Yarlagadda Rajkumar, Menda Yusuf, Graham Michael M
Department of Nuclear Medicine, University of Iowa Hospitals and Clinics, North Liberty, Iowa 52317, USA.
Clin Nucl Med. 2008 May;33(5):374-6. doi: 10.1097/RLU.0b013e31816a78e3.
Blue rubber bleb nevus syndrome, first discovered in 1860 by Gascoyen, is a rare syndrome characterized by multiple venous malformations (hemangiomas) of the skin and in the gastrointestinal tract. These hemangiomas may be found in the skin, GI tract, central nervous system, thyroid, parotid, eyes, oral cavity, musculoskeletal system, lungs, kidneys, liver, spleen, and bladder, and carry a significant potential for serious bleeding. We report a case of a 9-year-old patient who presented with bloody stools and was referred for localization of the bleeding site. A Tc-99m labeled red blood cell (RBC) scan showed no evidence of active lower GI bleeding but demonstrated multiple venous malformations throughout the body. Tc-99m labeled red blood cell imaging may be helpful to delineate the extent of involvement in patients with blue rubber bleb nevus syndrome.
蓝色橡皮疱痣综合征于1860年由加斯科因首次发现,是一种罕见的综合征,其特征为皮肤和胃肠道出现多发性静脉畸形(血管瘤)。这些血管瘤可见于皮肤、胃肠道、中枢神经系统、甲状腺、腮腺、眼睛、口腔、肌肉骨骼系统、肺、肾、肝、脾和膀胱,并有严重出血的重大风险。我们报告一例9岁患者,其出现便血并因出血部位定位而转诊。锝-99m标记红细胞(RBC)扫描未显示下消化道有活动性出血迹象,但显示全身有多处静脉畸形。锝-99m标记红细胞成像可能有助于明确蓝色橡皮疱痣综合征患者的受累范围。