Porokeratosis of Mibelli and HIV-infection.

Int J Dermatol

Department of Dermatology, Hospital General de Agudos, Juan A. Fernández, School of Medicine, University of Buenos Aires, Argentina.

Published: June 1996

Background: The exacerbation of porokeratosis of Mibelli associated with inmunosuppression has been well documented.

Materials And Methods: We describe the clinical and histologic data of three cases of HIV-infected patients, who developed porokeratosis following HIV-contact.

Results: The three reported patients were found to have the clinical and histologic features of porokeratosis of Mibelli. Either the exacerbation or development of the disease followed HIV infection.

Conclusion: Although porokeratosis is not a disease indicative of AIDS, its flare-up or its presence in HIV-infected patients may serve as a marker of inmunodeficiency.

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1365-4362.1996.tb03019.xDOI Listing

Publication Analysis

Top Keywords

porokeratosis mibelli
12
clinical histologic
8
hiv-infected patients
8
porokeratosis
5
mibelli hiv-infection
4
hiv-infection background
4
background exacerbation
4
exacerbation porokeratosis
4
mibelli associated
4
associated inmunosuppression
4

Similar Publications

Porokeratosis Ptychotropica.

J Cutan Med Surg

January 2025

Department of Dermatology, Beijing Hospital, National Center of Gerontology; Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, China.

View Article and Find Full Text PDF

Follicular porokeratosis (FPK) is a rare subtype of porokeratosis. Follicular porokeratosis mainly occurs in men and may be localized or diffuse. Involvement of the scalp is rarely reported, and we found only one case of alopecia due to scalp FPK.

View Article and Find Full Text PDF

Porokeratosis is a condition characterized by abnormal epidermal keratinization with a unique morphology of papules or plaques surrounded by a thread-like border of scale corresponding to the cornoid lamella on histology. Many established subtypes have been described; however, genitogluteal porokeratosis is a rare entity. We present the case of a 58-year-old male with pruritic reddish lesions affecting the genitals and thighs, diagnosed with genital porokeratosis.

View Article and Find Full Text PDF

The term autoinflammatory keratinization diseases (AIKDs) was recently proposed as a unifying concept for diseases characterized by inflammation in the epidermis and upper dermis which leads to hyperkeratosis, caused by genetic perturbations of the innate immune system. We present a case of a patient with hidradenitis suppurativa and porokeratosis, two AIKDs, followed by a review of these conditions as well as other AIKDs. This case was distinguished by hypertrophic porokeratoses involving cystic hair follicles, showing histopathologic features of both conditions within single biopsy specimens.

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!