Von Willebrand disease

A case report

https://doi.org/10.53730/ijhs.v6nS9.13575

Authors

  • Suraj Sasidharan Junior resident, Dept. of IHBT, VMKVMCH Salem, Tamilnadu
  • Arun M Senior resident, Dept. of IHBT, VMKVMCH Salem, Tamilnadu
  • Vignesh Balakrishnan Assistant Professor, Dept. of IHBT, VMKVMCH Salem, Tamilnadu
  • Anbu Lenin K Professor and HOD, Dept. of IHBT, VMKVMCH Salem, Tamilnadu
  • Thamil Selvi R Professor and HOD, Department of Pathology, VMKVMCH Salem, Tamilnadu

Keywords:

Von Willebrand Disease, bleeding patients, blood loss

Abstract

An hereditary bleeding illness is Von Willebrand Disease (vWD). Along with normal or declining factor VIII levels, von Willebrand factor (vWF) levels also fall. Clinical signs include bleeding that looks "platelet-like" and bleeds resemble factor VIII insufficiency. Life-threatening bleeding might result from the strategic position of the bleed, the volume of blood lost, or complications brought on by the significant blood loss. Treatment modalities include desmopressin (DDAVP) and replacement of vWF. The aim of this report is to make health professionals aware of this possibility that could be in operating on bleeding patients.

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References

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Published

30-09-2022

How to Cite

Sasidharan, S., Arun, M., Balakrishnan, V., Anbu, L. K., & Thamil, S. R. (2022). Von Willebrand disease: A case report. International Journal of Health Sciences, 6(S9), 4044–4047. https://doi.org/10.53730/ijhs.v6nS9.13575

Issue

Section

Peer Review Articles