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A case of severe allergic eosinophilic asthma with nasal polyposis in a patient affected by Birt-Hogg-Dubé syndrome successfully treated with benralizumab.
De Pace, C C; Scioscia, G; Lacedonia, D; Fuso, P; Lepore, G; Palumbo, M G; Foschino-Barbaro, M P.
Affiliation
  • De Pace CC; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
  • Scioscia G; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
  • Lacedonia D; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
  • Fuso P; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
  • Lepore G; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
  • Palumbo MG; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
  • Foschino-Barbaro MP; Department of Medical and Surgical Sciences, University of Foggia, Ospedali Riuniti c/o Colonnello D'Avanzo, Foggia, Italy.
Eur Ann Allergy Clin Immunol ; 53(6): 277-279, 2021 Nov.
Article in En | MEDLINE | ID: mdl-34148334
SUMMARY: Birt-Hogg-Dubé (BHD) syndrome is a rare genetic pathology characterized by cutaneous fibrofolliculomas, pulmonary cysts and kidney tumours. Severe asthma is the most serious form of asthma that does not respond to standard treatments. We present the case of a 68 years-old male patient who had frequent respiratory tract infections, shortness of breath and decline in lung function, nasal polyposis and hypertrophy of the nasal turbinates, for this reason was treated as a severe asthmatic patient for several years with ICS + LABA and high doses of OCS. When we tried to reduce OCS the patient had worsening of the symptoms, we requested a HRTC scan that showed presence of several cysts spread ubiquitously. The patient had a family history of pneumothorax, for this reason we requested a genetic test that resulted in a heterozygous point mutation on exon 12 (c.1429 C > T) of FLCN gene. Despite the diagnosis of BHD syndrome, the patient's clinical condition kept on suggesting an underlying severe asthma and the blood tests we requested pointed out a high percentage of eosinophils, for this reason we opted for the administration of benralizumab that resulted in an excellent asthma control and increased quality of life.
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Full text: 1 Database: MEDLINE Main subject: Asthma / Birt-Hogg-Dube Syndrome Type of study: Diagnostic_studies Limits: Aged / Humans / Male Language: En Journal: Eur Ann Allergy Clin Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2021 Type: Article Affiliation country: Italy

Full text: 1 Database: MEDLINE Main subject: Asthma / Birt-Hogg-Dube Syndrome Type of study: Diagnostic_studies Limits: Aged / Humans / Male Language: En Journal: Eur Ann Allergy Clin Immunol Journal subject: ALERGIA E IMUNOLOGIA Year: 2021 Type: Article Affiliation country: Italy