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Digital Papillary Adenocarcinoma at the Site of 5 Years of Recurrent Paronychia: Case Report and Literature Review.
Case Rep Oncol Med
December 2024
Hand and Upper Extremity Surgery, Barrington Orthopedic Specialists, Schaumburg, Illinois, USA.
Article Synopsis
- Digital papillary adenocarcinoma (DPA) is a rare and often misdiagnosed malignant tumor, commonly mistaken for benign conditions, leading to delayed diagnosis and treatment.
- A 57-year-old man with recurrent finger infections was ultimately diagnosed with DPA after a surgical evaluation and biopsy revealed both infection and the tumor, necessitating surgical removal.
- Accurate diagnosis is vital due to the tumor's tendency for recurrence and metastasis, particularly to the lungs and lymph nodes, and current treatment primarily involves surgical excision with focus on achieving negative margins.
Late-Onset Eruptive Clear Cell Syringoma: A Case Report and Literature Review.
Clin Cosmet Investig Dermatol
December 2024
Division of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Eruptive syringoma, a rare subtype of syringoma, is a benign adnexal tumor arising from the eccrine sweat glands. It is characterized by multiple asymptomatic, flat-topped, brown-pigmented papules. The disease typically occurs during adolescence and young adulthood.
View Article and Find Full Text PDFFamiliar cylindromatosis in a Colombian family caused by a mutation in CYLD.
Ecancermedicalscience
September 2024
Department of Human Genetics, Fundación Valle del Lili, Cali 760026, Colombia.
Article Synopsis
- The CYLD cutaneous syndrome leads to multiple skin tumors like cylindromas and spiradenomas, primarily affecting the face and head, with more frequent occurrence in women.
- A Colombian family spanning three generations showcased early onset of this syndrome, confirmed by genetic analysis identifying a specific variant in the CYLD gene.
- Understanding the genetic and environmental factors behind the syndrome is vital for developing better treatments and enhancing patient care.
Syringocystadenoma Papilliferum-Like Features in Poroma: An Unusual Morphologic Pattern of Poroma or True Synchronous Occurrence of 2 Distinct Neoplasms?
Am J Dermatopathol
December 2024
Department of Anatomical Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX; and.
Article Synopsis
- Poromas are benign skin tumors originating from sweat glands, often appearing as pink or red bumps primarily on hairless areas like palms and soles.
- A 70-year-old woman had a poroma on her abdomen that showed some histological features similar to another neoplasm, syringocystadenoma papilliferum (SCAP), but lacked certain defining characteristics of SCAP.
- This case, showing rare SCAP-like features within a poroma, emphasizes the need for careful diagnosis as it may simply reflect a variation of poromas, rather than representing two different tumors.
Article Synopsis
- Syringocystadenoma papilliferum is a rare benign tumor linked to sweat glands, often appearing as a slow-growing skin lesion.
- A 30-year-old woman had a 10-year history of an asymptomatic scalp nodule that developed after head trauma, which was examined and found to be 3 mm in size with specific features.
- A biopsy confirmed the diagnosis, and the patient successfully had the tumor removed through surgery.
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