Two Chronic Granulomatous Disease Diagnosed in Adult Age.

نویسندگان

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

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.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Colitis complicating chronic granulomatous disease. A clinicopathological case report.

BACKGROUND This report concerns a female patient now aged 24 years, diagnosed at the age of 7 years as suffering from chronic granulomatous disease. At age 20 she developed diarrhoea accompanied by rectal bleeding. Endoscopy showed extensive colitis. She failed to respond to medical treatment and underwent total colectomy two years later. AIMS To discuss the histological changes in the colon ...

متن کامل

Cytology of Idiopathic Granulomatous Mastitis : A Report of a Case Masquerading as Carcinoma

Idiopathic granulomatous mastitis is a rare condition of unknown aetiology, affecting women of childbearing age. Although many conditions mimic granulomatous mastitis, the cytologic pattern of epithelioid cells, multinucleated giant cells, neutrophils, macrophages and reactive epithelial cells, in absence of caseation necrosis and foam cells should prompt a diagnosis of granulomatous mastitis. ...

متن کامل

Chronic Granulomatous Disease, Case Report and Review of Literature

  Chronic granulomatous disease (CGD) is a rare inherited disorder characterized by inability of phagocytes to generate oxygen radicals needed for intracellular killing of phagocytic microorganisms. We report a 2.5-year-old Iranian female with multiple liver abscesses. She was admitted in surgical ward because of abdominal pain and fever for one month duration that had no response to conventio...

متن کامل

Pulmonary Aspergillosis in a Previously Healthy 13-Year-Old Boy

Chronic granulomatous disease (CGD) is a rare, polygenic primary immunodeficiency. In this case report, we describe a previously healthy 13-year-old boy who presented with multifocal pulmonary aspergillosis and was subsequently diagnosed with an autosomal recessive form of chronic granulomatous disease. CGD has a variable natural history and age of presentation and should be considered when inv...

متن کامل

A rare unusual case report of Hepatic Tuberculosis in a Yemeni Child, presented with Pyrexia of Unknown Origin

Hepatic Tuberculosis (HTB) is a rare form of tuberculosis. The disease presentation and characteristics have been described in a number of adult cases from low resource settings, however, little is known about the disease in children. We report a case of 9-year-old boy who had a prolonged history of fever. His clinical data were nonspecific. Laboratory and imaging data were not helpful. We did ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Turkish thoracic journal

دوره 17 4  شماره 

صفحات  -

تاریخ انتشار 2016