Marked Acanthocytosis Associated With Klipple Trenaunay Syndrom.

Syeda Mah Ali, Naila Raza, Eraj Aftab, Mahnoor Faisal Mohammad
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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.

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与Klipple Trenaunay综合征相关的显著棘细胞增多症。
kliple - trenaunay综合征(KTS)是一种极其罕见的先天性血管疾病,发病率和患病率不明确。我们报告一个病例的病人谁提出后道路交通事故的主要投诉,伤口愈合不良和持续出血的伤口部位。自出生以来明显存在的动静脉畸形和皮肤肥大导致Klipple-Trenaunay综合征(KTS)的诊断。偶然发现外周血膜棘细胞增多症,即使在患者临床好转后仍升高。本病例报告强调了红细胞棘细胞增多症与Klipple-Trenaunay综合征的密切联系。
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