Gao David X, Hussain Habiba, Bobber Brianna, Phan Peter
University of Illinois College of Medicine, One Illini Drive, Peoria, IL, 61605, USA.
Allergy Asthma Clin Immunol. 2022 Apr 5;18(1):31. doi: 10.1186/s13223-022-00673-3.
Common variable immunodeficiency (CVID) is a primary immunodeficiency disorder associated with a broad symptom presentation that is still being characterized. We report a rare case of recurrent mycoplasma skin abscesses in a patient with a history of autoimmune disorders and prolonged mycoplasma pneumonia who was diagnosed with CVID.
A 34-year-old woman presented with a history of recurrent abscesses previously confirmed positive for Mycoplasma pneumoniae. Her past medical history of recurrent mycoplasma abscesses, prolonged mycoplasma pneumonia, and autoimmune disorders (mixed connective tissue disease and immune thrombocytopenia) raised suspicion of CVID. Workup included negative anti-mycoplasma antibody titers, hypogammaglobulinemia, and negative anti-pneumococcal antibody titers despite prior vaccination, solidifying the diagnosis of CVID. The patient was discharged on antibiotic and intravenous immunoglobulin therapy and now follows allergy and immunology long-term for treatment.
Her diagnostic history underscores the importance of considering the various criteria of CVID for diagnosis, and her unique presentation of M. pneumoniae skin abscesses highlights the broad sequelae patients with CVID can manifest.
普通可变免疫缺陷(CVID)是一种原发性免疫缺陷疾病,其症状表现广泛,仍在研究之中。我们报告了一例罕见病例,一名有自身免疫性疾病病史且支原体肺炎病程迁延的患者被诊断为CVID,出现复发性支原体皮肤脓肿。
一名34岁女性,有复发性脓肿病史,此前确诊肺炎支原体阳性。她既往有复发性支原体脓肿、迁延性支原体肺炎及自身免疫性疾病(混合性结缔组织病和免疫性血小板减少症)病史,这引发了对CVID的怀疑。检查包括抗支原体抗体滴度阴性、低丙种球蛋白血症,以及尽管之前接种过疫苗但抗肺炎球菌抗体滴度仍为阴性,从而确诊为CVID。患者出院时接受抗生素和静脉注射免疫球蛋白治疗,目前长期在过敏与免疫学门诊接受治疗。
她的诊断病史强调了考虑CVID各种诊断标准的重要性,而她独特的肺炎支原体皮肤脓肿表现突出了CVID患者可能出现的广泛后遗症。