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DOI: 10.1055/s-0043-1778690
Giant Cutaneous Leiomyoma of Scalp
- Abstract
- Introduction
- Clinical Presentation
- Radiology
- Histopathology
- Discussion
- Conclusion
- References
Abstract
Leiomyomas are benign tumors arising from smooth muscle, most commonly seen in uterine myometrium, gastrointestinal tract, skin, and lower extremities of middle-aged women. Leiomyomas of head and neck region account for less than 1% of all leiomyomas. The most common site of leiomyoma in the head and neck region is the lips followed by tongue, and other maxillofacial regions. The clinical features, etiology, differential diagnosis, and treatment of leiomyoma are discussed in this case report. The aim of this case report is to raise awareness about a rare form of scalp giant leiomyoma. This could expand its consideration as a possible cause of uncertain neoplasms and promote accurate clinical diagnosis, leading to better treatment results.
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Introduction
Leiomyoma is a benign tumor that can occur in any location with smooth muscle with uterus being most common location of leiomyoma and scalp leiomyoma rarely reported.[1]
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Clinical Presentation
A 30-year-old woman presented with a painless swelling in the right occipital region. There were no complaints of headache, vomiting, and neuromuscular deficits. On examination, there was a 12 cm X 9cm X 6 cm sized freely mobile globular, smooth right occipital swelling with regular margins, firm to hard, and with normal skin. The swelling was in the subcutaneous plane, noncompressible, mobile from underlying bone with negative transillumination test ([Fig. 1]). Intraoperatively, the tumor was firm in consistency and vascular with scalloping of the occipital bone underneath ([Fig. 1]).
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Radiology
Preoperative computed tomography brain plain ([Fig. 2]) showed a swelling in the suboccipital region extending to the upper neck region with no intracranial extension.
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Histopathology
Tumor was encapsulated and composed of spindle cells arranged in interlacing fascicles and whorls, showing minimum pleomorphism without necrosis or an increase in mitotic activity ([Fig. 3]).
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Discussion
The characteristics of different types of cutaneous leiomyomas is depicted in [Table 1]. Solitary leiomyoma has indistinct boundaries and consists of intertwined smooth muscle bundles with mixed collagen bundles. They possess elongated nuclei with blunt edges and exhibit low mitotic activity. Previously five cases of scalp leiomyoma have been reported.[1] [2] [3] [4] [5] The reported cases of scalp leiomyoma are detailed in [Table 2]. Most patients had scalp lesions for a long time without pain. No mitotic figures were found in our case. Solitary lesions are usually amenable for complete surgical resection and recurrence is rare; however, complete excision is not possible with multiple lesions and they usually have higher rates of recurrence.[6] [7] Surgical excision is the best treatment for solitary scalp lesions.
Study Id |
Country |
Age/Gender |
Size (cm) |
Location |
Appearance |
Duration |
Pain |
Treatment |
Histopathology |
---|---|---|---|---|---|---|---|---|---|
Lotfi et al 2010[5] |
Iran |
5 months/male |
2 × 3 × 0.5 |
Occipital |
Smooth, firm, nontender, pink, and semimobile mass with ulcerated center and crusting |
Appeared 1 week after birth |
Absent |
Surgical excision |
Nonencapsulated mass in dermis composed of spindle cells with no mitotic activity. IHC positive for smooth muscle actin and vimentin, negative for S100. Masson trichrome staining was positive |
Kim et al 2011[4] |
Korea |
77 years/male |
5.5 × 4.5 |
Forehead |
Solitary erythematous indurated dermal nodule with yellowish papules and telangiectasia |
50 years |
Present |
Surgical excision |
Hyperplastic epidermis, muscles cells filled dermis and extended into subcutaneous fat, confirmed with Masson-trichome staining on IHC. No cellular atypia |
Arishima et al 2013[2] |
Japan |
6 years/male |
2 cm in diameter |
Top of head |
Hard, firm |
1 year |
Absent |
Surgical excision |
Spindle cell neoplasm with numerous blood vessels and < 1 mitosis/high power field. IHC positive for smooth muscle actin and negative for S100. Vascular leiomyoma |
Fatima et al 2015[1] |
India |
22 years/male |
5 × 3 × 2 |
Right scalp |
Solitary circumscribed red brown color, soft swelling |
6 months |
Present |
Surgical excision |
Well circumscribed and lobulated with cells arranged in a whorl like pattern. Tumor cells are composed of spindle cells and smooth muscle cells. No mitotic figures. Masson trichrome staining was positive |
Kim et al 2017[3] |
Korea |
31 years/male |
1 × 1 |
Frontal |
Firm and pinkish mass |
18 months |
Absent |
Surgical excision |
Non encapsulated spindle cells arranged in whorls. No mitotic figures. IHC positive for actin and negative for S100 |
Present case |
India |
30 years/female |
12 × 9 × 6 |
Occipital |
Globular, smooth firm with well-defined margins |
1 year |
Absent |
Surgical excision |
Spindle cells arranged in whorls. No mitotic figures |
Abbreviation: IHC, immunohistochemistry.
