A RARE OFUJI PAPULO-ERYTHRODERMA REVEALING A LANGERHANS CELL HISTIOCYTOSIS INVOLVING ONLY LYMPH NODES
作者: Nafissa Farid Said AmalOuafa Hocar
刊名: International Journal of Advanced Research (IJAR), 2020, Vol.8 (1)
来源数据库: International Journal of Advanced Research
原始语种摘要: Ofuji Papulo-erythroderma is a rare entity. Its origin is most often paraneoplasic: visceral neoplasias and blood diseases are the most frequently found. We report a case of Ofuji papuloerythroderma revealing langerhans cell histiocytosis involving only lymph nodes.We report the case of a 48-year-old man who presented a pruriginous papuloerythroderma, respecting skin folds, having progressed for 8 years in a context of deterioration of the general state, associated with bilateral inguinal lymphadenopathies. The patient had already had several skin biopsies that were inconclusive. The biological assessment revealed an inflammatory syndrome and a discreet hyper-eosinophilia. Lymph node biopsy confirmed the diagnosis of Langerhans cell histiocytosis. Clinical and imaging studies did not...
全文获取路径: IJAR 
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关键词翻译
关键词翻译
  • histiocytosis 组织细胞增多病
  • erythroderma 红皮病
  • chemotherapy 化学疗法
  • vinblastine 长春花碱
  • pruriginous 痒疹的
  • assessment 评价
  • inconclusive 不确定
  • literature 文献
  • lymph 淋巴
  • exceptionally 例外地