获得性常见可变型低丙种球蛋白血症和淋巴水肿。
Acquired common variable hypogammaglobulinaemia and lymphoedema.
作者信息
Lozewicz S, Morris G, Garbett N, Browse N, Slavin B, Cole P
机构信息
Department of Thoracic Medicine, Brompton Hospital, London, UK.
出版信息
Postgrad Med J. 1988 Jan;64(747):63-5. doi: 10.1136/pgmj.64.747.63.
Abstract
Two patients with lymphoedema of the legs developed recurrent respiratory infections and were found to have panhypogammaglobulinaemia. The early recognition and treatment of this form of immunity deficiency in patients with lymphoedema is important in order to prevent recurrent infections which could cause pulmonary damage and further lymphatic stasis.
摘要
两名患有腿部淋巴水肿的患者反复出现呼吸道感染，经检查发现患有全血细胞减少性低丙种球蛋白血症。对于淋巴水肿患者，早期识别和治疗这种免疫缺陷形式非常重要，以预防可能导致肺部损伤和进一步淋巴淤滞的反复感染。
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引用本文的文献
本文引用的文献
1
THE "YELLOW NAIL" SYNDROME.“黄甲”综合征
Br J Dermatol. 1964 Apr;76:153-7. doi: 10.1111/j.1365-2133.1964.tb14499.x.
2
Autoimmune blood dyscrasias in five patients with hypogammaglobulinemia: response of neutropenia to vincristine.
J Clin Immunol. 1981 Apr;1(2):113-8. doi: 10.1007/BF00915388.
3
Yellow nails, lymphoedema, and pleural effusions.黄甲、淋巴水肿和胸腔积液。
Thorax. 1966 May;21(3):247-53. doi: 10.1136/thx.21.3.247.
4
Lymphedema, pleural effusions and yellow nails: associated immunologic deficiency.
Dis Chest. 1969 Aug;56(2):114-7. doi: 10.1378/chest.56.2.114.
5
The gamma globulins. 3. The antibody deficiency syndromes.γ球蛋白。3. 抗体缺陷综合征。
N Engl J Med. 1966 Sep 29;275(13):709-15 contd. doi: 10.1056/NEJM196609292751307.
6
Pulmonary manifestations of the yellow nail syndrome.
Chest. 1972 May;61(5):452-8. doi: 10.1378/chest.61.5.452.
7
Pleural effusions and yellow nails of late onset.迟发性胸腔积液和黄甲
Postgrad Med J. 1973 May;49(571):364-5.
8
B and T lymphocytes in primary immunodeficiency disease in man.人类原发性免疫缺陷病中的B淋巴细胞和T淋巴细胞。
J Clin Invest. 1973 Apr;52(4):919-28. doi: 10.1172/JCI107257.
9
Sarcoidosis and primary hypogammaglobulinaemia: a report of two cases and a review of the literature.结节病与原发性低丙种球蛋白血症：两例报告及文献综述
Sarcoidosis. 1985 Sep;2(2):91-5.
10
Yellow-nail syndrome: report of three cases.黄甲综合征：三例报告。
Can Med Assoc J. 1976 Jul 3;115(1):46-8.
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