Aggressive superficial acral fibromyxoma of the great toe: A case report and mini-review of the literature
- Authors:
- Kazuhiko Hashimoto
- Shunji Nishimura
- Naohiro Oka
- Hiroki Tanaka
- Ryosuke Kakinoki
- Masao Akagi
View Affiliations
Affiliations: Department of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama, Osaka 589-8511, Japan
- Published online on: July 9, 2018 https://doi.org/10.3892/mco.2018.1669
-
Pages:
310-314
Metrics: Total
Views: 0 (Spandidos Publications: | PMC Statistics: )
Metrics: Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )
This article is mentioned in:
Abstract
Superficial acral fibromyxoma is a very rare soft tissue tumor. Fetsch et al first described the condition in 2001. It often occurs in the fingers and toes and has slow-progressive features. Since being described, a few cases occurring in the great toe have been reported. The present study indicated a case of a 37-year-old male kickboxer with a history of a rapid-growing lump under the nail of his left great toe with bone erosion. The patient was suspected to have a soft tissue tumor under the nail, such as a glomus tumor, as a differential diagnosis. However, a malignant soft tissue tumor as a differential diagnosis could not be ruled out because of the observed bone erosion. The patient underwent surgical excision, and pathologic analysis revealed superficial acral fibromyxoma. Twenty-four months after the treatment, he had no complaints or functional disorder and no recurrence was noted. Although an unusual diagnosis, surgeons should be aware of this tumor, which requires complete surgical excision and follow-up to detect recurrence. To the best of our knowledge, this is the first reported case of superficial acral fibromyxoma with bone erosion in a great toe.
View References
1
|
Fetsch JF, Laskin WB and Miettinen M:
Superficial acral fibromyxoma: A clinicopathologic and
immunohistochemical analysis of 37 cases of a distinctive soft
tissue tumor with a predilection for the fingers and toes. Hum
Pathol. 32:704–714. 2001. View Article : Google Scholar : PubMed/NCBI
|
2
|
Sawaya JL and Khachemoune A: Superficial
acral fibromyxoma. Int J Dermatol. 54:499–508. 2015. View Article : Google Scholar : PubMed/NCBI
|
3
|
Wakabayashi Y, Nakai N, Takenaka H and
Katoh N: Superficial acral fibromyxoma of the great toe: Case
report and mini-review of the literature. Acta Dermatovenerol
Croat. 20:263–266. 2012.PubMed/NCBI
|
4
|
Schwager ZA, Mannava KA, Mannava S, Telang
GH, Robinson-Bostom L and Jellinek NJ: Superficial acral
fibromyxoma and other slow-growing tumors in acral areas. Cutis.
95:E15–E19. 2015.PubMed/NCBI
|
5
|
Raghupathi DS, Krishnamurthy J and Kakoti
LM: Cytological diagnosis of superficial acral fibromyxoma: A case
report. J Cytol. 32:39–41. 2015. View Article : Google Scholar : PubMed/NCBI
|
6
|
Moon A, Yoon N and Kim HS: Myxoid
dermatofibroma on a great toe: A case report. Int J Clin Exp
Pathol. 8:7605–7609. 2015.PubMed/NCBI
|
7
|
Braga JM, Bartosch I, Baldaia H, Oliveira
I, Canelhas A and Silva Á: Superficial acral fibromyxoma: A rare
soft tissue tumor. J Foot Ankle Surg. 56:653–655. 2017. View Article : Google Scholar : PubMed/NCBI
|
8
|
Robati RM, Dadkhahfar S and Rakhshan A:
CD34 negative superficial acral fibromyxoma: A rare case report.
Indian Dermatol Online J. 8:45–47. 2017. View Article : Google Scholar : PubMed/NCBI
|
9
|
Hollmann TJ, Bovée JV and Fletcher CD:
Digital fibromyxoma (superficial acral fibromyxoma): A detailed
characterization of 124 cases. Am J Surg Pathol. 36:789–798. 2012.
View Article : Google Scholar : PubMed/NCBI
|
10
|
Kazakov DV, Mentzel T, Burg G and Kempf W:
Superficial acral fibromyxoma: Report of two cases. Dermatology.
205:285–288. 2002. View Article : Google Scholar : PubMed/NCBI
|