Observation of Angiolymphoid Hyperplasia with Eosinophilia (ALHE) at Three Arterial Sites and Its Association with Membranous Nephropathy
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- Ito Seigo
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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- Oda Takashi
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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- Matsuo Akiko
- Department of Cardiology, Japanese Red Cross Kyoto Daini Hospital, Japan
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- Takechi Hanako
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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- Uchida Takahiro
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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- Watanabe Atsushi
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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- Kono Takako
- Department of Laboratory Medicine, National Defense Medical College, Japan
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- Shimazaki Hideyuki
- Department of Laboratory Medicine, National Defense Medical College, Japan
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- Tamai Seiichi
- Department of Laboratory Medicine, National Defense Medical College, Japan
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- Oshima Naoki
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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- Kumagai Hiroo
- Department of Nephrology and Endocrinology, National Defense Medical College, Japan
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抄録
We herein report a case involving the systemic presentation of angiolymphoid hyperplasia with eosinophilia (ALHE) in association with membranous nephropathy (MN). A 34-year-old Japanese man presented with leg edema and bilateral temporal nodules. He had a history of Buerger's disease and recurrent coronary stenosis. A renal biopsy performed to assess nephrotic syndrome revealed MN. Furthermore, a temporal nodule was excised, and ALHE was diagnosed. We reevaluated the coronary and posterior tibial artery specimens obtained in his twenties and presumed that these lesions were also vascular tumors arising from ALHE. The association of ALHE and MN is quite rare.<br>
収録刊行物
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- Internal Medicine
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Internal Medicine 54 (15), 1933-1939, 2015
一般社団法人 日本内科学会
