Srinivasan R, Koliyadan K Sreedharan V, Krishnand Geetha, Bhat Sudha S
Department of Pathology, Kasturba Medical College, Manipal, Karnataka.
Indian J Pathol Microbiol. 2007 Jan;50(1):32-5.
Ganglioneuroma is a benign, most differentiated tumor of neural crest origin. These tumors though benign, can very rarely metastasize to regional lymphnodes or to distant sites. We report a case of a 52 year old lady who presented to the surgical OPD with dyspeptic symptoms of 2 months duration. Ultrasonography and CT scan of the abdomen showed a homogenous mass in the region of the right adrenal gland, extending between the inferior vena cava and the aorta. A clinical and radiological diagnosis of an adrenal tumor was made. Microscopically, the tumor histology was that of a ganglioneuroma (schwannian stroma-dominant) mature type. The lymph node attached to the tumor showed metastasis, the metastatic foci having the same morphology as the primary tumor. The right adrenal gland was free of tumor. The case is illustrative due to its clinical presentation mimicking an adrenal incidentaloma, and a rare phenomenon of a benign tumor exhibiting completely differentiated lymph node metastasis.
神经节神经瘤是一种起源于神经嵴的良性、高度分化的肿瘤。这些肿瘤虽然是良性的,但极罕见会转移至区域淋巴结或远处部位。我们报告一例52岁女性患者,因持续2个月的消化不良症状就诊于外科门诊。腹部超声和CT扫描显示右肾上腺区域有一个均匀的肿块,延伸于下腔静脉和主动脉之间。临床及影像学诊断为肾上腺肿瘤。显微镜下,肿瘤组织学表现为成熟型神经节神经瘤(雪旺氏基质为主型)。附着于肿瘤的淋巴结显示有转移,转移灶的形态与原发肿瘤相同。右肾上腺无肿瘤。该病例具有代表性,因其临床表现类似肾上腺偶发瘤,且存在良性肿瘤出现完全分化的淋巴结转移这一罕见现象。