Skin Metastasis of Cervical Cancer: About an Unusual Case

Autor: Tayeb Kebdani, Noureddine Benjaafar, Brahim El Gueddariv, Adama Diakité, Basma El Khannoussi, Sara Bellefqih, Imane Mezouri, J. Khalil
Rok vydání: 2013
Předmět:
Zdroj: Journal of Clinical Case Reports.
ISSN: 2165-7920
DOI: 10.4172/2165-7920.1000284
Popis: Congenital Chloride Diarrhoea (CCD) is a form of autosomal recessive disorder which is presented by persistent chloride rich watery diarrhea from birth. Diagnosis of CCD is simple but it needs early prediction and clinical and laboratory evaluation. It can be tentatively made from the typical history of polyhydramnios in antenatal period, prematurity, and watery diarrhea from the beginning and then confirmed by the high fecal concentration of Cl-. Serum electrolyte and pH changes are not reliable diagnostic criteria. Without early intervention most of the children will die in infancy, rest will achieve failure to thrive, and psychomotor developmental delay. .Although congenital chloride diarrhoea has been reported worldwide, but in Bangladesh, we have no reported cases. Here we have discussed two cases of CCD with their diagnostic and management outcome and also discuses about captopril and its effectiveness. Early diagnosis and treatment are essential for normal growth, development, and prevention of other severe complications of congenital chloride diarrhea.
Databáze: OpenAIRE