Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report

Acquired hemophilia is a rare disease that develops because of the synthesis of antibodies to endogenous VIII blood clotting factor. The most common symptom of acquired hemophilia is spontaneous bleeding. Acquired hemophilia is observed more frequently in older population and in 50% is secondary to...

Full description

Saved in:
Bibliographic Details
Main Authors: S. A. Alekseeva, N. I. Zozulya, T. M. Reshetnyak
Format: Article
Language:Russian
Published: IMA PRESS LLC 2025-07-01
Series:Научно-практическая ревматология
Subjects:
Online Access:https://rsp.mediar-press.net/rsp/article/view/3755
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849687848340422656
author S. A. Alekseeva
N. I. Zozulya
T. M. Reshetnyak
author_facet S. A. Alekseeva
N. I. Zozulya
T. M. Reshetnyak
author_sort S. A. Alekseeva
collection DOAJ
description Acquired hemophilia is a rare disease that develops because of the synthesis of antibodies to endogenous VIII blood clotting factor. The most common symptom of acquired hemophilia is spontaneous bleeding. Acquired hemophilia is observed more frequently in older population and in 50% is secondary to malignant tumors and autoimmune rheumatic diseases. In this article, we present a clinical case of autoimmune hemophilia that developed shortly before the onset of systemic lupus erythematosus.
format Article
id doaj-art-05f3a064cefa42a1ac4823e8b0613bac
institution DOAJ
issn 1995-4484
1995-4492
language Russian
publishDate 2025-07-01
publisher IMA PRESS LLC
record_format Article
series Научно-практическая ревматология
spelling doaj-art-05f3a064cefa42a1ac4823e8b0613bac2025-08-20T03:22:13ZrusIMA PRESS LLCНаучно-практическая ревматология1995-44841995-44922025-07-0163331832310.47360/1995-4484-2025-318-3233067Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case reportS. A. Alekseeva0N. I. Zozulya1T. M. Reshetnyak2V.A. Nasonova Research Institute of RheumatologyNational Medical Research Center for HematologyV.A. Nasonova Research Institute of RheumatologyAcquired hemophilia is a rare disease that develops because of the synthesis of antibodies to endogenous VIII blood clotting factor. The most common symptom of acquired hemophilia is spontaneous bleeding. Acquired hemophilia is observed more frequently in older population and in 50% is secondary to malignant tumors and autoimmune rheumatic diseases. In this article, we present a clinical case of autoimmune hemophilia that developed shortly before the onset of systemic lupus erythematosus.https://rsp.mediar-press.net/rsp/article/view/3755acquired hemophiliasystemic lupus erythematosusspontaneous bleedingautoantibodies
spellingShingle S. A. Alekseeva
N. I. Zozulya
T. M. Reshetnyak
Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report
Научно-практическая ревматология
acquired hemophilia
systemic lupus erythematosus
spontaneous bleeding
autoantibodies
title Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report
title_full Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report
title_fullStr Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report
title_full_unstemmed Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report
title_short Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report
title_sort acquired hemophilia in patient with systemic lupus erythematosus clinical case report
topic acquired hemophilia
systemic lupus erythematosus
spontaneous bleeding
autoantibodies
url https://rsp.mediar-press.net/rsp/article/view/3755
work_keys_str_mv AT saalekseeva acquiredhemophiliainpatientwithsystemiclupuserythematosusclinicalcasereport
AT nizozulya acquiredhemophiliainpatientwithsystemiclupuserythematosusclinicalcasereport
AT tmreshetnyak acquiredhemophiliainpatientwithsystemiclupuserythematosusclinicalcasereport