Published online May 26, 2020. doi: 10.12998/wjcc.v8.i10.1973
Peer-review started: February 5, 2020
First decision: March 18, 2020
Revised: April 3, 2020
Accepted: April 21, 2020
Article in press: April 21, 2020
Published online: May 26, 2020
Processing time: 110 Days and 7.2 Hours
Lymphangioma is a rare benign cystic tumor believed to be a proliferation of heterotopic lymphocytes. It is caused by congenital lymphatic dysplasia or other acquired factors related to surgery, trauma, infection, or cancer. In this article, we present the case of an adult patient who underwent multi-modal imaging and whose condition was finally confirmed to be multiple cystic lymphangiomas by pathological examination.
A 61-year-old man was referred to our hospital for having suffered from painless gross hematuria for 2 wk. Multiple masses rising from the retroperitoneum and pelvis were found incidentally by urinary ultrasonography. Contrast-enhanced abdominal-pelvic computed tomography showed multiple well-defined hypodense cystic lesions without enhancement. The lesions showed no uptake on F-18-fluorodeoxyglucose positron emission tomography/computed tomography images. Exploratory laparotomy was performed, and the case was confirmed as multiple cystic lymphangiomas.
When retroperitoneal and pelvic masses are found, clinicians should always consider cystic lymphangioma when making a differential diagnosis.
Core tip: Retroperitoneal and pelvic cystic lymphangioma, which is seldom seen in adults, has only rarely been reported. It is especially not often diagnosed by F-18-fluorodeoxyglucose (F-18 FDG) positron emission tomography/computed tomography (PET/CT). In addition, the features presented by F-18 FDG PET/CT are different. We here report an adult patient who underwent F-18 FDG PET/CT and was finally diagnosed with multiple cystic lymphangiomas, with an aim of improving the understanding of the disease.