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1.
Rev Pneumol Clin ; 72(4): 264-8, 2016 Aug.
Article in French | MEDLINE | ID: mdl-27368138

ABSTRACT

INTRODUCTION: Bone hydatidosis of the chest wall is rarely reported in the literature. Costal and sternal location are uncommon. Through 3 observations and literature review, we report particular pathophysiological and diagnostic aspects of costal and sternal hydatidosis. We also discuss therapeutic and prognostic aspects of this disease. OUR CASES: we report the cases of 45, 41 and 17 years old male patients, 2 of them had previous surgery for thoracic wall mass in general surgery service. Clinical presentation was thoracic wall painful mass sticking to bone. One patient had isolated costal location, the 2 others had sternal location; in one of them, the disease is located in sterno-costo-clavicular area. In all 3 cases, the disease was diagnosed by computed tomography (CT) scan, showing bone lysis or mediastinum enlargement. Patients undergo extended bone resection removing away all destructed parts of the bone. After surgery, albendazole has been prescribed to all patients. No recurrence was observed after 12 months follow-up. CONCLUSION: Chest wall bone hydatidosis is unusual even in endemic regions, with slow evolution and inconspicuous symptoms. Radiology plays a key role in the management of this disease. Extended surgical resection associated with medical treatment (albendazole) is a reliable treatment without recurrence.


Subject(s)
Echinococcosis/pathology , Thoracic Diseases/parasitology , Thoracic Wall/parasitology , Adolescent , Adult , Echinococcosis/diagnostic imaging , Echinococcosis/parasitology , Echinococcosis/surgery , Humans , Male , Middle Aged , Radiography, Thoracic , Ribs/diagnostic imaging , Ribs/parasitology , Ribs/pathology , Ribs/surgery , Sternum/diagnostic imaging , Sternum/parasitology , Sternum/pathology , Sternum/surgery , Thoracic Diseases/diagnostic imaging , Thoracic Diseases/pathology , Thoracic Diseases/surgery , Thoracic Wall/pathology
3.
Trop Doct ; 42(3): 174-5, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22785545

ABSTRACT

Rhinosporidiosis is a rare chronic granulomatous condition caused by a fungus (Rhinosporidium seeberi). It has been seen mainly in southern India, Sri Lanka and Pakistan. This is the first published report of a patient with multiple rhinosporidiosis. He had lesions in the nares, in multiple areas of the skin, in the external urethral meatus, glans of penis and the perineum.


Subject(s)
Rhinosporidiosis/pathology , Rhinosporidium/isolation & purification , Animals , Humans , Male , Middle Aged , Nose/parasitology , Nose/pathology , Penis/parasitology , Penis/pathology , Perineum/parasitology , Perineum/pathology , Rhinosporidiosis/parasitology , Rhinosporidium/pathogenicity , Scalp/parasitology , Scalp/pathology , Thoracic Wall/parasitology , Thoracic Wall/pathology
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