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Standardized surgical strategy for the treatment of preauricular sinus to reduce recurrence.
Arch Craniofac Surg
October 2023
Department of Plastic and Reconstructive Surgery, Daegu Fatima Hospital, Daegu, Korea.
Background: Preauricular sinus (PAS) is a common congenital anomaly, and complete excision is recommended to prevent recurrence. However, PAS has a high recurrence rate as a result of incomplete removal due to the high variability of the sinus ramifications, making its treatment challenging. In this study, we standardized the surgical procedure to reduce the complications and recurrence rate and compared the postoperative results between the non-standardized and the standardized groups.
View Article and Find Full Text PDFPorocarcinoma of the Ear Found to Have Cutaneous In-Transit and Regional Nodal Metastasis: Implications for Management and Importance of Clinical Examination.
Dermatol Surg
January 2024
Department of Dermatology, Lahey Hospital and Medical Center, Burlington, MA.
Eccrine poroma of the eyelid.
Orbit
August 2024
Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
Clinical and histopathologic case of an eyelid eccrine poroma, a benign adnexal neoplasm rarely found on the periorbital skin.
View Article and Find Full Text PDFBasal Cell Carcinoma and Eccrine Porocarcinoma of the Eyelid.
Ophthalmic Plast Reconstr Surg
April 2021
Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, Miami, Florida.
An 81-year-old woman presented with a progressively enlarging indurated, firm lesion encompassing one-third of the left upper eyelid. Four years prior, a similar lesion at that same site had been excised and diagnosed as a basal cell carcinoma. The patient underwent a full-thickness excision of the lesion with frozen section, cryotherapy, and reconstruction.
View Article and Find Full Text PDFYAP1-NUTM1 Gene Fusion in Porocarcinoma of the External Auditory Canal.
Head Neck Pathol
December 2020
Institute of Pathology and Molecular Diagnostics, University Hospital, Augsburg, Germany.
Gene fusions involving the NUTM1 gene (NUT) represent defining genetic markers of a highly aggressive carcinoma type with predilection for the midline structures of children and young adults, hence the original description as NUT midline carcinoma. Recent studies have increasingly documented involvement of the NUTM1 gene in the pathogenesis of other entities as well. We herein describe two cases of auditory canal carcinomas with features of porocarcinoma, both harboring a newly described YAP1-NUTM1 gene fusion.
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