scholarly journals Ligature of external carotid artery as an optional technique in a patient with von Willebrand disease

2011 ◽  
Vol 22 (5) ◽  
pp. 435-438 ◽  
Author(s):  
Leonardo Perez Faverani ◽  
Ellen Cristina Gaetti-Jardim ◽  
Gabriel Ramalho-Ferreira ◽  
Jessica Lemos Gulinelli ◽  
Thallita Pereira Queiroz ◽  
...  

The von Willebrand disease (vWD) is a hereditary coagulopathy. There is no gender predilection. Clinically characterized by mucocutaneous bleeding, especially nose bleeding, menorrhagia and bleeding after trauma. This article reports a case of a 52-year-old Caucasian male patient with vWD, who presented with extensive bleeding in the tongue after a lacerating injury caused by accidental biting, and describes some clinical, pathological and treatment aspects of vWD. After repeated attempts to suture the wound and replace clotting factors, a decision was made to perform the ligature of the external carotid artery ipsilateral to the injury. There was favorable resolution of the case, with a good aspect of the scar 2 months after ligation. This case reinforces that it is extremely important to make a thorough review of medical history of all patients, searching for possible bleeding disorders or previous family history.

Author(s):  
Nidal Karim Al-Rahal

Background: Consanguineous marriage is defined as inbreeding between second cousins or closer. In such families there will be a potential increase in the autosomal recessive traits with its lethal effect, with an increased risk of morbidity and mortality in the new generation.  Inherited bleeding disorders (InBDs) are rare complicated diseases, difficult and expensive to treat, the defect usually due to quantitative or qualitative deficiency of clotting factors, platelets or fibrinolysis. This study attempts to assess the diversity, the frequency and the clinical features of inherited bleeding disorders (InBDs) in central part of Iraq and to determine the state of consanguineous marriage. Materials and Methods: This is a prospective cross-sectional study conducted in the National Center of Hematology NCH, Baghdad, Iraq between June2014 and June 2017. In total, 256 pediatrics and adult patients were included. Full bleeding history, family history, drug history and consanguineous marriage were recorded and followed by medical examination.  First-line laboratory tests were performed and then were followed by further tests included mixing study, lupus anticoagulant testing, clotting factor activity assay, von Willebrand Antigen (VW: Ag), Ristocetin co factor vWF: RiCoF activity and platelet function test. Results: The range of age was from 1 month to 57 years, with mean age 8.424±8.623 years and median age of 6.5years. The male to female ratio was 1.1:1. The most common age group was in the range of 1-10 years (46.45%). Family history was positive in 55.07% of patients (P >0.05). The consanguinity was found in 76.95% of the families studied (P <0.0001).  The most prevalent InBD was von Willebrand disease (42.98%) with majority type 3VWD (86.4%). The second most prevalent was thrombasthenia (36.71%) and the majority had Glanzmann’s thrombosthenia (86.2%). Rare bleeding disorders (RBDs) were observed in 6.25% of patients and the most common factor deficiency was FVII.  Conclusion: Consanguinity is high in patients with inherited bleeding disorders in Iraq, leading to emergence of life-threatening autosomal recessive inherited diseases. Genetic counselling is recommended besides education and awareness to minimize such rare illnesses in the community.


2017 ◽  
Vol 01 (03) ◽  
pp. 184-189
Author(s):  
Rahul Kumar ◽  
Ankur Goyal ◽  
Ashu Bhalla ◽  
Sonia Sandip ◽  
Kapil Sikka

AbstractA 25-year-old patient presented with bleeding of right pinna arteriovenous malformation (AVM). There was history of ipsilateral external carotid artery (ECA) ligation 10 years back. Subsequent investigations (ultrasound, magnetic resonance imaging, digital subtraction angiography) showed recruitment of complex collaterals from the ipsilateral subclavian artery and vertebral artery feeding the recurrent nidus. The patient underwent two sessions of endovascular embolization and one session of percutaneous embolization. We wish to highlight the feasibility of antegrade embolization in such cases via collaterals and role of direct percutaneous treatment.


