Literature DB >> 31742640

Multicentric reticulohistiocytosis: the Mayo Clinic experience (1980-2017).

Catalina Sanchez-Alvarez1, Avneek Singh Sandhu2, Cynthia S Crowson1,3, David A Wetter4, Gavin A McKenzie5, Julia S Lehman4,6, Ashima Makol1.   

Abstract

OBJECTIVES: Multicentric reticulohistiocytosis (MRH), a rare histiocytic disease that can mimic other rheumatic conditions, may be associated with cancer and other autoimmune disorders. To better understand the disorder and its other associations, we aimed to evaluate clinical correlates and outcomes of all patients with MRH seen at Mayo Clinic, Rochester between 1980 and 2017.
METHODS: A retrospective medical record review was conducted to identify all patients with MRH between 1 January 1980 and 30 April 2017.
RESULTS: We identified 24 patients with biopsy-proven MRH (58% female, 75% Caucasian, median age at diagnosis 52 years, median follow-up of 2.3 years). All patients had cutaneous and articular involvement; 23 (96%) patients had papulonodular skin lesions (87% periungual and dorsal hand) and seven (30%) mucosal nodules; and 22 (92%) patients had arthralgias, 21 (88%) joint effusions and 13 (54%) synovitis. Most frequently used therapies included corticosteroids, cyclophosphamide, methotrexate and bisphosphonates. Biologics were used in four patients. Nine patients had symptomatic resolution at 1 year and 12 partial improvement. Radiological findings included erosive changes in three (60%) patients and arthritis mutilans in two patients (40%). Twenty-nine per cent of patients had a concomitant autoimmune disease and 25% malignancy including melanoma, endometrial, peritoneal and lung carcinoma. The 5-year survival rate was 85% (95% CI: 74, 100%).
CONCLUSION: To our knowledge, this is the largest single-centre series of patients with MRH highlighting the rarity of the condition and an unmet need for treatment options that can allow sustained disease remission. It also highlights the need for a high vigilance for malignancy and autoimmune diseases.
© The Author(s) 2019. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  MRH; arthritis; arthritis mutilans; histiocytic disorder; multicentric reticulohistiocytosis

Mesh:

Substances:

Year:  2020        PMID: 31742640     DOI: 10.1093/rheumatology/kez555

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  5 in total

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2.  Multicentric reticulohistiocytosis revealing breast cancer: Report of a case with dermoscopic, radiological and therapeutic aspects.

Authors:  Massimo Dell'Antonia; Laura Atzori; Luca Pilloni; Caterina Ferreli
Journal:  Australas J Dermatol       Date:  2021-08-16       Impact factor: 2.481

3.  Clinical characteristics of multicentric reticulohistiocytosis and distinguished features from rheumatoid arthritis: a single-center experience in China.

Authors:  Xiao-Juan Zou; Lin Qiao; Feng Li; Hua Chen; Yun-Jiao Yang; Dong Xu; Wen-Jie Zheng; Zhen-Yu Jiang; Li Wang; Qing-Jun Wu; Feng-Chun Zhang
Journal:  Orphanet J Rare Dis       Date:  2022-04-12       Impact factor: 4.123

4.  Multicentric Reticulohistiocytosis Exhibiting Positive HLA-B*07 and HLA-B*08: A Case Report.

Authors:  Elena Rezuș; Maria Alexandra Burlui; Anca Cardoneanu; Danisia Haba; Mihai Danciu; Romică Sebastian Cozma; Ciprian Rezuș
Journal:  Medicina (Kaunas)       Date:  2020-09-08       Impact factor: 2.430

5.  Case Report: Multicentric Reticulohistiocytosis Associated With Posterior Mediastinal Adenosquamous Carcinoma, Antinuclear Antibody Positivity and Lupus Anticoagulant Positivity.

Authors:  Ziyi Tang; Xiangpeng Wang; Zijing Xia; Zhongming Wang; Yi Zhao; Yi Liu
Journal:  Front Immunol       Date:  2022-01-07       Impact factor: 7.561

  5 in total

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