Archontovasilis Fotios, Markogiannakis Haridimos, Dikoglou Christina, Drimousis Panagiotis, Toutouzas Konstantinos G, Theodorou Dimitrios, Katsaragakis Stilianos
1st Department of Propaedeutic Surgery, Hippokrateion Hospital, Athens Medical School, University of Athens, Q, Sofias 114 avenue, 11527 Athens, Greece.
World J Surg Oncol. 2007 Aug 3;5:87. doi: 10.1186/1477-7819-5-87.
Extra-adrenal, intra-abdominal paraganglioma constitutes a rare neoplasm and, moreover, its location in the greater omentum is extremely infrequent.
A 46-year-old woman with an unremarkable medical history presented with an asymptomatic greater omentum mass that was discovered incidentally during ultrasonographic evaluation due to menstrual disturbances. Clinical examination revealed a mobile, non-tender, well-circumscribed mass in the right upper and lower abdominal quadrant. Blood tests were normal. Contrast-enhanced abdominal computed tomography (CT) scan confirmed a huge (15 x 15 cm), well-demarcated, solid and cystic, heterogeneously enhanced mass between the right liver lobe and right kidney. Exploratory laparotomy revealed a large mass in the greater omentum. The tumor was completely excised along with the greater omentum. Histopathology offered the diagnosis of benign greater omentum paraganglioma. After an uneventful postoperative course, the patient was discharged on the 4th postoperative day. She remains free of disease for 2 years as appears on repeated CT scans as well as magnetic resonance imaging (MRI) and scintigraphy performed with radiotracer-labeled metaiodobenzyl-guanidine (MIBG) scans.
This is the second reported case of greater omentum paraganglioma. Clinical and imaging data of patients with extra-adrenal, intra-abdominal paragangliomas are variable while many of them may be asymptomatic even when the lesion is quite large. Thorough histopathologic evaluation is imperative for diagnosis and radical excision is the treatment of choice. Since there are no definite microscopic criteria for the distinction between benign and malignant tumors, prolonged follow-up is necessary.
肾上腺外腹腔内副神经节瘤是一种罕见的肿瘤,此外,其位于大网膜的情况极为罕见。
一名46岁女性,既往病史无异常,因月经紊乱接受超声检查时偶然发现一个无症状的大网膜肿块。临床检查发现右上腹和右下腹象限有一个可移动、无压痛、边界清晰的肿块。血液检查正常。腹部增强计算机断层扫描(CT)证实,在右肝叶和右肾之间有一个巨大的(15×15厘米)、边界清晰、实性和囊性、不均匀强化的肿块。剖腹探查发现大网膜有一个大肿块。肿瘤连同大网膜被完整切除。组织病理学诊断为良性大网膜副神经节瘤。术后过程顺利,患者术后第4天出院。经重复CT扫描、磁共振成像(MRI)以及用放射性示踪剂标记的间碘苄胍(MIBG)扫描进行的闪烁显像检查显示,她已无病生存2年。
这是第二例报告的大网膜副神经节瘤病例。肾上腺外腹腔内副神经节瘤患者的临床和影像学数据各不相同,即使病变很大,许多患者可能也无症状。彻底的组织病理学评估对于诊断至关重要,根治性切除是首选治疗方法。由于良性和恶性肿瘤之间没有明确的微观标准,因此需要长期随访。