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Acquired Acrodermatitis enteropathica - an unusual cause of vulva ulceration in a post-operative patient: a case report.
Age Ageing
November 2022
Consultant Dermatologist, King's College Hospital London, SE5 9RS.
Article Synopsis
- Acrodermatitis enteropathica (AE) is a rare disorder that can either be inherited from birth or develop later, characterized by symptoms like skin inflammation around the mouth, diarrhea, skin issues on the extremities, and hair loss.
- The report emphasizes the importance of considering AE as a potential diagnosis in older patients who display mucosal infections or ulcers.
- It details the case of a 68-year-old woman with advanced liver disease who, after a fall resulting in a hip fracture, was found to have persistent mucosal ulcers upon hospital admission.
Vulvar and perineal verrucous changes complicating hidradenitis suppurativa after wide excision: a case and literature review.
Dermatol Online J
June 2020
Department of Dermatology, Duke University Medical Center, Durham, NC.
Poorly controlled and long-standing hidradenitis suppurativa (HS) increases the risk of squamous cell carcinoma (SCC). We report a 54-year-old woman with an over 20-year history of HS, who had previously undergone wide perineal excision with secondary intention healing and presented with a painful verrucous vulvar plaque and proximal non-healing perineal wound. The patient had four perineal scouting biopsies performed and excisional biopsy with no evidence of high-grade dysplasia or carcinoma on histology.
View Article and Find Full Text PDFNon-healing Vulval Ulcer in an Immunocompromised Female due to Concurrent Herpes Simplex Virus and Cytomegalovirus Co-infection Treated Effectively with Valganciclovir.
Indian Dermatol Online J
January 2020
Department of Dermatology, Armed Forces Medical College, Pune, Maharashtra, India.
Pseudoepitheliomatous hyperplasia causing a painful plaque in a HIV-infected female.
Int J STD AIDS
June 2017
1 Pacific Clinic Newcastle, HNE Sexual Health, Newcastle, NSW, Australia.
Dermatological conditions are more common and can present atypically, in human immunodeficiency virus-infected individuals. This case report describes a 22-year-old human immunodeficiency virus-positive Caucasian female who presented with a vulval lesion eight weeks after starting antiretroviral treatment. Clinical examination revealed a 2 cm well-demarcated plaque on the outer aspect of the left labium minus.
View Article and Find Full Text PDFExtramammary Paget's disease of vulva: A rare entity.
Indian J Sex Transm Dis AIDS
January 2017
Department of Dermatology, Shri Ram Murti Smarak Institute of Medical Sciences, Bhojipura, Bareilly, Uttar Pradesh, India.
Extramammary Paget's disease is a rare cutaneous, intraepithelial adenocarcinoma involving primarily the epidermis but occasionally extending into the underlying dermis. The condition typically presents as a red, velvety, pruritic skin rash of the vulva region which closely mimics a multitude of other, more common conditions. As a result, vulvar Paget's disease is frequently misdiagnosed, leading to an often lengthy lag time (an average of about 2-3 years) between the onset of symptoms and diagnosis.
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