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dc.creatorZapata, Juan Manuel
dc.creatorLillo, Fernando Andrés
dc.creatorCabezas, Antonio Fabian
dc.creatorRiquelme, Santiago Felipe Andrés
dc.date2019-03-01
dc.date.accessioned2021-07-23T21:55:53Z
dc.date.available2021-07-23T21:55:53Z
dc.identifierhttps://revistas.uautonoma.cl/index.php/ijmss/article/view/42
dc.identifier10.32457/ijmss.2019.006
dc.identifier.urihttps://hdl.handle.net/20.500.12728/9320
dc.descriptionCastleman’s disease (CD) or angiofollicular lymph node hyperplasia includes a heterogeneous mix of reactive lymphoproliferative processes with well-defined histological features. However, they differ in their localization patterns, clinical expression and etiopathogenesis. There are 4 types, one of them is the multicentric CD that is not associated with any viruses and has recently been called idiopathic MCD (iMCD). iMCD is a lymphoproliferative disorder with specific histopathological characteristics, more than one region of affected lymph nodes and absence of infection associated to human herpesvirus 8 and human immunodeficiency virus (HIV). iMCD covers multiple differential diagnoses and might simulate autoimmune diseases such as systemic lupus erythematosus. The aim of this article is to report the case of a patient with Castleman’s disease and lupus-like presentation. We present the case of a 38-year-old man without morbid history, who presented lumbago, fever, diaphoresis and asthenia with two months of evolution, associated to bilateral cervical adenopathies. General examinations result negative, antinuclear antibodies at a dilution of 1/640 were positive, and extractable nuclear antigens were positive suggesting moderate Systemic Lupus Erythematosus (SLE) plus secondary Sjögren’s. Methylprednisolone and Hydroxycloroquine boli were thus initiated. The patient evolved with anasarca, severe anemia, acidosis, polyserositis and multiple mediastinal adenopathies. Immunoglobulin and cyclophosphamide were thus initiated. He later presented fever, thrombocytopenia and nephrotic syndrome. Biopsy of cervical lymph node reported lymphadenitis with polyclonal plasmacytosis and concentric lymphoid hyperplasia, in agreement with iMCD. Treatment with Rituximab was initiated, which led to the favorable evolution of the patient. iMCD is a systemic inflammatory disease, its presentation corresponds to a constitutional syndrome resulting in a wide differential diagnosis. Every time suspicious adenopathies appear, they must be biopsied since this might lead to a definitive diagnosis.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherUniversidad Autónoma de Chileen-US
dc.relationhttps://revistas.uautonoma.cl/index.php/ijmss/article/view/42/37
dc.rightsCopyright (c) 2020 International Journal of Medical and Surgical Sciencesen-US
dc.sourceInternational Journal of Medical and Surgical Sciences; Vol. 6 No. 1 (2019): March 2019; 14-17en-US
dc.sourceInternational Journal of Medical and Surgical Sciences; Vol. 6 Núm. 1 (2019): March 2019; 14-17es-ES
dc.source0719-532X
dc.source0719-3904
dc.source10.32457/ijmss.v6i1
dc.subjectGiant lymph node hyperplasiaen-US
dc.subjectInterleukin-6en-US
dc.subjectSystemic Lupus Erythematosusen-US
dc.titleIdiopathic multicentric Castleman’s disease, infrequent cause of Lupus-like. Case Report.en-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typeCase Reporten-US


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