Cutaneous leiomyoma, also known as leiomyoma cutis,[1] or cutaneous leiomyomata,[2] is a benign skin tumor made of smooth muscle cells.[3] There are three different types of cutaneous leiomyomas, genital leiomyomas, angioleiomyomas, and piloleiomyomas. Cutaneous leiomyomas can occur sporadically or as a part of a genetic condition. Cutaneous leiomyomas are diagnosed by histopathology and treated by surgical excision.
Signs and symptoms
Piloleiomyomas can be single or many, and they are derived from the arrector pili muscles of the pilosebaceous unit.[1] The tumours are firm, reddish-brown to skin-colored papulonodules, ranging in diameter from few mm to 2 cm; older lesions exhibit progressive expansion.[4] Although lesions are immobile on the skin, they can move freely over deeply ingrained structures.[5]Blaschko's lines are frequently the center of many piloleiomyomas, while reports of linear, segmental, and zosteriform patterns have also been made.[6] Usually related to cold, pressure, or emotion, 90% of piloleiomyomas cause pain, characterized as burning, pinching, or stabbing.[4]
Genital leiomyomas are rare, solitary growths originating from dartoic, vulvar, or mammary smooth muscle that present similarly to piloleiomyomas, and they include tumors of the nipple.[4] Nonetheless, in contrast to piloleiomyomas, genitalia tumors usually do not cause discomfort and manifest as pedunculated papules on the scrotum, vulva, or nipple, or as unilateral papulonodules measuring less than 2 cm (scrotal and vulvar lesions can measure up to 9 and 15 cm, respectively).[7][8] The most common genital leiomyoma variations are scrotal and vulvar leiomyomas, with vulvar tumors exhibiting growth during pregnancy.[9][10][11]
Angioleiomyomas are uncommon extracutaneous tumors that arise from the tunica media of small- to medium-sized arteries and veins.[12][13] These tumors appear as firm nodules in the subcutaneous or, in rare cases, dermal regions of the extremities. They are well-circumscribed, vascularized, and differentiated.[14][15][16] Most lesions occur in the upper extremities of males and lower extremities of females, with around half of them being painful to the touch or extremely cold, particularly those of the solid and cavernous subtypes.[1][17][18]
The most effective treatment is surgery, despite its high recurrence rate following excision. However, a surgical treatment can be limited by numerous lesions or unsatisfactory aesthetic outcomes. Cryotherapy, intralesional BTA injection, and CO2 ablation laser have all demonstrated some degree of pain alleviation in these situations.[19]
Epidemiology
Adults are more prone than children to have cutaneous leiomyomas, which often appear in the fifth and sixth decades of life.[20] Seventy-five percent of extra-uterine leiomyomas are cutaneous and make up about 5% of all leiomyomas.[21]
^ abcdMalik, Kunal; Patel, Parth; Chen, Jin; Khachemoune, Amor (2015). "Leiomyoma Cutis: A Focused Review on Presentation, Management, and Association with Malignancy". American Journal of Clinical Dermatology. 16 (1): 35–46. doi:10.1007/s40257-015-0112-1. ISSN1175-0561. PMID25605645.
^ abcHolst, Valerie A.; Junkins-Hopkins, Jacqueline M.; Elenitsas, Rosalie (2002). "Cutaneous smooth muscle neoplasms: Clinical features, histologic findings, and treatment options". Journal of the American Academy of Dermatology. 46 (4). Elsevier BV: 477–494. doi:10.1067/mjd.2002.121358. ISSN0190-9622. PMID11907496.
^Kitoh, Akihiko; Akiyama, Hajime; Yoshida, Yoko; Tanaka, Toshihiro (2003). "Multiple Piloleiomyomas: Do They Follow Dermatomes or Blaschko Lines?". The Journal of Dermatology. 30 (11). Wiley: 851–852. doi:10.1111/j.1346-8138.2003.tb00493.x. ISSN0385-2407. PMID14684949.
^Fasih, Najla; Prasad Shanbhogue, Alampady K.; Macdonald, David B.; Fraser-Hill, Margaret A.; Papadatos, Demetrios; Kielar, Ania Z.; Doherty, Geoffrey P.; Walsh, Cynthia; McInnes, Matthew; Atri, Mostafa (2008). "Leiomyomas beyond the Uterus: Unusual Locations, Rare Manifestations". RadioGraphics. 28 (7). Radiological Society of North America (RSNA): 1931–1948. doi:10.1148/rg.287085095. ISSN0271-5333.
^Del Sordo, Rachele; Leite, Silvia; Petroni, Pietro Antonio; Sidoni, Angelo (2008). "Paratesticular angioleiomyoma with cytological atypia". International Journal of Urology. 15 (4). Wiley: 374–375. doi:10.1111/j.1442-2042.2008.02011.x. ISSN0919-8172. PMID18380834.
^Hanft, JR; Carbonell, JA; Do, HQ (1997-08-01). "Angioleiomyoma of the lower extremity". Journal of the American Podiatric Medical Association. 87 (8). American Podiatric Medical Association: 388–391. doi:10.7547/87507315-87-8-388. ISSN8750-7315. PMID9274095.
^Hwang, J W; Ahn, J M; Kang, H S; Suh, J S; Kim, S M; Seo, J W (1998). "Vascular leiomyoma of an extremity: MR imaging-pathology correlation". American Journal of Roentgenology. 171 (4). American Roentgen Ray Society: 981–985. doi:10.2214/ajr.171.4.9762979. ISSN0361-803X. PMID9762979.
^Ramesh, P.; Annapureddy, S.R.; Khan, F.; Sutaria, P.D. (2004-06-24). "Angioleiomyoma: a clinical, pathological and radiological review". International Journal of Clinical Practice. 58 (6). Hindawi Limited: 587–591. doi:10.1111/j.1368-5031.2004.00085.x. ISSN1368-5031. PMID15311559.
^LAWSON, G. M.; SALTER, D. M.; HOOPER, G. (1995). "Angioleiomyomas of the Hand". Journal of Hand Surgery. 20 (4). SAGE Publications: 479–483. doi:10.1016/s0266-7681(05)80157-3. ISSN0266-7681.
^ abStewart, Laveta; Glenn, Gladys; Toro, Jorge R. (2006). "Cutaneous leiomyomas: a clinical marker of risk for hereditary leiomyomatosis and renal cell cancer". Dermatology Nursing. 18 (4): 335–341, quiz 342. ISSN1060-3441. PMID16948378.
Marcoval, Joaquim; Llobera-Ris, Clàudia; Moreno-Vílchez, Carlos; Penín, Rosa María (2022). "Cutaneous Leiomyoma: A Clinical Study of 152 Patients". Dermatology. 238 (3): 587–593. doi:10.1159/000518542. ISSN1018-8665. PMID34569484.