Cytological Diagnosis of Ewing Sarcoma – Clavicle.

dc.contributor.authorPawar, V R
dc.contributor.authorPatil, P P
dc.contributor.authorMore, Sagar
dc.date.accessioned2015-04-10T11:19:54Z
dc.date.available2015-04-10T11:19:54Z
dc.date.issued2011-12
dc.description.abstractEwing sarcoma is a rare malignant round cell tumor of the bone. It is the second most common primary malignant tumor of bone found in children. It commonly affects long bones, pelvis and ribs. An 11 year old boy presented with painful swelling at the medial end of left clavicle. X-ray revealed a diaphyseal lesion of the medial end of the left clavicle with destruction of bone and mottled appearance. FNAC was done and reported as Malignant round cell tumor suggestive of Ewing sarcoma. Histopathologically the diagnosis of Ewing sarcoma was confirmed with special stains. Ewing sarcoma affecting clavicle is uncommon. Clavicle can be often resected with no need of reconstruction in young children.en_US
dc.identifier.citationPawar V R, Patil P P, More Sagar. Cytological Diagnosis of Ewing Sarcoma – Clavicle. Indian Medical Gazette. 2011 Dec ; 145 (12): 495-497.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/157366
dc.language.isoenen_US
dc.source.urihttps://medind.nic.in/ice/t11/i12/icet11i12p495.pdfen_US
dc.subjectewing sarcomaen_US
dc.subjectclavicleen_US
dc.subjectcancer in childrenen_US
dc.subject.meshChild
dc.subject.meshClavicle --pathology
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshSarcoma, Ewing --cytology
dc.subject.meshSarcoma, Ewing --diagnosis
dc.subject.meshSarcoma, Ewing --pathology
dc.subject.meshSarcoma, Ewing --radiography
dc.titleCytological Diagnosis of Ewing Sarcoma – Clavicle.en_US
dc.typeArticleen_US
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