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Journal of Clinical Immunology

, Volume 38, Issue 3, pp 257–259 | Cite as

Francisella philomiragia: Think of Chronic Granulomatous Disease

  • Angel Robles-Marhuenda
  • Marco Vaca
  • Pilar Romero
  • Antonio Ferreira
  • Eduardo López-Granados
  • Francisco Arnalich
Letter to Editor
  • 91 Downloads
A 20-year-old man was referred to our department with fever (about 38 °C), odynophagia, and dry cough for 2 weeks. He has a history of chronic granulomatous disease (CGD) linked X, diagnosed 18 months of birth, and he received primary prophylaxis with trimethoprim-sulfamethoxazole and itraconazole since. He had maternal uncle affection, being his mother the carrier of the mutation. He denied sore throat, neck pain, hoarseness, stridor, dyspnea, chest pain, arthralgia, or weight loss. He returned from recently holidays in Mediterranean beach. The examination revealed hyperemic pharynx, mild tonsillar hypertrophy, submandibular lymph nodes of 2 cm diameter and 1 cm at neck, mobile and not painful. Respiratory and systemic examination was normal. In the chest radiograph, a pulmonary nodule 2 cm in the right lower lobe was evident. Amoxicillin and clarithromycin were prescribed, but the fever and cough were not solved. A CT scan showed a nodular diffuse bilateral pattern more prevalent in...

Notes

Compliance with Ethical Standards

Conflict of Interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Internal Medicine DepartmentLa Paz Universitary HospitalMadridSpain
  2. 2.Microbiology DepartmentLa Paz Universitary HospitalMadridSpain
  3. 3.Immunology DepartmentLa Paz Universitary HospitalMadridSpain

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