Myeloma crystal tubulopathy and Fanconi syndrome: A rare histological finding

AppletonJ.P.; DayC.; NeilD.; WandrooF.A.

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Myeloma crystal tubulopathy and Fanconi syndrome: A rare histological finding

机译：骨髓瘤晶体肾小管病变和Fanconi综合征：罕见的组织学发现

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A 64-year-old man with a background of chronic renal impairment and ocular pemphigoid presented to the haema-tology clinic with a macrocytic anaemia (Hb 114 g/1, MCV 104·4 fl). He had a 16-month history of fatigue, arthralgia and bone pain following a viral illness and had lost 2 kg in weight in the preceding 6 months. General examination was unremarkable. Urine dipstick showed microscopic haematuria (+++), pro-teinuria (++) and glycosuria (+++). Previous urological investigations for microscopic haematuria 2 years previously were unremarkable.

机译：一名64岁的男子，患有慢性肾功能不全和眼天疱疮，因血红细胞性贫血（Hb 114 g / 1，MCV 104·4 fl）到血液病学诊所就诊。他患有病毒性疾病后有16个月的疲劳，关节痛和骨痛病史，并且在之前的6个月中体重减轻了2公斤。一般检查不明显。尿尺显示镜下血尿（+++），蛋白尿（++）和糖尿（+++）。之前2年前针对微血尿的泌尿外科检查并不明显。

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《British Journal of Haematology》 |2012年第1期|共1页
作者
AppletonJ.P.; DayC.; NeilD.; WandrooF.A.;
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正文语种 eng
中图分类血液及淋巴系疾病;
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1. Myeloma crystal tubulopathy and Fanconi syndrome: A rare histological finding [J] . AppletonJ.P., DayC., NeilD., British Journal of Haematology . 2012,第1期

机译：骨髓瘤晶体肾小管病变和Fanconi综合征：罕见的组织学发现
2. Crystal-storing histiocytosis with renal Fanconi syndrome: pathological and molecular characteristics compared with classicaln myeloma-associated Fanconi syndrome [J] . Guy Touchard Nephrology Dialysis Transplantation . 2010,第9期

机译：晶体存储组织细胞增生症与肾范可尼综合征：与经典骨髓瘤相关范可尼综合征相比的病理和分子特征
3. Crystal-storing histiocytosis with renal Fanconi syndrome: pathological and molecular characteristics compared with classical myeloma-associated Fanconi syndrome. [J] . El Hamel C, Thierry A, Trouillas P, Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association . 2010,第9期

机译：晶体储存组织细胞增生症伴肾Fanconi综合征：与经典骨髓瘤相关性Fanconi综合征相比，病理和分子特征。
4. Finding Needles in the Haystack: Identifying Patients with Rare Subtype of Multiple Myeloma Supported by a Data Warehouse and Information Extraction [C] . Jonathan KREBS, Max BITTRICH, Georg DIETRICH, GMDS 2018, Annual Meeting . 2018

机译：在干草堆中寻找针：鉴定数据仓库和信息提取支持的多发性骨髓瘤的罕见亚型患者
5. Crystal structures of the Fanconi anemia proteins: Structure of the interstrand cross-linking repair protein Fanconi anemia protein I (FANCI); structure of the human FANCF C-terminal domain; reconstitution and crystallilzation of the sub-complexes in the Fanconi anemia core complex. [D] . Xu, Guozhou. 2009

机译：Fanconi贫血蛋白的晶体结构：链间交联修复蛋白Fanconi贫血蛋白I（FANCI）的结构；人FANCF C末端结构域的结构； Fanconi贫血核心复合物中亚复合物的重组和结晶。
6. A case of Fanconi syndrome accompanied by crystal depositions in tubular cells in a patient with multiple myeloma [O] . Do Hee Kim, A Young Lim, Hye Bin Gwag, 2014

机译：多发性骨髓瘤患者的范科尼综合征一例伴有肾小管细胞内晶体沉积
7. A case of Fanconi syndrome accompanied by crystal depositions in tubular cells in a patient with multiple myeloma [O] . Do Hee Kim, A Young Lim, Hye Bin Gwag, 2014

机译：一例Fanconi综合征伴有多发性骨髓瘤患者肾小管细胞晶体沉积

Myeloma crystal tubulopathy and Fanconi syndrome: A rare histological finding

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