{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,28]],"date-time":"2025-10-28T05:49:10Z","timestamp":1761630550148,"version":"3.40.5"},"reference-count":14,"publisher":"FapUNIFESP (SciELO)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["An. Bras. Dermatol."],"published-print":{"date-parts":[[2010,4]]},"abstract":"<jats:p>As poroceratoses compreendem um grupo de doen\u00e7as da queratiniza\u00e7\u00e3o epid\u00e9rmica, heredit\u00e1rias ou adquiridas, caracterizadas histologicamente pela presen\u00e7a de lamela cornoide. A variante cl\u00ednica designada por poroceratose superficial disseminada tem sido descrita na literatura, associada a estados de imunossupress\u00e3o, como transplanta\u00e7\u00e3o de \u00f3rg\u00e3os, terap\u00eauticas imunossupressoras e infec\u00e7\u00f5es. A sua associa\u00e7\u00e3o a neoplasias s\u00f3lidas foi raramente descrita na literatura, estando publicados apenas 5 casos. Descrevemos o caso cl\u00ednico de um paciente que desenvolveu, subitamente, les\u00f5es de poroceratose superficial disseminada, concomitantemente ao diagn\u00f3stico de um colangiocarcinoma.<\/jats:p>","DOI":"10.1590\/s0365-05962010000200016","type":"journal-article","created":{"date-parts":[[2010,5,30]],"date-time":"2010-05-30T19:44:23Z","timestamp":1275248663000},"page":"229-231","source":"Crossref","is-referenced-by-count":11,"title":["Poroceratose superficial disseminada num doente com colangiocarcinoma: manifesta\u00e7\u00e3o paraneopl\u00e1sica?"],"prefix":"10.1590","volume":"85","author":[{"given":"Tiago","family":"Torres","sequence":"first","affiliation":[{"name":"Hospital de Santo Ant\u00f3nio,  Portugal"}]},{"given":"Gl\u00f3ria Cunha","family":"Velho","sequence":"additional","affiliation":[{"name":"Universidade do Porto; Hospital de Santo Ant\u00f3nio,  Portugal"}]},{"given":"Manuela","family":"Selores","sequence":"additional","affiliation":[{"name":"Universidade do Porto; 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