An Unusual Presentation of Primary Lymphoma of the Ilium
نویسندگان
چکیده
منابع مشابه
An Unusual Presentation of Primary Lymphoma of the Ilium
Primary bone lymphoma involving the pelvic bone is a rare entity. It does not have distinct clinical features or radiological features that are diagnostic. Biopsy is the gold standard investigation. We present a case of primary pelvic lymphoma with initial histopathological features of chronic osteomyelitis. Upon further clinical follow-up, repeat biopsy of the lesion revealed features of B-cel...
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Extramedullary plasmacytoma (EMP) is a rare neoplasm of soft tissue which usually arises in the respiratory tract, nasal cavity, sinuses and nasopharynx. Multiple extramedullary plasmacytomas are extremely rare, especially those that are not associated with multiple myeloma.We describe multiple primary EMP in a 37 year old man, without involvement of bone or bone marrow. EMP usually has a ...
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1. Wafflart E, Gibaud H, Lerat F, de Kersaint‐Gilly A, Leborgne J. Muscular metastasis of cancer of the pancreas. A propos of a case. J Chir (Paris) 1996;133:167‐70. 2. Garcia OA, Fernandez FA, Satue EG, Buelta L, Val‐Bernal JF. Metastasis of malignant neoplasms of skeletal muscle. Rev Esp Oncol 1984;31:57‐67. 3. Belloir A, Pujol J, Bruel JM, Rouanet JP, Lamarque JL. Muscular metastases: Uncomm...
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A 42-year-old woman presented with isolated right third nerve palsy and preceding lethargy. A previous head injury had required craniotomy, orbital reconstruction and medication to control the subsequent epilepsy. Apart from the pupillarysparing third nerve palsy, the general and neurological examinations were normal. Magnetic resonance imaging (MRI) revealed post-traumatic right frontal cortic...
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A patient with a thymic lymphoma invading both chest wall and lung is presented. Extensive systemic-pulmonary arterial communications had developed through this lymphoma. Hodgkin's disease should be included as a rare cause of systemic to pulmonary communications.
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ژورنال
عنوان ژورنال: Case Reports in Medicine
سال: 2014
ISSN: 1687-9627,1687-9635
DOI: 10.1155/2014/509837