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Sinus Histiocytosis with Massive Lymphadenopathy: A Case Report with Pleural Effusion and Cervical Lymphadenopathy

机译:窦性组织细胞增生伴大规模淋巴结肿大:胸腔积液和宫颈淋巴结肿大一例报告

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摘要

Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare disorder characterized by a nonneoplastic proliferation of distinctive histiocyte cells within lymph node sinuses and lymphatics in extranodal sites. SHML occurs worldwide and is primarily a disease of childhood and early adulthood. A 26-yr-old man presented with painless palpable lymph node in cervical area. Radiographic studies revealed pleural effusion with lymphadenopathy and calcification in mediastinum. The cervical lymph node biopsy showed dilated sinuses filled with histiocytes with clear cytoplasm. The cells stained positive with CD68 and S-100. These cytologic and immunohistochemical findings were considered consistent with the diagnosis of SHML.
机译:具有大量淋巴结病(SHML)的窦组织细胞增生症是一种罕见的疾病,其特征在于淋巴结窦和淋巴结外淋巴结部位的独特组织细胞发生非肿瘤性增殖。 SHML遍布世界各地,主要是儿童期和成年期疾病。一名26岁的男子在宫颈区域出现无痛可触及的淋巴结。影像学检查显示胸腔积液伴淋巴结肿大和纵隔钙化。宫颈淋巴结活检显示鼻窦扩张,充满了具有清晰细胞质的组织细胞。细胞被CD68和S-100染色阳性。这些细胞学和免疫组化发现被认为与SHML的诊断一致。

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