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1.
An Med Interna ; 14(4): 187-9, 1997 Apr.
Article in Spanish | MEDLINE | ID: mdl-9181815

ABSTRACT

Eosinophilic gastroenteritis is an uncommon disorder, characterised by eosinophilic infiltration of gut wall, with variable clinical features, depending affected layer of the wall and digestive area, but usually consisting in abdominal pain, diarrhoea, and vomiting. Etiopathogenesis is unknown, with a frequent allergic condition and good response to corticosteroids therapy. Although the existence of eosinophilic gastroenteritis may be suggested by abdominal manifestations, an allergic history with laboratory date and ESR normal, only the antral or intestinal biopsy might to confirm the diagnostic. We report a case of a patient with eosinophilic gastroenteritis and history of bronchial asthma, without evidence of intestinal parasitosis, and a spectacular response to corticosteroids therapy.


Subject(s)
Eosinophilia/diagnosis , Gastroenteritis/diagnosis , Biopsy , Duodenum/pathology , Eosinophilia/drug therapy , Eosinophilia/pathology , Gastric Mucosa/pathology , Gastroenteritis/drug therapy , Gastroenteritis/pathology , Glucocorticoids/administration & dosage , Humans , Male , Middle Aged , Prednisone/administration & dosage , Remission Induction
6.
J Clin Pathol ; 48(6): 579-82, 1995 Jun.
Article in English | MEDLINE | ID: mdl-7665707

ABSTRACT

A case of idiopathic granulomatous vasculitis (disseminated visceral giant cell arteritis) is described in an old woman, the seventh case of this rare disorder reported to date. The main organ affected was the liver and, to our knowledge, this is the first patient to be diagnosed while still alive and the only case to have received medical treatment. It is also the first time that muscular involvement has been documented in this condition. Cyclophosphamide treatment resulted in disappearance of symptoms and increase in weight. The patient died of an unrelated condition.


Subject(s)
Cyclophosphamide/therapeutic use , Giant Cell Arteritis/drug therapy , Liver Diseases/drug therapy , Muscular Diseases/drug therapy , Aged , Female , Humans
7.
An Med Interna ; 12(3): 130-2, 1995 Mar.
Article in Spanish | MEDLINE | ID: mdl-7795120

ABSTRACT

Langerhans' cell granulomatosis is a usually benign disease, characterized by the proliferation of Langerhans' cell containing S-100 protein. Disease is related with the smoking habit and immunological alterations, and is able to affect any organ in isolated or multisystem form. Diagnosis is provided by biopsy of the lesion and bronchoalveolar lavage if the lung is injured. We present a case of a smoker man with lytic lesion in the skull, which biopsy was diagnostic, and with an asymptomatic interstitial infiltrates lungs, with a restrictive spirometry. Remission was achieved with prednisone (0.75 mg x kg) and stop smoking.


Subject(s)
Bone Diseases/pathology , Histiocytosis, Langerhans-Cell/pathology , Lung/pathology , Adult , Histiocytosis, Langerhans-Cell/drug therapy , Humans , Male , Osteolysis/pathology , Prednisone/therapeutic use , Skull/pathology , Smoking/adverse effects
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