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[Intestinal hemorrhage for 21 years in a case of blue nevus syndrome]. / Sangrado intestinal de 21 años en un caso de síndrome de nevo azul.
Ramírez Mateos, C; Torres Salgado, F G; Bolaños Ulloa, F; Loría, A; Reynaga García, F J.
Afiliação
  • Ramírez Mateos C; Instituto Nacional de Nutrición Salvador Zubirán, México, D.F.
Rev Gastroenterol Mex ; 63(1): 37-40, 1998.
Article em Es | MEDLINE | ID: mdl-10068748
ABSTRACT

OBJECTIVE:

To report a case of gastrointestinal bleeding due to a blue rubber bleb nevus syndrome undiagnosed for 21 years. CASE A woman of 28 years of age suffered chronic gastrointestinal bleeding starting at seven years of age. During these 21 years she received various treatment with oral and parenteral iron and, in addition, four blood transfusions. We found her to be anemic with 7.8 g/dL of hemoglobin (HB), iron deficient and with skin lesions in tongue, right hand and lower extremities. A skin biopsy diagnosed the lesions as cavernous hemangiomas. Multiple intestinal hemangiomas seen by radiologic, endoscopic and colonoscopic studies, established the diagnosis. She was treated with oral iron; three months later she was asymptomatic and with higher levels of HB (9.1 g/dL).

CONCLUSION:

The rarity of the syndrome and the fact that, as far as we know, it is the first case reported in Mexico, probably led to a delay in its diagnosis and to potentially dangerous therapy in this patient in spite of the fact that the diagnosis was not difficult.
Assuntos
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Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neoplasias Gástricas / Hemangioma Cavernoso / Hemorragia Gastrointestinal / Neoplasias Intestinais Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: Es Ano de publicação: 1998 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neoplasias Gástricas / Hemangioma Cavernoso / Hemorragia Gastrointestinal / Neoplasias Intestinais Tipo de estudo: Diagnostic_studies Limite: Adult / Female / Humans Idioma: Es Ano de publicação: 1998 Tipo de documento: Article