Cargando…

Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report

Patient: Female, 42-year-old Final Diagnosis: Primary antiphospholipid antibody syndrome Symptoms: Coma Medication: — Clinical Procedure: Evacuation of the intracranial hematoma • suboccipital decompression • intraventricular catheter placement Specialty: Neurosurgery OBJECTIVE: Rare co-existance of...

Descripción completa

Detalles Bibliográficos
Autores principales: Tatsuoka, Yoshio, Mano, Yui, Ishikawa, Shuichi, Shinozaki, Shigeru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916662/
https://www.ncbi.nlm.nih.gov/pubmed/31822651
http://dx.doi.org/10.12659/AJCR.919649
_version_ 1783480277118484480
author Tatsuoka, Yoshio
Mano, Yui
Ishikawa, Shuichi
Shinozaki, Shigeru
author_facet Tatsuoka, Yoshio
Mano, Yui
Ishikawa, Shuichi
Shinozaki, Shigeru
author_sort Tatsuoka, Yoshio
collection PubMed
description Patient: Female, 42-year-old Final Diagnosis: Primary antiphospholipid antibody syndrome Symptoms: Coma Medication: — Clinical Procedure: Evacuation of the intracranial hematoma • suboccipital decompression • intraventricular catheter placement Specialty: Neurosurgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Antiphospholipid antibody syndrome (APS) is a systemic autoimmune disease associated with arterial and venous thromboembolism and pregnancy complications. There have been several reports of APS with systemic lupus erythematosus (SLE) complicated with aortic dissection. However, none of them has been primary APS, which is APS without SLE. CASE REPORT: A 42-year-old woman with primary APS and APS nephropathy on warfarin and aspirin therapy presented with coma due to cerebellar hemorrhage. The effect of warfarin was immediately reversed with prothrombin complex concentrate. We performed emergent evacuation of the hematoma, and her level of consciousness improved to normal on postoperative day (POD) 1. She had acute hypertension on arrival, which was resistant to multiple antihypertensives and was stabilized on POD 3. She also had exacerbation of chronic kidney disease after using contrast and prothrombin concentrate complex, and was on temporary renal replacement therapy from POD 3. Aortic dissection was found accidentally on echocardiography on POD 7, and she was subsequently treated medically. She was transferred to the rehabilitation hospital with mild dysarthria and truncal ataxia on POD 59. CONCLUSIONS: We report the first case in the English literature of primary APS complicated with cerebellar hemorrhage and aortic dissection. Acute hypertension following hemorrhage and exacerbation of APS nephropathy likely triggered the dissection of the aortic wall, the integrity of which might have been compromised by longstanding antiphospholipid antibody and vasa vasorum thrombosis.
format Online
Article
Text
id pubmed-6916662
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-69166622019-12-26 Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report Tatsuoka, Yoshio Mano, Yui Ishikawa, Shuichi Shinozaki, Shigeru Am J Case Rep Articles Patient: Female, 42-year-old Final Diagnosis: Primary antiphospholipid antibody syndrome Symptoms: Coma Medication: — Clinical Procedure: Evacuation of the intracranial hematoma • suboccipital decompression • intraventricular catheter placement Specialty: Neurosurgery OBJECTIVE: Rare co-existance of disease or pathology BACKGROUND: Antiphospholipid antibody syndrome (APS) is a systemic autoimmune disease associated with arterial and venous thromboembolism and pregnancy complications. There have been several reports of APS with systemic lupus erythematosus (SLE) complicated with aortic dissection. However, none of them has been primary APS, which is APS without SLE. CASE REPORT: A 42-year-old woman with primary APS and APS nephropathy on warfarin and aspirin therapy presented with coma due to cerebellar hemorrhage. The effect of warfarin was immediately reversed with prothrombin complex concentrate. We performed emergent evacuation of the hematoma, and her level of consciousness improved to normal on postoperative day (POD) 1. She had acute hypertension on arrival, which was resistant to multiple antihypertensives and was stabilized on POD 3. She also had exacerbation of chronic kidney disease after using contrast and prothrombin concentrate complex, and was on temporary renal replacement therapy from POD 3. Aortic dissection was found accidentally on echocardiography on POD 7, and she was subsequently treated medically. She was transferred to the rehabilitation hospital with mild dysarthria and truncal ataxia on POD 59. CONCLUSIONS: We report the first case in the English literature of primary APS complicated with cerebellar hemorrhage and aortic dissection. Acute hypertension following hemorrhage and exacerbation of APS nephropathy likely triggered the dissection of the aortic wall, the integrity of which might have been compromised by longstanding antiphospholipid antibody and vasa vasorum thrombosis. International Scientific Literature, Inc. 2019-12-11 /pmc/articles/PMC6916662/ /pubmed/31822651 http://dx.doi.org/10.12659/AJCR.919649 Text en © Am J Case Rep, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Tatsuoka, Yoshio
Mano, Yui
Ishikawa, Shuichi
Shinozaki, Shigeru
Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report
title Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report
title_full Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report
title_fullStr Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report
title_full_unstemmed Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report
title_short Primary Antiphospholipid Antibody Syndrome Complicated with Cerebellar Hemorrhage and Aortic Dissection: A Case Report
title_sort primary antiphospholipid antibody syndrome complicated with cerebellar hemorrhage and aortic dissection: a case report
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916662/
https://www.ncbi.nlm.nih.gov/pubmed/31822651
http://dx.doi.org/10.12659/AJCR.919649
work_keys_str_mv AT tatsuokayoshio primaryantiphospholipidantibodysyndromecomplicatedwithcerebellarhemorrhageandaorticdissectionacasereport
AT manoyui primaryantiphospholipidantibodysyndromecomplicatedwithcerebellarhemorrhageandaorticdissectionacasereport
AT ishikawashuichi primaryantiphospholipidantibodysyndromecomplicatedwithcerebellarhemorrhageandaorticdissectionacasereport
AT shinozakishigeru primaryantiphospholipidantibodysyndromecomplicatedwithcerebellarhemorrhageandaorticdissectionacasereport