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AJR 2005; 184:S110-S111
© American Roentgen Ray Society


Case Report

Primary Squamous Cell Carcinoma: An Incidental Toe Mass

Stavroula J. Theodorou1, Daphne J. Theodorou1, Susan J. Bona2 and Shella Farooki3

1 Department of Radiology, University of California School of Medicine, San Diego, CA.
2 Department of Pathology, The Ohio State University Medical Center, Columbus, OH.
3 Department of Radiology, The Ohio State University Medical Center, Columbus, OH.

Received January 5, 2004; accepted after revision April 3, 2004.

 
Address correspondence to D. J. Theodorou, 13 Papadopoulos St., Ioannina, 45444 Greece.


Introduction
Top
Introduction
Case Report
Discussion
References
 
Nonmelanoma skin cancer is the most common cancer in the United States [1]. Approximately 80% of the nonmelanoma skin cancers are basal cell carcinomas, and 20% are squamous cell carcinomas. Although most cases of squamous cell carcinomas of the skin are curable, some tumors may recur or metastasize. We describe the MRI findings of the toe in a patient with primary squamous cell carcinoma and correlate them with the histopathologic findings. To our knowledge, this is the first case of primary squamous cell carcinoma of the foot studied with MRI and histopathologic correlation.


Case Report
Top
Introduction
Case Report
Discussion
References
 
A 44-year-old woman presented with a 3-week history of intermittent, left-sided chest pain and exertional dyspnea. The patient was a heavy smoker (58 pack/year history). At the time of presentation, the patient complained incidentally of a soft-tissue mass in her right fifth toe that had been present for more than 15 years. In the previous 4 years, the mass had been slowly enlarging. The patient had recently noticed pain, ulceration, brown purulent discharge, and a foul smell from the mass.

A workup for coronary artery disease was negative. Physical examination of the right foot showed an ulcerated, fungating, painful 5-cm mass of the fifth digit. The patient was afebrile and a complete blood count was remarkable for a WBC of 11.8 x 109/L. Radiographs of the right foot showed no osseous abnormalities. A soft-tissue mass with no evidence of calcified or ossified matrix was present in the lateral aspect of the fifth toe. MR images of the right foot showed a soft-tissue mass measuring 4.5 x 2.5 x 2.8 cm in the dorsal, lateral, and plantar aspect of the fifth digit with homogeneously low T1-weighted and intermediate T2-weighted signal intensity (Figs. 1A and 1D). Abnormally high signal intensity in the mass was seen on the STIR sequences (Fig. 1B). After IV administration of a gadolinium-containing contrast medium, the mass showed heterogeneous striated enhancement (Fig. 1C). There was minimal increased intramedullary signal intensity consistent with adjacent bone marrow edema. The mass was considered to be of a soft-tissue origin. Because the tumor was in close proximity to the nail bed, it was difficult to exclude involvement of this structure.



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Fig. 1A. 44-year-old woman with painful soft-tissue mass in right fifth toe. Axial T1-weighted (TR/TE, 650/15) (A) and inversion recovery (4,820/25; TI = 180 msec) (B) MR images show abnormally low and high signal intensity, respectively, in soft-tissue mass of right fifth toe (arrow).

 


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Fig. 1D. 44-year-old woman with painful soft-tissue mass in right fifth toe. Coronal T2-weighted MR image (4,120/78) shows large mass of heterogeneous intermediate signal intensity in right fifth toe (arrow).

 


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Fig. 1B. 44-year-old woman with painful soft-tissue mass in right fifth toe. Axial T1-weighted (TR/TE, 650/15) (A) and inversion recovery (4,820/25; TI = 180 msec) (B) MR images show abnormally low and high signal intensity, respectively, in soft-tissue mass of right fifth toe (arrow).

 


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Fig. 1C. 44-year-old woman with painful soft-tissue mass in right fifth toe. Coronal T1-weighted MR image (650/20) with fat saturation after IV gadolinium administration reveals enhancement of soft-tissue mass in a striated pattern.

