Extranodal Rosai-Dorfman disease involving the pulmonary artery†

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Extranodal Rosai-Dorfman disease involving the pulmonary artery.

A 61-year-old woman underwent computed tomography (CT) angiography for evaluation of syncope and was found to have a central pulmonary artery filling defect (Fig. 1). During an attempted intravascular ultrasound-guided biopsy of the lesion, the patient coded and died. Autopsy confirmed the case as a rare presentation of Rosai-Dorfman disease (Fig. 2 and Supplementary Figs 1 and 2). Supplementar...

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Extranodal Rosai-Dorfman disease of the kidney

Ann Saudi Med 29(1) January-February 2009 www.saudiannals.net 55 Lampert and Lennert in 1961 were the first to describe what is now known as Rosai-Dorfman disease (RDD). Subsequently in 1969, Rosai and Dorfman described 4 cases of a disease they called sinus histocytosis with massive lymphadenopathy (better known as RDD).1 In 1972 they analyzed 30 additional cases, establishing RDD2 as a clinic...

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Rosai-Dorfman disease with extranodal involvement.

Rosai-Dorfman disease is a rare condition of marrow hematopoietic stem-cell origin. Patients can show extranodal involvement as well as lymphatic involvement, but only about 5% of extranodal cases involve intracranial lesions. A 53-year-old male was admitted to our hospital with bilateral cervical lymphadenopathy. Intracranial tumors and bone lesions were also detected. Cervical lymph node biop...

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Extranodal manifestation of Rosai-Dorfman disease in the breast tissue

A 71-year-old asymptomatic female with a history of breast cancer status after right total mastectomy had interval development of several new nodules in the left breast in a 1-year time span. Stereotactic biopsy was performed, which revealed multifocal Rosai Dorfman disease in the left breast. The patient was referred to hematology, and computed tomography of the chest/abdomen/pelvis did not de...

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Extranodal Rosai-Dorfman disease involving the right atrium in a 60-year-old male

UNLABELLED Rosai-Dorfman disease (RDD) involving the cardiovascular system is extremely rare; to our knowledge, there are only 9 cases in the literature. Here, a case of a 60-year-old male with RDD involving the right atrium is presented. A comprehensive literature review was undertaken to summarize the clinical and pathologic features of this disorder. VIRTUAL SLIDES The virtual slide(s) for...

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ژورنال

عنوان ژورنال: European Journal of Cardio-Thoracic Surgery

سال: 2013

ISSN: 1873-734X,1010-7940

DOI: 10.1093/ejcts/ezt202