Shiomi S, Moriyama Y, Oshitani N, Matsumoto T, Kuroki T, Kawabe J, Ochi H, Okuyama C
Third Department of Internal Medicine, Osaka City University Medical School, Osaka, Japan.
Clin Nucl Med. 1998 Aug;23(8):521-3. doi: 10.1097/00003072-199808000-00006.
Cap polyposis is a rare intestinal disease that can be difficult to differentiate from inflammatory bowel disease. When cap polyposis is suspected, it is important to confirm protein loss. A 54-year-old woman who had been treated for ulcerative colitis for 7 years had severe hypoproteinemia. Scintigraphy with Tc-99m-labeled DTPA complexed with human serum albumin showed protein loss from the descending colon. Left hemicolectomy and sigmoid colectomy were performed. Cap polyposis was diagnosed on the basis of histologic findings from an operative specimen. The patient's diarrhea resolved after surgery and her hypoproteinemia improved. Scintigraphy with this label gave information helpful in the diagnosis of cap polyposis.
卡普息肉病是一种罕见的肠道疾病,很难与炎症性肠病相鉴别。当怀疑患有卡普息肉病时,确认蛋白丢失很重要。一名接受溃疡性结肠炎治疗7年的54岁女性出现严重低蛋白血症。用与人类血清白蛋白络合的锝-99m标记的二乙三胺五乙酸进行闪烁扫描显示降结肠有蛋白丢失。实施了左半结肠切除术和乙状结肠切除术。根据手术标本的组织学检查结果诊断为卡普息肉病。术后患者的腹泻症状缓解,低蛋白血症有所改善。这种标记物的闪烁扫描为卡普息肉病的诊断提供了有用信息。