Abstract. Fibroepithelioma of Pinkus (FEP), which is considered to be an uncommon variant of basal cell carcinoma, has been described in association with other systemic diseases. However, no specific studies are currently available on this subject. The aim of our study was to evaluate the clinical and morphological characteristics of FEP and investigate whether this rare tumor is a single entity or seen in the context of a more complex syndrome. We retrospectively analyzed 49 cases of FEP diagnosed and excised in a single academic institution from 1995 to 2011. The tumors were mainly located on the trunk (77.55%), followed by the lower extremities (12.20%) and the head and neck (10.20%). In 9 of the 49 cases (18%), FEP was associated with gastrointestinal tumors. The abovementioned cases are presented in an attempt to make clinicians more aware of a possible association between FEP and gastrointestinal cancer. Although a possible underlying common genetic background between FEP and gastrointestinal tumors was not provided, our study suggests that patients with FEP should be screened for the occurrence of gastrointestinal tumors.
IntroductionFibroepithelioma of Pinkus (FEP) is considered to be an uncommon variant of basal cell carcinoma (BCC) (1), although it was recently described as a trichoblastoma (2,3). Clinically, FEP appears as a solitary non-pigmented or brownish to gray, well-outlined flat or polypoid lesion, with peculiar dermoscopic and confocal aspects (4) and with a predilection for the lower trunk (Fig. 1).Histopathologically, FEP is characterized by numerous thin anastomosing cords of basaloid cells extending downward from the epidermis into the dermis within a fibrotic stroma (Fig. 1).Unlike the common types of BCC, FEP exhibits an overwhelming predilection for the trunk (particularly the lower back) and the extremities, with only 5% of the tumors arising on sun-damaged skin. The clinical differential diagnosis includes a wide spectrum of lesions, such as skin tags or dermal nevi. However, the diagnosis is easier when the clinical examination is combined with dermoscopy and confocal microscopy (4,5).Although FEP was originally described by Pinkus as a variant of BCC, the nature of this tumor remains a subject of debate.The strong predilection for the lumbar region (not sun-exposed area) and for the female gender differentiates FEP from other BCC subtypes that usually arise on sun-exposed areas and̸or predominantly in men.Furthermore, FEP exhibits a peculiar histopathological architecture, as well as the presence of Merkel cells, which are usually absent in BCCs but found in trichoblastomas.Thus far, FEP has been described as a solitary lesion or in association with Paget's disease in a limited number of case series. However, no studies have been performed to investigate whether this lesion arises as an isolated rare tumor or in patients harboring specific diseases.The aim of our study was the characterization of a consecutive series of FEPs to identify a possible association of this tumor with con...