2002 ◽  
Vol 116 (12) ◽  
pp. 1053-1054 ◽  
Author(s):  
Furrat Amen ◽  
Amer A. Amen

We report the case of a 75-year-old man who presented with an ischaemic tongue. He was known to have external carotid artery stenosis and a history of a transient ischaemic attack. He was treated with a heparin infusion and the tongue healed well.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 2229-2229
Author(s):  
Veerle Labarque ◽  
Victor S. Blanchette ◽  
Dewi S. Clark ◽  
Paula D. James ◽  
Margaret L. Rand

Abstract Abstract 2229 Mucocutaneous bleeding symptoms, such as epistaxis and bruising, are frequent complaints in childhood; a detailed bleeding history is a crucial initial step in determining whether a child presenting with such symptoms has an underlying bleeding disorder. A Pediatric Bleeding Questionnaire (PBQ), based on the MCMDM-1 VWD Bleeding Questionnaire, incorporates 6 pediatric-specific bleeding symptoms (see below) to quantify bleeding severity in children. Bleeding symptoms are scored in a −1 to +4 range, with a −1 score assigned for tooth extraction or surgery if bleeding did not occur in at least 2 procedures, and are summed for all symptoms. An overall PBQ score of ≥2 predicts a diagnosis of von Willebrand disease (VWD). The PBQ has also been used to quantify the severity of bleeding symptoms in children with VWD or platelet function disorders (Bowman et al, J Thromb Haemost 2009;7:1418; Biss et al, J Thromb Haemost 2010;8:950; Biss et al, J Thromb Haemost 2010;8:1416). The ISTH has developed a Bleeding Assessment Tool (ISTH-BAT) to standardize the reporting of bleeding symptoms in adult and pediatric populations; bleeding symptoms are scored in a 0 to +4 range, and are summed (Rodeghiero et al, J Thromb Haemost 2010;8:2063). Criteria for scoring of each symptom are similar between the two questionnaires, but not identical. Here, we have performed a detailed comparison between PBQ and ISTH-BAT scores in a prospective study of children with mucocutaneous bleeding and/or a family history of VWD or a platelet function disorder referred to our tertiary-care pediatric bleeding disorders clinic. To date, we have enrolled 75 subjects, with a mean age of 9.9 yrs (range: 0.5–17.8 yrs), of whom 36 are males. The median overall PBQ score of these children was 3 (range: 0–12), as was the median overall ISTH-BAT score (range: 0–13). In 37/75 children (49%), the overall PBQ score was identical to the overall ISTH-BAT score. In the majority of these children (34/37; 92%), the individual scores for each symptom were identical. However, in 3 children, there were differences in the individual scores that balanced out, resulting in identical overall scores. For 38/75 children (51%), the overall PBQ and ISTH-BAT scores were different. In the majority of these children (33/38; 87%), the difference between the scores was only 1, with the ISTH-BAT being lower in 19/38 children, and higher in 14/38 children. In 2/38 children, the overall ISTH-BAT was lower by 2, in 2/38, higher by 2 and in 1/38, higher by 3. A lower overall ISTH-BAT score was mainly due to a lower score for cutaneous bleeding symptoms (14/21 children). A higher overall ISTH-BAT score was mainly due to a −1 PBQ score for a child who did not bleed on at least 2 tooth extractions or surgeries (observed in 11/17 children) and/or a higher ISTH-BAT score for menorrhagia (observed in 6/17 children, specifically, 6/9 postmenarchal adolescent females). 10/75 (13%) children had a normal overall PBQ score of 0 or 1 (median: 1). The median overall ISTH-BAT score in these children was also 1 (range: 0–3), but 5 children had a score of 2 or 3. In the remaining 65/75 children (87%) with a positive, abnormal PBQ score, the median score was 3 (range: 2–12), as was the median overall ISTH-BAT score (range: 2–13). In contrast with previous prospective studies using the PBQ/ISTH-BAT in which pediatric-specific symptoms were not observed (Bowman et al, J Thromb Haemost 2009;7:1418; Bidlingmaier et al, J Thromb Haemost 2012;10:1335), 12/75 children (16%) received scores for macroscopic hematuria, post-circumcision bleeding, cephalohematoma, umbilical stump bleeding, post-venipuncture bleeding, or conjunctival hemorrhage. In summary, in this prospective study, we have observed similar, but not identical, overall PBQ and ISTH-BAT scores and the occurrence of pediatric-specific bleeding symptoms in children referred to a tertiary-care bleeding disorders clinic with mucocutaneous bleeding and/or a family history of VWD or platelet dysfunction. Thus, the inclusion of pediatric-specific bleeding symptoms in the standardized questionnaires is useful, and if the ISTH-BAT is to be adopted for general use to aid in the evaluation of whether a child has an underlying bleeding disorder, it will be essential to determine the cut-off for an abnormal ISTH-BAT bleeding score in children <18 yrs of age. Disclosures: James: CSL-Behring, Baxter, Bayer: Honoraria, Research Funding.


