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1.
Przegl Epidemiol ; 62(2): 407-13, 2008.
Artículo en Polaco | MEDLINE | ID: mdl-18807488

RESUMEN

Toxocariasis in humans is a zoonosis due to the migration of Toxocara canis or T. cati larvae in human body. This review provides basic information on pathology of infection and clinical signs and symptoms of toxocariasis in children. The cases diagnosed in the recent years in central Poland are presented. The disease was recognised accidentally based on the results of laboratory analysis performed for other reasons, when abnormalities suggesting an active helminthiasis were found (eosinophilia, elevated IgE level and/or anemia). The high rate of soil contamination in households of the patients demonstrated elevated risk of infection and reinfection in both, rural and urban areas. Presented data show the need for educational programs which should be implemented for prevention of Toxocara infection in children.


Asunto(s)
Suelo/parasitología , Toxocara canis/aislamiento & purificación , Toxocariasis/diagnóstico , Toxocariasis/epidemiología , Animales , Antihelmínticos/uso terapéutico , Anticuerpos Antihelmínticos/sangre , Gatos , Niño , Protección a la Infancia/estadística & datos numéricos , Perros , Femenino , Educación en Salud/estadística & datos numéricos , Humanos , Larva Migrans Visceral/diagnóstico , Larva Migrans Visceral/epidemiología , Masculino , Polonia/epidemiología , Factores de Riesgo , Población Rural/estadística & datos numéricos , Toxocariasis/tratamiento farmacológico , Población Urbana/estadística & datos numéricos
2.
Klin Oczna ; 109(1-3): 18-21, 2007.
Artículo en Polaco | MEDLINE | ID: mdl-17687906

RESUMEN

PURPOSE: To estimate the state of the vision organ in the children treated for orbital rhabdomyosarcoma. Rhabdomyosarcoma (RMS) is the most common primary malignant orbital tumor in children. RMS usually manifest clinically as rapidly progressive exophthalmus and displacement of the globe. The diagnosis is based on biopsy, CT and MR images. The treatment includes radiation, chemotherapy, and surgery. MATERIAL AND METHODS: The retrospective review of data of 14 children between 0 and 11 years old with rhabdomyosarcmoa of orbit. After a biopsy, with precedent CT or MRI, all patients were treated with chemotherapy including or not including radiotherapy. RESULTS: 3 children died, orbital exentaration was necessary because of tumor recurrence in 3 cases, 8 children remained healthy (without recurrent disease). CONCLUSIONS: Fast diagnosis using CT, MRI and the result of biopsy, have a positive influence on the effect of neoplastic treatment and prognosis.


Asunto(s)
Neoplasias Orbitales/diagnóstico , Neoplasias Orbitales/terapia , Rabdomiosarcoma/diagnóstico , Rabdomiosarcoma/terapia , Biopsia con Aguja , Niño , Preescolar , Femenino , Humanos , Lactante , Recién Nacido , Imagen por Resonancia Magnética , Masculino , Neoplasias Orbitales/patología , Estudios Retrospectivos , Rabdomiosarcoma/patología , Tomografía Computarizada por Rayos X , Resultado del Tratamiento
3.
Klin Oczna ; 109(7-9): 337-9, 2007.
Artículo en Polaco | MEDLINE | ID: mdl-18260293

RESUMEN

Isolated posterior capsule rupture without penetrating injury has rarely been reported. Posterior capsule tears can be preexisting, spontaneous or intrasurgical. Authors report a case of progressing bilateral cataract in 3 months old boy, caused by posterior capsule rupture. Rapidly developing cataract with intumescent lens material in vitreous cavity required surgical procedure: pars plana lensectomy and vitrectomy in both eyes.


Asunto(s)
Catarata/etiología , Cápsula del Cristalino/cirugía , Subluxación del Cristalino/diagnóstico por imagen , Cuerpo Vítreo/diagnóstico por imagen , Extracción de Catarata/métodos , Humanos , Lactante , Cápsula del Cristalino/patología , Subluxación del Cristalino/cirugía , Masculino , Rotura Espontánea/diagnóstico , Resultado del Tratamiento , Ultrasonografía , Vitrectomía
4.
Klin Oczna ; 108(4-6): 170-3, 2006.
Artículo en Polaco | MEDLINE | ID: mdl-17019987

RESUMEN

PURPOSE: Presentation of diagnostic methods and results obtained in childre with nystagmus, with suspicion of ocular albinism. MATERIAL AND METHODS: Records of 9 children (range 0.2 to 5.5 years) are presented. In all cases family history, ophthalmic examination and visual evoked potentials were analyzed. RESULTS: Clinical signs of ocular albinism were found in all patients. 2 children had cutaneous albinism, VEP records of 7 children indicated abnormalities typical for albinism, clinical signs of gene carrying were found in 7 mothers. CONCLUSIONS: Clinical signs enable us to diagnose ocular albinism with relatively high probability, nevertheless characteristic VEP records confirm diagnosis in clinically difficult cases.


