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Anaplastic large cell lymphoma in a patient with MAGIC syndrome: a case and review of the literature

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Abstract

Mouth and genital ulcer with inflamed cartilage syndrome (MAGIC syndrome) is a rare autoinflammatory disorder with unknown etiology. Except for the common clinical manifestations mimicking Behçet’s disease and relapsing polychondritis, some other clinical entities are occasionally observed. In this report, we present a case in which a patient developed anaplastic large cell lymphoma 1 year after the diagnosis of MAGIC syndrome. Additionally, we review the clinical manifestations, management, and prognosis of MAGIC syndrome.

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The figures were created by the GraphPad Prism 8 software.

Funding

This work was supported by the National Natural Science Foundation of China [81871299], the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences [CIFMS 2017-I2M-1-008][CIFMS 2016-I2M-1-013] , National Key Research and Development Program: “Precise Medical Research” [2016YFC0906201].

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All authors were involved in drafting the article or revising it critically for important intellectual content, and all authors approved the final version to be published. ZC and JL performed the literature researching and summarizing. ZC, SZ, LW, YF, MS, JL, and WZ provided the patient medical care and assistance during the in-hospital period in our department. HW performed the pathological analysis and evaluation. JL and WZ designed this review initially.

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Correspondence to Jinjing Liu or Wenjie Zheng.

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The study was approved by the IRB of the Peking Union Medical College Hospital.

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Chen, Z., Zhang, S., Wang, L. et al. Anaplastic large cell lymphoma in a patient with MAGIC syndrome: a case and review of the literature. Clin Rheumatol 40, 2075–2082 (2021). https://doi.org/10.1007/s10067-020-05384-x

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