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Comprehensive Treatment and Gene Analysis of a Male Patient with Follicular Occlusion Tetrad with Fordyce Granules
Boce Liu1, Wenjing Wang1, Jianhai Bi2
1Department of Plastic Surgery, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, People's Republic of China.
Abstract:
Follicular occlusion tetrad (FOT) is a chronic inflammatory skin disease that seriously affects patients' quality of life. At present, there is no standard treatment plan for FOT. We report the case of a 50-year-old male patient diagnosed as having FOT with Fordyce granules and type 2 diabetes mellitus. During hospitalization, the patient received comprehensive and systematic treatment. The patient healed well after surgery and the 10-month follow-up revealed no recurrence. We found eight gene mutations by whole-exome sequencing (WES) of the patient's peripheral blood.
Insights
Follicular occlusion tetrad (FOT) is a chronic skin disease with no standard treatment. This case study details successful surgical management and identifies eight gene mutations in a patient with FOT, Fordyce granules, and diabetes.
Area of Science:
- Dermatology
- Genetics
- Surgical Oncology
Background:
- Follicular occlusion tetrad (FOT) presents a significant challenge due to the lack of standardized treatment protocols.
- Chronic inflammatory skin conditions like FOT can severely impair a patient's quality of life.
Observation:
- A 50-year-old male patient with FOT, Fordyce granules, and type 2 diabetes mellitus was treated comprehensively during hospitalization.
- The patient underwent surgical intervention for FOT.
Findings:
- Successful surgical treatment led to complete healing of FOT.
- A 10-month follow-up confirmed no recurrence of the condition.
- Whole-exome sequencing (WES) identified eight novel gene mutations in the patient's peripheral blood, potentially linked to FOT pathogenesis.
Implications:
- This case highlights the efficacy of surgical management for FOT.
- The identified gene mutations offer potential targets for future research into FOT etiology and personalized treatment strategies.
- Further investigation into the identified mutations could advance understanding and treatment of rare dermatological disorders.
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