Acquired Hemophilia presenting as Gross hematuria following Kidney Stone - A case report and review of the literature

被引:0
|
作者
Schmidt-Bowman, Max [1 ]
Reinstatler, Lael [2 ]
Raffin, Eric P. [2 ]
Yared, Joseph E. [2 ]
Seigne, John D. [2 ]
Sverrisson, Einar F. [2 ]
机构
[1] Geisel Sch Med Dartmouth, Hanover, NH USA
[2] Dartmouth Hitchcock Med Ctr, Sect Urol, Dept Surg, 1 Med Ctr Dr, Lebanon, NH 03756 USA
来源
INTERNATIONAL BRAZ J UROL | 2018年 / 44卷 / 02期
关键词
Hematuria; Nephrolithiasis; Factor; 8; deficiency; acquired [Supplementary Concept; GA-68-LABELED PSMA LIGAND; PROSTATE; BIOPSY; DIAGNOSIS; PET/CT;
D O I
10.1590/S1677-5538.IBJU.2017.0172
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
A rare condition in itself, acquired hemophilia A, seldom presents as isolated gross hematuria. It is a serious condition with a high mortality rate and thus clinical suspicion followed by prompt diagnosis is imperative (1). In fact, only 8 cases of such presentation of this condition have been reported thus far in the literature. Of these, none describe the initial presentation of hematuria with the inciting event of a kidney stone. We present a case of a 67-year-old man with signs and symptoms of nephrolithiasis accompanied by profuse hematuria, who was subsequently found to have developed expression of factor VIII inhibitor leading to acquired hemophilia A.
引用
收藏
页码:390 / 392
页数:3
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