scholarly journals Exercise induced anaphylaxis in kiwi allergic patient: case report

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Natalia Ukleja-Sokołowska ◽  
Robert Zacniewski ◽  
Kinga Lis ◽  
Magdalena Żbikowska-Gotz ◽  
Andrzej Kuźmiński ◽  
...  

Abstract Background An allergy to kiwi is rare in Poland. Most (65–72%) of the patients who are allergic to kiwi report symptoms of an oral allergy syndrome (OAS); however, systemic manifestations (18–28%) have also been reported. Case report A 27-year-old male patient, previously not suffering from chronic diseases, exercised in the gym. He began with isometric training and then continued with aerobic exercise on a treadmill. After exercise, he ate 2 kiwi (Actinidia deliciosa) fruits. He experienced a swelling of the lips after eating the fruit, followed by an itchy scalp and a swollen face. Approximately 60 min later, the symptoms worsened: the patient suffered from generalized hives, general weakness and a "rumbling" sensation in ears. The patient's condition improved upon the consumption of antihistamines. However, the swelling of the face persisted for 24 h despite previously eating a kiwi without any side effects. By means of diagnostics based on allergen components, an allergy to grass allergen components, especially timothy grass—Phl p 1, Phl p 2 and Phl p 5, was confirmed. The presence of IgE that is specific for Act d 2 kiwi was also found. The patient had an oral food challenge with kiwi fruit at rest and after exercise provocation test. The challenge was negative at rest and positive after exercise. A food-dependent exercise-induced anaphylaxis gathered with a kiwi sensitization was diagnosed. Conclusion To our knowledge, this case is the first report of a kiwi-allergic patient in whom exercise was a necessary cofactor to induce an anaphylactic reaction.

Head & Neck ◽  
1994 ◽  
Vol 16 (1) ◽  
pp. 75-78 ◽  
Author(s):  
Thiam Chye Lim ◽  
Walter Tiang Lee Tan ◽  
Yoke Sun Lee

2010 ◽  
Vol 163 (3) ◽  
pp. 638-640 ◽  
Author(s):  
T. Agostini ◽  
C. Catelani ◽  
A. Acocella ◽  
A. Franchi ◽  
R. Bertolai ◽  
...  

Lung ◽  
2014 ◽  
Vol 192 (2) ◽  
pp. 329-331 ◽  
Author(s):  
Amit Diwakar ◽  
Gregory A. Schmidt

2005 ◽  
Vol 57 (4) ◽  
pp. 305-313 ◽  
Author(s):  
Sunita Mathur ◽  
Donna L. MacIntyre ◽  
Bruce B. Forster ◽  
W. Darlene Reid

PEDIATRICS ◽  
1975 ◽  
Vol 56 (6) ◽  
pp. 1078-1079
Author(s):  
Abdul J. Khan ◽  
Hugh E. Evans ◽  
Marylu R. Macabuhay ◽  
Yu-En Lee ◽  
Robert Werner

Beta-hemolytic Streptococcus group G, a rare human pathogen, has long been implicated in human disease as causing pharyngitis, puerperal sepsis, empyema, and even septicemia. We are reporting a rare, life-threatening, acute illness, primary peritonitis, due to this organism, whose etiological source probably was a family dog. Case Report R.K., a 2-year-old girl, was admitted with the complaints of anorexia, vomiting of three days' duration, and severe abdominal distension of one day's duration. The symptoms started following a burn injury over the face and lips three days prior to admission. Past history was noncontributory. Physical examination revealed an ill child of average size, fully conscious.


2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841


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