Some of the largest lesions of KACM (measuring ≥20 cm) have been reported to occur on the lower extremities.3-6 The lesions enlarged over a period of 10 months to several years with no tendency to regress completely, similar to our patient. All of these reported large lesions of the legs were successfully treated surgically. The diagnostic difficulty was not addressed in these previously reported cases; in our case, however, the initial lack of the characteristic exophytic rolled and shiny peripheral border and the frequent secondary bacterial infections contributed to the difficulty in accurate diagnosis. Initially, an infectious etiology such as chromoblastomycosis and verrucous tuberculosis was suspected. Histopathologically, the distinguishing exoendophytic architecture present at the periphery of KACM was not present; instead, the pathologic changes were confined to the superficial dermis, which consisted of jagged outlined epithelial aggregations that were difficult to distinguish from pseuodoepitheliomatous hyperplasia secondary to deep fungal or mycobacterial infection or halogenoderma. The history, clinicopathologic correlation, and negative culture results eventually led to the diagnosis of KACM.
A variety of treatment modalities have been employed successfully for KAs, including surgical excision, intralesional MTX, intralesional and topical 5-FU, intralesional bleomycin, and isotretinoin.2 Isotretinoin has been advocated as both a prophylactic and therapeutic agent for skin cancers, especially in the setting of multiple lesions.7-9 A relatively high dose (1–3 mg/kg) is required, even for prophylactic outcome. A low dose, in the range of 5 to 10 mg/d, is neither prophylactic nor therapeutic.10,11 The side effects, which include elevated triglyceride levels, mucocutaneous reactions, and hyperostotic axial skeletal changes, limit the use of isotretinoin. The efficacy of retinoids in the prophylaxis and treatment of KA and KACM also has been reported by several authors.12-15 The dosage of isotretinoin ranged from 1 to 3 mg/kg per day with a response observed as early as within one week to several months. In our case, despite adequate duration and relative high doses of isotretinoin, there was no prophylactic or therapeutic effect as evidenced by the patient's continual development of nodular KAs without any of the existing KAs regressing while he was receiving isotretinoin therapy. The patient experienced the usual mucocutaneous side effects. His backache and the changes in his mood were suspected to be the side effects of isotretinoin, as well.
Intralesional MTX for the treatment of KAs has been reported to be effective with a regimen of 1 to 3 injections not exceeding a total dose of 100 mg, resulting in resolution of the KAs in 2 to 4 weeks.16-18 In our patient, although the 2 sites were injected with adequate amounts of MTX, the treatment was unsuccessful. In retrospect, intralesional therapy was unreasonable because of the large amounts of MTX that would have been required. The 2 treated sites accounted for less than 10% of the surface area of the lesions.
The rationale for imiquimod therapy in our patient was 2-fold. First, imiquimod is an immune response modifier emerging as an effective therapy for superficial carcinomas of the skin.19-22 Most therapies available for superficial skin carcinomas also have been applied to KAs. Second, because human papillomavirus has been found to be present in KA, though not consistently,23-26 we were hopeful that imiquimod would have a therapeutic effect for KACM similar to that for condyloma. Despite daily application of the cream for 7 months to some of the lesions, far beyond the 6 to 12 weeks' duration recommended for basal cell carcinomas,19,27 imiquimod had no effect.
Both topical and intralesional 5-FU, a thymine analog, have been reported to be effective therapies for solitary and multiple KAs, though there is no reported case of KACM treated with either topical or intralesional 5-FU. A dramatic resolution has been observed as early as one week after treatment using topical 5-FU, but the usual duration of therapy was 3 to 4 weeks.28-30 In contrast to these reports, encouraging signs of resolution were present in our patient after 2 months of therapy, and complete resolution occurred over a period of many months, not weeks. Despite the apparent efficacy of 5-FU, we cannot exclude the possibility that the regression of the lesions was the natural course of the neoplasm, especially when KAs are known to regress without any therapeutic intervention. The evidence supporting topical 5-FU being efficacious is that there was prompt resolution when the cream was applied to the new lesions.
The nature of KA and KACM, whether or not the neoplasm is a squamous cell carcinoma (SCC), has been controversial. A few authors assert that a KA is an SCC.5,31,32 We consider KA and its variants, including KACM, as one type of SCC encountered in the skin. A few well-documented cases of metastases of KAs to the lymph nodes have been reported.31,33 At the molecular level, KA has been shown to overexpress p53,34 a tumor suppressor gene that has been associated with a variety of malignant neoplasms. In contrast to other types of SCC, a complete regression, believed to be an immune-mediated process by some,35,36 is a unique characteristic of KA. The exact mechanism by which a KA regresses, however, remains largely a mystery. LeBoit37 has hinted that solving this mystery may have far-reaching applications. We agree.