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Tumor Discovery





                                        CASE REPORT
                                        A rare clinical observation of ureteral

                                        IgG4-related disease in urological practice:
                                        A case report



                                                                                               1,3
                                                          1,2
                                        Ekaterina Anikanova *, Daniel Yagudaev , Konstantin Firsov ,
                                                                            1,3
                                                     4,5
                                        Nina Kalyagina *, and Arina Plotnikova 5
                                        1 Department of Urology and Oncology, Central Clinical  Hospital  “Russian Railways-Medicine,”
                                        Moscow, Russia
                                        2 Department of Oncology and Radiology, Medical Faculty, A.I. Evdokimov Moscow State University
                                        of Medicine and Dentistry, Moscow, Russia
                                        3 Department of Endoscopic Urology, Faculty of Further Education, the Peoples’ Friendship University
                                        of Russia, Moscow, Russia
                                        4 Prokhorov General Physics Institute of the Russian Academy of Sciences, Moscow, Russia
                                        5 Engineering Physics Institute of Biomedicine, National Research Nuclear University MEPhI, Moscow,
                                        Russia




                                        Abstract

                                        IgG4-related disease (IgG4-RD) is a systemic immune-dependent pathology marked
                                        by infiltration of lymphocytes and plasma cells expressing IgG4 in affected tissues,
                                        leading to phlebitis and fibrosclerosis. In urological practice, diagnosing IgG4-RD of
            *Corresponding authors:     the ureter, which may resemble a malignant tumor, presents challenges. We present
            Ekaterina Anikanova
            (Anikanova1801@gmail.com)   a unique case: a 64-year-old patient (Patient P.) experienced left lumbar discomfort
            Nina Kalyagina              and a 4  kg weight loss over 2  months. A  computed tomography scan revealed a
            (Nina.Kalyagina@gmail.com)  111  mm tumor obstructing the left ureter, causing hydronephrosis and regional
            Citation: Anikanova E,      lymphadenopathy.  Suspecting  ureteral  urothelial  cancer,  the  patient  underwent
            Yagudaev D, Firsov K, et al.,   a left nephroureterectomy with lymphadenectomy. Microscopic analysis revealed
            2023, A rare clinical observation
            of ureteral IgG4-related disease in   fibrosis and inflammation infiltration (lymphocytes, plasma cells, and eosinophils) in
            urological practice: A case report.   the ureter wall, with no evidence of tumor growth. Immunohistochemistry confirmed
            Tumor Discov, 2(3): 1766.    IgG4-positive plasma cells. Serum IgG4 rose to 149 mg/dL. Morphological findings led
            https://doi.org/10.36922/td.1766
                                        to a diagnosis of IgG4-RD of the ureter. Clinically, it is crucial to recognize IgG4-RD in
            Received: September 5, 2023   ureteral neoplasms for early detection, to prevent unnecessary surgical intervention.
            Accepted: November 13, 2023
            Published Online: November 24,
            2023
                                        Keywords: IgG4-related diseases; IgG4; Ureter; Pseudotumor inflammation; Urothelial
            Copyright: © 2023 Author(s).   cancer
            This is an Open-Access article
            distributed under the terms of the
            Creative Commons Attribution
            License, permitting distribution,
            and reproduction in any medium,   1. Introduction
            provided the original work is
            properly cited.             IgG4-related disease (IgG4-RD) is a systemic immune-mediated pathology characterized
            Publisher’s Note: AccScience   by diffuse or focal infiltration of affected tissues by lymphocytes and plasma cells expressing
            Publishing remains neutral with   IgG4, with the absence of neutrophils (a moderate amount of eosinophils may be present).
            regard to jurisdictional claims in
            published maps and institutional   Subsequently, the  condition leads  to  the  development  of  phlebitis  and  fibrosclerosis,
            affiliations.               accompanied by an increase in IgG4 content in serum, serving as a laboratory sign [1-3] .



            Volume 2 Issue 3 (2023)                         1                          https://doi.org/10.36922/td.1766
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