Related Experiment Videos
Chromhidrosis: a rare diagnosis requiring clinicopathologic correlation
Ange Wang1, Ashley Wysong, Kristin M Nord
1*Department of Dermatology, Stanford University School of Medicine, Stanford, CA; †Department of Dermatology, Veterans Affairs Palo Alto Healthcare System, Palo Alto, CA; and ‡Department of Pathology, Veterans Affairs Palo Alto Healthcare System, Palo Alto, CA.
Chromhidrosis, a rare disorder causing colored sweat, is detailed in this case of a man with black cheek secretions. This report highlights a unique presentation of this condition in adult males.
Area of Science:
- Dermatology
- Histopathology
- Rare Diseases
Background:
- Chromhidrosis is a rare disorder characterized by colored sweat secretions.
- It typically affects the malar cheeks, axilla, or areolar regions.
- Histological findings include ectopic apocrine glands and lipofuscin pigments.
Observation:
- This case report details a 26-year-old man with a 2-3 year history of black secretions on his malar cheeks.
- Secretions were noted during exertion or when squeezing the cheeks.
- A biopsy confirmed histopathologic features consistent with chromhidrosis.
Findings:
- The patient presented with bilateral malar cheek black secretions.
- Histopathology confirmed chromhidrosis via H&E staining and UV fluorescence.
- This is the second reported case of chromhidrosis in an adult male.
Implications:
- This case represents the first report of an adult male with black malar cheek secretions due to chromhidrosis.
- It expands the known clinical spectrum of chromhidrosis.
- Further research into the specific mechanisms and triggers of chromhidrosis in males is warranted.
Related Concept Videos
Accessory Structures of the Skin: Sweat Glands
Sweat glands are classified as merocrine glands; that is, the secretions are excreted by exocytosis through a duct without affecting the cells of the gland. There...
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Hypertension III: Clinical Manifestations and Diagnostic Studies
Hyperthyroidism I: Introduction
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Cushing Syndrome I: Introduction