A case report of clitoral hood cyst in a pediatric patient with acute lymphoblastic leukemia and a review of the literature

IF 0.7 Q4 SURGERY
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.
小儿急性淋巴细胞白血病阴蒂包囊1例报告及文献复习。
简介和重要性:阴蒂囊肿是女性儿科人群阴蒂肿大的罕见原因,大多数报告的病例与创伤或生殖器切割有关。表皮样亚型是最常见的组织学类型,手术切除通常是首选的治疗方法。这个病例是独一无二的,因为它代表了第一例报道的阴蒂囊肿在儿科患者接受化疗急性淋巴细胞白血病(ALL)。我们强调免疫功能低下患者早期手术干预的重要性,并补充了指导儿科肿瘤学生殖器囊肿管理的有限文献。病例介绍:一名患有ALL的4岁女孩因大剂量甲氨蝶呤化疗而入院。在Foley导尿管插入时,在尿道附近发现一个可移动的、无触痛的阴蒂肿块。由于诊断不确定和免疫抑制状态,手术切除,组织病理学证实为表皮囊肿。化疗延迟了两周以允许愈合,患者完全恢复,随访时没有复发。临床讨论:广泛的鉴别诊断,包括激素和非激素原因,如表皮囊肿,在评估儿童阴蒂肿块时是必不可少的,特别是在复杂情况的患者中。早期识别和及时管理对于避免诊断延误和治疗中断至关重要。结论:这个病例说明了考虑罕见的,非激素的原因,特别是那些免疫功能低下的儿童患者阴蒂肿大的重要性。关键要点包括保持广泛的区别,优先考虑及时的多学科护理,并认识到手术干预何时可以预防并发症并避免化疗延迟。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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