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Sarcoidosis: a delayed or missed diagnosis in children
Annals of Saudi Medicine. 2006; 26 (3): 220-223
in English | IMEMR | ID: emr-75982
ABSTRACT
Sarcoidosis is an idiopathic granulomatous disease, most commonly affecting young adults and presenting with bilateral hilar lymphadenopathy and pulmonary infiltrates [1]. In children it is relatively rare and its clinical spectrum varies according to the age of onset [1-2] It is more common during adolescence and usually presents with clinical features similar to the adult type. In children under the age of 4 years it is rare and has a different presentation. Clinical features are characterized by a triad of rash, uveitis, and arthritis.[3] Sarcoidosis has a worldwide distribution, but is more frequently reported from developed countries.[4,5. To our knowledge, there are no reports of childhood Sarcoidosis from Saudi Arabia. We describe the clinical and laboratory features, treatment and outcome of 8 children with sarcoidosis seen at our hospital
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Index: IMEMR (Eastern Mediterranean) Main subject: Sarcoidosis / Biopsy / Incidence / Retrospective Studies / Diagnosis, Differential Type of study: Incidence study Limits: Female / Humans / Male Language: English Journal: Ann. Saudi Med. Year: 2006

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Index: IMEMR (Eastern Mediterranean) Main subject: Sarcoidosis / Biopsy / Incidence / Retrospective Studies / Diagnosis, Differential Type of study: Incidence study Limits: Female / Humans / Male Language: English Journal: Ann. Saudi Med. Year: 2006