Citations

Citations to this article as recorded by  

• Value of High‐Frequency Ultrasonography in the Qualitative and Semi‐Quantitative Assessment of Immunoglobulin G4‐Related Submandibular Sialadenitis
  Lei Chen, Lin Nong, Jumei Liu, Luzeng Chen, Yuhong Shao, Xiuming Sun
  Journal of Ultrasound in Medicine.2023; 42(10): 2235.     CrossRef
• IgG4-related pseudotumours: a series of 12 cases and a review of the literature
  Andrea Maccagno, Bianca Grosser, László Füzesi, Björn Konukiewitz, Dmytro Vlasenko, Dorothea Weckermann, Stephan Raab, Johannes Zenk, Abbas Agaimy, Bruno Märkl
  Pathology.2022; 54(5): 563.     CrossRef
• IgG4-Related Disease With Gastrointestinal Involvement: Case Reports and Literature Review
  Xinhe Zhang, Xing Jin, Lin Guan, Xuyong Lin, Xuedan Li, Yiling Li
  Frontiers in Immunology.2022;[Epub]     CrossRef
• Clinicopathological characteristics of gastric IgG4‐related disease: Systematic scoping review
  Haruki Sawada, Torrey Czech, Krixie Silangcruz, Landon Kozai, Adham Obeidat, Eric Andrew Wien, Midori Filiz Nishimura, Asami Nishikori, Yasuharu Sato, Yoshito Nishimura
  Journal of Gastroenterology and Hepatology.2022; 37(10): 1865.     CrossRef
• Utility of gastric biopsy in diagnosing IgG4‐related gastrointestinal disease
  Kaori Uchino, Kenji Notohara, Takeshi Uehara, Yasuhiro Kuraishi, Junya Itakura, Akihiro Matsukawa
  Pathology International.2021; 71(2): 124.     CrossRef
• A reappraisal of sclerosing nodular and/or polypoid lesions of the gastrointestinal tract rich in IgG4‐positive plasma cells
  Runjan Chetty
  Histopathology.2020; 76(6): 832.     CrossRef
• Gastric IgG4-related disease presenting as a mass lesion and masquerading as a gastrointestinal stromal tumor
  Banumathi Ramakrishna, Rohan Yewale, Kavita Vijayakumar, Patta Radhakrishna, Balakrishnan Siddartha Ramakrishna
  Journal of Pathology and Translational Medicine.2020; 54(3): 258.     CrossRef
• IgG4-related Sclerosing Disease Forming a Gastric Submucosal Tumor Diagnosed after Laparoscopic Endoscopic Cooperative Surgery—Report of a Case—
  Tatsuki ISHIKAWA, Katsunori NAKANO, Masafumi OSAKA, Yayoi KADOTANI, Kaori OKUGAWA, Kiyokazu AKIOKA, Kenta SHIGEMORI, Yohei HOSOKAWA
  Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2020; 81(2): 254.     CrossRef
• Calcifying fibrous tumor of the gastrointestinal tract: A clinicopathologic review and update
  Donald Turbiville, Xu-Chen Zhang
  World Journal of Gastroenterology.2020; 26(37): 5597.     CrossRef
• A Suspected Case of IgG4-Related Appendiceal Pseudotumor
  Yudai Hojo, Yoshiharu Shirakata, Ai Izumi, Jun Matsui, Tokuyuki Yamashita, Hikaru Aoki, Makoto Kurimoto, Masaaki Hirata, Naoki Goda, Hiroaki Ito, Jun Tamura
  The Japanese Journal of Gastroenterological Surgery.2020; 53(12): 976.     CrossRef
• Immunoglobulin G4-related gastric pseudotumor – An impostor: Case report
  Manuel Santiago Mosquera, Andrea Suarez Gómez, Hugo Herrera, Karen Moreno-Medina, Alejandro González-Orozco, Carlos J-Perez Rivera
