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1.
IRCMJ-Iranian Red Crescent Medical Journal. 2010; 12 (2): 190-194
em Inglês | IMEMR | ID: emr-93191

RESUMO

Bone hydatid disease is endemic in several regions worldwide and lacks a typical clinical appearance and image characteristics; therefore, its diagnosis is very difficult. A 49-year-old rural woman was referred with purulent discharge from sinus tract in the left ilium. X-ray and CT scan showed multiple lytic lesions with cortical destruction. She was scheduled for sequestrectomy with impression of chronic osteomyelitis but destroyed hydatid cysts were detected intraoperatively. Iliac wing excision from the iliac crest to the sacroiliac joint and supraacetabulum area was performed. Pathologic findings were in favor of bone hydatidosis. Postoperatively, albendazole and antibiotics were prescribed


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Ílio/patologia , Equinococose/cirurgia , Equinococose/tratamento farmacológico
2.
IJMS-Iranian Journal of Medical Sciences. 2005; 30 (3): 147-149
em Inglês | IMEMR | ID: emr-70850

RESUMO

Chronic inflammatory demyelinating polyneuroradiculopathy [CIDP] is an immune mediated disorder characterized by progressive developing or relapsing symmetrical motor or sensory symptoms in more than one limb over a period of two months. Achalasia, as a primary esophageal motility disorder, is also characterized by increasing the tone of lower esophageal sphincter, absence or incomplete sphincter relaxation in response to swallowing, loss of esophageal peristalsis and rising intra-esophageal pressure. Herein, a case of CIDP, dysmotility- like symptoms, and achalasia is presented


Assuntos
Humanos , Masculino , Acalasia Esofágica/diagnóstico , Transtornos da Motilidade Esofágica
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