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3.
Dermatol Online J ; 18(7): 5, 2012 Jul 15.
Article in English | MEDLINE | ID: mdl-22863627

ABSTRACT

Fibroepithelioma of Pinkus (FEP) is a rare cutaneous neoplasm. Evidence supports classification as a variant of either basal cell carcinoma (BCC) or trichoblastoma. Reports of FEP arising in sites of preceding radiation therapy have been documented in the literature, but the relationship between radiotherapy and the development of FEP has not yet been defined. We report a case of FEP following radiation therapy for testicular cancer.


Subject(s)
Carcinoma, Basal Cell/pathology , Neoplasms, Fibroepithelial/pathology , Neoplasms, Radiation-Induced/pathology , Skin Neoplasms/pathology , Testicular Neoplasms/radiotherapy , Aged, 80 and over , Carcinoma, Basal Cell/etiology , Carcinoma, Basal Cell/surgery , Curettage , Humans , Male , Neoplasms, Fibroepithelial/etiology , Neoplasms, Fibroepithelial/surgery , Neoplasms, Radiation-Induced/etiology , Neoplasms, Radiation-Induced/surgery , Skin Neoplasms/etiology , Skin Neoplasms/surgery , Treatment Outcome
4.
J Cutan Pathol ; 36(8): 906-9, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19586503

ABSTRACT

Lymphedematous fibroepithelial polyps of the penis are lesions that have only recently been described and are frequently associated with condom catheter use. We report an additional case of lymphedematous fibroepithelial polyps of the penis in association with long-term condom catheter use in a 36-year-old man. Local excision showed large polypoid nodules with compact orthohyperkeratosis and mild acanthosis. The stroma was hypercellular with spindled to stellate fibroblasts and occasional multinucleated cells. Proliferation of small linear to slightly arcuate vessels with some superficial dilatation was a prominent feature. Focal expression of smooth muscle actin and desmin was present in the stroma. Lymphedematous fibroepithelial polyps of the penis are rare lesions with only 11 cases previously reported. We present here an additional example of this entity to highlight the differential diagnosis, the association with condom catheter use and to raise awareness for this unusual diagnosis.


Subject(s)
Adenomatous Polyps/pathology , Catheterization/adverse effects , Lymphedema/pathology , Neoplasms, Fibroepithelial/pathology , Penile Neoplasms/pathology , Actins/biosynthesis , Adenomatous Polyps/etiology , Adenomatous Polyps/metabolism , Adult , Desmin/biosynthesis , Gene Expression Regulation , Humans , Lymphedema/etiology , Lymphedema/metabolism , Male , Neoplasm Proteins/biosynthesis , Neoplasms, Fibroepithelial/etiology , Neoplasms, Fibroepithelial/metabolism , Penile Neoplasms/etiology , Penile Neoplasms/metabolism , Time Factors
7.
Pediatr Dev Pathol ; 11(1): 30-4, 2008.
Article in English | MEDLINE | ID: mdl-18237238

ABSTRACT

A distinct group of fibroproliferative polyps of the tongue arising in immunosuppressed children and often associated with chromosomal breakpoints at chromosomes 9p34 or 22q11 was recently described. Based on this finding, we reviewed fibroepithelial polyps arising in nonlingual sites in the pediatric population to investigate a possible relationship with immunosuppression. We identified 8 fibroepithelial polyps arising in 6 immunosuppressed patients (4 males and 2 females, median age 17 years) in a wide range of mucocutaneous sites. Histologic features were identical to the common fibroepithelial polyp, or skin tag, with a variably collagenous fibrovascular core covered by unremarkable squamous epithelium. No viral cytopathic changes were identified in any case. Although cytogenetic studies were not performed on any of the biopsy material, 1 patient had a constitutional deletion of chromosome 22q11. We suggest that there may be a relationship between these polyps and the previously described tongue lesions and that immunosuppression may be an important factor in their pathogenesis.


Subject(s)
Immunosuppression Therapy/adverse effects , Mouth Neoplasms/etiology , Neoplasms, Fibroepithelial/pathology , Skin Neoplasms/etiology , Adolescent , Adult , Child , Chromosome Aberrations , Chromosomes, Human, Pair 22/genetics , Female , Humans , Lip/pathology , Male , Mouth Neoplasms/genetics , Mouth Neoplasms/pathology , Neoplasms, Fibroepithelial/etiology , Neoplasms, Fibroepithelial/genetics , Polyps , Skin/pathology , Skin Neoplasms/pathology
9.
Arch Dermatol ; 142(10): 1318-22, 2006 Oct.
Article in English | MEDLINE | ID: mdl-17043187

ABSTRACT

BACKGROUND: Fibroepithelioma of Pinkus (FeP) is a rare variant of basal cell carcinoma that may clinically mimic a number of benign skin tumors. While the dermoscopic features of basal cell carcinoma have been studied extensively, little is known about the dermoscopic features of FeP. OBSERVATIONS: Retrospective evaluation of clinical records and digital clinical dermoscopic images of 10 histopathologically proved FePs (6 nonpigmented and 4 pigmented) was performed. Clinically, no FeP was correctly identified and, in half of all patients, a clinical differential diagnosis of purely benign skin lesions was made. Dermoscopy enabled the correct diagnosis in 9 of 10 FePs, based on the presence of fine arborizing vessels, either alone or associated with dotted vessels, and white streaks (in 100%, 70%, and 90% of lesions, respectively). In the 4 pigmented FePs, a structureless gray-brown area of pigmentation and variable numbers of gray-blue dots were observed, in addition. CONCLUSIONS: Dermoscopy is helpful in diagnosing FeP and in differentiating this variant of basal cell carcinoma from other benign skin tumors commonly included in the clinical differential diagnosis. This presumes, however, that dermoscopy is used as a first-line examination for all skin lesions, not only for those that are clinically suspect.


Subject(s)
Neoplasms, Fibroepithelial/epidemiology , Neoplasms, Fibroepithelial/pathology , Skin Neoplasms/epidemiology , Skin Neoplasms/pathology , Adult , Aged , Carcinoma, Basal Cell/diagnosis , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/etiology , Carcinoma, Basal Cell/pathology , Dermoscopy/statistics & numerical data , Female , Humans , Italy/epidemiology , Male , Medical Records , Middle Aged , Neoplasms, Fibroepithelial/diagnosis , Neoplasms, Fibroepithelial/etiology , Retrospective Studies , Skin Neoplasms/diagnosis , Skin Neoplasms/etiology
10.
Hinyokika Kiyo ; 47(8): 579-82, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11579600

ABSTRACT

A 14-year-old boy complained of left flank pain. He had been given high-dose corticosteroid therapy for chronic inflammatory demyelinating polyneuropathy (CIDP). Retrograde pyelography revealed irregular defects at the left ureteropelvic junction (UPJ), and ureteroscopy demonstrated ureteral polyp. The polyp was removed and histologically diagnosed as fibroepithelial polyp. Hypercalciuria due to the corticosteroids and bedridden was assumed to have been a causative factor in the stone formation. To our knowledge, this is the first report of a ureteral fibroepithelial polyp in children associated with urolithiasis, and associated with CIDP.


Subject(s)
Methylprednisolone/adverse effects , Neoplasms, Fibroepithelial/etiology , Polyps/etiology , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/complications , Prednisolone/adverse effects , Ureteral Neoplasms/etiology , Urinary Calculi/etiology , Adolescent , Humans , Male , Methylprednisolone/administration & dosage , Polyradiculoneuropathy, Chronic Inflammatory Demyelinating/drug therapy , Prednisolone/administration & dosage
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