2003 ◽  
Vol 23 (03) ◽  
pp. 135-137
Author(s):  
B. Mansouri Taleghani ◽  
W. A. Wuillemin ◽  
N. X. von der Weid

SummaryThis case report of a school boy with a history of severe and repeated episodes of epistaxis presents a short overview of the clinical and laboratory findings which lead to confirm the suspected diagnosis of von Willebrand disease (vWD). Suspicion of defective primary haemostasis should arise when unusual (because of their number or duration) mucosal bleeds appear in an otherwise normal and healthy patient. Because of its definitive inhibitory effect on platelet aggregation, acetylsalicylic acid (more than other non-steroidal anti-inflammatory drugs exerting unselective inhibition of cyclooxygenase) is a strong factor in triggering or sustaining the bleeding disorders in these patients. Among the congenital disorder of primary haemostasis, vWD is by far the most frequent one.The difficulties of laboratory diagnosis of vWD are stressed; the promises and pitfalls of new in vitro methods for measuring primary haemostasis (PFA-100® analyzer) are discussed. An accurate diagnosis of the specific type of vWD is of critical importance for correct patient management as well as for genetic counseling.


2019 ◽  
Vol 2019 (6) ◽  
Author(s):  
Rajdeep Basu ◽  
Omkarr De Hazra ◽  
Sumantro Mondal ◽  
Srabani Ghosh ◽  
Soumitra Ghosh

Abstract Vascular complications in forms of venous and arterial thrombi are common scenario in antiphospholipid syndrome with raised titer of antibodies. Here we describe an 18 years old female who was admitted with right parotid swelling due to external carotid artery thrombi within gland parenchyma in antiphospholipid syndrome, with past history of right lower leg arterial occlusion and digital gangrene.


2006 ◽  
Vol 20 (4) ◽  
pp. 576-579
Author(s):  
Sana Ullah ◽  
Michael L. Schmitz ◽  
Kimo C. Stine ◽  
Charles E. Johnson ◽  
Sherry C. Faulkner ◽  
...  

Hematology ◽  
2003 ◽  
Vol 2003 (1) ◽  
pp. 559-574 ◽  
Author(s):  
Margaret E. Rick ◽  
Christopher E. Walsh ◽  
Nigel S. Key

Abstract Both clinical and basic problems related to the congenital bleeding disorders continue to confront hematologists. On the forefront are efforts to bring genetic correction of the more common bleeding disorders such as hemophilia A to the clinic in a safe and accessible manner. A second issue, particularly for patients with hemophilia, is the development of inhibitors—questions of how they arise and how to prevent and treat these problems that confound otherwise very successful replacement therapy and allow patients to maintain normal lifestyles. A third issue is the continuing question of diagnosis and management of von Willebrand disease, the most common congenital bleeding disorder, especially in individuals who have borderline laboratory values, but have a history of clinical bleeding. In Section I, Dr. Christopher Walsh discusses general principles of effective gene transfer for the hemophilias, specific information about viral vectors and non-viral gene transfer, and alternative target tissues for factor VIII and factor IX production. He highlights information about the immune response to gene transfer and reviews data from the hemophilia gene transfer trials to date. The future prospects for newer methods of therapy such as RNA repair and the use of gene-modified circulating endothelial progenitors are presented as possible alternatives to the more traditional gene therapy approaches. In Section II, Dr. Nigel Key focuses on inhibitor development in patients with hemophilia A. He reviews the progress in our understanding of the risk factors and presents newer information about the immunobiology of inhibitor development. He discusses the natural history of these inhibitors and the screening, laboratory diagnosis, and treatment, including the use of different modalities for the treatment of acute bleeding episodes. Dr. Key also presents information about the eradication of inhibitors by immune tolerance induction and reviews recent information from the international registries regarding the status and success of immune tolerance induction. In Section III, Dr. Margaret Rick discusses the diagnosis, classification, and management of von Willebrand disease. Attention is given to the difficulty of diagnosis in patients with mild bleeding histories and borderline laboratory test results for von Willebrand factor. She presents the value of different laboratory assays for both diagnosis and classification, and she relates the classification of von Willebrand disease to the choice of treatment and to the known genetic mutations. Practical issues of diagnosis and treatment, including clinical cases, will be presented.


Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 981-981
Author(s):  
Bhavya S Doshi ◽  
Rachel S Rogers ◽  
Hilary B Whitworth ◽  
Emily Stabnick ◽  
Jessica Britton ◽  
...  

Abstract Von Willebrand disease (VWD) is the most common inherited bleeding disorder and is diagnosed via 3 cardinal features: 1) personal history of bleeding, 2) laboratory assays and 3) family history of VWD. The diagnosis of VWD in pediatric patients is complicated by von Willebrand factor (VWF) inter- and intra-assay variability, phlebotomy-induced physiologic stress increasing VWF levels from baseline, and a lack of prior hemostatic challenges. Given these challenges, NHLBI guidelines recommend repeated testing in patients with mildly low or normal levels and a high suspicion of VWD. However, no studies to date have evaluated the utility of repeat VWF testing in pediatric patients. Currently, our center's standard of care is to complete 3 separate sets of VWF testing to rule out VWD. The primary objective of this study was to determine the clinical variables associated with requiring more than 1 test to diagnose VWD and to establish a cutoff value for the first set of VWF assays above which further testing would not be informative. This single center retrospective cohort study included patients ≤ 18 years of age who either had a diagnosis of or evaluation for VWD between January 2012 and July 2017. Patients were excluded if the VWD laboratory evaluation was completed at another institution or due to the presence of another bleeding disorder. Medical charts were abstracted for demographic information, medications, reason for testing, family history of VWD, results of VWF assays, and other illness at time of evaluation. All patients had a retrospective ISTH BAT score completed. Data were analyzed using SAS and are reported as median (IQR). Statistical analysis was done with non-parametric tests (Mann-Whitney or Wilcoxon sign-rank) for two groups comparisons. Odds ratios were calculated using Fisher's Exact test for clinical factors associated with a VWD diagnosis. Univariate logistic regression was performed, modeling the odds of requiring more than 1 diagnostic test to diagnose VWD. One thousand unique patients were evaluated and 189 excluded, yielding a final cohort of 811 patients. Of these, 631 (77.8%) did not have VWD and 180 (22.2%) were diagnosed with VWD. Patients diagnosed with VWD were younger than those without (median age 5.8 vs 8.5 years, p=0.0019) and were more likely to have a family history of VWD (38% vs 22%, p < 0.0001) but there was no difference in race or sex between cohorts. As expected, patients in the VWD cohort had lower VWF activity (34 vs 78 IU/dl, p < 0.0001), VWF antigen (45 vs 89 IU/dL, p < 0.0001) and FVIII (57 vs 100 IU/dL, p < 0.0001) than those without VWD. ISTH BAT scores were higher in the VWD cohort (2.47 vs. 2.07, p = 0.027). As shown in Table 1 and Figure 1, increased odds of VWD diagnosis were noted in those tested due to a family history of VWD (OR 1.75, 95% CI 1.21-2.51) or abnormal coagulation studies (OR 1.61, 95% CI 1.07-2.24). Subjects with VWD required fewer tests than those without VWD (median 1 vs 2, p < 0.001). Univariate analysis failed to identify any significant associations with needing > 1 test for the diagnosis of VWD (Table 1), so a multivariable model was not performed. In 69.4% (125/180) of subjects with VWD, the first test was diagnostic. In receiver-operating curve analysis, the first VWF antigen and activity have a high power for diagnosis of VWD with AUC of 0.88 and 0.92, respectively (Fig 1). A cutoff of 100 IU/dL for VWF antigen or activity on first test yielded a sensitivity of 95%, specificity of 38% and negative predictive value of 96.6% for VWF antigen compared to 98%, 38% and 98.6% for VWF activity, respectively. Here we demonstrate that the majority of pediatric subjects had diagnostic VWF values on the first set of testing. Unfortunately, no clinical variables were identified for patients with VWD who required > 1 test for diagnosis. However increased odds of VWD diagnosis were noted in those with a family history of VWD and abnormal coagulation studies. A cutoff of 100 IU/dL for VWF activity or antigen on the first test resulted in > 95% negative predictive value to rule out the diagnosis. Pediatric patients without a family history of VWD and VWF levels > 100 IU/dL on initial test may not need further testing to rule out the diagnosis of VWD. Disclosures Doshi: Bayer Hemophilia Awards Program: Research Funding. Butler:Pfizer: Consultancy; Genentech: Consultancy; HemaBiologics: Consultancy.


