Of the cases of regional enteritis reported since the description of that new disease entity in 1934, the greater percentage have involved the ileum. Until 1939 only 18 examples of regional enteritis of the upper small bowel had appeared in the literature (1, 2). To that number, 6 cases have subsequently been added. Regional jejunitis would thus appear to be a rare disease, but the question arises: Is it merely unrecognized? Regional jejunitis is a serious illness. Six out of 9 patients in whom the condition was surgically proved were incapacitated or dead within two years, according to Pemberton and Brown (3). Chronic regional enteritis is a definite pathological entity. Its etiology at the present time is undetermined. It is characterized by a chronic inflammatory process involving all layers in particular areas of the small intestine. In the early stages varying degrees of mucosal ulceration and destruction occur, followed later by thickening of the intestinal wall and loss of normal elasticity. The final results are narrowing of the lumen and obstruction. Numerous enlarged lymph nodes are always associated with the condition. We present 3 cases of regional jejunitis, of which 2 were diagnosed preoperatively by roentgen examination. All were proved surgically and all were seen within a three-month period. Case I: J. L. S., male, aged 31, was admitted on March 12, 1946, complaining of loss of appetite, moderate nausea, abdominal pain , and loose stools. The symptoms were of several months’ duration. The patient appeared in good physical condition, with tenderness to palpation in the right lower and middle abdominal areas. Laboratory findings were within normal limits. Roentgen examination of the upper gastro-intestinal tract revealed the diagnosis. Roentgen Findings: Fluoroscopically, spasticity and irritability were observed along the distal greater curvature of the stomach, and near the duodenal-jejunal junction. Marked loss of normal mucosal pattern was noted throughout the duodenum and upper jejunum. This was due in part to increased motility of the barium meal through the involved areas, and in part to spasticity. There was associated tenderness' on palpation. A tentative diagnosis of regional enteritis involving the proximal jejunum was made. Operation on April 13, 1946, revealed jejunitis. The entire jejunum was thickened and rubbery, from duodenum to ileum. Associated esenteric nodes were inflamed. There was no evidence of obstruction. A posterior gastro-low jejunostomy was performed. Eleven days later symptoms of obstruction developed, and an entero-enterostomy was done, bypassing the obstructed jejunal area. The patient recovered after two months' stormy convalescence, but never returned to full duty. Post-operative upper gastro-intestinal roentgenographic studies showed a normally functioning gastro-ileostomy. No further follow-up studies are available.