Sinus histiocytosis with massive lymphadenopathy, (Rosai-Dorfman Disease) with cholastatic jaundice in an HIV positive patient

K. Mpho, Elnagar Ali Ahmed, Mashoshoe Kgataki Sam, T. Preetha, Ngwata Portia, Bida Mishack
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Abstract

Introduction Sinus histiocytosis with massive lymphadenopathy is a rare histiocytic disease first described by Rosai and Dorfman in 1969. The typical presentation is that of cervical and often widespread painless lymphadenopathy. Case report We present a 33-year-old gentleman, with one-month history of pruritus, abdominal pain, jaundice and dark urine, jaundice, scratch marks, large inguinal lymph nodes, an enlarged liver and spleen. CT scan confirmed ultrasound findings and suggested that splenic lesions were microabscesses. Biopsy of the lymph nodes revealed features in keeping with sinus histiocytosis with dermatophatic lymphadenopathy. Discussion This is our second case of sinus histiocytosis in two years.
窦性组织细胞增多症伴大量淋巴结病变,(Rosai-Dorfman病)伴胆汁淤积性黄疸
窦性组织细胞增多症合并大量淋巴结病是一种罕见的组织细胞疾病,由Rosai和Dorfman于1969年首次报道。典型的表现是颈部无痛性淋巴结病,通常分布广泛。我们报告一位33岁的男性患者,有瘙痒、腹痛、黄疸及尿色深、黄疸、抓痕、腹股沟淋巴结大、肝脾肿大等病史一个月。CT扫描证实超声表现,提示脾病变为微脓肿。淋巴结活检显示的特征与皮肤淋巴病变的窦性组织细胞增多症一致。这是我们两年内第二例窦性组织细胞增多症。
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来源期刊
Australasian Medical Journal
Australasian Medical Journal MEDICINE, GENERAL & INTERNAL-
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