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Peri-clitoral Epidermal Inclusion Cyst as Initial Presentation of Lichen Sclerosus in a Pediatric Patient
Emily Huebner1, Kate Debiec2, Angela Hernandez2
1University of Washington School of Medicine, Department of Obstetrics and Gynecology, Seattle, Washington; Swedish Medical Center, Department of Obstetrics and Gynecology, Seattle, Washington.
Insights
Lichen sclerosus (LS) can cause vulvar masses in children. This case report describes a peri-clitoral epidermal inclusion cyst in a 5-year-old, potentially linked to LS inflammation and itching.
Area of Science:
- Dermatology
- Pediatric Surgery
- Gynecology
Background:
- Lichen sclerosus (LS) is a chronic inflammatory skin condition affecting the vulva and anogenital region, characterized by itching and hypopigmentation.
- LS typically presents with skin changes, but a peri-clitoral mass has not been previously documented.
Observation:
- A 5-year-old girl presented with vulvar itching and a homogenous mass on ultrasound, initially suspected to be clitoromegaly.
- Clinical examination revealed a soft, mobile, peri-clitoral mass with surrounding hypopigmentation consistent with LS.
- Surgical excision of the mass was performed, with pathology confirming an epidermal inclusion cyst.
Findings:
- The peri-clitoral mass was identified as an epidermal inclusion cyst.
- The patient's symptoms resolved after surgical excision and initiation of topical steroids for LS.
Implications:
- This case suggests that chronic inflammation and pruritus associated with Lichen sclerosus may lead to the development of peri-clitoral epidermal inclusion cysts in pediatric patients.
- Further investigation is warranted for clitoromegaly without hormonal causes to explore potential links to inflammatory dermatoses like LS.
Background:
Lichen sclerosus (LS) is a chronic inflammatory disorder, presenting with pruritis and hypopigmentation of the vulvar and anogenital skin. LS presenting as a peri-clitoral mass has not been previously described.
Case:
A 5-year-old patient with vulvar pruritis and ultrasound showing a homogenous mass was referred for suspected clitoromegaly with normal labs. Examination demonstrated a prepubertal patient with a mobile, soft, peri-clitoral mass and surrounding hypopigmentation consistent with LS. The cyst was excised surgically; pathology revealed an epidermal inclusion cyst. Postoperatively, she began using topical steroids for LS with symptom resolution.
Conclusion:
Thorough workup of clitoromegaly negative for hormonal causes requires further investigation to determine an alternative etiology of the mass. We suspect that inflammatory changes of LS and pruritus resulted in the peri-clitoral inclusion cyst.
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