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7 results on '"Razemon-Pinta M"'

3. [Zollinger-Ellison syndrome associated with Cushing's syndrome in a child (author's transl)].

Author

Loeuille GA, Debeugny P, Morel P, Razemon-Pinta M, Lefebvre J, Farriaux JP, and Fontaine G

Subjects
Celiac Artery diagnostic imaging, Child, Cyclophosphamide therapeutic use, Female, Fluorouracil therapeutic use, Gastrectomy, Humans, Male, Mesenteric Arteries diagnostic imaging, Paraneoplastic Syndromes etiology, Radiography, Zollinger-Ellison Syndrome diagnosis, Zollinger-Ellison Syndrome therapy, Cushing Syndrome etiology, Zollinger-Ellison Syndrome complications
Abstract

The Zollinger-Ellison syndrome with characteristic symptoms is described in an 11 year old girl. Coeliac and mesenteric arteriography showed a pancreatic gastrin-secreting tumor. After total gastrectomy the condition improved but the associated Cushing's syndrome deteriorated. Surgical removal of the tumor was not possible and the child was treated with chemotherapy (5-fluorouracil and cyclophosphamide) and OP'DDD.

Published
1980

4. [Association of congenital hypoaldosteronism and steatorrhoea].

Author

Loeuille G, Razemon-Pinta M, Lefebvre J, Racadot A, Farriaux JP, and Fontaine G

Subjects
Adult, Consanguinity, Failure to Thrive diagnosis, Female, Fetal Growth Retardation diagnosis, Follow-Up Studies, Humans, Infant, Infant, Newborn, Pedigree, Pregnancy, Steatorrhea diagnosis, Failure to Thrive genetics, Fetal Growth Retardation genetics, Hypoaldosteronism genetics, Steatorrhea genetics
Published
1977

5. [Fibroscopy and gastroesophageal reflux].

Author

Turck D, Maquet E, Razemon-Pinta M, Farriaux JP, and Fontaine G

Subjects
Adolescent, Child, Child, Preschool, Fiber Optic Technology, Humans, Infant, Infant, Newborn, Esophagitis, Peptic diagnosis, Esophagoscopy methods, Gastroesophageal Reflux complications
Published
1984

6. Hepatic porto-enterostomy or cholecystostomy in the treatment of extrahepatic biliary atresia. A study of 49 cases.

Author

Odiévre M, Valayer J, Razemon-Pinta M, Habib EC, and Alagille D

Subjects
Bile Ducts surgery, Cholangitis etiology, Humans, Infant, Liver Diseases etiology, Postoperative Complications, Sepsis etiology, Bile Ducts abnormalities, Gallbladder surgery, Intestines surgery, Liver surgery
Abstract

Hepatic porto-enterostomy or cholecystostomy (Kasai's procedure) was successful in restoring bile flow in 31 of 49 patients with "noncorrectable" extrahepatic biliary atresia. However, all but one of the 31 developed acute or chronic complications such as cholangitis, bile peritonitis, or portal hypertension. During a five-year follow-up period, 26 (53%) died while 9 of the 23 survivors continue to manifest chronic or recurrent cholangitis. Thirteen of the 19 survivors who are more than one year of age have developed portal hypertension. These complications limit the prognosis of infants with "noncorrectable" biliary malformations.

Published
1976
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7. [Byler's disease (familial fibrogenic cholestasis in children). Apropos of 7 cases].

Author

Razemon-Pinta M, Lecomte-Houcke M, Mary JP, and Loreille GA

Subjects
Child, Child, Preschool, Cholestasis, Intrahepatic complications, Cholestasis, Intrahepatic pathology, Female, Humans, Infant, Liver ultrastructure, Liver Cirrhosis pathology, Male, Cholestasis, Intrahepatic genetics, Liver pathology, Liver Cirrhosis etiology
Abstract

Seven cases presenting with the features of Byler's disease (BD) are reported. The diagnosis of BD can only be made after exclusion of other causes of cholestasis. It seems likely that BD is a syndrome and that more accurate biological and histological investigations will allow to differentiate several entities within this affection. At the present, liver transplantation appears to be the only rational treatment.

Published
1988

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