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"Jin Ah Park"

Case Reports
[English]
One Case of Buckwheat Allergy Proved by Oral Provacation Test
Eun Soon Hong, Jin Ah Park, Tae Rim Shin, Ki Youl Seo, Ga Eun Woo, Na Young Lee, Mi Sun Kim, Sun Hee Maeng, Young Joo Cho
Ihwa Ŭidae chi 1997;20(1):1-5.   Published online July 24, 2015
DOI: https://doi.org/10.12771/emj.1997.20.1.1

Buckwheat belongs to the Polygonacea or buckwheat family and is not a true cereral since it does not belong to the Graminiae, or grain family. Its products have long been considered excellent foods for both human and animal consumption.

The earlist reference to case of buckwheat sensitivity was a report by Smith in 1909. He accurately described a case of angionerotic edema and urticaria in a young man upon ingestion accurately described a case of angionerotic edema and urticaria in a young man upon ingestion of small amounts of buckwheat, and violent asthma on the ingestion of moderate quantities of buckwheat.

The authors have experienced one case of buckwheat allergy. The chief complaints were wheezing and dyspnea for several years. The skin tests showed positive reaction to the extracts of buckwheat flour and buckwheat husk. The buckwheat allergy is considered to be the model of the typeIallergy(that is lgE dependent type) proposed by Cooms and Gell. The antigenicity of buckwheat is extremely string, so oral provocation test must not easily be applied for fear of severe and dangerous reaction.

Citations

Citations to this article as recorded by  
  • Development of ultrafast PCR for rapid detection of buckwheat allergen DNA (fag e 1) in processed foods
    Mi-Ju Kim, Saet-Byul Park, Hyeon-Bee Kang, Kyung-Mi Lee, Hae-Yeong Kim
    Food Control.2021; 130: 108334.     CrossRef
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[English]
A Case of Autoimmune Hepatitis
Jin Ah Park, Il Hwan Moon, Doe Young Kim
Ihwa Ŭidae chi 1998;21(3):127-131.   Published online September 30, 1998
DOI: https://doi.org/10.12771/emj.1998.21.3.127

Autoimmune hepatitis is a rare cause of chronic hepatitis in Korea. The cause of autoimmune hepatitis is unknown. A loss of tolerance to autologous liver tissue is regarded as the primary pathogenetic mechanism. The clinical course of this disease is slowly progressive. The clinical picture of autoimmune hepatitis is also often associated with extrapehatic disease, many of which have a presumed autoimmune origin. Untreated patients have a poor prognosis, however immunosuppressive treatment prolongs survival.

In this report, we describe a 59-year-old female who had a history of hemolytic anemia. She was admitted to the hospital due to the jaundice, her liver function test had been known to be abnormal. Laboratory test showed hypergammaglobulinemia and autoantibody.

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