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成年期诊断出的两例慢性肉芽肿病

Two Chronic Granulomatous Disease Diagnosed in Adult Age.

作者信息

Akyıl Fatma Tokgöz, Sevim Tülin, Barış Safa, Aksoy Emine, Tokyay Dilem Anıl, Bodur Yasemin, Aktaş Oğuz

机构信息

Clinic of Chest Diseases, Süreyyapaşa Chest Diseases and Chest Surgery Training and Research Hospital, İstanbul, Turkey.

Clinic of Pediatric Allergy and İmmunology, Marmara University Hospital, İstanbul, Turkey.

出版信息

Turk Thorac J. 2016 Oct;17(4):163-167. doi: 10.5578/ttj.30515. Epub 2016 Oct 1.

Abstract

Chronic granulomatous disease (CGD) is a rare, inherited primary immunodeficiency that is usually diagnosed at adulthood and is presented with recurrent bacterial and fungal infections. In this case report, two adult cases of CGD have been presented. A 29-year-old woman was referred to our clinic with hypoxic respiratory failure, with a pre-diagnosis of multidrug resistant tuberculosis (TB). Her lung biopsy had been reported as granulomatous inflammation, she had not responded to a 5 month anti-TB treatment. A complete medical history consisted of 4 occasions of treatment with anti-TB drugs and that her sister and brother had undergone TB therapy. However, since childhood, a TB bacilli had never been isolated microbiologically in the siblings. Patient's parents were third degree consanguineous. The patient still had a purulent drainage around the operation site. Microbiological studies of the wound drainage and respiratory tract have not encountered any specific microorganism. Investigation of an immunodeficiency has proved CGD through nitroblue tetrazolium test. Her siblings has been diagnosed as CGD as well. Second case, a 19-year-old male, has been admitted to our clinic with complaints of fever, chest pain and an abscess lesion in the anterior chest wall. His medical history comprised 3 recurrences of pneumonia within last 2 years. In physical examination, a 3 × 5 cm fluctuant swelling lesion on the anterior chest wall. Radiologically, new pneumonic consolidations were detected. Sputum specimens did not provide any specific microorganism, cultures of the chest-wall abscess fluid grew aspergillus. His parents had been living in the same village but no consanguinity was known. Due to recurrent infections, immunodeficiency tests had been investigated. He was diagnosed as CGD due to dihydrorhodamin test. These two cases signify that, in our country where consanguinity is common, etiology of recurrent unexplained infections, abscesses and granulomas should be investigated and CGD should be in differantial diagnosis list.

摘要

慢性肉芽肿病(CGD)是一种罕见的遗传性原发性免疫缺陷病,通常在成年期被诊断出来,表现为反复出现细菌和真菌感染。在本病例报告中,介绍了两例成年CGD病例。一名29岁女性因低氧性呼吸衰竭被转诊至我们的诊所,初步诊断为耐多药结核病(TB)。她的肺活检报告为肉芽肿性炎症,接受了5个月的抗结核治疗但无反应。完整的病史包括4次抗结核药物治疗,她的姐姐和哥哥也接受过结核病治疗。然而,自童年以来,这些兄弟姐妹从未在微生物学上分离出结核杆菌。患者的父母是三级近亲。患者手术部位仍有脓性引流物。伤口引流物和呼吸道的微生物学研究未发现任何特定微生物。通过硝基蓝四唑试验证实免疫缺陷检查诊断为CGD。她的兄弟姐妹也被诊断为CGD。第二例,一名19岁男性,因发热、胸痛和前胸壁脓肿病变入住我们的诊所。他的病史包括过去2年内3次肺炎复发。体格检查发现前胸壁有一个3×5厘米的波动肿胀病变。放射学检查发现新的肺炎实变。痰标本未发现任何特定微生物,胸壁脓肿液培养出曲霉菌。他的父母住在同一个村庄,但不知是否有血缘关系。由于反复感染,进行了免疫缺陷检查。因二氢罗丹明试验,他被诊断为CGD。这两例病例表明,在我国近亲结婚很常见的情况下,对于反复出现的不明原因感染、脓肿和肉芽肿的病因应进行调查,CGD应列入鉴别诊断清单。

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本文引用的文献

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Chronic granulomatous disease.慢性肉芽肿病。
Clin Rev Allergy Immunol. 2010 Feb;38(1):3-10. doi: 10.1007/s12016-009-8136-z.
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Genetics and immunopathology of chronic granulomatous disease.慢性肉芽肿病的遗传学与免疫病理学
Semin Immunopathol. 2008 Jul;30(3):209-35. doi: 10.1007/s00281-008-0121-8. Epub 2008 May 29.
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BCG-osis and tuberculosis in a child with chronic granulomatous disease.一名患有慢性肉芽肿病儿童的卡介苗病和结核病
J Allergy Clin Immunol. 2007 Jul;120(1):32-8. doi: 10.1016/j.jaci.2007.04.034. Epub 2007 Jun 4.
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Nocardia infection in chronic granulomatous disease.慢性肉芽肿病中的诺卡菌感染。
Clin Infect Dis. 2002 Aug 15;35(4):390-4. doi: 10.1086/341416. Epub 2002 Jul 23.

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