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231224s2017 xx |||||o 00| ||jpn c |
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7 |
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|a 10.14989/ActaUrolJap_63_2_81
|2 doi
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|a jpn
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| 100 |
1 |
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|a Takada, Hideaki
|e verfasserin
|4 aut
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| 245 |
1 |
2 |
|a A Case of Hemodialysis-Associated Pelvic Amyloidoma Mimicking Renal Cancer-Associated Etiology
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| 264 |
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1 |
|c 2017
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| 336 |
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|a Text
|b txt
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|a Date Completed 24.08.2017
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|a Date Revised 23.10.2018
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|a published: Print
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|a Citation Status MEDLINE
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|a Patients with renal insufficiency receiving long-term hemodialysis often develop so-called hemodialysis amyloidosis characterized by systemic β 2-microglobulin amyloid lesions, while patients with renal cell carcinoma may develop amyloid A(AA) amyloidosis. Herein, we present a 67-year-old man on thirty-yearlong hemodialysis who was diagnosed to have left renal cell carcinoma coincident with a large spaceoccupying lesion adjacent to the psoas muscle in the pelvic cavity. An ultrasound-guided percutaneous needle biopsy was performed at the time of laparoscopic radical nephrectomy. The pathological work-up on the needle biopsy specimen revealed that the lesion was not an AA amyloidoma but a β2-microglobulin amyloidoma, which is a rare manifestation of hemodialysis amyloidosis
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| 650 |
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|a Case Reports
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| 650 |
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4 |
|a Journal Article
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| 700 |
1 |
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|a Nagahama, Kanji
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Nakashima, Yoshiharu
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Yoshimura, Koji
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Nishio, Yasunori
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Matsuo, Ken
|e verfasserin
|4 aut
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| 700 |
1 |
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|a Mori, Noriko
|e verfasserin
|4 aut
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| 773 |
0 |
8 |
|i Enthalten in
|t Hinyokika kiyo. Acta urologica Japonica
|d 1962
|g 63(2017), 2 vom: 28. Feb., Seite 81-85
|w (DE-627)NLM012631779
|x 0018-1994
|7 nnns
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| 773 |
1 |
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|g volume:63
|g year:2017
|g number:2
|g day:28
|g month:02
|g pages:81-85
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| 856 |
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|u http://dx.doi.org/10.14989/ActaUrolJap_63_2_81
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