  International Journal of Surgery Case Reports.2020; 75: 333.     CrossRef
• Imaging and pathological features of gastric lesion of immunoglobulin G4-related disease: A case report and review of the recent literature
  Dai Inoue, Norihide Yoneda, Kotaro Yoshida, Hiromi Nuka, Jun Kinoshita, Sachio Fushida, Fumihito Toshima, Tetsuya Minami, Masayuki Takahira, Shoko Hamaoka, Hiroko Ikeda, Toshifumi Gabata, Mitsuhiro Kawano
  Modern Rheumatology.2019; 29(2): 377.     CrossRef
• Immunoglobulin G4-Related Gastric Ulcer Mimicking Advanced Stomach Cancer in a Patient with Type I Autoimmune Pancreatitis
  Joung Ha Park, Jin Hee Noh, Jang ho Lee, Goeun Lee, Seung-Mo Hong, Kwang Bum Cho, Myung-Hwan Kim
  The Korean Journal of Medicine.2019; 94(3): 287.     CrossRef
• Review of IgG4-related disease
  Raquel Sánchez-Oro, Elsa María Alonso-Muñoz, Lidia Martí Romero
  Gastroenterología y Hepatología (English Edition).2019; 42(10): 638.     CrossRef
• Revisión de la enfermedad relacionada con la IgG4
  Raquel Sánchez-Oro, Elsa María Alonso-Muñoz, Lidia Martí Romero
  Gastroenterología y Hepatología.2019; 42(10): 638.     CrossRef
• Gastrointestinal manifestation of immunoglobulin G4-related disease: clarification through a multicenter survey
  Kenji Notohara, Terumi Kamisawa, Kazushige Uchida, Yoh Zen, Mitsuhiro Kawano, Satomi Kasashima, Yasuharu Sato, Masahiro Shiokawa, Takeshi Uehara, Hajime Yoshifuji, Hiroko Hayashi, Koichi Inoue, Keisuke Iwasaki, Hiroo Kawano, Hiroyuki Matsubayashi, Yukitos
  Journal of Gastroenterology.2018; 53(7): 845.     CrossRef
• IgG4-Related Disease Mimicking Crohn’s Disease: A Case Report and Review of Literature
  Fabiana Ciccone, Antonio Ciccone, Mirko Di Ruscio, Filippo Vernia, Gianluca Cipolloni, Gino Coletti, Giuseppe Calvisi, Giuseppe Frieri, Giovanni Latella
  Digestive Diseases and Sciences.2018; 63(4): 1072.     CrossRef
• IgG4-related Disease in the Stomach which Was Confused with Gastrointestinal Stromal Tumor (GIST): Two Case Reports and Review of the Literature
  Ho Seok Seo, Yoon Ju Jung, Cho Hyun Park, Kyo Young Song, Eun Sun Jung
  Journal of Gastric Cancer.2018; 18(1): 99.     CrossRef
• Multivisceral IgG4-related disease presenting as recurrent massive gastrointestinal bleeding: a case report and literature review
  Xuexue Deng, Ronghua Fang, Jianshu Zhang, Rongqiong Li
  BMC Gastroenterology.2018;[Epub]     CrossRef
• IgG4-Related Sclerosing Disease Presenting as a Gastric Submucosal Tumor
  Takashi Masuda, Toshifumi Matsumoto, Yushi Kaishakuji, Hirotada Tajiri, Akinori Egashira, Hirofumi Kawanaka
  The Japanese Journal of Gastroenterological Surgery.2018; 51(10): 599.     CrossRef
• A rare case of IgG4-related disease: a gastric mass, associated with regional lymphadenopathy
  Dimitar Bulanov, Elena Arabadzhieva, Sasho Bonev, Atanas Yonkov, Diana Kyoseva, Tihomir Dikov, Violeta Dimitrova
  BMC Surgery.2016;[Epub]     CrossRef

