Published online May 26, 2020. doi: 10.12998/wjcc.v8.i10.2044
Peer-review started: January 21, 2020
First decision: February 26, 2020
Revised: April 1, 2020
Accepted: April 15, 2020
Article in press: April 15, 2020
Published online: May 26, 2020
Processing time: 124 Days and 18.3 Hours
Ileocecal intussusception caused by two different tumors is rare, according to a literature review. We describe a case of a male patient with a cauliflower-like mass in the middle of the transverse colon observed by colonoscopy before surgery. It was considered to be intussusception caused by colon cancer. However, a substantial lipomatous mass was seen in the distal end of the intussusception by computed tomography before surgery, which posed a challenge in the preoperative diagnosis.
We report a 72-year-old male patient with intussusception. The patient underwent right hemicolectomy and cholecystectomy in our hospital on April 29, 2019. During operation, the ileum was inserted into the ascending colon by about 15 cm, and a tumor with a diameter of approximately 3.0 cm was observed in the distal part of the intestine. An atypical liposarcoma/highly differentiated liposarcoma in the adipose tissue was suspected in the postoperative pathology, and a lipoma was diagnosed after MDM2 gene testing. A 4.0 cm × 5.0 cm polypoid mass was seen immediately adjacent to the mass, and the postoperative pathology report suggested a high-level tubular adenoma. The patient was eventually cured and discharged with an uneventful follow-up.
Intussusception caused by two different types of masses is extremely rare. At present, surgery is the best treatment once intussusception is diagnosed.
Core tip: Ileocecal intussusception caused by two different tumors is rare. We report a 72-year-old male with intussusception. A cauliflower-like mass was observed in the transverse colon by colonoscopy before surgery. It was considered to be intussusception caused by colon cancer. However, a substantial lipomatous mass was seen in the distal end of the intussusception by computed tomography before surgery. The patient underwent a right hemicolectomy and cholecystectomy in our hospital. The benign and malignant fatty masses were sent for microscopic/immunohistochemical examination and MDM2 fluorescence in situ hybridization diagnosis after surgery. The patient was eventually cured and discharged with an uneventful follow-up.