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Dtsch Med Wochenschr ; 131(33): 1803-6, 2006 Aug 18.
Artigo em Alemão | MEDLINE | ID: mdl-16902903

RESUMO

HISTORY: A 52-year-old woman with chronic anaemia presented with recurrent epistaxis, telangiectasias and haemangiomas, suggesting the presence of hereditary haemorrhagic telangiectasia (Osler-Rendu-Weber disease). Moreover, previous investigations had also shown multiple polyps of the stomach. INVESTIGATIONS: A severe microcytic iron deficiency anaemia in combination with hepatic haemangiomas and duodenal angio-dysplasia were detected. Gastrointestinal endoscopy revealed multiple juvenile polyps in the gastric fundus and body, indicating the diagnosis of hereditary haemorrhagic telangiectasia in combination with juvenile polyposis. THERAPY AND COURSE: A gastrectomy was performed because of recurrent gastrointestinal bleeding and the malignant potential of juvenile gastric polyposis. Histopathology confirmed the diagnosis and did not reveal any malignancy. CONCLUSION: The association of hereditary haemorrhagic telangiectasia and juvenile polyposis, as seen in this patient, has been reported repeatedly. A diagnosis of one of the described entities should initiate the screening for evidence of the other one to prevent (life-threatening) complications.


Assuntos
Anemia Ferropriva/etiologia , Gastrectomia/métodos , Pólipos/diagnóstico , Gastropatias/diagnóstico , Telangiectasia Hemorrágica Hereditária/complicações , Anemia Ferropriva/diagnóstico , Diagnóstico Diferencial , Epistaxe/etiologia , Feminino , Hemorragia Gastrointestinal/etiologia , Hemorragia Gastrointestinal/prevenção & controle , Hemorragia Gastrointestinal/cirurgia , Humanos , Pessoa de Meia-Idade , Pólipos/cirurgia , Prevenção Secundária , Gastropatias/cirurgia , Neoplasias Gástricas/prevenção & controle , Telangiectasia Hemorrágica Hereditária/diagnóstico , Resultado do Tratamento
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