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MR Vol.12 No.1 indexに戻る
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MODERN RHEUMATOLOGY
Vol.12 No.1 |
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Pulmonary AL amyloidosis in a patient
with primary Sjogren syndrome |
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| S. Banno2, Y. Matsumoto1, Y. Hayami1,
Y. Sugiura1, T. Yoshinouchi1 , R. Ueda1 |
(1)Second Department of Internal Medicine,
Medical School, Nagoya City University, Nagoya, Japan
(2) Department of Clinical Laboratory Medicine, Medical School, Nagoya City
University, 1 Kawasumi, Mizuho-ku, Nagoya 460-8601, Japan |
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| Abstract |
| Abstract The condition of a 29-year-old woman
with primary Sjogren syndrome (SS) was complicated by amyloid light
chains- (AL-) type amyloidosis in the paranasal sinus. She had
not complained of respiratory symptoms, but her chest computed
tomography (CT) scan revealed bilateral multiple nodular shadows.
Lung biopsy specimens using video-associated thoracoscopy showed
amyloidoma in a subpleural nodular lesion and amyloid deposits
in the interstitial parenchymal walls and pulmonary vessels. Pulmonary
AL amyloidosis, presumably related to a chronic inflammatory lymphoproliferative
process in SS, has rarely been reported. |
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| Key words |
| Key words Pulmonary amyloidosis ・ Sjogren
syndrome (SS) |
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