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Intravascular lymphoma presenting as a specific pulmonary embolism and acute respiratory failure: a case report.

作者信息

Georgin-Lavialle Sophie, Darmon Michael, Galicier Lionel, Fysekidis Marinos, Azoulay Elie

出版信息

J Med Case Rep. 2009 May 12;3:7253. doi: 10.1186/1752-1947-3-7253.

Abstract

INTRODUCTION

The occurrence of an intravascular lymphoma with severe pulmonary involvement mimicking pulmonary embolism is described.

CASE PRESENTATION

A 38-year-old man was referred to our intensive care unit with acute respiratory failure and long lasting fever. Appropriate investigations failed to demonstrate any bacterial, viral, parasitic or mycobacterial infection. A chest computed tomography scan ruled out any proximal or sub-segmental pulmonary embolism but the ventilation/perfusion lung scan concluded that there was a high probability of pulmonary embolism. The cutaneous biopsy pathology diagnosed intravascular lymphoma.

CONCLUSION

Intravascular lymphoma is a rare disease characterized by exclusive or predominant growth of neoplastic cells within the lumina of small blood vessels. Lung involvement seems to be common, but predominant lung presentation of this disease is rare. In our patient, urgent chemotherapy, along with adequate supportive care allowed complete recovery.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5041/2726505/5b54623020fd/1752-1947-0003-0000007253-1.jpg

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本文引用的文献

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Intravascular lymphomatosis presenting as reversible severe pulmonary hypertension.
Int J Cardiol. 2000 Sep 15;75(2-3):283-4. doi: 10.1016/s0167-5273(00)00311-9.
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Capillary leak syndrome in patients with hemophagocytic lymphohistiocytosis.
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