Orbital Rosai-Dorfman disease initially diagnosed as IgG4-related disease: a case report
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D. Staffenberg | D. Golub | Michelle W. McQuinn | D. Harter | Travis C Hill | C. Sen | I. Belinsky | Karen H. K. Tang | N. Iyengar | K. Thomas | Zachary Elkin | Christopher M William | Sharon L Gardner
[1] F. Vega,et al. Primary cutaneous Rosai-Dorfman disease; a case-based review of a diagnostically and therapeutically challenging rare variant. , 2019, Annals of diagnostic pathology.
[2] S. Heegaard,et al. Diagnosis of Orbital Mass Lesions Clinical, Radiological and Pathological Recommendations. , 2019, Survey of ophthalmology.
[3] D. Salomão,et al. Distinguishing IgG4-Related Ophthalmic Disease From Graves Orbitopathy. , 2019, Ophthalmic plastic and reconstructive surgery.
[4] R. Verdijk,et al. The treatment outcomes in IgG4‐related orbital disease: a systematic review of the literature , 2019, Acta ophthalmologica.
[5] G. Tirelli,et al. Head and neck immunoglobulin G4 related disease: systematic review , 2018, The Journal of Laryngology & Otology.
[6] E. Jacobsen,et al. Consensus recommendations for the diagnosis and clinical management of Rosai-Dorfman-Destombes disease. , 2018, Blood.
[7] D. Rontogianni,et al. Ocular manifestations of IgG4-related disease in children. More common than anticipated? Review of the literature and case report , 2018, Clinical Rheumatology.
[8] Bernie Chang,et al. How accurate is the clinical and radiological evaluation of orbital lesions in comparison to surgical orbital biopsy? , 2018, Eye.
[9] S. Staibano,et al. Inflammatory myofibroblastic tumor of the orbit: A clinico-pathological study of 25 cases , 2018, Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society.
[10] R. Senetta,et al. A 68‐Year‐Old Woman with A Left Orbital and Temporal Mass , 2018, Brain pathology.
[11] Larissa A Habib,et al. Spontaneous regression of inflammatory myofibroblastic tumor of the orbit: A case report and review of literature , 2017, Orbit.
[12] V. Surabhi,et al. Inflammatory Myofibroblastic Tumors: Current Update. , 2016, The Radiologic clinics of North America.
[13] R. Verdijk,et al. IgG4-related disease: a systematic review of this unrecognized disease in pediatrics , 2016, Pediatric Rheumatology.
[14] T. Al-Khateeb. Cutaneous Rosai-Dorfman Disease of the Face: A Comprehensive Literature Review and Case Report. , 2016, Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons.
[15] J. Stone,et al. International Consensus Guidance Statement on the Management and Treatment of IgG4‐Related Disease , 2015, Arthritis & rheumatology.
[16] P. Satija,et al. Immunoglobulin G4-related diseases in the head and neck: a systematic review , 2015, Journal of Otolaryngology - Head & Neck Surgery.
[17] V. Deshpande. IgG4 Related Disease of the Head and Neck , 2015, Head and Neck Pathology.
[18] J. Stone,et al. Rituximab for IgG4-related disease: a prospective, open-label trial , 2015, Annals of the rheumatic diseases.
[19] V. Dutta,et al. ALK negative inflammatory myofibroblastic tumor of the orbit: A masquerading entity , 2014, Indian journal of ophthalmology.
[20] E. Jaffe,et al. A subset of Rosai–Dorfman disease cases show increased IgG4‐positive plasma cells: another red herring or a true association with IgG4‐related disease? , 2014, Histopathology.
[21] D. Weisenburger,et al. Relationship between Rosai-Dorfman disease and IgG4-related disease: study of 32 cases. , 2013, American journal of clinical pathology.
[22] J. Vardiman,et al. A subset of Rosai-Dorfman disease exhibits features of IgG4-related disease. , 2013, American journal of clinical pathology.
[23] C. V. van Hasselt,et al. Rosai–dorfman disease: Presentation, diagnosis, and treatment , 2013, Head & neck.
[24] D. Sahani,et al. Consensus statement on the pathology of IgG4-related disease , 2012, Modern Pathology.
[25] C. Edelsten,et al. Inflammatory lesions of the orbit: a single paediatric rheumatology centre experience , 2011, Rheumatology.
[26] B. Petersen,et al. Differences in clinical profile and relapse rate of type 1 versus type 2 autoimmune pancreatitis. , 2010, Gastroenterology.
[27] T. Kamisawa,et al. Autoimmune pancreatitis and IgG4-related sclerosing disease , 2010, Nature Reviews Gastroenterology &Hepatology.
[28] Li‐yu Lee,et al. IgG4‐positive plasma cells in cutaneous Rosai‐Dorfman disease: an additional immunohistochemical feature and possible relationship to IgG4‐related sclerosing disease , 2009, Journal of cutaneous pathology.
[29] S. Honavar,et al. Rosai dorfman disease of the orbit , 2008, Journal of hematology & oncology.
[30] Y. Nakanuma,et al. Th2 and regulatory immune reactions are increased in immunoglobin G4‐related sclerosing pancreatitis and cholangitis , 2007, Hepatology.
[31] A. Vincent-Salomon,et al. Ocular adnexal lymphoma: a review of clinicopathologic features and treatment options. , 2006, Blood.
[32] J. Rootman,et al. The Spectrum of Orbital Rosai-Dorfman Disease , 2006, Ophthalmic plastic and reconstructive surgery.
[33] C. Shields,et al. Survey of 1264 patients with orbital tumors and simulating lesions: The 2002 Montgomery Lecture, part 1. , 2004, Ophthalmology.
[34] F. Mandelli,et al. Treatment of sinus histiocytosis with massive lymphadenopathy (rosai‐dorfman disease): Report of a case and literature review , 2002, American journal of hematology.
[35] G. Harris,et al. ORBITAL VASCULAR LESIONS , 2000 .
[36] J. Rosai,et al. Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease): review of the entity. , 1990, Seminars in diagnostic pathology.
[37] J. Rosai,et al. The ophthalmologic manifestations of sinus histiocytosis with massive lymphadenopathy. , 1979, American journal of ophthalmology.
[38] R. Jaffe,et al. Pathology of Histiocytic Disorders and Neoplasms and Related Disorders , 2018 .
[39] Hilde van der Togt,et al. Publisher's Note , 2003, J. Netw. Comput. Appl..
[40] L. Bilaniuk,et al. Orbital vascular lesions. Role of imaging. , 1999, Radiologic clinics of North America.