| Literature DB >> 26581887 |
Erika Mori1, Terumi Kamisawa2, Taku Tabata1, Satomi Shibata1, Kazuro Chiba1, Sawako Kuruma1, Go Kuwata1, Tomoko Onishi1, Takashi Fujiwara1, Junko Fujiwara1, Takeo Arakawa1, Kumiko Momma1, Koichi Koizumi1, Hiroshi Matsumoto3, Shinichiro Horiguchi4.
Abstract
IgG4-related disease is a newly recognized fibroinflammatory condition characterized by tumefaction consisting of fibrosis with dense infiltration of IgG4-positive plasma cells; affecting various organs. A case of IgG4-related sclerosing mesenteritis is reported. A 64-year-old man was admitted to our hospital with a suspected tumor of the small intestine. Abdominal computed tomography demonstrated a 6-cm soft tissue mass in the right lower mesentery compressing the jejunum, which also showed accumulation of fluorodeoxyglucose uptake on fluorine-18 fluorodeoxyglucose positron emission tomography. With a preoperative diagnosis of suspected malignant lymphoma with lymphadenopathy in the mesentery, partial small bowel resection was performed. Macroscopically, a hard mass, including several swollen lymph nodes, was detected in the mesentery. Microscopically, marked fibrosis showing partially storiform pattern, obstructive phlebitis, follicular hyperplasia, and abundant infiltration of IgG4-positive plasma cells were detected. IgG4-related mesenteritis was diagnosed histopathologically, but the serum IgG4 level was 81 mg/dl postoperatively. Five months after the surgery, an 11-cm soft tissue mass involving the left ureter appeared. Histological examination of a biopsy specimen from the retroperitoneal mass showed fibrosis with inflammatory infiltration. Although IgG4-related retroperitoneal fibrosis could not be confirmed histologically, the tumor responded well to steroid therapy.Entities:
Keywords: IgG4; Retroperitoneal fibrosis; Sclerosing mesenteritis
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Year: 2015 PMID: 26581887 DOI: 10.1007/s12328-015-0617-4
Source DB: PubMed Journal: Clin J Gastroenterol ISSN: 1865-7265