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Immunoglobulin G4‐related disease accompanying a small intestinal ulcer: A case
Author(s) -
Yoshidome Yuta,
Mizoguchi Akinori,
Narimatsu Kazuyuki,
Takahashi Shun,
Hirata Dai,
Ono Shinji,
Onoyama Yusuke,
Suzuki Seiya,
Horiuchi Tomoaki,
Chiya Nanoka,
Ikeyama Keisuke,
Tahara Hiroyuki,
Tomioka Akira,
Ito Suguru,
Tanemoto Rina,
Nishii Shin,
Inaba Kenichi,
Sugihara Nao,
Hanawa Yoshinori,
Horiuchi Kazuki,
Wada Akinori,
Akita Yoshihiro,
Higashiyama Masaaki,
Komoto Shunsuke,
Tomita Kengo,
Yoshimatsu Shinya,
Matsukuma Susumu,
Hokari Ryota
Publication year - 2022
Publication title -
den open
Language(s) - English
Resource type - Journals
ISSN - 2692-4609
DOI - 10.1002/deo2.76
Subject(s) - medicine , igg4 related disease , colonoscopy , prednisolone , gastroenterology , antibody , ileum , gastrointestinal tract , disease , pathology , immunology , colorectal cancer , cancer
Immunoglobulin (Ig)G4‐related disease (IgG4‐RD) is a systemic condition associated with fibroinflammatory lesions and is characterized by elevated serum IgG4 levels and IgG4‐positive cell infiltration into the affected tissues. It has been reported that IgG4‐RD affects a variety of organs but uncommonly affects the gastrointestinal tract. In particular, there are few cases of lesions in the small intestine, except for sclerosing mesenteritis, which were mostly diagnosed from surgical specimens. Herein, we describe the case of a 70‐year‐old man who initially presented with abdominal pain, headache, later cognitive decline, and gait disturbance caused by IgG4‐RD. Colonoscopy revealed irregular ulcers in the terminal ileum, and computed tomography of the head showed hypertrophic pachymeningitis. Numerous IgG4‐positive cells were detected in the ileal and dural biopsies. We diagnosed the patient with IgG4‐RD and started steroid pulse therapy. After initiation of treatment, the symptoms quickly improved. The patient was discharged from the hospital after starting oral prednisolone treatment (30 mg). The dosage was gradually reduced to 10 mg. A follow‐up colonoscopy revealed scarring of the ileal ulcers. This case may provide valuable information regarding the endoscopic findings of small intestinal lesions in IgG4‐RD.

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