Takahashi Toshiaki, Nouso Hiroshi, Yamoto Masaya, Fukumoto Koji, Urushihara Naoto
Department of Pediatric Surgery, Shizuoka Children's Hospital, 860 Urushiyama, Aoi-ku, Shizuoka City, Shizuoka Prefecture, 420-8660, Japan.
Surg Case Rep. 2018 Sep 4;4(1):109. doi: 10.1186/s40792-018-0514-4.
Primary adenocarcinoma of the appendix is a rare disease in clinical practice. Moreover, primary adenocarcinoma of the appendix in the pediatric age group is even rarer with very little cases being published. Here, we report a case of primary adenocarcinoma of the appendix with local invasion into adjacent organs in a child who was initially diagnosed as having an acute appendicitis.
A 13-year-old girl presented with abdominal pain of 3-month duration. Imaging study showed a mass including the fecalith that occupied her pelvic and right lower abdominal cavity. Drainage of the abscess and appendectomy were performed by the preoperative diagnosis of an acute appendicitis with an appendiceal mass. Postoperative histopathological examinations revealed the appendiceal adenocarcinoma. She then received the whole mass resection, ileocecal resection with lymph node dissection. The masses were tightly adherent with infiltration into the sigmoid colon, uterus, and right ovary. These organs were all dissected, and subsequent sigmoid colostomy was performed. We preserved the left ovary for her fertility. The pathological findings demonstrated negative margins and no lymph node invasions, and final pathological stage was pT4(SI)N0M0, stage II. After the operation, she received the chemotherapy with 6 cycles of 5-fluorouracil (5-FU), leucovorin (LV), and oxaliplatin (mFOLFOX6) and subsequent 6 cycles of simplified LV and 5-FU (sLV5FU2). The patient is doing well till today on follow-up without progression of the disease 5 years after the operation.
Primary adenocarcinoma of the appendix is exceedingly rare in children. In this report, we described one of the youngest primary adenocarcinomas of an appendix case ever reported. When encountering atypical cases of the appendicitis, we should consider the possibility of primary adenocarcinoma of the appendix as it has an extremely poor prognosis and is usually diagnosed in advanced stages.
原发性阑尾腺癌在临床实践中是一种罕见疾病。此外,小儿年龄组的原发性阑尾腺癌更为罕见,仅有极少病例被报道。在此,我们报告一例小儿原发性阑尾腺癌,其局部侵犯相邻器官,该患儿最初被诊断为急性阑尾炎。
一名13岁女孩出现持续3个月的腹痛。影像学检查显示一个包含粪石的肿块占据盆腔和右下腹。根据术前诊断为急性阑尾炎伴阑尾肿块,进行了脓肿引流和阑尾切除术。术后组织病理学检查显示为阑尾腺癌。随后她接受了整块切除、回盲部切除及淋巴结清扫。肿块与乙状结肠、子宫和右卵巢紧密粘连并浸润。对这些器官均进行了切除,并随后进行了乙状结肠造口术。我们保留了左侧卵巢以维持其生育能力。病理结果显示切缘阴性且无淋巴结侵犯,最终病理分期为pT4(SI)N0M0,II期。术后,她接受了6周期的5-氟尿嘧啶(5-FU)、亚叶酸钙(LV)和奥沙利铂(mFOLFOX6)化疗,随后接受了6周期简化的LV和5-FU(sLV5FU2)化疗。术后5年随访至今,患者情况良好,疾病无进展。
小儿原发性阑尾腺癌极为罕见。在本报告中,我们描述了有史以来报道的最年轻的原发性阑尾腺癌病例之一。遇到阑尾炎非典型病例时,应考虑原发性阑尾腺癌的可能性,因为其预后极差且通常在晚期才被诊断出来。