Multicentric reticulohistiocytosis: a case report
نویسندگان
چکیده
منابع مشابه
multicentric reticulohistiocytosis: a case report
multicentric reticulohistiocytosis (mrh) is a rare proliferative histiocytic disease of unknown cause with potentially disabling nature. primary manifestations are involvement of skin and joints. the articular destruction can lead to permanent joint deformities. our patient was a 47 year-old woman with bilateral symmetrical polyarthritis and reddish- brown papulonodular cutaneous lesions. t...
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Multicentric reticulohistiocytosis (MRH) is a very rare systemic disease with variable phenotypic presentation and a high rate of misdiagnosis. Here we describe a patient with MRH and extra-mammillary Paget's disease (EMPD), a diagnosis that has not previously been described in the literature.
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We report a unique case of multicentric reticulohistiocytosis (MRH) associated with liver carcinoma. A 61-year-old man presented with a 4-month history of nonpruritic, generalized, ruby-red papules and nodules, accompanied by fever, joint swelling and difficulty in swallowing. Skin histology showed polymorphic histiocyte infiltration with typical 'ground glass' cytoplasm. Further immunohistoche...
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Multicentric reticulohistiocytosis is a very rare systemic disease that affects skin, mucosa and joints. We reported a case of a woman with multicentric reticulohistiocytosis who presented typical skin syndromes and arthralgia. Immunohistochemical analysis showed positive staining for S100 protein, which was reported negative in the majority of previously presented cases. Other immunohistochemi...
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ژورنال
عنوان ژورنال: BMC Research Notes
سال: 2018
ISSN: 1756-0500
DOI: 10.1186/s13104-018-3753-3