Appendiceal adenocarcinoma associated with Amyand's hernia: a case report.

IF 0.9 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Kotaro Momota, Koji Shibata, Hideo Miyake, Hidemasa Nagai, Yuichiro Yoshioka, Norihiro Yuasa, Hideki Murakami
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Abstract

We encountered a rare case of appendiceal carcinoma associated with Amyand's hernia, which was difficult to diagnose preoperatively. A 74-year-old man presented to our hospital with right lower abdominal pain. A hard mass was palpable in the right lower abdomen, and blood tests showed a slightly elevated inflammatory response. Computed tomography revealed a 7 × 5 cm mass with indistinct borders and heterogeneous internal density extending from the cecum to the right lower abdominal wall. We diagnosed appendiceal abscess, however, percutaneous biopsy which was performed for differential diagnosis with appendiceal carcinoma showed no malignancy. Thereafter, the patient was followed up. Two months later, a blood test showed insignificant changes in the inflammatory response and a high serum carcinoembryonic antigen level (48.6 ng/mL). An ultrasound showed a mass contiguous to the appendix, extending to the abdominal wall, with abundant blood flow signals. Fluorodeoxyglucose-positron emission tomography showed a high accumulation of fluorodeoxyglucose in the mass. Four months after the initial visit, the patient had an open ileocecal resection combined with an abdominal wall resection based on the preoperative diagnosis of appendiceal carcinoma invading the abdominal wall. During laparotomy, an enlarged appendix tip extended from the internal inguinal ring outside the inferior epigastric artery to the abdominal wall. Histopathological examination of the appendiceal tumor revealed well-differentiated adenocarcinoma, T4b (abdominal wall), N0, Ly0, and V0. When a right lower abdominal mass extends from the cecum to the abdominal wall, appendiceal tumors associated with Amyand's hernia should be considered.

阑尾腺癌伴发阿米氏疝:病例报告。
我们遇到了一例罕见的阑尾癌伴有阿米恩疝的病例,术前很难确诊。一名 74 岁的男性因右下腹疼痛来我院就诊。右下腹可触及硬块,血液检查显示炎症反应略有升高。计算机断层扫描显示,肿块大小为 7 × 5 厘米,边界不清,内部密度不均,从盲肠一直延伸到右下腹壁。我们诊断为阑尾脓肿,但为与阑尾癌进行鉴别诊断而进行的经皮活检显示没有恶性肿瘤。此后,我们对患者进行了随访。两个月后,血液检查显示炎症反应无明显变化,血清癌胚抗原水平较高(48.6 纳克/毫升)。超声波检查显示,肿块与阑尾毗连,并延伸至腹壁,伴有大量血流信号。氟脱氧葡萄糖正电子发射断层扫描显示,肿块内有大量氟脱氧葡萄糖聚集。首次就诊四个月后,根据术前阑尾癌侵犯腹壁的诊断,患者接受了开腹回盲部切除术和腹壁切除术。在开腹手术中,肿大的阑尾尖端从腹股沟内环外下腹股沟动脉延伸至腹壁。阑尾肿瘤的组织病理学检查显示为分化良好的腺癌,T4b(腹壁),N0,Ly0,V0。当右下腹肿块从盲肠延伸至腹壁时,应考虑阑尾肿瘤伴发Amyand疝。
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
Nagoya Journal of Medical Science
Nagoya Journal of Medical Science MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
1.30
自引率
0.00%
发文量
65
审稿时长
>12 weeks
期刊介绍: The Journal publishes original papers in the areas of medical science and its related fields. Reviews, symposium reports, short communications, notes, case reports, hypothesis papers, medical image at a glance, video and announcements are also accepted. Manuscripts should be in English. It is recommended that an English check of the manuscript by a competent and knowledgeable native speaker be completed before submission.
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