Delsol G, Familiades J, Voigt J J, Gorguet B, Pris J, Laurent G, Fabre J
Ann Anat Pathol (Paris). 1977;22(1):61-74.
Besides the dysimmunitary and pseudo-lymphomatous adenopathies rich in immunoblasts and plasmocytes (ADPL type I) five cases showed similar clinical and biological data but with frequently otorhinolaryngologic location. The lesions are characterized by important structural changes and abundant epithelioid cells are comparable to Lukes' type III immunoblastic lymphadenopathies and to Lennert's lymphoepithelioid lymphomas. They must be distinguished from Hodgkin's granulomas which are rich in epithelioid cells. They are perhaps due to a disturbancy bearing mainly on the cellular immunity.
除了富含免疫母细胞和浆细胞的免疫失调性和假淋巴瘤性腺病(ADPL I型)外,5例患者具有相似的临床和生物学数据,但病变部位常位于耳鼻喉科。这些病变的特征是有重要的结构改变,大量上皮样细胞可与卢克斯III型免疫母细胞性淋巴结病和 Lennert 淋巴上皮样淋巴瘤相媲美。它们必须与富含上皮样细胞的霍奇金肉芽肿相鉴别。它们可能主要是由于细胞免疫紊乱所致。