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3.
An Med Interna ; 14(4): 187-9, 1997 Apr.
Artículo en Español | MEDLINE | ID: mdl-9181815

RESUMEN

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.


Asunto(s)
Eosinofilia/diagnóstico , Gastroenteritis/diagnóstico , Biopsia , Duodeno/patología , Eosinofilia/tratamiento farmacológico , Eosinofilia/patología , Mucosa Gástrica/patología , Gastroenteritis/tratamiento farmacológico , Gastroenteritis/patología , Glucocorticoides/administración & dosificación , Humanos , Masculino , Persona de Mediana Edad , Prednisona/administración & dosificación , Inducción de Remisión
5.
An Med Interna ; 13(12): 595-7, 1996 Dec.
Artículo en Español | MEDLINE | ID: mdl-9063936

RESUMEN

Primary adrenal insufficiency is a non frequent disease, that is declared in young adults and in the most of the cases is produced from an autoimmune mechanism or a tuberculous disease. The incidence of these forms in the different geographic areas is dependent of degree of irradication of the tuberculosis. We report the case of a patient with latent chronic adrenal insufficiency of tuberculous origin who was affected for an addisonian crisis during an intercurrent infectious disease, which permitted the diagnosis of the addisonian crisis, and Mal of Pott was moreover detected. Evolution with corticosteroid and specific treatment was very favorable.


Asunto(s)
Enfermedad de Addison/etiología , Insuficiencia Suprarrenal/etiología , Tuberculosis Endocrina/diagnóstico , Tuberculosis de la Columna Vertebral/diagnóstico , Enfermedad de Addison/diagnóstico , Anciano , Enfermedad Crónica , Humanos , Masculino , Tuberculosis Endocrina/complicaciones , Tuberculosis de la Columna Vertebral/complicaciones
10.
J Clin Pathol ; 48(6): 579-82, 1995 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-7665707

RESUMEN

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.


Asunto(s)
Ciclofosfamida/uso terapéutico , Arteritis de Células Gigantes/tratamiento farmacológico , Hepatopatías/tratamiento farmacológico , Enfermedades Musculares/tratamiento farmacológico , Anciano , Femenino , Humanos
13.
An Med Interna ; 12(3): 130-2, 1995 Mar.
Artículo en Español | MEDLINE | ID: mdl-7795120

RESUMEN

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.


Asunto(s)
Enfermedades Óseas/patología , Histiocitosis de Células de Langerhans/patología , Pulmón/patología , Adulto , Histiocitosis de Células de Langerhans/tratamiento farmacológico , Humanos , Masculino , Osteólisis/patología , Prednisona/uso terapéutico , Cráneo/patología , Fumar/efectos adversos
14.
An Med Interna ; 12(2): 82-4, 1995 Feb.
Artículo en Español | MEDLINE | ID: mdl-7749016

RESUMEN

The finding of a cardiac tamponade (CT) as initial manifestation of lung cancer is rare, being its most frequent manifestations dyspnea, cough and edemas. The presence of alithiasic acute cholecystitis (AAC) as early manifestation of CT is extremely rare, despite this having being described related to other situations of low cardiac output. We present the case of a patient who underwent emergency surgery due to AAC as a form of presentation of CT, this being the initial manifestation of a pulmonary adenocarcinoma. The histopathological study of the liver and the vesicle were compatible with signs of short evolution venous stasis, and the diagnosis was established through pericardium biopsy and thoracic CAT.


Asunto(s)
Adenocarcinoma/complicaciones , Taponamiento Cardíaco/complicaciones , Colecistitis/diagnóstico , Neoplasias Pulmonares/complicaciones , Enfermedad Aguda , Adenocarcinoma/diagnóstico , Adulto , Biopsia , Taponamiento Cardíaco/diagnóstico , Taponamiento Cardíaco/etiología , Colecistitis/cirugía , Urgencias Médicas , Vesícula Biliar/patología , Humanos , Hígado/patología , Neoplasias Pulmonares/diagnóstico , Masculino , Pericardio/patología
17.
An Med Interna ; 9(12): 610-2, 1992 Dec.
Artículo en Español | MEDLINE | ID: mdl-1486170

RESUMEN

Endocarditis is the first manifestation of Q fever in its chronic form, generally affecting prosthetic cardiac valves or previously injured valves. Its clinical presentation is an endocarditis with negative culture and there is not agreement with regard to the most adequate antimicrobial treatment and its duration. Frequently, the valve has to be replaced. We present a case of a patient with double aortic lesion, in whom endocarditis by Q fever was diagnosed and treated with doxycycline, initially with success. However, she relapsed one year later, being then resistant to the medical treatment (doxycycline, ciprofloxacine plus rifampicine). It was not possible to replace the valve and the patient died two months later due to cardiac failure.


Asunto(s)
Endocarditis Bacteriana/etiología , Fiebre Q/complicaciones , Anciano , Válvula Aórtica , Enfermedad Crónica , Terapia Combinada , Quimioterapia Combinada , Endocarditis Bacteriana/diagnóstico , Endocarditis Bacteriana/terapia , Femenino , Enfermedades de las Válvulas Cardíacas/diagnóstico , Enfermedades de las Válvulas Cardíacas/etiología , Enfermedades de las Válvulas Cardíacas/terapia , Humanos , Fiebre Q/diagnóstico , Fiebre Q/terapia , Recurrencia
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