A 45 year-old man and known case of IPSID (Immunoproliferative small intestine disorder) was referred for follow-up to our GI (gastrointestinal) clinic. He presented with a 22-year history of intractable watery diarrhea along with slight weight loss. Chronic diarrhea had gradual onset, most of times, as often as 6 to 10 times a day and three times in the recent months. He never noticed pus or mucus in his stools. Nevertheless, 16 years ago, he had reported a slight fresh rectal bleeding in early phase of disease for at least a few months when hemorrhoidectomy and perianal fistulectomy were performed. Consequently, rectal bleeding improved completely but diarrhea was continued. This was relatively a painless condition. The patient underwent his first colonoscopy 13 years ago when just a solitary ulcer in descending colon was seen. Three years later, he was admitted to a hospital with a history of severe abdominal pain along with distension. Physical examination revealed a moderately tender definite mass at the right lower quadrant of his abdomen.
2.1. Ultrasonography Reported
A mass (50 × 70 mm) was found at his right lower quadrant suggestive of abscess. Therefore, laparotomy was performed regarding a suspicious appendicular mass. However, surgeon discovered a cecum mass and extended adhesion during laparotomy. According to the diagnosis of cecum tumor (IPSID), right hemicolectomy was performed which was confirmed by a pathologist. As a result, he was referred to an oncologist and received chemotherapy for six sessions. After chemotherapy, he was under close follow-up with colonoscopy each year and biopsy had been obtained at every session. In each follow-up session, he was introduced with IPSID diagnosis to gastroenterologist and pathologist by oncologist. Pathologist reported some infiltration of inflammatory and lymphocyte cells and confirmed IPSID again. Although alkaline phosphates gradually increased, alpha heavy chain had negative results in several times. Two years later, he was diagnosed with bilateral renal stones and received medical therapy. In addition, he had to do transurethral lithotomy due to hydronephrosis and multiple bilateral renal stones. One year later, he had arthritis in his left foot for a few days, which his joint pain was subsided after a week. Laboratory data reported normal ANA (anti-nuclear antibody), Complement 3, 4, 50, Anti CCP (Antibodies to cyclic citrullinated polypeptides), and RF (Rheumatic factor). Wright and coombs tests had negative results. Although he was gradually complicated by diarrhea, clinicians did not consider any diagnosis for his condition except IPSID and then he just was followed by supportive medicine.
On physical examination, the patient was thin, weak, depressed and pale. Vital signs were as follows: Blood Pressure: 118/72 mmHg; Pulse Rate: 74/min; Respiratory Rate: 16/min; Temperature: 37°C. A midline laparotomy scar was seen in abdominal examination. Rectal examination revealed no masses, partially formed stools and no localized tenderness. Sarcopenia was present, but temporal wasting was not significant. Other examinations had normal findings. We as gastroenterologists reviewed his history carefully this time and requested a revision of all his histopathology results by GI pathologist to conclude IBD. Pathologist revised them and confirmed IBD (CD, Crohn's disease) from the first pathology (
Figure 1). Magnetic resonance (MR) enterography showed multiple strictures in anastomosis site (ileocolic), in transverse and left parts of colon (
Figure 2).
There is considerable mural thickening with mass like appearance at ileocolic anastomotic area with intense contrast enhancement leading to luminal stricture (thin arrow). Adjacent mesenteric enlarged lymph nodes are also depicted (curved arrow). Another short segment mural thickening is evident in mid ileum with predominant involvement of mesenteric side showing increased contrast enhancement (thick arrow).
A focal short segment mural thickening is seen in distal ileum mostly mesenteric border with marked contrast enhancement (thin arrow), which is accompanied with adjacent increased mesenteric vascularity. There is also circumferential mural thickening of sigmoid, which shows typical target appearance in post contrast image in favor of active Crohn’s disease (thick arrow).
Multiple biopsies were taken from stenotic lesion in descending colon through flexible sigmoidoscopy, but pathology did not show any malignant cell. Last laboratory data were as follows: Creatinine: 1 ng/mL (GFR: 66 mL/min, MDRD: 85.6 mL/min), AST: 20 IU/L, ALT: 13 IU/L, Total Bilirubin: 0.7 g/dL, Direct Bilirubin: 0.1 gr/dL, LDH: 296 IU/L, WBC: 10600/mm3, HB: 9 g/dL, Ferritin: 5 μg/L, PLT: 422000/mm3, Albumin: 1.8 g/dL, ESR: 21 mm 1st hour, ALP: 396 IU/L (350), Gamma glutamyl transpeptidase: 26 U/L (normal), CA 19-9: 8.8 U/mL (normal), CEA: 3.9 ng/mL (normal). Urine analysis showed excretion of moderate calcium oxalate and proteinuria (250 mg/24 hours). Prednisolone 40 mg daily, Mesalamine 4 g daily, Folic acid 5 mg daily and Ca-D twice daily were ordered immediately. His general condition improved after 1 month and then corticosteroid was tapered and replaced with Azathioprine 100 mg daily later in a few months.