Mostrar el registro sencillo del ítem

dc.creatorSegura Vílchez, John
dc.creatorGonzález Rojas, Paulina
dc.creatorRetana Moreira, Lissette
dc.date.accessioned2023-02-14T19:26:24Z
dc.date.available2023-02-14T19:26:24Z
dc.date.issued2013-01
dc.identifier.citationhttps://www.scielo.sa.cr/pdf/amc/v55n1/en_art10v55n1.pdfes_ES
dc.identifier.issn0001-6012
dc.identifier.urihttps://hdl.handle.net/10669/88194
dc.description.abstractThe case of a 19–year–old male patient from a rural area is presented. He had a 3-year history of nasal obstruction, episodes of facial inflammation, epistaxis, fetid rhinorrhea, hearing loss in the right ear, bilateral axillary and multiple facial bilateral lymphadenopathies. He was referred for consultation to the Mexico Hospital due to an obstructive granulomatous lesion of the nasal septum. The first biopsy revealed the presence of chronic inflammatory infiltrate, with predominance of macrophages with foamy appearance. A second biopsy was positive for Klebsiellapneumoniae subsp. rhinoscleromatis, described histologically as a pseudoepitheliomatouse hyperplasia with dense inflammatory infiltrate and the analysis of lamina propria showed dense inflammatory infiltrate with lymphocytes, plasmatic cells, Russell bodies and macrophages with vacuolated cytoplasm, with microorganisms and debris. The patient was treated with oral ciprofloxacin therapy for seven months, after which the patient was considered cured from the etiological point of view.es_ES
dc.language.isoenges_ES
dc.sourceActa Médica Costarricense vol.55(1), pp. 48-50es_ES
dc.subjectKlebsiellaes_ES
dc.subjectChronic granulomatose diseasees_ES
dc.subjectBiopsyes_ES
dc.titleCaso clínico: Rinoescleromaes_ES
dc.typeartículo originales_ES
dc.description.procedenceUCR::Vicerrectoría de Docencia::Salud::Facultad de Microbiologíaes_ES


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem