Hidradenoma papilliferum is a rare tumor that occurs almost exclusively in females on the anogenital area. Rare cases of ectopic (nongenital) hidradenoma papilliferum have been described. The lesions usually present as an asymptomatic slow-growing, red, firm, mobile, well-delimitated nodule that grows for a long time before resection. We describe a case of an 26-year-old man that presented with an enlarging nodule on his right eyelid. The histological findings revealed a hidradenoma papilliferum. So far, among the very few reports of ectopic hidradenoma papilliferum, only a very small number were localized to the eyelid.
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http://dx.doi.org/10.1155/2010/709371 | DOI Listing |
J Med Case Rep
November 2024
Surgery Department, Guelmim Military Hospital Moulay El Hassan General, Guelmim, Morocco.
Introduction: Syringocystadenocarcinoma papilliferum is an extremely rare malignant adnexal tumor that typically arises from a papilliferous syringocystadenoma (World Health Organization classification of skin tumors, 2018.). This tumor predominantly occurs in the cephalic region.
View Article and Find Full Text PDFAm J Surg Pathol
January 2025
Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX.
Sialadenoma papilliferum is a tumor characterized by surface papillary projections and glandular/microcystic proliferation at the lesion base. Cases in which surface involvement is absent have been termed "sialadenoma papilliferum-like intraductal papillary tumor." Similar tumors that are present in the mandible have been termed "tubulopapillary hidradenoma-like tumor of the mandible.
View Article and Find Full Text PDFAm J Dermatopathol
December 2024
Department of Anatomical Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX; and.
J Clin Ultrasound
January 2025
Department of Ultrasound, Shaoxing People's Hospital, Shaoxing, China.
Hidradenoma papilliferum is a rare superficial mass with distinct ultrasonic features. It originates from mammary structures and is commonly observed in the anogenital region of women. We report a hidradenoma papilliferum with clear ultrasound images which have never be described before.
View Article and Find Full Text PDFLaryngoscope
February 2025
Department of Otorhinolaryngology, Sengkang General Hospital, Singapore.
Benign cutaneous apocrine sweat gland adenomas in the nose are rare. We present the novel case of a nasal ala cutaneous sweat gland lesion. A 43-year-old male presents with a one year history of a right nostril mass with intermittent clear discharge, triggered by periods of hot weather and increased humidity.
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