Pulmonary T-cell Lymphoma with Pulmonary Arterial Hypertension

We report on a 73-year-old man with systemic lymphadenopathy and chest computed tomography (CT) findings of bilateral diffuse ground-glass opacities and interlobular septal thickening. He also had pulmonary arterial hypertension (PAH). Several lymph node biopsies were attempted, without a definitive...

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Veröffentlicht in:Internal Medicine 2011, Vol.50(16), pp.1733-1736
Hauptverfasser: Watanabe, Satoshi, Takato, Hazuki, Waseda, Yuko, Tokuda, Akira, Katayama, Nobuyuki, Kondo, Yukio, Fujimura, Masaki, Nakao, Shinji
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Sprache:eng
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Zusammenfassung:We report on a 73-year-old man with systemic lymphadenopathy and chest computed tomography (CT) findings of bilateral diffuse ground-glass opacities and interlobular septal thickening. He also had pulmonary arterial hypertension (PAH). Several lymph node biopsies were attempted, without a definitive diagnosis. A thoracoscopic lung biopsy was performed, and the specimen was diagnosed as peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS). Lymphoma cells had invaded lung vessels, resulting in PAH. We should include pulmonary lymphoma in the differential diagnosis of patients with PAH and chest CT findings of diffuse ground-glass opacities and interlobular septal thickening.
ISSN:0918-2918
1349-7235
1349-7235
DOI:10.2169/internalmedicine.50.5329