Insulin therapy in patients with systemic insulin allergy

1975 ◽  
Vol 135 (6) ◽  
pp. 818-821 ◽  
Author(s):  
J. R. Mattson
PEDIATRICS ◽  
1982 ◽  
Vol 70 (1) ◽  
pp. 137-138
Author(s):  
Kathleen L. Wishner ◽  
Lynda K. Fisher ◽  
Dinesh Kumar

Systemic insulin allergy is rare and usually occurs in adults with diabetes mellitus following reinstitution of insulin therapy.1,2 The present case is unusual in that the systemic symptoms appeared 23 days after initial continuous treatment with insulin in a very young child. CASE REPORT An 18-month-old boy was seen by his pediatrician six weeks after a severe episode of varicella, with a monilial diaper rash and a three-week history of polyuria, polydipsia, polyphagia, and weight loss. The blood glucose concentration was 534 mg/100 ml and serum ketones were present. Diabetes mellitus was diagnosed. He was hospitalized and insulin therapy was instituted without incident; the patient was discharged on a daily mixed dose of regular and isophane (NPH) insulins (single-peak, beef-pork mixture, Eli Lilly & Co).


2020 ◽  
Vol 57 (8) ◽  
pp. 1025-1026
Author(s):  
Tomohiko Kimura ◽  
Yoshiro Fushimi ◽  
Hiroaki Hayashi ◽  
Fuminori Tatsumi ◽  
Yukiko Kanda-Kimura ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-9 ◽  
Author(s):  
Joselyn Rojas ◽  
Marjorie Villalobos ◽  
María Sofía Martínez ◽  
Mervin Chávez-Castillo ◽  
Wheeler Torres ◽  
...  

Introduction. Insulin allergy is a rare complication of insulin therapy, especially in type 1 diabetes mellitus (T1DM). Key manifestations are hypersensitivity-related symptoms and poor metabolic control. T1DM, as well as insulin allergy, may develop in the context of autoimmune polyendocrine syndrome (APS), further complicating management.Case Report. A 17-year-old male patient, diagnosed with T1DM, was treated with various insulin therapy schemes over several months, which resulted in recurrent anaphylactoid reactions and poor glycemic control, after which he was referred to our Endocrinology and Immunology Department. A prick test was carried out for all commercially available insulin presentations and another insulin scheme was designed but proved unsuccessful. A desensitization protocol was started with Glargine alongside administration of Prednisone, which successfully induced tolerance. Observation of skin lesions typical of vitiligo prompted laboratory workup for other autoimmune disorders, which returned positive for autoimmune gastritis/pernicious anemia. These findings are compatible with APS type 4.Discussion. To our knowledge, this is the first documented case of insulin allergy in type 4 APS, as well as this particular combination in APS. Etiopathogenic components shared by insulin allergy and APS beg for further research in immunogenetics to further comprehend pathophysiologic aspects of these diseases.


2008 ◽  
Vol 32 (6) ◽  
pp. 529 ◽  
Author(s):  
Jun Hwa Hong ◽  
Ji Hye Lee ◽  
Jong Ho Shin ◽  
Dong Pil Kim ◽  
Bong Suk Ko ◽  
...  

2010 ◽  
Vol 44 (11) ◽  
pp. 45
Author(s):  
MIRIAM E. TUCKER
Keyword(s):  

2008 ◽  
Vol 41 (10) ◽  
pp. 8
Author(s):  
MARTIN J. ABRAHAMSON ◽  
BARRY J. GOLDSTEIN

2017 ◽  
Vol 23 ◽  
pp. 314
Author(s):  
Israel Hodish ◽  
Mary Johnson ◽  
Eran Bashan ◽  
Davida Kruger ◽  
Anuj Bhargava ◽  
...  

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