We describe a rare case of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) associated with a six-year history of autoimmune pancreatitis, which was controlled by steroid treatment. The patient presented with multiple, cervical and thoracic lymphadenopathy and abnormal, nodular opacities in the lung. Histologically, Rosai-Dorfman disease with numerous IgG4-positive cells was identified in a subcutaneous lymph node in the patient's left forearm. The patient recovered uneventfully with steroid treatment.

Citations

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• Lung Involvement in Destombes-Rosai-Dorfman Disease
  Quentin Moyon, Samia Boussouar, Philippe Maksud, Jean-François Emile, Frédéric Charlotte, Nathalie Aladjidi, Grégoire Prévot, Jean Donadieu, Zahir Amoura, Philippe Grenier, Julien Haroche, Fleur Cohen Aubart
  Chest.2020; 157(2): 323.     CrossRef
• Rosai-Dorfman Disease: Rare Pulmonary Involvement Mimicking Pulmonary Langerhans Cell Histiocytosis and Review of the Literature
  Rashid AL Umairi, Danielle Blunt, Wedad Hana, Matthew Cheung, Anastasia Oikonomou
  Case Reports in Radiology.2018; 2018: 1.     CrossRef
• IgG4‐related skin disease may have distinct systemic manifestations: a systematic review
  Adam E. Bennett, Neil A. Fenske, Paul Rodriguez‐Waitkus, Jane L. Messina
  International Journal of Dermatology.2016; 55(11): 1184.     CrossRef
• Nosology and Pathology of Langerhans Cell Histiocytosis
  Jennifer Picarsic, Ronald Jaffe
  Hematology/Oncology Clinics of North America.2015; 29(5): 799.     CrossRef
• A subset of Rosai–Dorfman disease cases show increased IgG4‐positive plasma cells: another red herring or a true association with IgG4‐related disease?
  Madhu P Menon, Moses O Evbuomwan, Juan Rosai, Elaine S Jaffe, Stefania Pittaluga
  Histopathology.2014; 64(3): 455.     CrossRef

Rosai-Dorfman disease (RDD) can present in any anatomic site, but breast involvement is rarely reported. Recently, a relationship between RDD and IgG4-related sclerosing disease has been suggested. Here we report another case of RDD with overlapping features of IgG4-related sclerosing disease occurring in a right breast of a 62-year-old female. On microscopic examination, the mass demonstrated a characteristic zonal pattern of proliferation of large polygonal histiocytes and lymphoplasma cells with stromal fibrosis. Emperipolesis was observed in histiocytes with abundant cytoplasm, which showed immunoreactivity for S-100 protein and CD68; the diagnosis of RDD was made. Sheets of plasma cells in the fibrotic stroma demonstrated positive reactions for IgG and IgG4. The mean count of IgG4-positive plasma cells was 100.2/high power field, and the ratio of IgG4/IgG was 56.7%. Additional findings of stromal fibrosis and obliteration of preexisting breast lobules suggested overlapping features with IgG4-related sclerosing disease.

