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Synchronous Primary Perianal Paget's Disease and Rectal Adenocarcinoma: Report of a Hitherto Undescribed PhenomenonDepartment of Pathology, The Johns Hopkins Medical Institutions, Baltimore, Maryland, Department of Oncology, The Johns Hopkins Medical Institutions, Baltimore, Maryland
Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, Maryland, pargani{at}jhmi.edu Perianal Paget's disease is rare. It usually represents intraepidermal extension of an invasive carcinoma from an adjacent internal organ, but some cases represent primary intraepithelial cutaneous apocrine adenocarcinomas. Here, we report a unique case, which we interpret as synchronous primary perianal Paget's disease and lower rectal adenocarcinoma. Immunohistochemical stains demonstrated that the Paget's cells were CK7+/ CK20–/GCDFP+, whereas the rectal adenocarcinoma was CK7+(variable)/CK20+/GCDFP –. This discordant immunoprofile supported our impression that the Paget's disease in this patient was of cutaneous apocrine origin rather than a pagetoid extension from the patient's nearby rectal adenocarcinoma—to our knowledge a hitherto undocumented occurrence.
Key Words: primary Paget's disease perianal rectal adenocarcinoma
This version was published on February
1, 2009 International Journal of Surgical Pathology, Vol. 17, No. 1,
42-45 (2009) |
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