Zeeshan Zubair , Mary B. Ross , Janeen Buonaccorsi , Ali El Ghazzaoui
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Abstract
Introduction and importance
Clitoral cysts are a rare cause of clitoromegaly in the female pediatric population, with the majority of reported cases linked to trauma or genital mutilation. The epidermoid subtype is the most common histological type, and surgical excision is generally the preferred treatment. This case is unique as it represents the first reported instance of a clitoral cyst in a pediatric patient undergoing chemotherapy for Acute Lymphoblastic Leukemia (ALL). We highlight the importance of early surgical intervention in immunocompromised patients and add to the limited literature guiding management of genital cysts in pediatric oncology.
Presentation of case
A 4-year-old girl with ALL was admitted for high-dose methotrexate chemotherapy. During Foley catheter insertion, a mobile, non-tender clitoral mass was found near the urethra. Surgical excision was performed due to diagnostic uncertainty and immunosuppressed status, and histopathology confirmed an epidermal cyst. Chemotherapy was delayed for two weeks to allow healing, and the patient recovered fully, with no recurrence at follow-up.
Clinical discussion
A broad differential diagnosis, including hormonal and non-hormonal causes like epidermal cysts, is essential when evaluating pediatric clitoral masses, particularly in patients with complex conditions. Early recognition and timely management are critical to avoid diagnostic delays and treatment interruptions.
Conclusion
This case illustrates the importance of considering rare, non-hormonal causes of clitoromegaly in pediatric patients, particularly those with immunocompromised states. Key takeaways include maintaining a broad differential, prioritizing timely multidisciplinary care, and recognizing when surgical intervention may prevent complications and avoid chemotherapy delays.