Cutaneous spindle cell squamous cell carcinoma.

Abstract

Dear Editor: Spindle cell squamous cell carcinoma (SpSCC) is a rare variant of squamous cell carcinoma (SCC). Despite having clinical attributes that overlap conventional SCC, these lesions are pathologically distinct and are comprised of spindled cells that infiltrate the dermis as single cells or cohesive nests; that lack features of keratinization. SpSCC most commonly occurs in the larynx, and less often in the hypopharynx, oropharynx, and nasal cavity1. It is extremely rare to find SpSCC confined to the cutaneous lesion, and only three cases have previously been reported in Korea. A 73-year-old woman presented with a 1-year history of a pruritic, solitary mass on the face. Physical examination revealed an irregular-shaped, erythematous, firm, fixed mass with a yellowish crust on her left upper perioral area. The mass was 1.3 cm in diameter and was slowly expanding (Fig. 1). The patient had a history of a wide excision of basal cell carcinoma on her nose 2 years previously, and no relapse has been observed. Fig. 1 (A, B) Solitary, 1.3 cm-sized, irregular-shaped, erythematous, firm mass with a yellowish crust on the left upper perioral area. Histologic examination of the lesion showed spindle-shaped cells with hyperchromatic nuclei infiltrating the dermis in a whorl-like pattern (Fig. 2). Furthermore, immunohistochemical investigation revealed the specimen was positive for cytokeratins (34βE12, CK5/6, AE1/3) and vimentin, but was negative for smooth muscle actin (SMA), S-100, and CD68. Through histologic features and immunohistochemical evaluation, she was diagnosed with SpSCC. The lesion was surgically removed 13 months previously and no relapse has been observed. Fig. 2 (A) Diffuse dermal infiltrates of spindle cells (HE B: ×200, C: ×400). (D) Positive immunostaining for 34βE12, ... Cutaneous SpSCC presents as a raised or exophytic nodule accompanied by spontaneous bleeding and central ulceration similar to conventional SCC2. It is usually confined to sun-damaged sites such as the head, neck, chest, and upper extremities or areas that have received prior ionizing radiation2,3. Although the rarity of these tumors makes difficult to study patient survival rates, the literature suggests an overall prognosis similar to that of conventional SCC. SpSCC must be distinguished from other spindle cell lesions such as atypical fibroxanthoma (AFX), spindle cell/desmoplastic melanoma, cutaneous leiomyosarcoma, and scars. Immunohistochemistry has become the essential method in the pathologic workup of these tumors. The spindle cells in SpSCC stained positively for one or more of the cytokeratins (34βE12, AE1/3, cam 5.2, low molecular weight keratin) and the mesenchymal marker, vimentin. Each of these neoplasms stained negatively for S-100, CD68, and SMA; whereas AFX showed positivity for CD68, but lacked keratin and S-100. The spindle cell melanomas showed a connection with the epithelium that was contiguous with similar junctional cells possessing cytoplasmic melanin and S-100 immunostaining, but lacking keratins. The leiomyosarcomas showed positivity with SMA and vimentin, and were negative for keratins and S-100. The scars were negative for all immunohistochemical stains4. Cutaneous SpSCC is so rare subtype of SCC that pathophysiology, prognostic factors, and metastatic risk are not well-established. It is known that SpSCCs that are associated with radiation, burn scars, and immunosuppression may correlate with aggressive clinical courses5. Further studies of this rare entity are needed to establish its biological behavior, and the accumulation of more case reports will aid in determining a precise prognosis.