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1
Adult Fanconi syndrome and multiple myelomatosis.成人范科尼综合征与多发性骨髓瘤
J Clin Pathol. 1969 Jul;22(4):414-6. doi: 10.1136/jcp.22.4.414.
2
[Fanconi syndrome in an adult coincident with early myeloma with monoclonal IgG, type kappa, anomaly (author's transl)].成人范科尼综合征合并早期骨髓瘤伴单克隆IgG(κ型)异常(作者译)
Dtsch Med Wochenschr. 1980 Sep 26;105(39):1355-9. doi: 10.1055/s-2008-1070871.
3
V-domain deposition of lambda Bence Jones protein in the renal tubular epithelial cells in a patient with the adult Fanconi syndrome with myeloma.一名患有成人范可尼综合征合并骨髓瘤患者的肾小管上皮细胞中λ轻链型本-周蛋白的V区沉积
Amyloid. 1998 Jun;5(2):117-20. doi: 10.3109/13506129808995289.
4
Adult Fanconi syndrome with monoclonal abnormality of immunoglobulin light chain.成人范科尼综合征伴免疫球蛋白轻链单克隆异常。
J Clin Pathol. 1967 Jan;20(1):42-8. doi: 10.1136/jcp.20.1.42.
5
Adult Fanconi syndrome secondary to kappa-light chain myeloma: improvement of tubular functions after treatment for myeloma.继发于κ轻链骨髓瘤的成人范科尼综合征:骨髓瘤治疗后肾小管功能的改善
Nephron. 1990;55(3):332-5. doi: 10.1159/000185986.
6
Bence Jones myelomatosis and intravenous pyelography.本斯·琼斯骨髓瘤病与静脉肾盂造影术
S Afr Med J. 1977 Apr 23;51(17):574-6.
7
Multiple myeloma presenting as adult Fanconi syndrome.表现为成人范可尼综合征的多发性骨髓瘤。
Clin Chem. 1972 Mar;18(3):293-5.
8
[A case of IgG-kappa type multiple myeloma complicated by Fanconi syndrome].1例IgG-κ型多发性骨髓瘤合并范科尼综合征
Rinsho Ketsueki. 1994 Aug;35(8):786-91.
9
[General pain during exertion, percussion pain of the bone, proteinuria and glycosuria (thoracic radiography, serum electrolyte levels and kidney biopsy): (myeloma of Bence Jones K type and an adult type of Fanconi syndrome)].[运动时全身疼痛、骨叩击痛、蛋白尿和糖尿(胸部X光检查、血清电解质水平及肾活检):(本斯·琼斯K型骨髓瘤及成人型范科尼综合征)]
Nihon Rinsho. 1977 Fall;35 Suppl 2:3252-3, 3622-3.
10
[A case of renal Fanconi syndrome due to Bence Jones' protein K-type multiple myeloma].
Nihon Jinzo Gakkai Shi. 2016;58(7):1088-1094.

引用本文的文献

1
Adult Fanconi syndrome progressing to multiple myeloma.成人范科尼综合征进展为多发性骨髓瘤。
J Clin Pathol. 1984 Nov;37(11):1256-8. doi: 10.1136/jcp.37.11.1256.
2
Isocyanates in industry: environmental control.工业中的异氰酸酯:环境控制
Proc R Soc Med. 1970 Apr;63(4):368-72. doi: 10.1177/003591577006300416.
3
Rickets (and osteomalacia), nutritional and metabolic (1919-69).佝偻病(及骨软化症),营养性与代谢性(1919 - 1969年)
Proc R Soc Med. 1970 Apr;63(4):401-8. doi: 10.1177/003591577006300432.
4
[Myeloma-kidney. II. Correlation of structure and function with special reference to acute renal failure (author's transl)].骨髓瘤肾病。II. 结构与功能的相关性,特别提及急性肾衰竭(作者译)
Klin Wochenschr. 1974 Aug 15;52(16):771-80. doi: 10.1007/BF01468737.

本文引用的文献

1
The adult Fanconi syndrome. Report of two cases, one with multiple myeloma.成人范科尼综合征。两例报告,其中一例合并多发性骨髓瘤。
Med Clin North Am. 1963 Jan;47:191-206. doi: 10.1016/s0025-7125(16)33629-x.
2
Myelomatosis associated with glycosuria and aminoaciduria.伴有糖尿和氨基酸尿的骨髓瘤病
Scott Med J. 1959 Feb;4(2):89-93. doi: 10.1177/003693305900400206.
3
[Multiple myelomas & the De Toni-Fanconi syndrome].[多发性骨髓瘤与德托尼 - 范科尼综合征]
Ned Tijdschr Geneeskd. 1958 Aug 30;102(35):1690-3.
4
Multiple myeloma and the adult Fanconi syndrome. I. Report of a case with crystal-like deposits in the tumor cells and in the epithelial cells of the kidney.多发性骨髓瘤与成人范科尼综合征。I. 一例肿瘤细胞及肾上皮细胞内有晶体样沉积物的病例报告。
Am J Med. 1957 Jan;22(1):5-23. doi: 10.1016/0002-9343(57)90333-9.
5
The association of the Fanconi syndrome with malignant disease.范科尼综合征与恶性疾病的关联。
Dan Med Bull. 1956 Sep;3(6):177-9.
6
Renal function studies in a adult subject with the Fanconi syndrome.对一名患有范科尼综合征的成年受试者的肾功能研究。
Am J Med. 1954 Jan;16(1):138-52. doi: 10.1016/0002-9343(54)90329-0.
7
Abnormal proteins in myeloma.骨髓瘤中的异常蛋白质。
Adv Intern Med. 1952;5:398-440.
8
Adult Fanconi syndrome with monoclonal abnormality of immunoglobulin light chain.成人范科尼综合征伴免疫球蛋白轻链单克隆异常。
J Clin Pathol. 1967 Jan;20(1):42-8. doi: 10.1136/jcp.20.1.42.
9
Paraproteins, benign or malignant?副蛋白,良性还是恶性?
Br Med J. 1967 Sep 16;3(5567):699-704. doi: 10.1136/bmj.3.5567.699.

成人范科尼综合征与多发性骨髓瘤

Adult Fanconi syndrome and multiple myelomatosis.

作者信息

Horn M E, Knapp M S, Page F T, Walker W H

出版信息

J Clin Pathol. 1969 Jul;22(4):414-6. doi: 10.1136/jcp.22.4.414.

DOI:10.1136/jcp.22.4.414
PMID:5798628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC474200/
Abstract

A case is described of a 59-year-old woman presenting with multiple renal tubular defects. The aminoaciduria was of a generalized type. When investigated initially the only feature of myelomatosis was urinary Bence-Jones protein. Two years later radiologically classical multiple myelomatosis developed and rapidly progressed to the patient's death nine months later.

摘要

本文描述了一例59岁女性,其表现为多种肾小管缺陷。氨基酸尿为全身性类型。最初检查时,骨髓瘤病的唯一特征是尿本-周蛋白。两年后,影像学显示典型的多发性骨髓瘤病,九个月后病情迅速进展导致患者死亡。