Download full-text PDF

Source
http://dx.doi.org/10.1111/1346-8138.14183DOI Listing

Publication Analysis

Top Keywords

case warty
4
warty dyskeratoma
4
dyskeratoma anterior
4
anterior chest
4
chest relationship
4
relationship dermoscopic
4
dermoscopic histopathological
4
histopathological findings
4
case
1
dyskeratoma
1

Similar Publications

Article Synopsis
  • Trichilemmomas are rare, benign tumors that develop from hair follicles and appear as warty nodules made up of clear and intermediate cells.
  • A 34-year-old Indian man's scalp lesion was initially misdiagnosed as a pyogenic granuloma due to its bleeding tendency.
  • After surgical removal and histopathological analysis confirmed it as a trichilemmoma, the patient has been monitored for six months without any recurrence.
View Article and Find Full Text PDF

Acquired epidermodysplasia verruciformis is a rare condition, secondary to a state of acquired immunosuppression and is characterized by a susceptibility to infection by human papillomavirus of the beta genus, which carries an increased risk of developing non-melanoma skin cancer. We report the case of a 39-year-old woman receiving a kidney transplant, treated with prednisone and tacrolimus, who after starting immunosuppressive therapy developed papules and warty plaques in the inguinal region. A skin biopsy was performed that was consistent with epidermodysplasia verruciformis, so it was decided to adjust immunosuppressive therapy to everolimus, which achieved a reduction in lesions.

View Article and Find Full Text PDF
Article Synopsis
  • The report discusses a unique case of invasive acantholytic anaplastic extramammary Paget disease (AAEMPD) found in an 87-year-old woman after multiple treatments for a persistent vulvar lesion.
  • Microscopic examination revealed unusual features such as intraepidermal acantholysis and atypical cell growth, raising concerns of both EMPD and invasive carcinoma.
  • Accurate diagnosis of AAEMPD is essential as it has different treatment strategies compared to other potential conditions, highlighting the need for careful assessment in clinical practice.
View Article and Find Full Text PDF
Article Synopsis
  • The case report details a rare instance of vulvar lymphangioma in a 29-year-old woman with May-Thurner syndrome (MTS), a vascular condition causing left iliac vein obstruction.
  • Lymphangioma, a benign lesion characterized by abnormal lymphatic channel dilation, is noted to be rare in the vulvar area.
  • The report aims to highlight this unique association between vulvar lymphangioma and MTS, discussing the clinical aspects, causes, and potential connections between the two conditions.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!