Literature DB >> 26755916

Successful treatment of multiple cutaneous leiomyomas with carbon dioxide laser ablation.

Igor Michajłowski1, Izabela Błażewicz1, Gabrielle Karpinsky2, Michał Sobjanek1, Roman Nowicki1.   

Abstract

Entities:  

Year:  2015        PMID: 26755916      PMCID: PMC4697020          DOI: 10.5114/pdia.2015.48058

Source DB:  PubMed          Journal:  Postepy Dermatol Alergol        ISSN: 1642-395X            Impact factor:   1.837


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Leiomyomas are rare, benign neoplasms that arise from smooth muscles. The condition was first reported in 1854 by Rudolf Virchow [1, 2]. According to the site of origin we can distinguish piloleiomyoma (deriving from the arrector pili muscles of hair follicles), genital leiomyoma (originating from the tunica dartos of the scrotum, and mammary muscles of nipples), and angioleiomyoma (arising from smooth muscles of blood vessels) [3]. The most common locations include the uterus (about 95% of cases) and the skin, which accounts for 75% of extra-uterine leiomyomas [4]. According to Malhotra, the average age of onset is 38.9 years for solitary leiomyomas and 43.8 years for multiple lesions [5]. Herein we report a 41-year-old man with multiple, painful, well-demarcated, oval, red papules localized within the region of the left scapula. The lesions had appeared progressively over the past 6 months. They measured 5 mm to 20 mm and were increasing in size and number (Figure 1). The intensity of the pain was aggravated by pressure and exposure to low temperature. The level of pain was preventing him from sleeping, sitting and participating in normal everyday activities. Family history of similar lesions and physical examination were unremarkable. Based on the clinical picture we assumed multiple leiomyoma. The final diagnosis of leiomyoma was based on histopathological examination of the lesional tissue. It revealed a well-demarcated lobulated tumor located in the reticular dermis. It consisted of bundles of smooth muscle fibers. Tumor cells had eosinophilic cytoplasm and blunt-ended vesicular nuclei. There was no cytologic atypia or mitotic activity (Figure 2). Routine hematological, urine and ultrasound examination of the abdomen did not reveal any abnormalities.
Figure 1

A – Multiple cutaneous leiomyomas within the region of the left scapula at initial presentation. B – The clinical appearance 1 month after the initial lesions were treated. C – The clinical appearance 6 months postoperative

Figure 2

The histopathological examination of the lesional tissue revealed a well-demarcated lobulated tumor located in the reticular dermis. It consisted of bundles of smooth muscle fibers. Tumor cells had eosinophilic cytoplasm and blunt-ended vesicular nuclei. There was no cytologic atypia or mitotic activity

A – Multiple cutaneous leiomyomas within the region of the left scapula at initial presentation. B – The clinical appearance 1 month after the initial lesions were treated. C – The clinical appearance 6 months postoperative The histopathological examination of the lesional tissue revealed a well-demarcated lobulated tumor located in the reticular dermis. It consisted of bundles of smooth muscle fibers. Tumor cells had eosinophilic cytoplasm and blunt-ended vesicular nuclei. There was no cytologic atypia or mitotic activity Because of the huge number of leiomyomas, surgical removal was impossible. Treatment with carbon dioxide laser ablation was performed under local anesthesia with 2% lignocaine. We used the following settings: total power output – 10 W, spot size – 1 mm. We performed four procedures with monthly intervals and no side effects had been reported. During a 6-month follow up, the patient was completely asymptomatic and occurrence of new leiomyomas had not been noticed (Figures 1 B, C). Although the cosmetic outcome was not perfect, the resolution of pain seemed to be more important. Cutaneous leiomyomas are benign tumors of smooth muscle bundles [4]. Piloleiomyomas are the most common type of leiomyomas. They may be either solitary or multiple. Solitary cutaneous piloleiomyomas are usually asymptomatic and larger in size. Multiple piloleiomyomas occur more often and can be inherited as an autosomal-dominant trait with variable penetrance, or they can occur spontaneously. The pathogenesis of leiomyomas remains obscure. Multiple cutaneous leiomyomas may occur in conjunction with uterine leiomyomas, also known as multiple cutaneous and uterine leiomyomatosis (MCUL), familial leiomyomatosis cutis et uteri, Reed syndrome, or multiple leiomyomatosis [2]. Some patients with Reed syndrome also were found to have aggressive forms of renal cell carcinoma, which is known as hereditary leiomyomatosis and renal cell cancer (HLRCC) [6]. In the case of our patient, the family history of similar lesions was unremarkable. Piloleiomyomas usually present as small, red-brown, firm papules. Individual lesions range in size from few millimeters to 1 cm and are fixed to the skin [7]. They are freely movable over underlying deeper structures. The most common location includes the trunk and extensor surfaces of upper extremities, however, involvement of the face, breast and scrotum have also been described [5, 8]. Various distribution patterns have been reported: symmetrical, Blaschkoid, diffuse (disseminated), and segmental (zosteriform) [2, 5, 9–11]. Piloleiomyomas can be asymptomatic or very painful. Approximately 50% to 72% of patients complain of pain [5, 7]. They tend to occur more frequently in diffuse and segmental forms [2]. The origin of pain is not fully understood. It may be spontaneous or secondary to local pressure by the tumor on cutaneous nerves [3]. Other authors have suggested that it is due to muscle contraction mediated via a-adrenergic receptors [12]. The diagnosis of pilar leiomyoma may be suspected clinically, but the final diagnosis is based on the histopathological examination of lesional tissue. It shows proliferation of smooth muscle bundles which are described as cigar-shaped. The cells have eosinophilic cytoplasm and elongated nuclei with blunt ends. They stain positively for markers of smooth muscle differentiation (desmin and actin) [5, 9, 13, 14]. In the case of solitary leiomyomas, the first line of therapy is surgical excision of tumor. Due to numerous lesions and frequent recurrences after surgical removal of multiple leiomyomas, we decided to avoid surgical procedures. Various medications have been used with diverse response to alleviate pain connected with cutaneous leiomyomas. These include calcium channel blockers [3, 10, 11], α-adrenergic blocking agents [15], anticonvulsants [3], serotonin reuptake inhibitors, and topical 9% hyoscine hydrobromide, hyoscine butyl bromide. There is a single report of carbon dioxide laser ablation with significant improvement [4]. The carbon dioxide laser is the most versatile laser used in the treatment of cutaneous lesions. It is unique in that it can be used for resurfacing as well as excisional and even incisional procedures. The localized tissue destruction produced by carbon dioxide laser may make this technique superior to other destructive methods and allows the scarring to be limited. As in the case described by Christenson et al. [4], we observed resolution of pain in all treated lesions. Although the cosmetic outcome was not perfect, the resolution of pain seemed to be more important. The follow up period is required to assess the long-term results. Multiple leiomyomas can arise in hundreds and because of that, surgical procedures are not a viable option. Carbon dioxide laser ablation may be one of the therapeutic options in the case of multiple and painful leiomyomas.
  14 in total

