Hyperpigmentation coexisted with hypopigmentation is classified in this chapter⁚ familial progressive hypo- and hyperpigmentation, cutis tricolor parvimaculata, reticulate genital pigmentation associated with localized depigmentation, pigmentary twin spotting, acromelanosis albo-punctata, acquired brachial cutaneous dyschromatosis, graft-versus-host disease, leopard skin eruption, superficial ․․․
Definition and Classification
Progressive acromelanosis is an inherited pigment disorder characterized by dark pigmentation on the fingers and toes that may spread to other areas of the body․ It falls under various classifications, including familial progressive hypo- and hyperpigmentation, cutis tricolor parvimaculata, and other pigmentary disorders․
Clinical Presentation and Features
Features of progressive acromelanosis include dark pigmentation on the fingers and toes with potential spread to other body areas, notably the neck, face, and limbs․
Patients with progressive acromelanosis may exhibit dark pigmentation on the fingers and toes that can extend to other body areas, such as the neck, face, and limbs․ The condition can present as dark patches on the skin, often starting at the extremities․
Progression of the Disease
Progressive acromelanosis typically begins with dark pigmentation on the fingers and toes and may gradually spread to involve other parts of the body, such as the neck, face, and limbs․ The condition may show variable progression in affected individuals over time․
Signs and Symptoms
Dark pigmentation on fingers and toes is a common sign of progressive acromelanosis, with potential extension to other body areas over time․
In Progressive Acromelanosis, SNOMED CT classifies it as Acromelanosis (239089006)․ Review classifications for Acromelanosis in Orphanet for more detailed information․
Case Studies and Reported Cases
Reported cases include a 2-year-old Puerto Rican boy and a Japanese child showing distinctive pigmentation patterns on the fingers․
SNOMED CT and Orphanet Classifications
Research shows that Progressive Acromelanosis is classified under SNOMED CT as Acromelanosis (239089006)․ For more detailed classifications, refer to Orphanet’s guidelines․
Furuya and Mishima’s Reports
Cases reported by Furuya and Mishima detailed unique pigment patterns in a 2-year-old Puerto Rican boy and a Japanese child, showcasing distinctive features of progressive acromelanosis․
Treatment and Management
Treatment for progressive acromelanosis aims to manage the symptoms and may involve topical medications and phototherapy to help improve skin pigmentation․
Current Approaches
The current approaches for treating progressive acromelanosis may involve topical medications and phototherapy to manage skin pigmentation and improve symptoms․ Individualized treatment plans are recommended based on the patient’s specific needs․
Research and Resources
PubMed articles and medical literature provide insights into the progressive acromelanosis condition, offering valuable resources for understanding the disorder and its management․
PubMed Articles and Medical Literature
Resources like PubMed provide valuable insights into progressive acromelanosis through articles and literature, aiding in better understanding and management of the condition․
Resources for Further Information
Additional resources on progressive acromelanosis can be found, providing more detailed information on the condition and associated symptoms․ These resources may contain scientific language that helps in understanding the disorder․
Conclusion
As evidenced by reported cases and ongoing research, understanding the intricacies of progressive acromelanosis is vital for accurate diagnosis and effective management․ Through resources like PubMed and medical literature, further insights into this condition can be gained, aiding in improved patient care and outcomes․