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Conclusion
Diagnosis of cutaneous leiomyomas relies more on histological examination. Complete excision of solitary scalp leiomyoma with clear margins is the appropriate treatment.
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Conflict of Interest
None declared.
Ethical Approval Statement
The study was started after the approval from institutional ethical committee.
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References
- 1 Fatima Q, Singh O, Kothari DC, Godara SK. Cutaneous leiomyoma of scalp: a rare case report with review of literature. Intern J Res Med Sci 2014; 3 (04) 993-997
- 2 Arishima H, Takeuchi H, Kitai R, Yamauchi T, Kikuta K. Vascular leiomyoma of the scalp with a small deformity on the skull mimicking a dermoid cyst. Pediatr Dermatol 2013; 30 (03) e27-e29
- 3 Kim DH, Lee JS, Kim JA, Lee JH. Solitary piloleiomyoma in the scalp. Arch Craniofac Surg 2017; 18 (01) 62-64
- 4 Kim GW, Park HJ, Kim HS. et al. Giant piloleiomyoma of the forehead. Ann Dermatol 2011; 23 (Suppl. 02) S144-S146
- 5 Lotfi S, Ghalamkarpour F, Rahimi H, Kani ZA, Yousefi M, Qaisari M. An ulcerated tumor in an infant. Dermatol Online J 2010; 16 (04) 9
- 6 Veeresh M, Sudhakara M, Girish G, Naik C. Leiomyoma: a rare tumor in the head and neck and oral cavity: report of 3 cases with review. J Oral Maxillofac Pathol 2013; 17 (02) 281-287
- 7 Holst VA, Junkins-Hopkins JM, Elenitsas R. Cutaneous smooth muscle neoplasms: clinical features, histologic findings, and treatment options. J Am Acad Dermatol 2002; 46 (04) 477-490 , quiz, 491–494
Address for correspondence
Publikationsverlauf
Artikel online veröffentlicht:
20. März 2024
© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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References
- 1 Fatima Q, Singh O, Kothari DC, Godara SK. Cutaneous leiomyoma of scalp: a rare case report with review of literature. Intern J Res Med Sci 2014; 3 (04) 993-997
- 2 Arishima H, Takeuchi H, Kitai R, Yamauchi T, Kikuta K. Vascular leiomyoma of the scalp with a small deformity on the skull mimicking a dermoid cyst. Pediatr Dermatol 2013; 30 (03) e27-e29
- 3 Kim DH, Lee JS, Kim JA, Lee JH. Solitary piloleiomyoma in the scalp. Arch Craniofac Surg 2017; 18 (01) 62-64
- 4 Kim GW, Park HJ, Kim HS. et al. Giant piloleiomyoma of the forehead. Ann Dermatol 2011; 23 (Suppl. 02) S144-S146
- 5 Lotfi S, Ghalamkarpour F, Rahimi H, Kani ZA, Yousefi M, Qaisari M. An ulcerated tumor in an infant. Dermatol Online J 2010; 16 (04) 9
- 6 Veeresh M, Sudhakara M, Girish G, Naik C. Leiomyoma: a rare tumor in the head and neck and oral cavity: report of 3 cases with review. J Oral Maxillofac Pathol 2013; 17 (02) 281-287
- 7 Holst VA, Junkins-Hopkins JM, Elenitsas R. Cutaneous smooth muscle neoplasms: clinical features, histologic findings, and treatment options. J Am Acad Dermatol 2002; 46 (04) 477-490 , quiz, 491–494