Review 1.  Cutaneous smooth muscle neoplasms: clinical features, histologic findings, and treatment options.

Authors:  Valerie A Holst; Jacqueline M Junkins-Hopkins; Rosalie Elenitsas
Journal:  J Am Acad Dermatol       Date:  2002-04       Impact factor: 11.527

Review 2.  Cutaneous leiomyomas: a clinical marker of risk for hereditary leiomyomatosis and renal cell cancer.

Authors:  Laveta Stewart; Gladys Glenn; Jorge R Toro
Journal:  Dermatol Nurs       Date:  2006-08

3.  Disseminated cutaneous leiomyomatosis treated with oral amlodipine.

Authors:  Saurabh Aggarwal; Dipankar De; Amrinder J Kanwar; Uma Nahar Saikia; Geeti Khullar; Rahul Mahajan
Journal:  Indian J Dermatol Venereol Leprol       Date:  2013 Jan-Feb       Impact factor: 2.545

4.  Inherited susceptibility to uterine leiomyomas and renal cell cancer.

Authors:  V Launonen; O Vierimaa; M Kiuru; J Isola; S Roth; E Pukkala; P Sistonen; R Herva; L A Aaltonen
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-27       Impact factor: 11.205

5.  Treatment of multiple cutaneous leiomyomas with CO2 laser ablation.

Authors:  L J Christenson; K Smith; C J Arpey
Journal:  Dermatol Surg       Date:  2000-04       Impact factor: 3.398

6.  Cutaneous leiomyoma: novel histologic findings for classification and diagnosis.

Authors:  Alireza Ghanadan; Ata Abbasi; Kambiz Kamyab Hesari
Journal:  Acta Med Iran       Date:  2013

7.  Cutaneous piloleiomyomata.

Authors:  Gideon Smith; Noushin Heidary; Rishi Patel; Karla Rosenman; Shane A Meehan; Hideko Kamino; Miguel Sanchez
Journal:  Dermatol Online J       Date:  2009-08-15

8.  Leiomyoma of scrotum.

Authors:  R K Sherwani; K Rahman; K Akhtar; S Zaheer; M J Hassan; A Haider
Journal:  Indian J Pathol Microbiol       Date:  2008 Jan-Mar       Impact factor: 0.740

Review 9.  Bilateral segmental leiomyomas: a case report and review of the literature.

Authors:  Pitiporn Suwattee; Cari Dakin
Journal:  Cutis       Date:  2008-07

10.  Cutaneous leiomyoma in a child: A case report.

Authors:  Nursel Dilek; Derya Yüksel; Ibrahim Sehitoğlu; Yunus Saral
Journal:  Oncol Lett       Date:  2013-02-15       Impact factor: 2.967

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