Sclerosing Mesenteritis Presenting as Protein-losing Enteropathy: a Fatal Case

• Published in: Internal Medicine Vol. 50; no. 22; pp. 2845 - 2849
• Main Authors: Kida, Takashi, Suzuki, Kentaro, Matsuyama, Tatsuzo, Okita, Mika, Isozaki, Yutaka, Matsumoto, Naoyuki, Miki, Shigeyuki, Nagao, Yasutaka, Kawabata, Kenji, Kohno, Masataka, Oyamada, Hirokazu
• Format: Journal Article
• Language: English
• Published: Japan The Japanese Society of Internal Medicine 01.01.2011
• Subjects: Adipose Tissue - pathology; Aged; Autopsy; Diagnosis, Differential; Fatal Outcome; Humans; Male; Mesentery - pathology; panniculitis; Panniculitis, Peritoneal - complications; Panniculitis, Peritoneal - diagnosis; Panniculitis, Peritoneal - pathology; Protein-Losing Enteropathies - diagnosis; Protein-Losing Enteropathies - etiology; protein-losing enteropathy; retractile mesenteritis; sclerosing mesenteritis
• ISSN: 0918-2918; 1349-7235
• DOI: 10.2169/internalmedicine.50.5251

Sclerosing mesenteritis is a rare, benign disorder characterized by non-specific and chronic inflammation of the mesenteric adipose tissue. The disease usually presents with gastrointestinal symptoms and abdominal masses. The long-term prognosis is favorable, but it often becomes severe. In the present report we describe a 77-year-old man who presented with diarrhea, massive ascites and an abdominal mass. The rapid deterioration of the general condition of the patient limited invasive examinations and left the primary disease unclear. Despite symptomatic therapy, malnutrition and hypovolemia were prolonged, and he died. The definitive diagnosis of sclerosing mesenteritis and the cause of the fatal outcome were disclosed at autopsy. This case indicates that sclerosing mesenteritis is a potentially-fatal disease and the need for aggressive treatment should be discussed.