A Giant Cystic Pheochromocytoma of the Adrenal Gland

被引:0
作者
Zenggang Pan
Susan Repertinger
Caishu Deng
Poonam Sharma
机构
[1] Creighton University Medical Center,Department of Pathology
来源
Endocrine Pathology | 2008年 / 19卷
关键词
pheochromocytoma; giant; adrenal gland;
D O I
暂无
中图分类号
学科分类号
摘要
Adrenal pheochromocytomas are rare catecholamine-secreting tumors that originate from chromaffin cells in the adrenal medulla, and giant pheochromocytomas with cystic changes are particularly rare. We report a case of a 46-year-old man who presented with episodic hypertension and headache. Radiographic studies showed an 18-cm cystic mass in the left upper quadrant of the abdomen; further workups, which included light microscopy, immunohistochemical, and electron microscopic analysis, revealed a pheochromocytoma of the left adrenal gland. Cytogenetic analysis and genetic mutation analyses for von-Hippel–Lindau (VHL), rearranged during transfection (RET), and succinate dehydrogenase complex subunit B (SDHB) genes were also performed but failed to reveal any abnormalities within the tumor cells.
引用
收藏
页码:133 / 138
页数:5
相关论文
共 77 条
[1]  
Safar A(2000)Recurrent anomalies of 6q25 in chondromyxoid fibroma Human Pathol. 31 306-311
[2]  
Nelson M(2003)Pheochromocytoma Curr Treatm Opt Oncol. 4 329-337
[3]  
Neff JR(1984)Current concepts. Pheochromocytoma: diagnosis, localization and management N Engl J Med. 311 1298-1303
[4]  
Pederson LC(2006)Evolving concepts in pheochromocytoma and paraganglioma Curr Opin Oncol. 18 1-8
[5]  
Lee JE(2005)Pheochromocytoma and functional paraganglioma syndrome: no longer the 10% tumor J Surg Oncol. 89 193-201
[6]  
Bravo EL(1993)Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel–Lindau disease N Engl J Med. 329 1531-1538
[7]  
Gifford RW(1999)Clinical and genetic characterization of pheochromocytoma in von Hippel–Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma J Urol. 162 659-664
[8]  
Dahia PL(1996)Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung’s disease N Engl J Med. 335 943-951
[9]  
Elder EE(2000)Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma Science. 287 848-851
[10]  
Elder G(2001)Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma Am J Hum Genet. 69 49-54