Poroma ecrino pigmentado en region abdominal, una rara presentacion.
Herein, we present a case of a 56-year-old female with a pigmented and painful nodule with progressive growth in the abdominal region with 15-year evolution, which presented easy bleeding in the last month prior to consultation. Upon physical exam, a hyperpigmented and angiomatous pedunculated nodule was found with hyperkeratotic surface (Fig. 1).
The following were considered as presumptive diagnoses: irritated seborrheic keratosis, epithelialized pyogenic granuloma, inflamed intradermal nevus, and nodular melanoma. A skin excision biopsy was carried out, whose report was a dermal tumor mass from the lower portion of the epidermis, well de fined, formed by small cuboidal cells without atypia, arranged in well-defined bands that anastomose without barricade, with pigmented areas and few dilated ducts, which are in contact with the resection margins, compatible with eccrine poroma (Fig. 2). Immunohistochemistry was also performed, highlighting Carcinoembryonic Antigen (CEA) with elongated cells that line the cavities that support glandular differentiation. S100 staining was observed in the dendritic cells and melanocytes in the thickness of the cell proliferation (Fig. 2).
The patient attended clinical controls post intervention, with out lesion recurrence.
Eccrine poroma is a benign adnexal tumor, of rare occurrence, with an incidence of 0.001 to 0.008%, first reported by Pinkus in 1956 (1). It originates as from the epithelium of the intra-epidermal portion of the eccrine duct.
It typically appears as a papule or solitary nodule, euchromatic or red in the sole or lateral border of the feet, corresponding to 2/3 of the cases; as with other eccrine gland tumors, a pigmented variant of rare presentation exists (2,3) other sites affected are: the distal extremities, palms, and fingers, and less likely in the forearms, eyelids, thorax, scalp, external auditory canal, hip, gluteus, and abdomen (4-9).
Melanocytes and melanin are rare in eccrine poroma and two hypotheses are posed regarding its presence originating the pigmentation: the first is that it comes from melanocytes present in cell primordia of eccrine ducts during the 14th week of gestation that were not eliminated during the maturity process; the other hypothesis is that it comes from epidermal melanocytes (9).
This benign tumor has a favorable prognosis, without recurrence after complete resection and low risk of malignancy (1).
A case is presented of a patient diagnosed with pigmented eccrine poroma on abdominal skin, of unusual presentation and location, with only one case found in the literature (10).
Conflict of interest
The authors declare having no conflict of interest regarding this case
Received Sep 7 2011
Received in revised form Oct 12 2011
Accepted Feb 2 2012
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(9.) Pechere M, Roten S, Piletta P, Harms M, Krischer J. Pigmented eccrine poroma. Ann Dermatol Venereol. 1998; 125:281.
(10.) Hu SC, Chen GS, Wu CS, Chai CY, Chen WT, Lan CC. Pigmented eccrine poromas: expression of melanocyte stimulating cytokines by tumor cells does not always result in melanocyte colonization. J Eur Acad Dermatol Venereol.2008; 22:303-10.
Cardenas, Monica Lorena [a]; Diaz, Claudia Juliana [a]; Rueda Plata, Ricardo [b]
[a] School of Dermatology and Dermatological Surgery, Department of Internal Medicine, Faculty of Health, Universidad del Valle, Cali, Colombia.
[b] Hospital Universitario del Valle, Department of Clinical Pathology, Cali, Colombia.
* Corresponding Author.
E-mail Address :monilorena @hotmail.com(Cardenas ML) firstname.lastname@example.org (Diaz CJ) email@example.com (RuedaR)
Cardenas ML, Diaz CJ, Rueda Plata R. Pigmented Eccrine Poroma in abdominal region, a rarepresentation.Colomb.Med. 2013; 44(2): 115-7
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|Title Annotation:||articulo en ingles|
|Author:||Cardenas, Monica Lorena; Diaz, Claudia Juliana; Rueda Plata, Ricardo|
|Date:||Apr 1, 2013|
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