CUTANEOUS ROSAI-DORFMAN DISEASE – A CLINICAL CASE

V. Pătrașcu, Alexandra Filculescu, C. C. Georgescu, R. Ciurea
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Abstract

Introduction. Rosai-Dorfman disease is a benign condition, characterized by self limiting proliferation of non-Langerhans histiocytes insidelymph nodes but also in extranodal areas. Clinical case. A 54-year-old patient, diagnosed with arterial hypertension since 2011, is hospitalised in the Dermatology Department of the Emergency County Hospital, Craiova, Romania, in March 2016, for a polymorphous rash composed of violet-erythematous papulonodules with sizes ranging between 0.2 cm and 2 cm, slightly itchy, located in the latero-thoracic region, lumbar region and in the area around the menton area. The lesions appeared 18 months prior to hospitalization. Clinical and paraclinical investigations as well as interdisciplinary consultations revealed no associated pathologies. Histopathological and immunohistochemical examinations confirmed the diagnostic of cutaneous Rosai-Dorfman disease, imaging investigations excluding other localizations. Treatment with Doxycycline, in combination with 20 mg of Rutoside and 50 mg of ascorbic acid, Pentoxifylline and Levocetirizine resulted in remission of the skin lesions. Discussion. Rosai-Dorfman disease is a rare condition, having a reported incidence rate of 1:200.000. It generally affects males, being more frequent in young males and people of African descent. The pathogenesis of Rosai-Dorfman disease is still not fully understood, although immunological and infectious factors may play an important role. Foucar has divided this condition into three types: nodal, extranodal and mixed. Cutaneous lesions have been described in 3% of cases of Rosai-Dorfman disease of the extranodal type. It is more frequent in females (sex ratio of 2/1) and in adults of Asian descent, with a mean age at onset of 45 years. Treatment options include: oral and intralesional corticosteroids, alfa-interferon, retinoids, dapsone, methotrexate, thalidomide, cryo- and radiotherapy. Conclusions. The presented case is an atypical one because of the three locations of the skin lesions. Although we obtained remission of the disease, the patient would remain in direct observation because of the risk of recurrence. Key words :  Rosai-Dorfman disease; cutaneous form; treatment.
皮肤蔷薇-多夫曼病1例临床分析
介绍。Rosai-Dorfman病是一种良性疾病,其特点是淋巴结内和结外区域非朗格汉斯组织细胞的自限性增殖。临床病例。一名54岁的患者,自2011年以来被诊断为动脉高血压,于2016年3月在罗马尼亚克拉约瓦急诊县医院皮肤科住院,因其多形态皮疹,由紫色红斑丘疹组成,大小在0.2 cm至2 cm之间,轻微瘙痒,位于胸后区、腰椎区和颏区周围区域。病变出现于住院前18个月。临床和临床旁调查以及跨学科会诊未发现相关病理。组织病理学和免疫组织化学检查证实了皮肤Rosai-Dorfman病的诊断,影像学检查排除了其他局限性。多西环素联合20毫克乳托苷和50毫克抗坏血酸、己酮可可碱和左西替利嗪治疗可缓解皮肤病变。讨论。罗赛-多夫曼病是一种罕见的疾病,据报道发病率为1:20万。它通常影响男性,在年轻男性和非洲人后裔中更为常见。Rosai-Dorfman病的发病机制仍不完全清楚,尽管免疫和感染因素可能起重要作用。福卡将这种情况分为三种类型:结节性、结外性和混合性。结节外型Rosai-Dorfman病有3%的病例有皮肤病变。它在女性(性别比例为2/1)和亚裔成年人中更为常见,平均发病年龄为45岁。治疗方案包括:口服和局部皮质类固醇、α -干扰素、类维生素a、氨苯砜、甲氨蝶呤、沙利度胺、冷冻和放疗。结论。本病例为非典型病例,有三个部位的皮肤病变。虽然我们获得了疾病的缓解,但由于复发的风险,患者将继续接受直接观察。关键词:Rosai-Dorfman病;皮肤的形式;治疗。
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