[合并不寻常特征的可变型免疫缺陷。病例报告]
[Combined variable immunodeficiency with unusal features. A case report].
作者信息
De Charry F, Peterschmitt Tonetti A, De Charry C, Baseggio L, Pasquet F, Khenifer S, Rassat R, Pavic M
机构信息
Service de médecine interne-oncologie, HIA Desgenettes, 108, boulevard Pinel, 69003 Lyon, France.
Service médecine interne, groupe hospitalier mutualiste, 8, rue Docteur-Calmette, 38000 Grenoble, France.
出版信息
Rev Med Interne. 2015 May;36(5):359-62. doi: 10.1016/j.revmed.2014.02.003. Epub 2014 Mar 12.
INTRODUCTION
The association granulomatosis - combined variable immunodeficiency (CVID) - is well known from the clinicians. However, the association with a large granular lymphocyte (LGL) leukemia has not been yet reported.
CASE REPORT
We report a 50-year-old woman, followed for CVID associated with a granulomatous disease. During the follow-up, the patient developed a granulomatous lymphocytic interstitiel lung disease (GLILD). Secondarily, she presented a LGL leukemia.
CONCLUSION
To our knowledge, this is the first reported case of an association between CVID and LGL leukemia.
引言
肉芽肿病与联合可变免疫缺陷（CVID）的关联在临床医生中广为人知。然而，与大颗粒淋巴细胞（LGL）白血病的关联尚未见报道。
病例报告
我们报告一名50岁女性，因与肉芽肿病相关的CVID接受随访。在随访期间，患者发展为肉芽肿性淋巴细胞间质性肺病（GLILD）。其次，她出现了LGL白血病。
结论
据我们所知，这是首例报道的CVID与LGL白血病相关联的病例。
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