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首页> 外文期刊>European Journal of Case Reports in Internal Medicine >Sinus Histiocytosis with Massive Lymphadenopathy (Rosai Dorfman Disease) and Anaplastic Large Cell Lymphoma
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Sinus Histiocytosis with Massive Lymphadenopathy (Rosai Dorfman Disease) and Anaplastic Large Cell Lymphoma

机译:窦性组织细胞增生伴大规模淋巴结病(罗赛·多夫曼病)和间变性大细胞淋巴瘤

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摘要

Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare and benign source of lymphadenopathy first described in 1969. This disease commonly presents in children and young adults with supra-diaphragmatic lymphadenopathy mainly at cervical nodal sites, composed of a polyclonal population of histiocytes. Since its description greater than 400 cases have been described, however the literature is quiet scanty when it comes to its association with lymphomas. This case report describes a case with co-existing SHML and anaplastic large cell lymphoma (ALCL). The diagnosis of SHML in our patient did not alter the clinical outcome and patient responded well to treatment of ALCL. Clinicians should maintain a high index of suspicion in cases of infra-diaphragmatic SHML for the presence of occult lymphoma.
机译:窦性组织细胞增生伴大量淋巴结肿大(SHML)是一种罕见且良性的淋巴结病来源,最早于1969年描述。这种疾病通常存在于dia上淋巴结淋巴结肿大的儿童和年轻人中,主要存在于颈部淋巴结部位,由多克隆的组织细胞组成。由于已经描述了超过400例病例,但是,与淋巴瘤相关的文献很少。该病例报告描述了SHML与间变性大细胞淋巴瘤(ALCL)并存的病例。我们患者中SHML的诊断没有改变临床结果,并且患者对ALCL的治疗反应良好。对于dia下SHML患者是否存在隐匿性淋巴瘤,临床医生应保持高度怀疑。

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