Asunto(s)
Albinismo Oculocutáneo/complicaciones , Albinismo Oculocutáneo/diagnóstico , Nistagmo Congénito/complicaciones , Nistagmo Congénito/diagnóstico , Albinismo Oculocutáneo/genética , Preescolar , Potenciales Evocados Visuales , Femenino , Humanos , Lactante , Masculino , Estimulación Luminosa , Agudeza Visual
5.
Klin Oczna ; 108(4-6): 202-5, 2006.
Artículo en Polaco | MEDLINE | ID: mdl-17019996

RESUMEN

The authors describe the case of bilateral optic nerve sheath meningioma /ONSM/ in 14 years old girl. When being hospitalized at the Neurology Clinic with paresis n.VII, the patient was examined by ophthalmologist. The diagnosis was made on the basis of clinical and characteristic changes revealed by USG, CT and MRI. The very first ophthalmologic examination confirmed a visual acuity 5/5 OD and hand movements OS, associated with papilloedema OD and edematous optic atrophy OS. The use of USG, CT and MRI revealed bilateral tubular thickening of the optic nerves (8mm), with calcification. After the period of one year, clinical progression was observed. The intracranial tumor extended. It was shown in diagnostic imaging. The patient was operated on by neurosurgeons with histopathology verification. In the later stage she underwent radiotherapy. The case has been described because of its diagnostic and therapeutic difficulties.


Asunto(s)
Meningioma/diagnóstico , Meningioma/radioterapia , Neoplasias de la Vaina del Nervio/diagnóstico , Neoplasias de la Vaina del Nervio/radioterapia , Neoplasias del Nervio Óptico/diagnóstico , Neoplasias del Nervio Óptico/radioterapia , Adolescente , Femenino , Humanos , Imagen por Resonancia Magnética , Meningioma/complicaciones , Meningioma/cirugía , Neoplasias de la Vaina del Nervio/complicaciones , Neoplasias de la Vaina del Nervio/cirugía , Neoplasias del Nervio Óptico/complicaciones , Neoplasias del Nervio Óptico/cirugía , Radiocirugia , Técnicas Estereotáxicas , Tomografía Computarizada por Rayos X , Resultado del Tratamiento , Trastornos de la Visión/etiología
6.
Klin Oczna ; 108(7-9): 316-8, 2006.
Artículo en Polaco | MEDLINE | ID: mdl-17290832

RESUMEN

Retinopathy of prematurity is a serious disease which may cause blindness. Modern laser treatment is effective but must be done in right time. The aim of the work is to answer the question: what principles should be used in ophthalmic screening in Poland. 267 premature newborn with 3rd stage of ROP treated with laser coagulation were taken into account. Birth weight of treated children ranged from 490 to 1980 grams, gestation age ranged from 23 to 34 weeks. Laser photocoagulation was carried out between 25 and 147 days of life. Analysis of the above data leads to the following conclusions: compulsory screening for ROP in Poland should be limited to all children born before or in 34 week of gestation and children with birth weight less than 2000 grams; first examination should take place in the 4th week of life.


Asunto(s)
Peso al Nacer , Técnicas de Diagnóstico Oftalmológico , Tamizaje Neonatal/métodos , Retinopatía de la Prematuridad/diagnóstico , Femenino , Edad Gestacional , Humanos , Lactante , Recién Nacido , Recien Nacido Prematuro , Recién Nacido de muy Bajo Peso , Masculino , Polonia/epidemiología , Guías de Práctica Clínica como Asunto/normas , Retinopatía de la Prematuridad/epidemiología , Estudios Retrospectivos
7.
Klin Oczna ; 106(3 Suppl): 509-11, 2004.
Artículo en Polaco | MEDLINE | ID: mdl-15636252

RESUMEN

Authors present diagnostic procedures and dinical features of the congenital stationary night blindness (CSNB) in 19 patients. Effective therapy of the concomitant ophthalmological pathologies usually improves patient's vision ability.


Asunto(s)
Ceguera Nocturna/congénito , Ceguera Nocturna/diagnóstico , Adolescente , Niño , Electrorretinografía , Femenino , Humanos , Masculino , Ceguera Nocturna/terapia , Resultado del Tratamiento , Agudeza Visual
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