Cesar E. Larancuent , Mandolin Ziadie , Noor Kassira
{"title":"Hepatic epidermoid cyst in a pediatric patient: A case report","authors":"Cesar E. Larancuent , Mandolin Ziadie , Noor Kassira","doi":"10.1016/j.epsc.2024.102796","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>Hepatic epidermoid cysts are uncommon benign liver lesions that infrequently manifest in pediatric populations. Out of the limited reported cases, only 11 are pediatric. Despite their rarity, their potential for various clinical presentations necessitates careful examination and understanding.</p></div><div><h3>Case presentation</h3><p>A 10-year-old female with a history of constipation presented with persistent abdominal pain. Initial suspicions, influenced by her travel history to Dubai and interactions with camels and dolphins, led to considerations of infectious etiologies like echinococcosis. Imaging revealed a complex cystic mass in the liver's right lobe, measuring 4.5 x 5.2 × 6.0 cm. Despite a range of diagnostic efforts, including imaging with ultrasound and MRI as well as infectious disease and gastroenterology consults, the cyst's nature remained ambiguous. After interventional radiology (IR) drainage, symptoms continued and the cyst remained visible on imaging, but cytology of the fluid revealed it to be a benign epidermoid cyst. Surgical intervention, specifically a laparoscopic deroofing, was performed, resulting in symptom relief and prevention of potential future complications. Six months post-surgery, no further dominant cyst was present.</p></div><div><h3>Conclusion</h3><p>This case accentuates the diagnostic complexities surrounding hepatic epidermoid cysts in pediatric patients. A multidisciplinary approach, along with surgical intervention, proved instrumental in diagnosing and managing this rare condition. It reinforces the importance of careful examination and collaboration in managing atypical pediatric liver conditions.</p></div>","PeriodicalId":45641,"journal":{"name":"Journal of Pediatric Surgery Case Reports","volume":null,"pages":null},"PeriodicalIF":0.2000,"publicationDate":"2024-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213576624000241/pdfft?md5=77e5b925b8150596eac0940f00c1e932&pid=1-s2.0-S2213576624000241-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213576624000241","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
Hepatic epidermoid cysts are uncommon benign liver lesions that infrequently manifest in pediatric populations. Out of the limited reported cases, only 11 are pediatric. Despite their rarity, their potential for various clinical presentations necessitates careful examination and understanding.
Case presentation
A 10-year-old female with a history of constipation presented with persistent abdominal pain. Initial suspicions, influenced by her travel history to Dubai and interactions with camels and dolphins, led to considerations of infectious etiologies like echinococcosis. Imaging revealed a complex cystic mass in the liver's right lobe, measuring 4.5 x 5.2 × 6.0 cm. Despite a range of diagnostic efforts, including imaging with ultrasound and MRI as well as infectious disease and gastroenterology consults, the cyst's nature remained ambiguous. After interventional radiology (IR) drainage, symptoms continued and the cyst remained visible on imaging, but cytology of the fluid revealed it to be a benign epidermoid cyst. Surgical intervention, specifically a laparoscopic deroofing, was performed, resulting in symptom relief and prevention of potential future complications. Six months post-surgery, no further dominant cyst was present.
Conclusion
This case accentuates the diagnostic complexities surrounding hepatic epidermoid cysts in pediatric patients. A multidisciplinary approach, along with surgical intervention, proved instrumental in diagnosing and managing this rare condition. It reinforces the importance of careful examination and collaboration in managing atypical pediatric liver conditions.
导言肝表皮样囊肿是一种不常见的肝脏良性病变,很少发生在儿童身上。在有限的报道病例中,仅有 11 例为儿科病例。尽管肝表皮样囊肿非常罕见,但其潜在的各种临床表现却需要仔细检查和了解。由于她曾到迪拜旅行,并与骆驼和海豚有过接触,最初怀疑是感染性病因,如棘球蚴病。影像学检查发现肝脏右叶有一个复杂的囊性肿块,大小为 4.5 x 5.2 x 6.0 厘米。尽管进行了一系列诊断,包括超声波和核磁共振成像以及传染病和消化内科会诊,但囊肿的性质仍然不明确。经介入放射学(IR)引流后,症状仍在持续,囊肿在影像学上仍清晰可见,但液体的细胞学检查显示这是一个良性表皮样囊肿。经过手术治疗,特别是腹腔镜下切除术,症状得到缓解,并避免了今后可能出现的并发症。结论:该病例凸显了儿科肝表皮样囊肿诊断的复杂性。事实证明,多学科方法和手术干预有助于诊断和处理这一罕见病症。该病例强调了仔细检查和合作治疗非典型儿科肝病的重要性。