MARKED ACANTHOCYTOSIS ASSOCIATED WITH KLIPPLE-TRENAUNAY SYNDROME

Authors

  • Syeda Mah Ali Liaquat National Hospital
  • Naila Raza Liaquat National Hospital
  • Eraj Aftab
  • Mahnoor Faisal Mohammad

DOI:

https://doi.org/10.55519/JAMC-01-11307

Keywords:

Klipple Trenaunay Syndrome, Acanthocytosis, Arteriovenous malformation, Skin hypertrophy

Abstract

Klipple-Trenaunay syndrome (KTS) is an extremely rare congenital vascular disorder with poorly defined incidence and prevalence. We report a case of a patient who presented after road traffic accident with primary complaints of poor wound healing and persistent bleeding from wound site. Discernible presence of arteriovenous malformation and skin hypertrophy since birth lead to the diagnosis of Klipple-Trenaunay syndrome (KTS). There was an incidental finding of acanthocytosis on peripheral film of blood which remained elevated even after clinical improvement of the patient. This case report highlights a close association of marked acanthocytosis of red blood cells and Klipple-Trenaunay syndrome.

Author Biography

Naila Raza, Liaquat National Hospital

Consultant and Head of the department of Hematology and blood bank.

References

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Published

2023-01-02

How to Cite

Ali, S. M., Raza, N., Aftab, E., & Faisal Mohammad, M. (2023). MARKED ACANTHOCYTOSIS ASSOCIATED WITH KLIPPLE-TRENAUNAY SYNDROME. Journal of Ayub Medical College Abbottabad, 35(1), 182–185. https://doi.org/10.55519/JAMC-01-11307

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