Citations

Citations to this article as recorded by  

• Pathology of IgG4-related sclerosing mastitis
  Polycarp Erivwo, Gulisa Turashvili
  Journal of Clinical Pathology.2021; 74(8): 475.     CrossRef
• Rosai–Dorfman Disease: Breast Involvement—Case Report and Literature Review
  George Iancu, Nicolae Gica, Laura Mihaela Mustata, Anca Maria Panaitescu, Danut Vasile, Gheorghe Peltecu
  Medicina.2021; 57(11): 1167.     CrossRef
• Sonographic features of Rosai‐Dorfman disease in the breast: A case report
  Gi W. Shin, Young M. Park, Young J. Heo, Jin W. Baek, Yoo J. Lee, Ji Y. Han, Hayoung Park
  Journal of Clinical Ultrasound.2020; 48(2): 108.     CrossRef
• Rosai-Dorfman Disease of the Breast With Variable IgG4+ Plasma Cells
  Jenny C. Hoffmann, Chieh-Yu Lin, Siddhartha Bhattacharyya, Olga K. Weinberg, Karen M. Chisholm, Michael Bayerl, Michael Cascio, Girish Venkataraman, Kimberly Allison, Megan Troxell, Chung-Che Chang, Adam Bagg, Tracy I. George, Dennis O’Malley, Robert S. O
  American Journal of Surgical Pathology.2019; 43(12): 1653.     CrossRef
• Rosai-Dorfman disease presenting as a breast mass
  Dai Ding*, Cai Qi, Vohra Nasreen A. , Wong Jan, Therien Zsuzsanna P. , Hewan-Lowe Karlene , Sutton Ann
  Archives of Pathology and Clinical Research.2019; 3(1): 008.     CrossRef
• Erdheim-Chester Disease Involving Lymph Nodes and Liver Clinically Mimicking Lymphoma: A Case Report
  Yeoun Eun Sung, Yoon Seo Lee, Jieun Lee, Kyo Young Lee
  Journal of Pathology and Translational Medicine.2018; 52(3): 183.     CrossRef
• Enfermedad de Rosai-Dorfman en mama de paciente masculino: una entidad rara
  Paola Iturralde Rosas-Priego, José Daniel Flores-Alatriste, Daniela Stuht López, Javier Gómez Pedroso-Rea, Cecilia Ortiz-de-Iturbide, Jorge Valenzuela-Tamariz, Manuel Ubiergo-García
  Revista de Senología y Patología Mamaria.2018; 31(2): 72.     CrossRef
• Increased Immunoglobulin G4-positive Plasma Cells in Lymphadenoma of the Salivary Gland: An Immunohistochemical Comparison Among Lymphoepithelial Lesions
  Jiyoon Kim, Joon Seon Song, Jong-Lyel Roh, Seung-Ho Choi, Soon Yuhl Nam, Sang Yoon Kim, Kyung-Ja Cho
  Applied Immunohistochemistry & Molecular Morphology.2018; 26(6): 420.     CrossRef
• IgG4-Related Sclerosing Disease of the Breast in a Male Patient
  Taisia Vitkovski, Galina S. Marder, Dominic A. Filardi, Ekta Gupta, Frank Breuer
  International Journal of Surgical Pathology.2017; 25(8): 711.     CrossRef
• Extranodal manifestation of Rosai-Dorfman disease in the breast tissue
  Qiao Zhou, Umer Ansari, Nandan Keshav, Fiona Davis, Maria Cundiff
  Radiology Case Reports.2016; 11(3): 125.     CrossRef
• Rosai-Dorfman Disease with Massive Cutaneous Nodule on the Shoulder and Back
  Han Ma, Yue Zheng, Guoxing Zhu, Jie Wu, Chun Lu, Wei Lai
  Annals of Dermatology.2015; 27(1): 71.     CrossRef
• IgG4-related disease of the breast: a systemic disease whose mammary manifestations mimic breast cancer
  Takuya Moriya, Hisashi Hirakawa, Maki Nagashima, Mitsuhiko Yasuda, Izo Kimijima
  International Cancer Conference Journal.2015; 4(2): 67.     CrossRef
• Primary Cutaneous Marginal IgG4 Lymphoma and Rosai–Dorfman's Disease Coexisting in Several Lesions of the Same Patient
  Salma Machan, Camino Medina, Socorro María Rodríguez-Pinilla, José M. Suárez-Peñaranda, Yolanda Castro, Paula Molés, Celia Requena, Carles Saus, Luis Requena, Carlos Santonja
  The American Journal of Dermatopathology.2015; 37(5): 413.     CrossRef
• A subset of Rosai–Dorfman disease cases show increased IgG4‐positive plasma cells: another red herring or a true association with IgG4‐related disease?
  Madhu P Menon, Moses O Evbuomwan, Juan Rosai, Elaine S Jaffe, Stefania Pittaluga
  Histopathology.2014; 64(3): 455.     CrossRef
• Freiburg Neuropathology Case Conference: A Partially Calcified, Dura-based Tumour of the Frontal Lobe
  C. A. Taschner, O. Staszewski, R. Jabbarli, A. Keuler, M. Prinz
  Clinical Neuroradiology.2013; 23(1): 63.     CrossRef