Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/15251
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dc.contributor.authorKrsteska, Blagicaen_US
dc.contributor.authorIlievski, Boroen_US
dc.contributor.authorJovanovikj, Rubensen_US
dc.contributor.authorRistovski, Gligoren_US
dc.contributor.authorKostadinova Kunovska, Slavicaen_US
dc.date.accessioned2021-10-18T09:16:30Z-
dc.date.available2021-10-18T09:16:30Z-
dc.date.issued2021-08-31-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/15251-
dc.description.abstractBackground and objective: Primary melanomas of breast and carcinomas with pigment rich melanocytes are well known entities. Melanoma in nipple-areola complex is extremely rare and in differential diagnosis must be distinguished between Paget disease, melanoma from extramammary sites and other invasive carcinomas. We present a case of invasive papillary carcinoma of male nipple with melanin laden tumor cells. Methods: A 71-year old male patient presents with lobulated grayish tumor of the right nipple measuring 2x1, 3 cm elevated above the skin surface 1cm. The lesion was surgically removed with skin excision 0,7x 0,5x 0,5cm. The specimen was formalin-fixed and paraffin-embedded, routinely stained with HE. Additional immunohistochemical analysis was performed with CK7, ER, SMA, S-100, and Melan A. Results: The gross specimen on cut sections revealed solid white to brown tumor, well demarcated at the base and ulceration of overlying epidermis. Histomorphology of the sections showed papillary structures with tall columnar cells overlying fibrovascular cores, as well as micropapillary formations. There were areas of solid and cribriform growth pattern. Microcalcifications were diffusely present. There were accumulated melanophages in subepithelial tissue and melanin granules were also found in tumor cells. Immunohistochemical analysis showed that tumor cells were positive for CK7, with strong and diffuse nuclear stain for ER, with complete absence of myoepithelial cell on SMA stain. Melan A and S-100 were negative. Although rare, a diagnosis of pigmented papillary carcinoma was made. Conclusion: Pigmented carcinomas of breast are rare. When they are localized in areolar region the diagnosis should be carefully made to exclude lesions with melanocytic differentiation. The pigmentation should be considered also as a result by proximity to epidermis. The distinction between benign and malignant papillary lesions is quite difficult in most cases. The prognosis of patients with papillary carcinoma is relatively favorable.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofVirchows Archiven_US
dc.subjectMelanomaen_US
dc.subjectPigmenteden_US
dc.subjectPapillary carcinomaen_US
dc.subjectBreasten_US
dc.titlePigmented papillary carcinoma of male nipple mimicking melanomaen_US
dc.typeProceeding articleen_US
dc.relation.conference33rd European Congress of Pathologyen_US
dc.identifier.doi10.1007/s00428-021-03157-8-
item.grantfulltextopen-
item.fulltextWith Fulltext-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Conference papers
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