scholarly journals Hypertriglyceridaemic pancreatitis with eruptive xanthomas

2021 ◽  
Vol 14 (7) ◽  
pp. e241970
Author(s):  
Gorrepati Rohith ◽  
Bachavarahalli Sriramareddy Rajesh ◽  
Andi Rajendhran Keerthi ◽  
Amaranathan Anandhi
Keyword(s):  
Author(s):  
Rosita Saraceno ◽  
Annunziata Dattola ◽  
Lucia Pietroleonardo ◽  
Rossella Pitocco ◽  
Monika Fida ◽  
...  

Author(s):  
Yoshihiro Nakamura ◽  
Tsuyoshi Watanabe ◽  
Naoho Takizawa ◽  
Yoshiro Fujita

PEDIATRICS ◽  
1970 ◽  
Vol 46 (6) ◽  
pp. 925-929
Author(s):  
John T. Cuttino ◽  
George K. Summer ◽  
Hoyle D. Hill ◽  
B. Jean Mitchell

Dietary studies have been carried out on the effects of ingested carbohydrate and fat (as MCT and LCT) on hyperlipemia in a patient with von Gierke's disease. Increased carbohydrate in the diet resulted in increased serum lipid levels represented predominantly in the triglyceride fraction. Substitution of MCT for LCT in the diet when carbohydrate consumption was at normal levels resulted in significantly decreased serum lipid levels, disappearance of eruptive xanthomas, and reduction in liver size. We suggest on the basis of this preliminary study that excess carbohydrate should be avoided in the diet and substitution of MCT for LCT should be considered as a rational approach to management of lipid abnormalities in von Gierke's disease.


2001 ◽  
Vol 7 (2) ◽  
Author(s):  
Narayan S. Naik
Keyword(s):  

2020 ◽  
pp. 59-66

This chapter describes many of the skin diseases associated with diabetes, thyroid, pituitary, and sex hormone disorders and includes some useful treatment tips and clinical images. Diabetic reactions include skin infections, granuloma annulare, necrobiosis, eruptive xanthomas, and insulin injection site reactions. Brief descriptions of skin problems encountered in hyper- and hypothyroidism are included. The rarer but important skin changes seen in pituitary disorders such as Cushing’s syndrome, Addison’s disease, and acromegaly are described. The role of androgens on the skin and problems created from androgen or oestrogen deficiencies/excess are elaborated. The very rare polyglandular autoimmune type 1 and multiple endocrine neoplasia syndromes are also briefly discussed.


2015 ◽  
Vol 187 (5) ◽  
pp. 356-356 ◽  
Author(s):  
Hui Gao ◽  
Jing Chen
Keyword(s):  

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