic prognostic factors in soft tissue sarcomas. Cancer. 1988;62(5):994–8.

18. Ueda T, Aozasa K, Tsujimoto M, et al. Multivariate analysis for clinical prognostic factors in 163 patients with soft tissue sarcoma. Cancer. 1988;62(7):1444–50.

19.Spencer JM, Amonette RA. Tumors with smooth muscle differentiation. Dermatol Surg. 1996;22(9):761–8.

20.Cook TF, Fosko SW. Unusual cutaneous malignancies. Semin Cutan Med Surg. 1998;17(2):114–32.

21.Bernstein SC, Roenigk RK. Leiomyosarcoma of the skin. Treatment of 34 cases. Dermatol Surg. 1996;22(7):631–5.

22. Chow J, Sabet LM, Clark BL, Coire CI. Cutaneous leiomyosarcoma: case reports and review of the literature. Ann Plast Surg. 1987;18(4):319–22.

23.Fish FS. Soft tissue sarcomas in dermatology. Dermatol Surg. 1996;22(3):268–73.

24.Iacobucci JJ, Stevenson TR, Swanson NA, Headington JT. Cutaneous leiomyosarcoma. Ann Plast Surg. 1987;19(6): 552–4.

25.Vujevich JJ, Goldberg LH, Kimyai-Asadi A, Law R. Recurrent nodule on the nasal columella: a good reason to re-biopsy. Int J Dermatol. 2008;47(7):728–31.

26. Brown MD, Zachary CB, Grekin RC, Swanson NA. Genital tumors: their management by micrographic surgery. J Am Acad Dermatol. 1988;18(1 Pt 1):115–22.

27. Davidson LL, Frost ML, Hanke CW, Epinette WW. Primary leiomyosarcoma of the skin. Case report and review of the literature. J Am Acad Dermatol. 1989;21(5 Pt 2):1156–60.

28.Huether MJ, Zitelli JA, Brodland DG. Mohs micrographic surgery for the treatment of spindle cell tumors of the skin. J Am Acad Dermatol. 2001;44(4):656–9.

29.Humphreys TR, Finkelstein DH, Lee JB. Superficial leiomyosarcoma treated with Mohs micrographic surgery. Dermatol Surg. 2004;30(1):108–12.

30. Montes LF, Ocampo J, Garcia NJ, et al. Response of leiomyosarcoma to cryosurgery: clinicopathological and ultrastructural study. Clin Exp Dermatol. 1995;20(1):22–6.

31. Hwang ES, Gerald W, Wollner N, Meyers P, La Quaglia MP. Leiomyosarcoma in childhood and adolescence. Ann Surg Oncol. 1997;4(3):223–7.

32.Guron G, Neugut AI. Soft tissue sarcomas. Is adjuvant chemotherapy indicated? N Y State J Med. 1993;93(3): 156–8.

33. Haffner AC, Zepter K, Fritz T, Dummer R, Lejeune FJ, Burg G. Complete remission of advanced cutaneous leiomyosarcoma following isolated limb perfusion with high-dose tumour necrosis factor-alpha and melphalan. Br J Dermatol. 1999;141(5):935–6.