Epidermoid Cyst of the Cecum Treated by Laparoscopic Colectomy: A Case Report With Histopathology and Literature Review.

IF 0.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastrointestinal Medicine Pub Date : 2025-06-13 eCollection Date: 2025-01-01 DOI:10.1155/crgm/6326844
Ada Firrincieli, Eleonora Nardi, Lavinia Pugliese, Chiara Marconcini, Giovanni Alemanno, Luca Messerini
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Abstract

Introduction: Cecal epidermoid cyst (CEC) is a rare and benign lesion; the origin can be acquired or congenital, but the pathogenesis remains unclear. We present a case report of a patient with a cecal cyst treated by hemicolectomy. Histopathology revealed an epidermoid cyst (EC) of the cecum. Case Presentation: A 28-year-old woman was admitted to the hospital with abdominal pain, without significant past medical history. CT and MRI scans were performed, and a large cystic mass in the anterior portion of the pelvic region was detected. Imaging techniques managed to localize the site and dimensions of the neoplasm; however, they did not provide a conclusive diagnosis. The differential diagnosis was made with appendiceal mucocele, duplication cyst, or endometriotic cyst formation. Laparoscopic right hemicolectomy was performed; the mass did not present with any adhesions with the surrounding organs. Macroscopically, the mass appears as irregular extraluminal cystic lesion arising from the cecal wall of 104 × 83 × 68 mm. Microscopically, the cystic wall was lined by keratinized stratified squamous epithelium. No malignant findings were identified. Thus, the histopathologic evaluation leads to the final diagnosis of EC. Conclusions: ECs are rare benign neoplasms that can be acquired or congenital. They can vary both in their clinical and imaging presentation; the lesion can be associated with nonspecific symptoms or be asymptomatic. A wide heterogeneity both in sex distribution and age is observed. Imaging techniques are useful, but the final diagnosis can be made only after the complete surgical excision of the neoplasm and its histopathological examination.

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腹腔镜结肠切除术治疗盲肠表皮样囊肿1例组织病理学报告并文献复习。
盲肠表皮样囊肿(CEC)是一种罕见的良性病变;起源可为获得性或先天性,但发病机制尚不清楚。我们提出一个病例报告,病人与盲肠囊肿治疗半结肠切除术。组织病理学显示盲肠表皮样囊肿(EC)。病例介绍:一名28岁女性因腹痛入院,无明显既往病史。行CT和MRI扫描,发现盆腔前部有一个大的囊性肿块。成像技术能够定位肿瘤的位置和大小;然而,他们并没有提供一个结论性的诊断。鉴别诊断为阑尾黏液囊肿、重复囊肿或子宫内膜异位囊肿形成。行腹腔镜右半结肠切除术;肿块未与周围脏器粘连。宏观表现为104 × 83 × 68 mm盲肠壁上的不规则腔外囊性病变。镜下,囊壁内衬角化层状鳞状上皮。未发现恶性肿瘤。因此,组织病理学评估导致最终诊断EC。结论:ECs是一种罕见的良性肿瘤,可以是后天的,也可以是先天性的。它们在临床和影像学表现上各不相同;病变可伴有非特异性症状或无症状。在性别分布和年龄上都有很大的异质性。影像技术是有用的,但最终的诊断只能在肿瘤完全手术切除和组织病理学检查后才能做出。
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来源期刊
Case Reports in Gastrointestinal Medicine
Case Reports in Gastrointestinal Medicine GASTROENTEROLOGY & HEPATOLOGY-
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发文量
33
审稿时长
14 weeks
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