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 4939-4939
Author(s):  
Shamsa Alkaabi ◽  
Aala Alzadjali ◽  
Mustafa Wasifuddin ◽  
Ibrahim Suliman Masoud Alghaithi ◽  
Murtadha Al-Khabori ◽  
...  

Introduction: Von Willebrand Disease (VWD) is the second most common inherited bleeding disorder. There is paucity of the literature describing the prevalence and clinical characteristics of VWD in this part of the world. The aim of the current study is to detect the prevalence, describe the spectrum of the different types of VWD, their mode of presentation, bleeding phenotype and outcome in Oman. Methods: A retrospective cross-sectional study was carried out in the 2 available referral tertiary care facilities in Oman namely; Sultan Qaboos University and the Royal Hospitals. The study included all children and adults diagnosed with VWD in Oman until June 2019. The patients were subtyped as per the International Society of Thrombosis and Haemostasis (ISTH) criteria. Data was collected from the electronic hospital systems in both hospitals. Out of 700 entries of VWD in both hospitals, only 140 were true cases and 560 were tested negative but wrongly labelled. Patients or their next of ken were called and interviewed to obtain the necessary information that was not documented in the electronic system. Results: A total of 140 patients are confirmed to have VWD giving a prevalence of 1:20000. Fifty eight patients are males (41.5%), 82 patients are females (58.5%). Sixty six patients have type I (47%), 38 patients have type II (27%) and 36 patients have type III (26%). The majority of patients 90 (64%) were diagnosed before the age of 20 years and 62 of them (68%) had positive family history of the disease. The most common presentation was recurrent unexplained bruising. As expected, patients with type III tend to have a significant bleeding phenotype with a bleeding score more than 5 in adults and 3 for paediatric patients. All of them were admitted to hospital at some point electively (for surgery) or for bleeding control, however, they were not put on prophylaxis. None of the patients had serious or intra-cranial bleeding. Conclusion: Von Willebrand Disease is not uncommon in Oman with an overall prevalence of 1:20000, however, it is much less than what was originally reported in previous studies in developing countries and the WFH website. The majority of patients are type 1 and have a positive family history of the disease. The disease is more common in females. All patients with type III have abnormal bleeding score and required VW factor replacement at one point. None of the patients had a serious bleed and they are not on prophylaxis. Keywords: Von Willebrand disease, Prevalence, Oman. Disclosures Al-Khabori: AstraZeneca: Honoraria; Amgen: Membership on an entity's Board of Directors or advisory committees; Novartis: Honoraria, Membership on an entity's Board of Directors or advisory committees; SOBI: Honoraria; NovoNardisk: Membership on an entity's Board of Directors or advisory committees; Shire (Takeda): Membership on an entity's Board of Directors or advisory committees; Servier: Membership on an entity's Board of Directors or advisory committees; Roche: Membership on an entity's Board of Directors or advisory committees; Abbvie: Membership on an entity's Board of Directors or advisory committees.


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