Protein-losing enteropathy cured by resection of adenomatous goiter: report of a case

被引:0
作者
Takada J. [1 ]
Araki H. [1 ]
Kubota M. [1 ]
Ibuka T. [1 ]
Shiraki M. [1 ]
Shimizu M. [1 ]
Moriwaki H. [1 ]
机构
[1] Department of Gastroenterology, Gifu University Graduate School of Medicine, 1-1 Yanagido, Gifu
关键词
Adenomatous goiter; Double balloon enteroscopy; Protein-losing enteropathy;
D O I
10.1007/s12328-015-0565-z
中图分类号
学科分类号
摘要
A 51-year-old Japanese woman presented to our hospital with systemic edema and general fatigue. Her serum albumin level was very low (1.5 g/dL). Technetium-99 m-human serum albumin (99mTc-HSA) scintigraphy showed albumin leakage from the upper small bowel. Magnetic resonance lymphangiography showed dilated lymphatic vessels in the chest, whereas double-balloon enteroscopy (DBE) showed white villi and chyle leakage in the deeper part of the duodenal mucosa. A duodenal mucosa biopsy specimen revealed lymphangiectasia. She was diagnosed with protein-losing enteropathy (PLE). Treatment with a fat-restricted diet and tranexamic acid—previously reported to be effective against PLE—was attempted, but was ineffective. A thyroid tumor was simultaneously detected in her left neck, and was found to extend to the mediastinum on computed tomography. The tumor (size, >5 cm) was resected, and a pathological diagnosis of adenomatous goiter was made. The patient’s serum albumin level increased to normal levels within 1 month postoperatively. After 6 months, 99mTc-HSA scintigraphy showed no albumin leakage from the gastrointestinal tract, and disappearance of white villi and chyle leakage on DBE. No lymphangiectasia was noted in the biopsy specimen. Adenomatous goiter was thus considered the cause of the PLE, possibly through lymph flow obstruction in the mediastinum. © 2015, Springer Japan.
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页码:120 / 125
页数:5
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共 11 条
  • [1] Umar S.B., DiBaise J.K., Protein-losing enteropathy: case illustrations and clinical review, Am J Gastroenterol., 105, 1, pp. 43-49, (2010)
  • [2] Aoyagi K., Iida M., Yao T., Matsui T., Okada M., Oh K., Et al., Characteristic endoscopic features of intestinal lymphangiectasia: correlation with histological findings, Hepatogastroenterology, 44, 13, pp. 133-138, (1997)
  • [3] Takenaka H., Ohmiya N., Hirooka Y., Nakamura M., Ohno E., Miyahara R., Et al., Endoscopic and imaging findings in protein-losing enteropathy, J Clin Gastroenterol, 46, 7, pp. 575-580, (2012)
  • [4] Lai Y., Yu T., Qiao X.Y., Zhao L.N., Chen Q.K., Primary intestinal lymphangiectasia diagnosed by double-balloon enteroscopy and treated by medium-chain triglycerides: a case report, J Med Case Rep, 7, (2013)
  • [5] Ingle S.B., Hinge Ingle C.R., Primary intestinal lymphangiectasia: minireview, World J Clin Cases, 2, 10, pp. 528-533, (2014)
  • [6] Mine K., Matsubayashi S., Nakai Y., Nakagawa T., Intestinal lymphangiectasia markedly improved with antiplasmin therapy, Gastroenterology, 96, 6, pp. 1596-1599, (1989)
  • [7] MacLean J.E., Cohen E., Weinstein M., Primary intestinal and thoracic lymphangiectasia: a response to antiplasmin therapy, Pediatrics, 109, 6, pp. 1177-1180, (2002)
  • [8] Kaneko H., Yamashita M., Ohshiro M., Ohkawara Y., Matsumoto Y., Nomura K., Et al., Protein-losing enteropathy in a case of nodal follicular lymphoma without a gastrointestinal mucosal lesion, Intern Med, 47, 24, pp. 2171-2173, (2008)
  • [9] Konar A., Brown C.B., Hancock B.W., Moss S., Protein losing enteropathy as a sole manifestation of non-Hodgkin’s lymphoma, Postgrad Med J, 62, 727, pp. 399-400, (1986)
  • [10] Laharie D., Degenne V., Laharie H., Cazorla S., Belleannee G., Couzigou P., Et al., Remission of protein-losing enteropathy after nodal lymphoma treatment in a patient with primary intestinal lymphangiectasia, Eur J Gastroenterol Hepatol, 17, 12, pp. 1417-1419, (2005)