 

Surgical treatment consisted of amputation of the fifth toe. A friable soft-tissue mass measuring 5 x 5.5 x 1 cm was removed. The mass had invaded the nail bed but not the underlying bone. The surgical margins were free of tumor. Histopathologic examination of the amputated fifth toe revealed a florid proliferation of squamous epithelial cells showing low-grade cytologic atypia and keratinization with infiltration of the dermis (Figs. 1E and 1F). The final pathologic diagnosis was invasive, well-differentiated, primary squamous cell carcinoma of the toe—a common cutaneous malignancy unusual in this anatomic location.



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Fig. 1E. 44-year-old woman with painful soft-tissue mass in right fifth toe. Photomicrograph of histopathologic specimen at low power reveals normal dermis and epidermis (left) and invasive squamous cell carcinoma (right). Note infiltration of tumor into deep dermis (arrow). (H and E, x2)

 


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Fig. 1F. 44-year-old woman with painful soft-tissue mass in right fifth toe. Photomicrograph at medium power shows infiltrating islands of well-differentiated neoplasm and squamous epithelium within dermis. Foci of keratin are also seen (thick arrow). (H and E, x10)

 


Discussion
Top
Introduction
Case Report
Discussion
References
 
Squamous cell carcinoma of the skin is the second most common cancer that affects Caucasians, with 200,000 new diagnoses each year in the United States [1]. Metastatic disease is uncommon, with an overall rate of 2%, although the incidence can be higher for primary tumors in certain anatomic locations [2]. Squamous cell carcinoma originates from the squamous epithelium of the surface epidermis and may show varying degrees of differentiation and keratinization [2]. The clinical appearance is variable, and the tumor may present as a skin-colored, red, or brown nodule with or without scaling, a focus of induration, an ulcerated lesion, plaque, or an exophytic cauliflower-like growth [2]. Primary squamous cell carcinoma may grow slowly or rapidly with invasion of the neighboring structures. Although the MRI appearance of verrucous carcinoma, a rare subtype of locally invasive squamous cell carcinoma of the foot, has been reported [3], our case is the first to describe the MRI findings of primary squamous cell carcinoma (nonverrucous, or the usual type) of the foot.

The importance of this case from a diagnostic-imaging perspective is the presentation of a soft-tissue neoplasm unfamiliar to many radiologists. Differential diagnostic considerations for squamous cell carcinoma of skin include keratoacanthoma, basal cell carcinoma, verrucous carcinoma, deep mycosis, eccrine poroma, sweat gland carcinoma, amelanotic melanoma, pyogenic granuloma, reactive epidermal hyperplasias overlying sites of infection, chronic mechanical trauma changes, and cutaneous Hodgkin's disease. Although the MRI appearance of squamous cell carcinoma of skin may be nonspecific, placing the MRI findings in clinical context and assessment of histopathologic findings is helpful for establishing the correct diagnosis. MRI helps to determine the presence and extent of disease in the skin, surrounding soft tissue, and subjacent bone, and therefore aids in surgical planning. Based on the experience with this case, the presence of a soft-tissue mass in the foot exhibiting characteristics of a chronic inflammatory process associated with new pain or recent ulceration warrants diagnostic imaging, biopsy, or both to avoid a misdiagnosis of malignancy. Given the potential for local destruction and the potential risk, albeit small, for metastasis with squamous cell carcinoma of the skin, this entity should be considered in the differential diagnosis of soft-tissue masses in the foot.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Alam M, Ratner D. Cutaneous squamous cell carcinoma. N Engl J Med 2001;344:975 -983[Free Full Text]
  2. Barnhill RL. Tumors of the epidermis. In: Barnhill RL, ed. Textbook of dermatopathology. New York, NY: McGraw Hill, 1998: 521-525
  3. Bhushan M, Ferguson J, Hutchinson C, Muston H. Carcinoma cuniculatum of the foot assessed by magnetic resonance scanning. Clin Exp Dermatol2001; 26:419 -422[Medline]

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