Evans J D, Wilson P G, Barber P C, Neoptolemos J P
Department of Surgery, Queen Elizabeth Hospital, Edgbaston, Birmingham, UK.
Int J Pancreatol. 1996 Oct;20(2):131-4. doi: 10.1007/BF02825512.
We report a case of a duodenal gangliocytic paraganglioma that had an unusual clinical presentation and atypical immunohistochemical features.
Duodenal gangliocytic paragangliomas are rare tumors of the gastrointestinal tract with approx 70 cases reported in the literature. The most common presentation is with gastrointestinal bleeding, whereas obstructive jaundice is very uncommon. Immunohistochemistry typically shows positive epithelial cell staining for somatostatin, pancreatic polypeptide, and other neuroendocrine markers.
A 56-yr-old man presented with intermittent episodes of epigastric pain, vomiting, and obstructive jaundice. Upper gastrointestinal endoscopy revealed a pedunculated ampullary tumor that was subsequently confirmed by computed tomography. At operation, there was marked secondary obstructive chronic pancreatitis in the remaining pancreas necessitating a pylorus-preserving total pancreatectomy.
Histology confirmed typical features of a duodenal gangliocytic paraganglioma, but immunohistochemistry demonstrated negative staining for somatostatin and other polypeptides, which is in contrast to most other reported cases. Two years after surgery, the patient remains alive and well on medical treatment with no evidence of recurrent tumor.
我们报告一例十二指肠神经节细胞性副神经节瘤,其具有不寻常的临床表现和非典型免疫组化特征。
十二指肠神经节细胞性副神经节瘤是胃肠道罕见肿瘤,文献报道约70例。最常见的表现是胃肠道出血,而梗阻性黄疸非常少见。免疫组化通常显示上皮细胞对生长抑素、胰多肽和其他神经内分泌标志物呈阳性染色。
一名56岁男性出现上腹部疼痛、呕吐和梗阻性黄疸的间歇性发作。上消化道内镜检查发现一个带蒂的壶腹肿瘤,随后经计算机断层扫描证实。手术时,剩余胰腺存在明显的继发性梗阻性慢性胰腺炎,需要行保留幽门的全胰切除术。
组织学证实为十二指肠神经节细胞性副神经节瘤的典型特征,但免疫组化显示生长抑素和其他多肽呈阴性染色,这与大多数其他报道的病例不同。手术后两年,患者经药物治疗后仍存活且状况良好,无肿瘤复发迹象。