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Adult-Onset Primary Intestinal Lymphangiectasia With Liver Enzymes Elevation.
Nguyen, Chuong Dinh; Buchman, Alan; Bui, Hoang Huu; Thi-Lan Pham, Anh; Thi-Ngoc Vo, Diem; Dang, Luan Minh; Vo, Van Huy.
Afiliação
  • Nguyen CD; Department of Gastroenterology, University Medical Center Ho Chi Minh City, Vietnam.
  • Buchman A; Intestinal Rehabilitation and Transplant Center, Department of Surgery/UI Health, University of Illinois at Chicago, Chicago, IL.
  • Bui HH; Department of Gastroenterology, University Medical Center Ho Chi Minh City, Vietnam.
  • Thi-Lan Pham A; Department of Internal Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Vietnam.
  • Thi-Ngoc Vo D; Department of Nutrition and Dietary, University of Medicine and Pharmacy at Ho Chi Minh City, Vietnam.
  • Dang LM; Department of Pathology, University of Medicine and Pharmacy at Ho Chi Minh City, Vietnam.
  • Vo VH; Department of Gastroenterology, University Medical Center Ho Chi Minh City, Vietnam.
ACG Case Rep J ; 9(12): e00939, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36600788
ABSTRACT
Primary intestinal lymphangiectasia is a rare disorder that may result in protein-losing enteropathy. We report a 21-year-old man with malabsorption syndrome, an unintentional weight loss of 30 kg over 10 months, lymphocytopenia, and hepatic aminotransferase elevation. His diagnosis was established by a combination of enteroscopy, histopathology, and secondary etiology exclusion. Institution of parenteral nutrition, followed by a low-fat diet, medium-chain triglycerides, and octreotide, resulted in the resolution of his symptoms and laboratory abnormalities and led to weight gain. Aminotransferase abnormalities are an atypical finding in primary intestinal lymphangiectasia and were most likely due to nonalcohol steatohepatitis after rapid weight loss. Primary intestinal lymphangiectasia should be considered in patients with protein-losing enteropathy and lymphocytopenia.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article