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1.
Eur Ann Allergy Clin Immunol ; 50(1): 42-44, 2018 01.
Article in English | MEDLINE | ID: mdl-29350021

ABSTRACT

Summary: We report a case of a previously healthy 24-year-old man with a 3-month history of gastrointestinal symptoms during exercise and also few minutes after the ingestion of cow's milk (CM) without exercise. He reported the ingestion of a blend of hydrolyzed whey and casein proteins for bodybuilding for the last 2 years. The in vivo tests showed positivity to CM, α-lactalbumin, ß-lactoglobulin and casein extracts, and also to the protein supplement. The serum specific IgE was positive for CM, ß-lactoglobulin and α-lactalbumin. The in vivo and in vitro tests results suggested an IgE-mediated CMA. Adult-onset CMA has been rarely reported, and to our knowledge this is the first case possibly related to bodybuilding supplements. The authors theorize that the presentation of large amounts of proteins in the gastrointestinal tract may favor sensitization.


Subject(s)
Allergens/immunology , Caseins/immunology , Exercise/physiology , Gastrointestinal Diseases/diagnosis , Milk Hypersensitivity/diagnosis , Milk/immunology , Whey/immunology , Adult , Animals , Cattle , Dietary Supplements/adverse effects , Humans , Immunoglobulin E/blood , Male , Young Adult
2.
Eur Ann Allergy Clin Immunol ; 50(3): 141-144, 2018 05.
Article in English | MEDLINE | ID: mdl-29384119

ABSTRACT

Summary: Aquagenic urticaria (AU) is a rare form of chronic inducible urticaria elicited by water at any temperature. We describe the case of a 25-year-old atopic woman who presented to our unit with a 4-year history of recurrent urticarial rashes, highly pruritic, confined to the neck and lower part of the face, occurring solely on contact with sea water. The lesions were reproduced by challenge tests with aqueous 3.5% NaCl and other hypertonic aqueous solutions but not with 20% glucose neither tap water. Our case supports the existence of a distinct salt-dependent subtype of aquagenic urticaria (SDAU), which seems to be triggered mostly by sea bathing, affects young women and has a characteristic localization on the inferior facial contours and neck. To the best of our knowledge, only eight cases of SDAU have been reported in the literature.


Subject(s)
Hypersensitivity, Immediate/diagnosis , Seawater/adverse effects , Urticaria/diagnosis , Adult , Female , Humans , Hypersensitivity, Immediate/immunology , Rhinitis, Allergic/complications , Sodium Chloride , Urticaria/immunology , Chronic Inducible Urticaria
3.
Eur Ann Allergy Clin Immunol ; 50(6): 277-280, 2018 11.
Article in English | MEDLINE | ID: mdl-29384113

ABSTRACT

Summary: Background. Antiretroviral therapy (ART) may be responsible for hypersensitivity reactions varying in severity, clinical manifestations and frequency. Case report. We report the case of a 47-year-old woman with HIV infection who developed a delayed mucocutaneous reaction after treatment with ART. Hypersensitivty reaction (HR) to emtricitabine and tenofovir was considered probable based on positive patch tests (PT) and hypersensitivity reaction to nevirapine was confirmed by drug provocation test. Discussion. The diagnosis of HR to ART remains a diagnostic challenge, partly due to unknown mechanism and the absence of validated diagnostic tools. Patch testing may represent a useful method for confirming hypersensitivity. Further investigation in this area is required, so that successful management strategies can be offered, preventing loss of potent and viable antiretroviral agents.


Subject(s)
Anti-HIV Agents/immunology , Drug Hypersensitivity/diagnosis , Drug Hypersensitivity/immunology , Emtricitabine/immunology , Nevirapine/immunology , Tenofovir/immunology , Anti-HIV Agents/adverse effects , Anti-HIV Agents/therapeutic use , Emtricitabine/adverse effects , Emtricitabine/therapeutic use , Female , HIV Infections/drug therapy , Humans , Male , Middle Aged , Nevirapine/adverse effects , Nevirapine/therapeutic use , Skin Tests , Tenofovir/adverse effects , Tenofovir/therapeutic use
4.
Eur Ann Allergy Clin Immunol ; 48(6): 242-246, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27852430

ABSTRACT

BACKGROUND: Omalizumab is indicated to treat chronic spontaneous urticaria (CSU) refractory to antihistamines. We aim to describe the experience of our department in the treatment of CSU with omalizumab. MATERIALS AND METHODS: Retrospective review of the clinical records of patients. RESULTS: Six patients (5 females, median age 33 years) treated with omalizumab for a median of 17.5 months were evaluated. All patients had improvement of symptoms after the first dose. In one case, the treatment was suspended after 7 months, but in 9 weeks there was recurrence of symptoms. The main side effect was headache in the drug administration's day. Currently, all patients maintain therapy with omalizumab and are clinically stable. CONCLUSION: Omalizumab proved to be an effective and safe drug for the treatment of patients with refractory CSU.


Subject(s)
Anti-Allergic Agents/therapeutic use , Omalizumab/therapeutic use , Urticaria/drug therapy , Adult , Chronic Disease , Female , Humans , Male , Middle Aged , Retrospective Studies , Treatment Outcome , Young Adult
5.
Eur Ann Allergy Clin Immunol ; 46(1): 53-5, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24702878

ABSTRACT

Clopidogrel is an antiplatelet drug widely used for treatment and prevention of a variety of cardiovascular diseases. We report a successful desensitization to clopidogrel in a 70-year-old Caucasian man with delayed hypersensitivity (HS) reaction. He developed lip, hand and foot swelling, erythematous papular non-pruritic lesions and arthralgias 2 weeks after starting treatment with clopidogrel 75 mg/d. A 3-hour desensitization protocol was started, achieving a cumulative dose of 154 mg without any reaction, and a daily dose of 75 mg was recommended. On the 4th day, the patient developed skin lesions similar to the previously described. He was treated with topical steroids and oral antihistamines, and the daily dose of clopidogrel was reduced to 20 mg. A new desensitization protocol was established, with a slow dose increment, according to the patient's response. It was only possible to achieve the dose of 75 mg/d after 2 months. Although well tolerated by most patients, HS reactions with clopidogrel may occur and desensitization is rising as a safe alternative in those patients. In delayed reactions with cutaneous lesions, a slower desensitization protocol may be necessary, as in this case.


Subject(s)
Desensitization, Immunologic , Drug Hypersensitivity/therapy , Platelet Aggregation Inhibitors/adverse effects , Ticlopidine/analogs & derivatives , Aged , Clopidogrel , Humans , Male , Ticlopidine/adverse effects
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