Background: X-linked reticulate pigmentary disorder is a very rare cutaneous condition characterized by different clinical manifestations according to sex.

Methods: We report a 31-year-old woman with X-linked reticulate pigmentary disorder.

Results: On examination, there were multiple, asymptomatic, brownish macules in linear and whorled patterns over the trunk, axillae, groin, and extremities. The woman had not experienced any systemic manifestations involving the gastrointestinal, pulmonary, or ocular systems. Her hair, teeth, and nails were normal on close observation. All laboratory data were within the normal range. A genetic study was not performed.

Conclusions: Although a genetic study was not performed, we believe that our patient can be diagnosed with X-linked reticulate pigmentary disorder according to the clinical and histopathologic findings.

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1365-4632.2010.04102.xDOI Listing

Publication Analysis

Top Keywords

x-linked reticulate
16
reticulate pigmentary
16
pigmentary disorder
12
genetic study
8
x-linked
4
pigmentary
4
disorder female
4
female patient
4
patient background
4
background x-linked
4

Similar Publications

Article Synopsis
  • * A literature review was conducted to develop a user-friendly diagnostic algorithm to help clinicians identify these disorders and determine appropriate genetic testing.
  • * The research included a comprehensive search of databases, resulting in 625 relevant articles that discuss the different diseases and contributed to forming a clear approach for provisional diagnosis based on specific clinical factors.
View Article and Find Full Text PDF

X-Linked Reticulate Pigmentary Disorder.

JAMA Dermatol

December 2023

Department of Dermatology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, State Key Laboratory of Complex Severe and Rare Diseases, National Clinical Research Center for Dermatologic and Immunologic Diseases, Beijing, China.

View Article and Find Full Text PDF

Inherited Reticulate Pigmentary Disorders.

Genes (Basel)

June 2023

Department of Dermatology, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.

Article Synopsis
  • Reticulate pigmentary disorders (RPDs) are skin conditions that can be either inherited or acquired, featuring areas of hyperpigmentation or hypopigmentation.
  • There are several inherited types of RPDs, with varying pigmentation patterns and additional symptoms, including DSH, DUH, and RAK primarily affecting East Asian populations, while DDD is more common in Caucasians.
  • The article examines the different clinical, histological, and genetic characteristics of these inherited RPDs.
View Article and Find Full Text PDF

To quantitatively analyze the number and density of macrophage-like cells (MLCs) at the vitreoretinal interface at macular region in diabetic retinopathy (DR) with and without diabetic macular edema (DME). This cross-sectional study involved 240 eyes of 146 treatment-naïve DR patients, including 151 eyes with DME. The number and density of MLCs were analyzed quantitatively using optical coherence tomography angiography (OCTA) and were compared between DME and non-DME eyes as well as proliferative DR (PDR) and non-PDR (NPDR) eyes.

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!