Einsele H, Saal J G, Dopfer R, Niethammer D, Waller H D, Müller C A
Abteilung Innere Medizin II, Universität, Tübingen.
Dtsch Med Wochenschr. 1990 Jul 27;115(30):1141-4. doi: 10.1055/s-2008-1065133.
A largely symptom-free swelling of the right submandibular lymph nodes developed in a 23-year-old woman with hyper-IgE syndrome who had suffered from recurrent staphylococcal abscesses since childhood. Histological examination of the lymph nodes revealed highly malignant non-Hodgkin lymphoma of centroblastic type. Extensive staging tests did not reveal any further tumour manifestations. Because granulocyte chemotaxis is abnormal in hyper-IgE syndrome and the patient also had an infection of an old lung cyst, treatment was restricted to local radiotherapy of the cervical lymph nodes. Since 12 months there has been no recurrence. There is probably no connection between the hyper-IgE syndrome and the development of a malignant non-Hodgkin lymphoma, judging by the results of immunological and immunoelectrophoretic findings.
一名23岁患有高IgE综合征的女性,自童年起就反复出现葡萄球菌脓肿,右侧颌下淋巴结出现了一个基本无症状的肿大。淋巴结组织学检查显示为中心母细胞型高度恶性非霍奇金淋巴瘤。广泛的分期检查未发现任何其他肿瘤表现。由于高IgE综合征中粒细胞趋化性异常,且该患者还患有一个陈旧性肺囊肿感染,治疗仅限于颈部淋巴结局部放疗。12个月来未再复发。从免疫学和免疫电泳结果判断,高IgE综合征与恶性非霍奇金淋巴瘤的发生可能没有关联。