Comparison of Gastrointestinal Loss of Alpha-1-Antitrypsin and Chromium-51-Albumin in Ménétrier’s Disease and the Influence of Ranitidine

Digestion ◽  
1983 ◽  
Vol 26 (4) ◽  
pp. 192-196 ◽  
Author(s):  
W.H. Reinhart ◽  
K. Weigand ◽  
M. Kappeler ◽  
H. Roesler ◽  
F. Halter
2021 ◽  
Vol 8 ◽  
Author(s):  
Ana Barrés-Fernández ◽  
Andrés Piolatti-Luna ◽  
José Rafael Bretón-Martínez ◽  
Elena Crehuá-Gaudiza ◽  
Carmen Quiñones-Torrelo ◽  
...  

Introduction: Primary peritonitis (PP) and Ménétrier's Disease (MD) are both rare conditions among pediatric population. Although about 150 MD cases have been described in the scientific literature to date, its onset with a PP is an unusual condition.Case Presentation: We present a case of an 11-year-old boy who was admitted to our unit because of abdominal pain and distension. Complementary tests showed ascites, bilateral pleural effusion, leukocytosis, increased acute phase reactants and hypoproteinemia with hypoalbuminemia. Laparoscopy ruled out appendicitis or visceral perforations and exposed purulent peritoneal fluid, compatible with PP. Biochemical stool analysis showed increased clearance of alpha-1-antitrypsin, which was consistent with a protein-losing enteropathy. Gastroscopy findings were compatible with MD. The clinical course was favorable and he had no recurrence after 12 months of follow-up.Conclusion: PP can be the first clinical manifestation of pediatric MD. Knowledge of MD and its generally benign nature in children is important in order to avoid excessive testing and unnecessary treatment.


1960 ◽  
Vol 39 (3) ◽  
pp. 347-350 ◽  
Author(s):  
Earl E. Gambill ◽  
Donald C. Campbell ◽  
Donald C. Balfour ◽  
John M. Waugh ◽  
Malcolm B. Dockerty

2009 ◽  
Vol 195 (1-6) ◽  
pp. 247-252 ◽  
Author(s):  
Heino Raotma ◽  
Lennart Angervall ◽  
Ingvar Dahl ◽  
Gerhard Dotevall

2021 ◽  
Vol 14 (10) ◽  
pp. e246137
Author(s):  
Sofia Rao ◽  
Anna Viola ◽  
Omar Ksissa ◽  
Walter Fries

Ménétrier’s disease (MD) is a rare disease of the stomach, characterised by hypertrophic gastric folds leading to protein loss. The association with ulcerative colitis (UC) is rare but has been reported in the literature. We report a case of a 29-year-old male affected by UC with an additional diagnosis of MD 3 years after UC diagnosis. UC was refractory to several treatment lines (thiopurines, infliximab, vedolizumab and ustekinumab), and the patient underwent colectomy. Octreotide was administered for MD normalising blood biochemistry, but it was not effective in inducing endoscopic remission of the stomach. Treatment options in patients with MD and UC are discussed.


Gut ◽  
2010 ◽  
Vol 59 (12) ◽  
pp. 1617-1624 ◽  
Author(s):  
Amy Rich ◽  
Tania Zuluaga Toro ◽  
Jarred Tanksley ◽  
William H Fiske ◽  
Christopher D Lind ◽  
...  

1997 ◽  
Vol 27 (2) ◽  
pp. 178-180 ◽  
Author(s):  
Junji Takaya ◽  
Yuhmi Kawamura ◽  
Minoru Kino ◽  
Yosihiko Kawashima ◽  
Akitsugu Yamamoto ◽  
...  

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