Skip to main navigation menu Skip to main content Skip to site footer

Fibrosis quística del páncreas con test de iontoforesis negativo. Presentación de un caso y revisión de la literatura.

Fibrosis quística del páncreas con test de iontoforesis negativo. Presentación de un caso y revisión de la literatura.




Section
Presentación de casos

How to Cite
Fibrosis quística del páncreas con test de iontoforesis negativo. Presentación de un caso y revisión de la literatura.
rev. colomb. neumol. [Internet]. 2000 Mar. 1 [cited 2024 Dec. 22];12(1):37-40. Disponible en: https://doi.org/10.30789/rcneumologia.v12.n1.2000.1175

Dimensions
PlumX
license
Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

Ninguna publicación, nacional o extranjera, podrá reproducir ni traducir sus artículos ni sus resúmenes sin previa autorización escrita del editor; sin embargo  los usuarios pueden descargar la información contenida en ella, pero deben darle atribución o reconocimiento de propiedad intelectual, deben usarlo tal como está, sin derivación alguna.

Lina Jaramillo B.

    Lina Jaramillo B.,

    Profesora Asistente Universidad Nacional de Colombia. Departamento de Patología, Hospital Pediátrico de la Misericordia.


    A case study is presented about a 6-month-old intant with repetitive respiratory symptoms. lt is documented as cystic fibrosis, even though traditional diagnostic criteria are not met, such as a negative iontophoresis. The possible causes ot this case are discussed, as well as diagnostic alternatives in these circumstances. Even though the iontophoresis test is negative the need to not elíminate this disease especially when the symptoms are very suspicious, is insisted greatly.


    Article visits 0 | PDF visits 0


    Downloads

    Download data is not yet available.
    1. Marino CR, Gorelick FS. Scientific advances in cystic fibrosis. Gastroenterology 1992; 103:681-93. Oppenheimer E.H. Esterly JR
    2. Pathology of Cystic Fibrosis. Review of the Literature and Comparison with 146 Autopsied Cases. Perspectives in Pediatric Pathology. Year Book, 1975;2:241-75.
    3. Stern RC. et al. lntermediate range sweat chloride concentration and Pseudomonas bronchitis: a cystic fibrosis variant with preservation of exocrine pancreatic function JAMA 1978;239:2676-80.
    4. Davis PB, Hubbard VS, Sant'agnese PA. Low Sweet Electrolytes in a patient with Cystic Fibrosis. Am J Med. 1980;69: 6436-46.
    5. Highsmith WE. et al. A novel mutation in the cystic Fibrosis gene in patients with pulmonary disease but normal sweat chloride conc~ntrations. N Engl J Med. 1994;331 :974-80.
    6. Strong TV. et, al. Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels. N Engl J Med. 1991;325:1630-4.
    7. Augarten A et al, Mild cystic fibrosis and normal or borderline sweat test in patients with the 31849 + 1 O kb C-T mutat/pn, Lancet 1993; 342:25-6. ·
    8. Zielenski J, Tsui LC. Cystic Fibrosis. Genotypic and Phenotypic variations. Annu Rev Genet 1995;29:777-807.
    9. Stern RC. et al. The Diagnosis of Cystic Fibrosis. N Engl. J Med. 1997; 336:487-91.
    10. Denning CR. et al. Cooperative study Comparing three Methods of Performing sweet tests to Diagnose Cystic Fibrosis. Pediatrics 1980;66:752-7.
    11. LeGrys V A. Sweet testing for the diagnosis of Cystic fibrosis: Practica! considerations. J. Pediatric 1996; 129:892-7.
    12. Stern Rx, BoatTR, Doershuk. Óbstructive azoospermia as diagnostic criterion far the cystic fibrosis syndrome. Lancet 1982;1 :1401-4.
    Sistema OJS 3.4.0.7 - Metabiblioteca |