Tumor in the plantar region: dermatofibrosarcoma protuberans in an infrequent topography^☆,☆☆

Abstract

Dermatofibrosarcoma protuberans is a rare mesenchymal tumor; it is locally aggressive and presents high rates of local recurrence. It may present as a nodular or plaque vegetating lesion. It mainly affects the trunk and proximal limbs, being rare in the distal extremities. Biopsy and immunohistochemistry help confirm the diagnosis. The authors report a case of dermatofibrosarcoma protuberans with plantar region involvement, a rare presentation. To the best of the authors’ knowledge, only 11 cases of involvement of the feet were described in the international literature.

KEYWORDS
Dermatofibrosarcoma; Immunohistochemistry; Sarcoma

Introduction

Dermatofibrosarcoma protuberans (DFSP) is a mesenchymal neoplasm of slow growth, locally aggressive and with low metastatic potential. It has several presentations and can be characterized as a hardened plaque, nodule, or vegetating lesion.¹ Local trauma has been described as a potential risk factor for tumor onset.² The most common sites of involvement are the trunk (40%–50%), the proximal limbs (30%–40%), and the head and cervical region (10%–15%). In the literature review, 11 reports of tumors located in the plantar region were retrieved. Due to the rarity of the presentation on the distal limbs, the authors believe that reporting this case is relevant.

Case report

Male patient, 35 years old, previously healthy, complained of painful lesion on the left plantar region with progressive growth over six months; he denied trauma. On physical examination, he presented an erythematous, exophytic, vegetating, and ulcerated tumor on the first metatarsal joint (Fig. 1). Histopathological examination of the lesion revealed a fusocellular proliferation with a focal storiform pattern (Fig. 2). In the immunohistochemical study, a diffuse positivity for CD34 + cells was observed. The findings were compatible with low-grade fusocellular mesenchymal neoplasia, favoring the diagnosis of DFSP (Fig. 3). Surgical treatment involved amputation of the hallux and part of the left forefoot; no tumor recurrence was observed after four months of post-operative follow-up.

Figure 1
Exophytic and ulcerated tumor lesion.

Figure 2
Histopathology: fusocellular proliferation with a focal storiform pattern (Hemathoxylin & eosin ×40).

Figure 3
Immunohistochemistry: diffuse positivity for CD34 in spindle cells with storiform pattern.

Discussion

DFSP is a rare mesenchymal tumor with low rates of aggressiveness. It presents slow progression, with high rates of local recurrence and rare cases of distant metastases. An American study conducted between 2000 and 2010 found an incidence of 41 cases in 10 million patients.³ Some studies observed a higher incidence in women and black people. It mostly affects the trunk (40%–50%), the proximal limbs (30%–40%), and the head and cervical region (10%–15%).³

A literature review published in 2019 described 11 cases of dermatofibrosarcoma that affected the feet. The mean age observed was 41 years; it was more frequent in men than in women (8:3) and the most frequent location of the tumor was the dorsum of the feet. The mean growth period was 3.5 years. The mean DFSP size at diagnosis was approximately 3.5 cm. Clinical diagnosis is difficult given the variety of presentations. Dermoscopy has been described as a useful tool to aid diagnosis.¹ In a review based on the analysis of 32 dermatofibrosarcomas, the most common features described in dermoscopy were the presence of vessels (81%), followed by a pigment network (78%) and a pinkish background (66%).³

Histologically, dermatofibrosarcoma presents monomorphic spindle cells with little atypia and mitotic activity, arranged in irregular and multidirectional (storiform) fascicles. The tumor infiltrates the subcutaneous tissue, creating the characteristic honeycomb pattern. The histological differential diagnoses of other spindle cell tumors are dermatofibroma, malignant fibrous histiocytoma, atypical fibroxanthoma, desmoplastic melanoma, Kaposi's sarcoma, and solitary fibrous tumor.¹

Immunohistochemistry becomes an important resource for differential diagnosis, as DFSP is positive for CD34 and negative for S 100 protein, factor XIIIA, and desmin.¹ All the cases described in the literature were tested for CD34 and were positive.³

The recommended treatment is lesion excision with 2–3 cm of safety margins.⁴ Involvement of margins is associated with local recurrence.⁴ Another therapeutic option is Mohs micrographic surgery. Management with radiotherapy and imatinib has been described. The use of imatinib is indicated for metastases, local recurrences, as neoadjuvancy, or when the tumor is unresectable.⁵

Attention should be paid to this disease, even in unusual anatomical areas, as the prognosis depends on the early diagnosis and treatment.

• Financial support
  None declared.
• ☆
  How to cite this article: Perazzoli S, Bonamigo RR, HeckR, Cartell AS. Tumor in the plantar region: dermatofibrosar-coma protuberans in an infrequent topography. An Bras Dermatol.2020;95:728-730.
• ☆☆
  Study conducted at the Sanitary Dermatology OutpatientClinic, Porto Alegre, RS, Brazil.

References

• ¹
  Escobar FG, Ribeiro CK, Leite LL, Barone CR, Cartell A. Dermoscopy of dermatofibrosarcoma protuberans: what do we know? Dermatol Pract Concept. 2019;9:139-45.
• ²
  Lee SW, Zaesim A, Jackson A, Borkat M. Fibrosarcomatous dermatofibrosarcoma protuberans from scar following trauma. Autops Case Rep. 2018;8:e2018039.
• ³
  Madden C, Spector A, Siddiqui S, Mirkin G, Yim J, Hao X. Dermatofibrosarcoma protuberans on adult toes: a case report and review of the literature. Anticancer Res. 2019;39:2105-11.
• ⁴
  Gladdy RA, Wunder JS. Risk-stratified surveillance in dermatofibrosarcoma protuberans: less is more. Cancer. 2019;125:670-2.
• ⁵
  Navarrete-Dechent C, Mori S, Barker CA, Dickson MA, Nehal KS. Imatinib treatment for locally advanced or metastatic dermatofi-brosarcoma protuberans: a systematic review. JAMA Dermatol. 2019;155:361-9.

Publication Dates

• Publication in this collection
  30 Nov 2020
• Date of issue
  Nov-Dec 2020

History

• Received
  27 Jan 2020
• Accepted
  2 May 2020