Nuño-Guzmán Carlos M, Arróniz-Jáuregui José, Alvarez-López Francisco, Corona Jorge L, Cerda-Camacho Felipe, Rostro Rodrigo, Gutiérrez-Manjarrez Juan I
Department of General Surgery, Antiguo Hospital Civil de Guadalajara 'Fray Antonio Alcalde', Guadalajara, Mexico.
Case Rep Gastroenterol. 2012 May;6(2):489-95. doi: 10.1159/000341586. Epub 2012 Jul 24.
Gangliocytic paragangliomas are infrequent tumors almost exclusively found in the second portion of the duodenum. An unusual case of a gangliocytic paraganglioma in the third portion of the duodenum with obstructive symptoms is herein reported. A 16-year-old male patient presented with epigastric pain, postprandial plenitude and reflux. A barium swallow failed to demonstrate abnormalities. Endoscopy showed a pedunculated submucosal tumor, originating at the third duodenal portion and causing partial obstruction. Biopsy was not performed due to the risk of bleeding. CT scan demonstrated a polypoid lesion. Through a transmesocolic approach and an anterior duodenotomy, resection of the tumor was performed. No lymph node or other organ affection was found. Histologic examination revealed a gangliocytic paraganglioma. Immunohistochemical examination was performed. Gangliocytic paragangliomas originating in the third or fourth portion of the duodenum, as in the present case, are extremely rare. Characteristic histologic features including epithelioid cells, spindle-shaped cells and ganglion-like cells were met. The majority of cases manifest with a similar benign behavior. Local resection of the tumor is recommended for these cases. An infrequent case of a gangliocytic paraganglioma located in the third portion of the duodenum, with a less common clinical presentation, is herein reported.
神经节细胞性副神经节瘤是一种罕见肿瘤,几乎仅见于十二指肠第二部。本文报告了一例发生于十二指肠第三部且伴有梗阻症状的神经节细胞性副神经节瘤罕见病例。一名16岁男性患者出现上腹部疼痛、餐后饱胀感和反流症状。上消化道钡餐检查未显示异常。内镜检查发现一个带蒂的黏膜下肿瘤,起源于十二指肠第三部并导致部分梗阻。由于有出血风险,未进行活检。CT扫描显示一个息肉样病变。通过经结肠系膜途径和十二指肠前路切开术,对肿瘤进行了切除。未发现淋巴结或其他器官受累。组织学检查显示为神经节细胞性副神经节瘤。进行了免疫组化检查。如本病例所示,起源于十二指肠第三部或第四部的神经节细胞性副神经节瘤极为罕见。可见到包括上皮样细胞、梭形细胞和神经节样细胞在内的特征性组织学特征。大多数病例表现出类似的良性行为。对于这些病例,建议对肿瘤进行局部切除。本文报告了一例位于十二指肠第三部的神经节细胞性副神经节瘤罕见病例,其临床表现较少见。